| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207711004-207711168 | Rare:19 | ||||
| chr2:207711239-207711674 | Common:5; Rare:509 | ||||
| chr2:207711585-207712243 | Common:2; Rare:285 | ||||
| chr2:207769370-207770240 | Common:15; Rare:1040 | ||||
| chr2:208025400-208025840 | Common:11; Rare:279 | ||||
| chr2:208254046-208254525 | Common:5; Rare:496 | ||||
| chr2:208254980-208255380 | Common:14; Rare:464 | ||||
| chr2:208255437-208255537 | Common:2; Rare:18 | ||||
| chr2:208255440-208255580 | Common:4; Rare:43 | ||||
| chr2:208265511-208265916 | Common:3; Rare:191 | ||||
| chr2:208265898-208266391 | Common:61; Rare:818; Clinvar:7; Clinvar (benign):14 | ||||
| chr2:208489264-208489664 | Rare:106 | ||||
| chr2:210002350-210002750 | Common:24; Rare:434 | ||||
| chr2:210169926-210170367 | Common:4; Rare:148 | ||||
| chr2:210170410-210170530 | Rare:22 |