ID: 127887730 | H3K4me1 hESC enhancer GRCh37_chr17:67209122-67210042 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (69212981..69213901) | | |
ID: 125316785 | Sharpr-MPRA regulatory region 12537 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (69141788..69142082) | | |
ID: 124900401 | uncharacterized LOC124900401 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (69355133..69355283, complement) | | |
ID: 112533663 | Sharpr-MPRA regulatory region 12590 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (69103648..69103942) | | |
ID: 105371878 | uncharacterized LOC105371878 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (69331844..69358961) | | |
ID: 100133319 | uncharacterized LOC100133319 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (69232975..69235012, complement) | | |
ID: 100130368 | small nuclear ribonucleoprotein polypeptide G pseudogene 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (69318690..69319127) | | |
ID: 23461 | ATP binding cassette subfamily A member 5 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (69244311..69327133, complement) | ABC13, EST90625, HTC3 | 612503 |
ID: 23460 | ATP binding cassette subfamily A member 6 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (69078702..69141895, complement) | EST155051 | 612504 |
ID: 10349 | ATP binding cassette subfamily A member 10 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (69148007..69244848, complement) | EST698739 | 612508 |