| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17207910-17208111 | Common:2; Rare:76 | ||||
| chr11:17276564-17276828 | Common:4; Rare:70; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18012911-18013241 | Common:6; Rare:110 | ||||
| chr11:18322113-18322332 | Common:5; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322521-18322672 | Common:1; Rare:59 | ||||
| chr11:18394294-18394633 | Common:1; Rare:127; Clinvar (benign):1 | ||||
| chr11:18396102-18396435 | Common:1; Rare:120 | ||||
| chr11:18526835-18527014 | Common:1; Rare:90 | ||||
| chr11:18588656-18588941 | Common:4; Rare:95 | ||||
| chr11:18634287-18634548 | Common:3; Rare:92 | ||||
| chr11:18698539-18698772 | Common:4; Rare:62 | ||||
| chr11:18791768-18791912 | Rare:45 | ||||
| chr11:19201932-19202166 | Rare:48; Clinvar (benign):5 | ||||
| chr11:20363650-20363798 | Common:4; Rare:29 | ||||
| chr11:20387407-20387765 | Common:8; Rare:115 |