| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73376190-73376438 | Common:1; Rare:87 | ||||
| chr11:73597953-73598328 | Common:3; Rare:94 | ||||
| chr11:73760650-73760741 | Common:2; Rare:18 | ||||
| chr11:73760831-73761176 | Common:3; Rare:103 | ||||
| chr11:73787813-73787974 | Common:1; Rare:46 | ||||
| chr11:73876610-73877049 | Common:5; Rare:132 | ||||
| chr11:73982825-73982962 | Common:6; Rare:44 | ||||
| chr11:73983238-73983649 | Common:2; Rare:87 | ||||
| chr11:74170831-74171427 | Common:3; Rare:192 | ||||
| chr11:74398373-74398575 | Common:3; Rare:48 | ||||
| chr11:74493061-74493363 | Common:1; Rare:102; Clinvar (pathogenic):1 | ||||
| chr11:74592504-74592679 | Common:1; Rare:61 | ||||
| chr11:74949043-74949392 | Common:6; Rare:108 | ||||
| chr11:74988614-74988703 | Rare:14 | ||||
| chr11:74988782-74988949 | Rare:44 |