| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:11465860-11466286 | Common:6; Rare:123 | ||||
| chr2:11746517-11746655 | Common:1; Rare:43; Clinvar:2 | ||||
| chr2:12716555-12716611 | Common:1; Rare:24 | ||||
| chr2:12716643-12717091 | Common:3; Rare:136 | ||||
| chr2:12717123-12717320 | Common:1; Rare:41 | ||||
| chr2:12717502-12718015 | Common:1; Rare:106 | ||||
| chr2:12718073-12718250 | Common:2; Rare:34 | ||||
| chr2:15561294-15561421 | Rare:49 | ||||
| chr2:17518438-17518653 | Common:2; Rare:59 | ||||
| chr2:17753702-17754187 | Common:5; Rare:150; Clinvar (benign):1 | ||||
| chr2:18560647-18560801 | Rare:44 | ||||
| chr2:19901634-19901803 | Common:1; Rare:94 | ||||
| chr2:19901936-19902056 | Common:1; Rare:41 | ||||
| chr2:19989605-19989688 | Rare:15 | ||||
| chr2:19990011-19990231 | Rare:63 |