| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67606681-67607027 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:67629324-67629537 | Common:1; Rare:48 | ||||
| chr11:67629885-67629983 | Rare:25 | ||||
| chr11:67630167-67630577 | Common:7; Rare:72 | ||||
| chr11:67650231-67650356 | Common:2; Rare:30 | ||||
| chr11:67650981-67651032 | Rare:9 | ||||
| chr11:68003138-68003303 | Rare:37; Clinvar (benign):1 | ||||
| chr11:68003464-68003798 | Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68004018-68004215 | Common:1; Rare:59 | ||||
| chr11:68030341-68030795 | Common:3; Rare:128; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68030833-68030988 | Common:6; Rare:59 | ||||
| chr11:68038853-68039120 | Rare:79; Clinvar:1 | ||||
| chr11:68120416-68120521 | Rare:24 | ||||
| chr11:68120718-68120882 | Rare:53 | ||||
| chr11:68121304-68121713 | Common:6; Rare:157 |