| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34105362-34105835 | Common:4; Rare:140 | ||||
| chr11:34106009-34106118 | Common:1; Rare:26 | ||||
| chr11:34357967-34358327 | Common:2; Rare:108 | ||||
| chr11:34358399-34358571 | Rare:36 | ||||
| chr11:34438720-34439023 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr11:34439161-34439201 | Common:1; Rare:8 | ||||
| chr11:34915702-34915734 | Rare:6 | ||||
| chr11:34915997-34916200 | Common:3; Rare:62; Clinvar (benign):2 | ||||
| chr11:34916219-34916688 | Common:11; Rare:189; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:35138737-35138906 | Common:2; Rare:38 | ||||
| chr11:35139039-35139196 | Common:1; Rare:29 | ||||
| chr11:35139691-35139761 | Common:2; Rare:12 | ||||
| chr11:35525595-35525871 | Common:1; Rare:62 | ||||
| chr11:35618218-35618550 | Common:3; Rare:100 | ||||
| chr11:35618819-35619009 | Common:1; Rare:65 |