ID: 130067337 | ATAC-STARR-seq lymphoblastoid active region 18942 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36921489..36921868) | | |
ID: 130067336 | ATAC-STARR-seq lymphoblastoid silent region 13671 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36775681..36775740) | | |
ID: 129664845 | ReSE screen-validated silencer GRCh37_chr22:37275012-37275204 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36878970..36879162) | | |
ID: 127896065 | H3K4me1 hESC enhancer GRCh37_chr22:37318330-37318900 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36922288..36922858) | | |
ID: 127896064 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:37307503-37308204 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36911461..36912162) | | |
ID: 127896063 | H3K27ac hESC enhancer GRCh37_chr22:37297463-37298028 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36901364..36901986) | | |
ID: 127896062 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:37296897-37297462 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36900855..36901420) | | |
ID: 127896061 | OCT4-NANOG hESC enhancer GRCh37_chr22:37291564-37292117 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36895522..36896075) | | |
ID: 127896060 | H3K4me1 hESC enhancer GRCh37_chr22:37267835-37268373 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36871793..36872331) | | |
ID: 127896059 | NANOG-H3K4me1 hESC enhancer GRCh37_chr22:37203445-37204171 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36807401..36808127) | | |
ID: 127896058 | H3K4me1 hESC enhancer GRCh37_chr22:37194619-37195541 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36798575..36799497) | | |
ID: 127896057 | H3K27ac hESC enhancer GRCh37_chr22:37172992-37173555 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36776948..36777511) | | |
ID: 127896056 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr22:37171863-37172426 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36775819..36776420) | | |
ID: 126863140 | BRD4-independent group 4 enhancer GRCh37_chr22:37321546-37322745 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36925504..36926703) | | |
ID: 126863139 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr22:37161913-37163112 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36765869..36767068) | | |
ID: 107985578 | NCF4 antisense RNA 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36847372..36870443, complement) | | |
ID: 105373023 | uncharacterized LOC105373023 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36918472..36925943, complement) | | |
ID: 105373022 | uncharacterized LOC105373022 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36888028..36889304, complement) | | |
ID: 105373021 | CACNG2 divergent transcript [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36703876..36767089) | | |
ID: 11020 | intraflagellar transport 27 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36758211..36776119, complement) | BBS19, CFAP156, FAP156, RABL4, RAYL | 615870 |