Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116754347-116754469 | Rare:36 | ||||
chr1:117368205-117368307 | Rare:25 | ||||
chr1:117929560-117929800 | Common:2; Rare:70 | ||||
chr1:119140616-119140675 | Rare:31 | ||||
chr1:145823839-145824251 | Rare:147 | ||||
chr1:145845568-145845636 | Common:2; Rare:16 | ||||
chr1:145858996-145859184 | Rare:54 | ||||
chr1:145918680-145919022 | Common:2; Rare:79 | ||||
chr1:145927364-145927644 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:145958000-145958223 | Rare:53 | ||||
chr1:145964567-145964767 | Rare:48 | ||||
chr1:145994913-145995479 | Rare:233 | ||||
chr1:145995998-145996369 | Rare:158 | ||||
chr1:145996412-145996901 | Common:2; Rare:178 | ||||
chr1:147172093-147172283 | Rare:47 |