ID: 130067336 | ATAC-STARR-seq lymphoblastoid silent region 13671 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36775681..36775740) | | |
ID: 130067335 | ATAC-STARR-seq lymphoblastoid active region 18938 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36529037..36529436) | | |
ID: 130067334 | ATAC-STARR-seq lymphoblastoid active region 18937 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36528677..36528726) | | |
ID: 130067333 | ATAC-STARR-seq lymphoblastoid active region 18936 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36511344..36511423) | | |
ID: 129664844 | ReSE screen-validated silencer GRCh37_chr22:37104667-37104810 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36708622..36708765) | | |
ID: 127896056 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr22:37171863-37172426 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36775819..36776420) | | |
ID: 127896055 | H3K4me1 hESC enhancer GRCh37_chr22:37121981-37122481 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36725936..36726436) | | |
ID: 127896054 | H3K4me1 hESC enhancer GRCh37_chr22:37080862-37081403 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36684817..36685358) | | |
ID: 127896053 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:37006222-37006886 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36610175..36610839) | | |
ID: 127896052 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:37005558-37006221 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36609511..36610174) | | |
ID: 127896051 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:37004893-37005557 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36608846..36609510) | | |
ID: 127896050 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:36966399-36966990 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36570352..36570943) | | |
ID: 127896049 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:36959107-36959622 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36563060..36563575) | | |
ID: 126863139 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr22:37161913-37163112 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36765869..36767068) | | |
ID: 125446228 | Sharpr-MPRA regulatory region 13009 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36544402..36544696) | | |
ID: 124905112 | uncharacterized LOC124905112 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36744175..36746341, complement) | | |
ID: 105373021 | CACNG2 divergent transcript [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36703876..36767089) | | |
ID: 100500719 | HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36536609..36537756, complement) | | |
ID: 11020 | intraflagellar transport 27 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36758211..36776119, complement) | BBS19, CFAP156, FAP156, RABL4, RAYL | 615870 |
ID: 10369 | calcium voltage-gated channel auxiliary subunit gamma 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36560857..36703752, complement) | MRD10 | 602911 |