Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112466536-112466718 | Common:3; Rare:29 | ||||
chr1:112618787-112619261 | Rare:151 | ||||
chr1:112619341-112619463 | Common:1; Rare:28 | ||||
chr1:112619618-112619882 | Common:2; Rare:92 | ||||
chr1:112674601-112674792 | Common:1; Rare:38 | ||||
chr1:112693890-112694057 | Common:3; Rare:34 | ||||
chr1:112698018-112698356 | Common:1; Rare:96 | ||||
chr1:112706546-112706781 | Rare:46 | ||||
chr1:112707030-112707281 | Rare:80 | ||||
chr1:112715289-112715614 | Common:1; Rare:96 | ||||
chr1:112922019-112922250 | Rare:49 | ||||
chr1:112935983-112936044 | Common:1; Rare:9 | ||||
chr1:112956004-112956827 | Common:8; Rare:235; Clinvar:12; Clinvar (benign):3 | ||||
chr1:112957413-112957694 | Common:1; Rare:43 | ||||
chr1:113073043-113073285 | Common:1; Rare:99 |