| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1180343-1180649 | Rare:61 | ||||
| chr11:1181057-1181388 | Common:3; Rare:79 | ||||
| chr11:1181390-1181732 | Common:2; Rare:57 | ||||
| chr11:1193464-1193933 | Common:3; Rare:144 | ||||
| chr11:1194137-1194737 | Common:4; Rare:242 | ||||
| chr11:1194901-1195653 | Common:9; Rare:234 | ||||
| chr11:1195769-1195854 | Rare:21 | ||||
| chr11:1195857-1196265 | Common:2; Rare:115 | ||||
| chr11:1196279-1196908 | Common:2; Rare:196 | ||||
| chr11:1197363-1197667 | Common:5; Rare:85 | ||||
| chr11:1197884-1198658 | Common:12; Rare:197 | ||||
| chr11:1198810-1199037 | Common:2; Rare:71 | ||||
| chr11:1199356-1199560 | Common:2; Rare:72 | ||||
| chr11:1199623-1199980 | Common:5; Rare:122 | ||||
| chr11:1231225-1231558 | Common:2; Rare:85; Clinvar (benign):2 |