Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:209771719-209772060 | Common:2; Rare:94 | ||||
chr2:210002525-210002678 | Common:4; Rare:63 | ||||
chr2:210170712-210170921 | Rare:86 | ||||
chr2:210171230-210171532 | Common:4; Rare:114 | ||||
chr2:213151521-213151982 | Common:2; Rare:163 | ||||
chr2:213284232-213284494 | Rare:85 | ||||
chr2:215311970-215312145 | Common:7; Rare:76 | ||||
chr2:215436066-215436253 | Common:2; Rare:63 | ||||
chr2:216081728-216081966 | Common:1; Rare:73 | ||||
chr2:216082921-216083056 | Rare:18 | ||||
chr2:216371412-216371721 | Common:2; Rare:76 | ||||
chr2:216371865-216371918 | Rare:15 | ||||
chr2:216372291-216372591 | Rare:71 | ||||
chr2:216412272-216412549 | Common:3; Rare:65; Clinvar (benign):2 | ||||
chr2:216412671-216412786 | Rare:13 |