| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66677765-66678032 | Common:1; Rare:105 | ||||
| chr11:66744650-66744883 | Common:3; Rare:96 | ||||
| chr11:67353484-67353785 | Common:2; Rare:81 | ||||
| chr11:67401789-67402075 | Common:3; Rare:103 | ||||
| chr11:67428331-67428531 | Rare:69 | ||||
| chr11:67443419-67443698 | Common:2; Rare:95 | ||||
| chr11:67482954-67483192 | Rare:54; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:68010153-68010354 | Common:1; Rare:50 | ||||
| chr11:68030381-68030733 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038925-68039079 | Rare:48; Clinvar:1 | ||||
| chr11:68043488-68043858 | Common:1; Rare:129; Clinvar:6; Clinvar (pathogenic):1 | ||||
| chr11:68271865-68272134 | Common:2; Rare:109 | ||||
| chr11:68903795-68903943 | Common:4; Rare:67; Clinvar (benign):6 | ||||
| chr11:69013214-69013276 | Common:1; Rare:13 | ||||
| chr11:69675309-69675519 | Rare:56 |