| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111766345-111766415 | Rare:40 | ||||
| chr11:111871254-111871378 | Rare:40; Clinvar:1 | ||||
| chr11:111878989-111879027 | Rare:21 | ||||
| chr11:111879152-111879556 | Common:1; Rare:123 | ||||
| chr11:111912730-111912758 | Rare:4 | ||||
| chr11:111913138-111913281 | Rare:43 | ||||
| chr11:111937138-111937198 | Common:1; Rare:11 | ||||
| chr11:112025293-112025464 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:112073980-112074351 | Common:1; Rare:80 | ||||
| chr11:112086709-112086907 | Rare:84; Clinvar:1 | ||||
| chr11:112226320-112226650 | Common:1; Rare:138; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:113314411-113314602 | Rare:66 | ||||
| chr11:113875486-113875768 | Common:4; Rare:101 | ||||
| chr11:114059410-114060034 | Common:1; Rare:132 | ||||
| chr11:114400444-114400748 | Common:2; Rare:123 |