| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118621116-118621516 | Rare:79 | ||||
| chr11:118790911-118791259 | Rare:99 | ||||
| chr11:118997980-118998264 | Common:4; Rare:94 | ||||
| chr11:119018280-119018452 | Common:6; Rare:71 | ||||
| chr11:119018620-119018808 | Common:5; Rare:76 | ||||
| chr11:119057048-119057448 | Common:3; Rare:153 | ||||
| chr11:119067618-119067866 | Common:3; Rare:79 | ||||
| chr11:119084792-119084908 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr11:119206211-119206391 | Common:4; Rare:79; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119311784-119312187 | Common:1; Rare:139 | ||||
| chr11:119317034-119317303 | Rare:84 | ||||
| chr11:119340548-119340875 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:120336221-120336556 | Rare:136 | ||||
| chr11:122655575-122655807 | Common:2; Rare:57 | ||||
| chr11:123062403-123062663 | Common:4; Rare:120 |