| ID: 130010082 | ATAC-STARR-seq lymphoblastoid active region 7975 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102970704..102970903) | | |
| ID: 130010081 | ATAC-STARR-seq lymphoblastoid active region 7974 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102966086..102966135) | | |
| ID: 130010080 | ATAC-STARR-seq lymphoblastoid active region 7973 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102916349..102916458) | | |
| ID: 130010079 | ATAC-STARR-seq lymphoblastoid silent region 5487 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102846771..102846820) | | |
| ID: 130010078 | ATAC-STARR-seq lymphoblastoid silent region 5486 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102800316..102800745) | | |
| ID: 130010077 | ATAC-STARR-seq lymphoblastoid silent region 5485 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102800236..102800285) | | |
| ID: 130010076 | ATAC-STARR-seq lymphoblastoid silent region 5484 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102799406..102799675) | | |
| ID: 130010075 | ATAC-STARR-seq lymphoblastoid active region 7970 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102799126..102799345) | | |
| ID: 129663377 | ReSE screen-validated silencer GRCh37_chr13:103485696-103485895 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102833346..102833545) | | |
| ID: 127826818 | H3K27ac hESC enhancers GRCh37_chr13:103497312-103498136 and GRCh37_chr13:103498137-103498959 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102844962..102846609) | | |
| ID: 127826817 | NANOG hESC enhancer GRCh37_chr13:103478160-103478661 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102825810..102826311) | | |
| ID: 126861834 | BRD4-independent group 4 enhancer GRCh37_chr13:103518038-103519237 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102865688..102866887) | | |
| ID: 100533467 | BIVM-ERCC5 readthrough [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102807146..102875995) | ERCC5-202 | |
| ID: 100380878 | RNY5 pseudogene 8 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102819999..102820066) | | |
| ID: 121952 | methyltransferase like 21E, pseudogene [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102880099..102896033) | METTL21CP1 | |
| ID: 79070 | protein O-glucosyltransferase 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102784281..102798976, complement) | EP58, ERp58, KDEL1, KDELC1 | 611613 |
| ID: 54841 | basic, immunoglobulin-like variable motif containing [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102799119..102841533) | | 619006 |
| ID: 6555 | solute carrier family 10 member 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (103043998..103066417, complement) | ASBT, IBAT, ISBT, NTCP2, PBAM, PBAM1 | 601295 |
| ID: 2073 | ERCC excision repair 5, endonuclease [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102846032..102875995) | COFS3-201, ERCM2, UVDR, XPG, XPGC, ERCC5 | 133530 |