| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174634532-174634633 | Rare:23 | ||||
| chr2:175168098-175168558 | Common:2; Rare:122 | ||||
| chr2:176002229-176002414 | Common:3; Rare:80 | ||||
| chr2:176129635-176129753 | Rare:62 | ||||
| chr2:176130559-176130804 | Common:1; Rare:139 | ||||
| chr2:176188487-176188668 | Common:1; Rare:70 | ||||
| chr2:177212416-177212831 | Common:4; Rare:166 | ||||
| chr2:177219102-177219313 | Rare:67 | ||||
| chr2:177263412-177263709 | Common:1; Rare:72 | ||||
| chr2:177263814-177263891 | Rare:18 | ||||
| chr2:177264048-177264177 | Rare:42 | ||||
| chr2:177264533-177264828 | Common:2; Rare:85 | ||||
| chr2:177392651-177392823 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:177552761-177552838 | Common:1; Rare:29 | ||||
| chr2:177618702-177618989 | Common:7; Rare:81 |