ID: 129935616 | ATAC-STARR-seq lymphoblastoid silent region 12327 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218871507..218871576) | | |
ID: 129935615 | ATAC-STARR-seq lymphoblastoid silent region 12326 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218711177..218711226) | | |
ID: 129935614 | ATAC-STARR-seq lymphoblastoid silent region 12325 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218711117..218711166) | | |
ID: 129660902 | ReSE screen-validated silencer GRCh37_chr2:219584289-219584586 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218719566..218719863) | | |
ID: 127275780 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:219736377-219737323 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218871655..218872601) | | |
ID: 126806514 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr2:219687585-219688784 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218822862..218824061) | | |
ID: 126806513 | BRD4-independent group 4 enhancer GRCh37_chr2:219611731-219612930 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218747008..218748207) | | |
ID: 126806512 | MED14-independent group 3 enhancer GRCh37_chr2:219609538-219610737 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218744815..218746014) | | |
ID: 124907983 | uncharacterized LOC124907983 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218709602..218711484, complement) | | |
ID: 103504730 | microRNA 9500 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218823090..218823154) | hsa-mir-9500 | |
ID: 100271460 | ribosomal protein L23a pseudogene 31 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218841586..218842119) | RPL23A_13_326 | |
ID: 80326 | Wnt family member 10A [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218874116..218893928) | ECTD16, OODD, SSPS, STHAG4 | 606268 |
ID: 53632 | protein kinase AMP-activated non-catalytic subunit gamma 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218822308..218831803, complement) | AMPKG3, SMGMQTL | 604976 |
ID: 9654 | tubulin tyrosine ligase like 4 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218710835..218759724) | | 618738 |
ID: 7475 | Wnt family member 6 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218859805..218874233) | | 604663 |
ID: 1593 | cytochrome P450 family 27 subfamily A member 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218782147..218815293) | CP27, CTX, CYP27 | 606530 |