Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37692229-37692558 | Common:4; Rare:71 | ||||
chr1:40257936-40258255 | Common:4; Rare:80; Clinvar:6 | ||||
chr1:42767030-42767292 | Common:3; Rare:73 | ||||
chr1:42958862-42959031 | Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
chr1:43358768-43359006 | Common:2; Rare:64 | ||||
chr1:43367989-43368235 | Rare:67 | ||||
chr1:43389768-43389913 | Common:3; Rare:55 | ||||
chr1:45521843-45522013 | Common:1; Rare:70 | ||||
chr1:45687090-45687294 | Common:1; Rare:50 | ||||
chr1:46303239-46303321 | Rare:41 | ||||
chr1:46303378-46303730 | Common:2; Rare:88 | ||||
chr1:52055158-52055261 | Common:1; Rare:23 | ||||
chr1:52056153-52056337 | Rare:59 | ||||
chr1:52404467-52404618 | Common:1; Rare:45 | ||||
chr1:53946262-53946431 | Rare:65 |