ID: 129934651 | ATAC-STARR-seq lymphoblastoid silent region 11898 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118881765..118881824) | | |
ID: 129660796 | ReSE screen-validated silencer GRCh37_chr2:119843263-119843429 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119085687..119085853) | | |
ID: 127274518 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:119914695-119915505 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119157119..119157929) | | |
ID: 127274517 | H3K4me1 hESC enhancer GRCh37_chr2:119892423-119892923 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119134847..119135347) | | |
ID: 127274516 | H3K4me1 hESC enhancer GRCh37_chr2:119891922-119892422 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119134346..119134846) | | |
ID: 127274515 | H3K4me1 hESC enhancer GRCh37_chr2:119870527-119871192 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119112951..119113616) | | |
ID: 127274514 | H3K4me1 hESC enhancer GRCh37_chr2:119746563-119747064 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118988987..118989488) | | |
ID: 127274513 | H3K4me1 hESC enhancer GRCh37_chr2:119616527-119617286 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118858951..118859710) | | |
ID: 127274512 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:119615765-119616526 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118858189..118858950) | | |
ID: 127274511 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:119615003-119615764 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118857427..118858188) | | |
ID: 127274510 | H3K4me1 hESC enhancer GRCh37_chr2:119610971-119611506 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118853395..118853930) | | |
ID: 127274509 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:119607811-119608363 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118850235..118850787) | | |
ID: 127274508 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:119599819-119600399 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118842243..118842823) | | |
ID: 127274507 | H3K4me1 hESC enhancer GRCh37_chr2:119590580-119591348 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118833004..118833772) | | |
ID: 126806330 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:119868745-119869944 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119111169..119112368) | | |
ID: 126806329 | MED14-independent group 3 enhancer GRCh37_chr2:119807422-119808621 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (119049846..119051045) | | |
ID: 126806328 | MED14-independent group 3 enhancer GRCh37_chr2:119749973-119751172 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118992397..118993596) | | |
ID: 126806327 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr2:119711468-119712667 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118953892..118955091) | | |
ID: 126806326 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:119671170-119672369 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118913594..118914793) | | |
ID: 124906072 | uncharacterized LOC124906072 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (118990207..118993318, complement) | | |