ID: 127896409 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:42026409-42027062 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41630405..41631058) | | |
ID: 107985567 | protein LLP homolog [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41675202..41677160, complement) | | |
ID: 106479777 | RNA, U6 small nuclear 476, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41679711..41679817) | | |
ID: 150365 | meiotic double-stranded break formation protein 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41699503..41799454) | HYDM3, SPATA38 | 608797 |
ID: 79640 | chromosome 22 open reading frame 46, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41688937..41698136) | C22orf46 | |
ID: 23606 | high mobility group nucleosomal binding domain 2 pseudogene10 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41709025..41709585, complement) | HMG17L2, HMGN2L10, bK216E10 | |
ID: 4809 | small nuclear ribonucleoprotein 13 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41673933..41690480, complement) | 15.5K, FA-1, FA1, NHP2L1, NHPX, OTK27, SNRNP15-5, SPAG12, SSFA1 | 601304 |
ID: 2547 | X-ray repair cross complementing 6 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41621295..41664041) | CTC75, CTCBF, G22P1, KU70, ML8, TLAA | 152690 |