| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:114400370-114400765 | Common:2; Rare:145 | ||||
| chr11:117144191-117144362 | Common:2; Rare:89 | ||||
| chr11:117232504-117232723 | Common:2; Rare:70 | ||||
| chr11:118790888-118791031 | Rare:34 | ||||
| chr11:119018364-119018497 | Common:3; Rare:45 | ||||
| chr11:119018616-119018795 | Common:5; Rare:72 | ||||
| chr11:119057048-119057442 | Common:3; Rare:149 | ||||
| chr11:119206175-119206266 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chr11:123062126-123062361 | Rare:87 | ||||
| chr11:124673700-124673943 | Common:4; Rare:74 | ||||
| chr11:124762233-124762391 | Rare:44 | ||||
| chr11:125887513-125887737 | Common:2; Rare:66 | ||||
| chr11:126211625-126211807 | Rare:84 | ||||
| chr11:126268814-126269190 | Common:1; Rare:144; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:126355554-126355725 | Rare:40 |