| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111541063-111541400 | Common:1; Rare:87 | ||||
| chr11:111541401-111541560 | Common:2; Rare:28 | ||||
| chr11:111602180-111602571 | Common:1; Rare:125 | ||||
| chr11:111766338-111766415 | Rare:46 | ||||
| chr11:111871254-111871378 | Rare:40; Clinvar:1 | ||||
| chr11:111871488-111871753 | Rare:76; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:111878815-111879011 | Common:2; Rare:69 | ||||
| chr11:111879148-111879548 | Common:1; Rare:124 | ||||
| chr11:111912116-111912234 | Rare:14 | ||||
| chr11:111912724-111912820 | Rare:12 | ||||
| chr11:111913106-111913292 | Rare:47 | ||||
| chr11:111937120-111937403 | Common:6; Rare:86 | ||||
| chr11:111988853-111989001 | Rare:29 | ||||
| chr11:112025315-112025486 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:112073995-112074364 | Common:1; Rare:77 |