ID: 132089408 | Neanderthal introgressed variant-containing enhancer experimental_92170 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53207665..53207834) | | |
ID: 124901513 | uncharacterized LOC124901513 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53147829..53147929, complement) | | |
ID: 123744824 | Sharpr-MPRA regulatory region 2296 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53119791..53120456) | | |
ID: 106481632 | RNA, U1 small nuclear 136, pseudogene [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53219261..53219420) | | |
ID: 106479771 | RNA, U6 small nuclear 464, pseudogene [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53153795..53153898, complement) | | |
ID: 106479311 | RNA, 7SL, cytoplasmic 244, pseudogene [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53090961..53091257) | | |
ID: 106479055 | superoxide dismutase 1 pseudogene 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53196720..53197159, complement) | | |
ID: 26268 | F-box protein 9 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53064998..53100873) | FBX9, NY-REN-57, VCIA1, dJ341E18.2 | 609091 |
ID: 8521 | glial cells missing transcription factor 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53126961..53148841, complement) | GCMA, hGCMa | 603715 |