| ID: 127896411 | NANOG hESC enhancer GRCh37_chr22:42219786-42220287 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41823782..41824283) | | |
| ID: 127896410 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:42195504-42196490 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41799500..41800491) | | |
| ID: 106479777 | RNA, U6 small nuclear 476, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41679711..41679817) | | |
| ID: 106479553 | RNA, U6atac small nuclear 22, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41722043..41722131, complement) | | |
| ID: 150365 | meiotic double-stranded break formation protein 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41699503..41799454) | HYDM3, SPATA38 | 608797 |
| ID: 79879 | coiled-coil domain containing 134 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41800679..41832164) | OI22 | 618788 |
| 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 |