| ID: 130057482 | ATAC-STARR-seq lymphoblastoid active region 9726 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72628451..72628520) | | |
| ID: 130057481 | ATAC-STARR-seq lymphoblastoid active region 9725 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72615841..72615980) | | |
| ID: 129390718 | MPRA-validated peak2381 silencer [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72706384..72706584) | | |
| ID: 127830088 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:72963099-72964076 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72670758..72671735) | | |
| ID: 127830087 | H3K27ac hESC enhancer GRCh37_chr15:72955117-72955616 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72662776..72663275) | | |
| ID: 127830086 | H3K27ac hESC enhancer GRCh37_chr15:72954615-72955116 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72662274..72662775) | | |
| ID: 127830085 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr15:72942597-72943114 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72650256..72650773) | | |
| ID: 127830084 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:72939289-72940171 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72646948..72647830) | | |
| ID: 127830083 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:72920983-72921575 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72628642..72629234) | | |
| ID: 127830082 | H3K27ac hESC enhancer GRCh37_chr15:72902139-72902639 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72609798..72610298) | | |
| ID: 112268145 | uncharacterized LOC112268145 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72628766..72649543) | | |
| ID: 106481153 | RNA, 7SL, cytoplasmic 853, pseudogene [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72664577..72664799) | | |
| ID: 102723640 | long intergenic non-protein coding RNA 2259 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72608481..72636955, complement) | | |
| ID: 646665 | golgin A6 family member A pseudogene [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72605178..72612324) | | |
| ID: 123346 | HIG1 hypoxia inducible domain family member 2B [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72675798..72686182, complement) | HIGD2BP | |
| ID: 55889 | golgin A6 family member B [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72654697..72669599) | GOLGA, GOLGA6D | |
| ID: 585 | Bardet-Biedl syndrome 4 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72686207..72738473) | | 600374 |