| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:33476240-33476309 | Rare:21 | ||||
| chr2:33476464-33476749 | Common:4; Rare:60 | ||||
| chr2:33599154-33599640 | Common:1; Rare:172 | ||||
| chr2:36355482-36355731 | Common:1; Rare:83 | ||||
| chr2:36355745-36355849 | Common:1; Rare:53 | ||||
| chr2:36356329-36356437 | Common:1; Rare:40 | ||||
| chr2:36597700-36597930 | Common:4; Rare:95 | ||||
| chr2:36598094-36598279 | Common:15; Rare:86 | ||||
| chr2:36966466-36967049 | Common:7; Rare:227 | ||||
| chr2:37084269-37084573 | Common:4; Rare:117 | ||||
| chr2:37156810-37157157 | Common:4; Rare:111 | ||||
| chr2:37196406-37196717 | Common:5; Rare:106 | ||||
| chr2:37197077-37197189 | Rare:22 | ||||
| chr2:37231313-37231369 | Common:1; Rare:22 | ||||
| chr2:37231493-37231780 | Common:6; Rare:159; Clinvar:1; Clinvar (benign):5 |