| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111913167-111913451 | Rare:72 | ||||
| chr11:112073994-112074341 | Common:1; Rare:71 | ||||
| chr11:112086726-112086893 | Rare:69 | ||||
| chr11:113314406-113314603 | Rare:69 | ||||
| chr11:114296251-114296609 | Rare:69 | ||||
| chr11:114400450-114400755 | Common:2; Rare:122 | ||||
| chr11:117199015-117199422 | Common:6; Rare:131 | ||||
| chr11:117200008-117200253 | Common:6; Rare:50 | ||||
| chr11:117232526-117232725 | Common:2; Rare:68 | ||||
| chr11:118790888-118791255 | Rare:108 | ||||
| chr11:119018375-119018514 | Common:3; Rare:50 | ||||
| chr11:119018617-119018808 | Common:5; Rare:76 | ||||
| chr11:119057025-119057437 | Common:3; Rare:149 | ||||
| chr11:119067662-119067822 | Common:2; Rare:59 | ||||
| chr11:119101392-119101493 | Rare:28; Clinvar:1; Clinvar (pathogenic):1 |