ID: 127829667 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:62457535-62458134 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62165336..62165935) | | |
ID: 127829666 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:62456935-62457534 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62164736..62165335) | | |
ID: 127829665 | H3K4me1 hESC enhancer GRCh37_chr15:62359400-62359915 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62067201..62067716) | | |
ID: 124903502 | uncharacterized LOC124903502 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62165413..62166594) | | |
ID: 107984784 | uncharacterized LOC107984784 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62196161..62203318, complement) | | |
ID: 100129972 | nucleophosmin 1 pseudogene 47 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62082149..62083330, complement) | | |
ID: 388125 | C2 calcium dependent domain containing 4B [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62163535..62165285, complement) | FAM148B, NLF2 | 610344 |
ID: 145741 | C2 calcium dependent domain containing 4A [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62066977..62070917) | FAM148A, NLF1 | 610343 |