ID: 132090627 | Neanderthal introgressed variant-containing enhancer experimental_62558 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19135625..19135794) | | |
ID: 130066951 | ATAC-STARR-seq lymphoblastoid silent region 13454 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19122297..19122736) | | |
ID: 130066950 | ATAC-STARR-seq lymphoblastoid silent region 13452 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19109713..19109762) | | |
ID: 127895277 | H3K27ac hESC enhancer GRCh37_chr22:19159167-19160103 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19171576..19172590) | | |
ID: 127895276 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:19156355-19157292 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19168842..19169779) | | |
ID: 127895275 | H3K4me1 hESC enhancer GRCh37_chr22:19136757-19137256 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19149244..19149743) | | |
ID: 127895274 | H3K4me1 hESC enhancer GRCh37_chr22:19131233-19131739 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19143720..19144226) | | |
ID: 127895273 | H3K27ac hESC enhancer GRCh37_chr22:19109284-19109785 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19121771..19122272) | | |
ID: 127895272 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:19101726-19102620 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19114213..19115107) | | |
ID: 127895271 | H3K4me1 hESC enhancer GRCh37_chr22:19097874-19098375 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19110361..19110862) | | |
ID: 127895270 | H3K4me1 hESC enhancer GRCh37_chr22:19097371-19097873 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19109858..19110360) | | |
ID: 127895269 | H3K4me1 hESC enhancer GRCh37_chr22:19093647-19094147 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19106134..19106634) | | |
ID: 127895268 | H3K4me1 hESC enhancer GRCh37_chr22:19074057-19074556 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19086544..19087043) | | |
ID: 127895267 | H3K4me1 hESC enhancer GRCh37_chr22:19073555-19074056 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19086042..19086543) | | |
ID: 124905078 | uncharacterized LOC124905078 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19094687..19100184, complement) | | |
ID: 112268297 | uncharacterized LOC112268297 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19136209..19136946) | | |
ID: 100652736 | long intergenic non-protein coding RNA 1311 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19171706..19172832) | | |
ID: 100129262 | ribosomal protein L28 pseudogene 6 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19055841..19056187) | | |
ID: 23752 | testis specific serine kinase 1A (pseudogene) [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19124874..19125887) | SPOGA1, STK22A, TSSK1P, TSSK1b, TSSK7P, TSSK1A | |
ID: 23617 | testis specific serine kinase 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19131308..19132622) | DGS-G, SPOGA2, STK22B, TSK2 | 610710 |