| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37231451-37231712 | Common:5; Rare:133; Clinvar (benign):3 | ||||
| chr2:37324698-37324909 | Common:1; Rare:82 | ||||
| chr2:37344513-37344759 | Common:2; Rare:83 | ||||
| chr2:37671514-37671782 | Common:2; Rare:109 | ||||
| chr2:37925202-37925418 | Common:3; Rare:93 | ||||
| chr2:38076149-38076255 | Rare:26 | ||||
| chr2:38602867-38602949 | Rare:39 | ||||
| chr2:38602951-38603192 | Common:4; Rare:93 | ||||
| chr2:38875886-38876055 | Common:1; Rare:63 | ||||
| chr2:39120992-39121137 | Rare:52 | ||||
| chr2:39436995-39437469 | Common:5; Rare:176 | ||||
| chr2:40511904-40512027 | Rare:21 | ||||
| chr2:40512401-40512515 | Rare:27 | ||||
| chr2:42169162-42169468 | Common:1; Rare:145 | ||||
| chr2:42282726-42282836 | Rare:37 |