Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:46198368-46198525 | Common:2; Rare:113; Clinvar:2 | ||||
chr1:46247270-46247795 | Common:8; Rare:175 | ||||
chr1:46247820-46248180 | Common:3; Rare:123 | ||||
chr1:46303089-46303745 | Common:6; Rare:375 | ||||
chr1:46340543-46340881 | Common:10; Rare:175 | ||||
chr1:46604196-46604458 | Common:2; Rare:134 | ||||
chr1:46616809-46616944 | Common:2; Rare:34 | ||||
chr1:47314014-47314514 | Common:7; Rare:209; Clinvar:6; Clinvar (benign):1 | ||||
chr1:47333752-47334090 | Common:6; Rare:188 | ||||
chr1:47334170-47334350 | Common:3; Rare:103 | ||||
chr1:48222607-48222770 | Common:2; Rare:63 | ||||
chr1:50959020-50959520 | Common:5; Rare:92 | ||||
chr1:50960000-50960381 | Rare:198 | ||||
chr1:50970121-50970256 | Rare:22 | ||||
chr1:51236193-51236368 | Common:2; Rare:66 |