| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111871256-111871391 | Rare:40; Clinvar:1 | ||||
| chr11:111871494-111871652 | Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:111878815-111878981 | Common:2; Rare:51 | ||||
| chr11:111879152-111879554 | Common:1; Rare:122 | ||||
| chr11:111912718-111912807 | Rare:12 | ||||
| chr11:111913138-111913260 | Rare:39 | ||||
| chr11:112025293-112025477 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:112073995-112074364 | Common:1; Rare:77 | ||||
| chr11:112086703-112086905 | Rare:87; Clinvar:1 | ||||
| chr11:112226319-112226837 | Common:1; Rare:187; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961329-112961661 | Common:4; Rare:153 | ||||
| chr11:113314448-113314602 | Rare:54 | ||||
| chr11:113875480-113875765 | Common:4; Rare:102 | ||||
| chr11:114059421-114059725 | Rare:66 | ||||
| chr11:114400444-114400765 | Common:2; Rare:125 |