| ID: 127829137 | H3K4me1 hESC enhancer GRCh37_chr15:30852659-30853158 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30560456..30560955) | | |
| ID: 127829136 | H3K4me1 hESC enhancer GRCh37_chr15:30659757-30660257 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30367554..30368054) | | |
| ID: 124900358 | U8 small nucleolar RNA [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30581184..30581316) | | |
| ID: 107080653 | RNA, 7SL, cytoplasmic 796, pseudogene [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30560644..30560934) | | |
| ID: 106783506 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:30917238-30918231 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30625035..30626187) | | |
| ID: 106736480 | 15q13 proximal microdeletion recombination region [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30614939..30628733) | | |
| ID: 106736468 | 15q13.2-13.3 gamma inversion proximal recombination region [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30565815..30597289) | | |
| ID: 106736465 | 15q13.2 beta inversion distal recombination region [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30542345..30554283) | | |
| ID: 106479451 | RNA, 7SL, cytoplasmic 628, pseudogene [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30612724..30612960) | | |
| ID: 105370751 | uncharacterized LOC105370751 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30362811..30374794) | | |
| ID: 102725021 | ARHGAP11B divergent transcript [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30591195..30625778, complement) | | |
| ID: 101927579 | dynamin 1 pseudogene 50 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30568598..30571721, complement) | | |
| ID: 100288380 | ULK4 pseudogene 2 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30572555..30600708) | D-X, FAM7A2 | |
| ID: 728498 | golgin A8 family member H [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30604028..30617752) | GOLGA6L11 | |
| ID: 727909 | golgin A8 family member Q [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30552050..30565684) | | |
| ID: 89839 | Rho GTPase activating protein 11B [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30626128..30649229) | B'-T, FAM7B1, GAP (1-8) | 616310 |
| ID: 89832 | CHRNA7 (exons 5-10) and FAM7A (exons A-E) fusion [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (30360566..30393900, complement) | CHRNA7, CHRNA7-DR1, D-10, NACHRA7 | 609756 |