| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111541295-111541367 | Rare:22 | ||||
| chr11:111602271-111602481 | Common:1; Rare:72 | ||||
| chr11:111766338-111766415 | Rare:46 | ||||
| chr11:111871254-111871332 | Rare:20 | ||||
| chr11:111879154-111879542 | Rare:116 | ||||
| chr11:111913138-111913281 | Rare:43 | ||||
| chr11:112025319-112025486 | Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:112073987-112074356 | Common:1; Rare:78 | ||||
| chr11:112086665-112086941 | Rare:126; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr11:112226314-112226650 | Common:1; Rare:140; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:113314408-113314609 | Rare:71 | ||||
| chr11:113875503-113875783 | Common:4; Rare:105 | ||||
| chr11:114059392-114059728 | Rare:75 | ||||
| chr11:114295597-114295782 | Common:2; Rare:34 | ||||
| chr11:114296170-114296578 | Common:1; Rare:77 |