| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215436017-215436375 | Common:2; Rare:106 | ||||
| chr2:216013248-216013821 | Common:4; Rare:146 | ||||
| chr2:216081761-216081920 | Common:1; Rare:54 | ||||
| chr2:216412217-216412561 | Common:3; Rare:80; Clinvar (benign):2 | ||||
| chr2:216412700-216412786 | Rare:11 | ||||
| chr2:216497925-216497968 | Rare:10 | ||||
| chr2:216498689-216499055 | Common:13; Rare:139 | ||||
| chr2:217905433-217905594 | Rare:32 | ||||
| chr2:218217049-218217234 | Common:1; Rare:66 | ||||
| chr2:218270095-218270573 | Common:5; Rare:153; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218287270-218287427 | Common:1; Rare:25 | ||||
| chr2:218292479-218292614 | Rare:37 | ||||
| chr2:218322953-218323275 | Common:7; Rare:104 | ||||
| chr2:218568276-218568966 | Common:5; Rare:181 | ||||
| chr2:218659600-218659755 | Rare:40 |