| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18394331-18394641 | Common:1; Rare:122; Clinvar (benign):1 | ||||
| chr11:18396084-18396408 | Common:1; Rare:120 | ||||
| chr11:18455791-18455925 | Rare:26 | ||||
| chr11:18526527-18526695 | Common:2; Rare:31 | ||||
| chr11:18526821-18527077 | Common:2; Rare:115 | ||||
| chr11:18588656-18588905 | Common:2; Rare:90 | ||||
| chr11:18634263-18634592 | Common:3; Rare:120 | ||||
| chr11:18634805-18634845 | Rare:6 | ||||
| chr11:18698520-18698747 | Common:3; Rare:51 | ||||
| chr11:19116996-19117245 | Common:1; Rare:68 | ||||
| chr11:19712662-19712954 | Common:2; Rare:97 | ||||
| chr11:20387399-20387806 | Common:8; Rare:134 | ||||
| chr11:20668861-20669101 | Common:3; Rare:71 | ||||
| chr11:20669442-20669682 | Common:3; Rare:97 | ||||
| chr11:22625468-22625639 | Rare:84; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 |