| ID: 130057217 | ATAC-STARR-seq lymphoblastoid silent region 6505 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62068317..62068806) | | |
| ID: 130057216 | ATAC-STARR-seq lymphoblastoid silent region 6504 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62068127..62068266) | | |
| ID: 130057215 | ATAC-STARR-seq lymphoblastoid silent region 6503 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62067947..62067996) | | |
| ID: 129663611 | ReSE screen-validated silencer GRCh37_chr15:62407814-62408044 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62115615..62115845) | | |
| ID: 129390712 | MPRA-validated peak2366 silencer [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62109876..62110076) | | |
| ID: 127829669 | H3K4me1 hESC enhancer GRCh37_chr15:62535215-62535715 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62243016..62243516) | | |
| ID: 127829668 | H3K4me1 hESC enhancer GRCh37_chr15:62534714-62535214 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62242515..62243015) | | |
| 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: 125078094 | Sharpr-MPRA regulatory region 14002 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62066790..62067084) | | |
| ID: 124903502 | uncharacterized LOC124903502 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62165413..62166594) | | |
| ID: 113939945 | Sharpr-MPRA regulatory region 15238 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62253736..62254644) | | |
| 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: 255180 | GOLGA2 pseudogene 11 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62241721..62257703, complement) | | |
| ID: 145741 | C2 calcium dependent domain containing 4A [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (62066977..62070917) | FAM148A, NLF1 | 610343 |