Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25819878-25820038 | Common:3; Rare:49 | ||||
chr1:25820830-25820860 | Common:1; Rare:8 | ||||
chr1:25859359-25859578 | Common:3; Rare:92 | ||||
chr1:25906397-25906590 | Rare:75 | ||||
chr1:26233896-26234254 | Common:2; Rare:112 | ||||
chr1:26279928-26280127 | Rare:100 | ||||
chr1:26306546-26306843 | Common:13; Rare:84 | ||||
chr1:26317820-26317976 | Common:2; Rare:22 | ||||
chr1:26432091-26432403 | Common:5; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472270-26472532 | Common:4; Rare:85 | ||||
chr1:26545696-26545876 | Common:1; Rare:37 | ||||
chr1:26787870-26788225 | Common:3; Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26900420-26900481 | Rare:26 | ||||
chr1:26921554-26921869 | Common:3; Rare:99 | ||||
chr1:27322020-27322305 | Common:1; Rare:97 |