ID: 127896388 | H3K4me1 hESC enhancer GRCh37_chr22:41704863-41705362 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41308859..41309358) | | |
ID: 127896387 | H3K4me1 hESC enhancer GRCh37_chr22:41704361-41704862 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41308357..41308858) | | |
ID: 127896386 | H3K27ac hESC enhancer GRCh37_chr22:41697637-41698138 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41301633..41302134) | | |
ID: 127896385 | H3K27ac hESC enhancer GRCh37_chr22:41685594-41686193 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41289590..41290189) | | |
ID: 127896384 | H3K4me1 hESC enhancer GRCh37_chr22:41667991-41668491 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41271987..41272487) | | |
ID: 127896383 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:41660124-41660999 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41264120..41264995) | | |
ID: 127896382 | H3K4me1 hESC enhancer GRCh37_chr22:41654013-41654555 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41258009..41258551) | | |
ID: 127896381 | H3K4me1 hESC enhancer GRCh37_chr22:41652925-41653468 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41256921..41257464) | | |
ID: 127896380 | H3K4me1 hESC enhancer GRCh37_chr22:41652381-41652924 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41256377..41256920) | | |
ID: 127896379 | H3K4me1 hESC enhancer GRCh37_chr22:41637039-41637539 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41241035..41241535) | | |
ID: 127896378 | H3K4me1 hESC enhancer GRCh37_chr22:41636538-41637038 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41240534..41241034) | | |
ID: 125446243 | Sharpr-MPRA regulatory region 10804 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41296805..41297099) | | |
ID: 112695097 | Sharpr-MPRA regulatory region 14092 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41290645..41291387) | | |
ID: 102466758 | microRNA 6889 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41252992..41253050, complement) | hsa-mir-6889 | |
ID: 150356 | chondroadherin like [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41229513..41240931, complement) | SLRR4B | 616236 |
ID: 23264 | zinc finger CCCH-type containing 7B [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41301525..41360147) | ROXAN1, RoXaN | 618206 |
ID: 5905 | Ran GTPase activating protein 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41244779..41302369, complement) | Fug1, RANGAP, SD | 602362 |