| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118224984-118225193 | Common:1; Rare:31 | ||||
| chr11:118264284-118264383 | Rare:19 | ||||
| chr11:118344315-118344365 | Rare:8 | ||||
| chr11:118401320-118401710 | Rare:133 | ||||
| chr11:118621176-118621509 | Rare:68 | ||||
| chr11:118790894-118791316 | Rare:144 | ||||
| chr11:118997980-118998200 | Common:4; Rare:68 | ||||
| chr11:119018280-119018811 | Common:13; Rare:204 | ||||
| chr11:119057120-119057438 | Common:3; Rare:124 | ||||
| chr11:119067756-119067862 | Rare:34 | ||||
| chr11:119206175-119206383 | Common:5; Rare:96; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119311407-119311652 | Rare:84 | ||||
| chr11:119317097-119317275 | Rare:59 | ||||
| chr11:120128448-120128534 | Common:1; Rare:29 | ||||
| chr11:120336235-120336556 | Rare:128 |