ID: 130003642 | ATAC-STARR-seq lymphoblastoid silent region 2280 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31928503..31929002) | | |
ID: 130003641 | ATAC-STARR-seq lymphoblastoid active region 3243 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31760431..31760520) | | |
ID: 130003640 | ATAC-STARR-seq lymphoblastoid active region 3242 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31707696..31707885) | | |
ID: 129390162 | MPRA-validated peak921 silencer [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31851388..31851588) | | |
ID: 127817547 | H3K4me1 hESC enhancer GRCh37_chr10:32189989-32190489 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31901061..31901561) | | |
ID: 127817546 | H3K4me1 hESC enhancer GRCh37_chr10:32062977-32063974 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31774049..31775046) | | |
ID: 127817545 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:32054478-32055115 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31765550..31766187) | | |
ID: 127817544 | H3K27ac hESC enhancer GRCh37_chr10:32048354-32049250 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31759426..31760350) | | |
ID: 127817543 | H3K4me1 hESC enhancer GRCh37_chr10:31984137-31984698 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31695209..31695770) | | |
ID: 127817542 | H3K4me1 hESC enhancer GRCh37_chr10:31983575-31984136 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31694647..31695208) | | |
ID: 127817541 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:31966287-31966838 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31677359..31677910) | | |
ID: 127817540 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:31955149-31956018 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31666221..31667090) | | |
ID: 127817539 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:31954277-31955148 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31665349..31666220) | | |
ID: 126860906 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr10:32229391-32230590 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31940463..31941662) | | |
ID: 107984219 | uncharacterized LOC107984219 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31922852..32020399) | | |
ID: 107080654 | RNA, 7SL, cytoplasmic 825, pseudogene [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31992087..31992381, complement) | | |
ID: 105376485 | uncharacterized LOC105376485 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31980782..31996595, complement) | | |
ID: 105376484 | uncharacterized LOC105376484 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31603034..31620973, complement) | | |
ID: 101929951 | macrophage enriched lincRNA repressor of IFN-gamma signaling [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31693082..31707447, complement) | | |
ID: 100420044 | high mobility group box 1 pseudogene 7 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (31913149..31913754) | | |