| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207625197-207625498 | Common:1; Rare:86 | ||||
| chr2:207711582-207711785 | Rare:59 | ||||
| chr2:208025466-208025612 | Common:1; Rare:38 | ||||
| chr2:208255003-208255234 | Common:2; Rare:59 | ||||
| chr2:208266053-208266341 | Common:8; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002462-210002659 | Common:5; Rare:62 | ||||
| chr2:210477580-210477690 | Rare:38 | ||||
| chr2:213150393-213150535 | Common:2; Rare:32 | ||||
| chr2:213284210-213284493 | Rare:92 | ||||
| chr2:215311859-215312139 | Common:8; Rare:106 | ||||
| chr2:215370292-215370593 | Common:10; Rare:94 | ||||
| chr2:215435646-215436180 | Common:3; Rare:137 | ||||
| chr2:216081756-216081920 | Common:1; Rare:57 | ||||
| chr2:216498740-216498894 | Common:6; Rare:65 | ||||
| chr2:216694415-216694484 | Rare:12 |