Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209652421-209652618 | Common:2; Rare:42; Clinvar:1 | ||||
chr1:209675268-209675539 | Common:2; Rare:73 | ||||
chr1:209704790-209704908 | Rare:29 | ||||
chr1:209784546-209784721 | Common:1; Rare:55 | ||||
chr1:209806050-209806301 | Common:5; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
chr1:209827869-209828076 | Common:1; Rare:58 | ||||
chr1:210328864-210329013 | Rare:50 | ||||
chr1:211258991-211259449 | Common:1; Rare:154 | ||||
chr1:212035497-212035732 | Common:1; Rare:67 | ||||
chr1:212414833-212415111 | Common:2; Rare:74 | ||||
chr1:212608472-212608763 | Common:1; Rare:75 | ||||
chr1:212791741-212791930 | Common:4; Rare:81 | ||||
chr1:212858070-212858273 | Common:3; Rare:53; Clinvar:1 | ||||
chr1:213051218-213051351 | Rare:47 | ||||
chr1:214280923-214281266 | Common:4; Rare:140 |