| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118621215-118621503 | Rare:60 | ||||
| chr11:118790894-118791263 | Rare:107 | ||||
| chr11:118997980-118998185 | Common:4; Rare:60 | ||||
| chr11:119018292-119018425 | Common:6; Rare:54 | ||||
| chr11:119018449-119018795 | Common:7; Rare:128 | ||||
| chr11:119057068-119057438 | Common:3; Rare:142 | ||||
| chr11:119067624-119067817 | Common:3; Rare:63 | ||||
| chr11:119206180-119206367 | Common:5; Rare:84; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119311618-119311951 | Common:2; Rare:100 | ||||
| chr11:119317053-119317282 | Rare:70 | ||||
| chr11:122882845-122882932 | Rare:22 | ||||
| chr11:123062398-123062639 | Common:4; Rare:103 | ||||
| chr11:123741627-123741731 | Common:1; Rare:29 | ||||
| chr11:124673706-124673935 | Common:4; Rare:71 | ||||
| chr11:124762209-124762451 | Rare:64 |