| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46564615-46564756 | Rare:16 | ||||
| chr11:46675066-46675216 | Rare:38 | ||||
| chr11:46675267-46675519 | Rare:47 | ||||
| chr11:46686816-46687119 | Rare:50 | ||||
| chr11:46687525-46687733 | Common:1; Rare:39 | ||||
| chr11:46916905-46916974 | Rare:20 | ||||
| chr11:47189444-47189547 | Rare:11 | ||||
| chr11:47194154-47194398 | Rare:49 | ||||
| chr11:47204680-47204907 | Common:1; Rare:38 | ||||
| chr11:47216227-47216394 | Common:1; Rare:51; Clinvar:2 | ||||
| chr11:47241098-47241239 | Rare:25 | ||||
| chr11:47242579-47242676 | Rare:16 | ||||
| chr11:47355251-47355479 | Rare:43 | ||||
| chr11:47400209-47400336 | Common:1; Rare:43 | ||||
| chr11:47407842-47407938 | Rare:15 |