| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118401320-118401661 | Rare:109 | ||||
| chr11:118572281-118572447 | Common:3; Rare:54 | ||||
| chr11:118621251-118621384 | Rare:20 | ||||
| chr11:118790919-118791255 | Rare:96 | ||||
| chr11:118997980-118998193 | Common:4; Rare:66 | ||||
| chr11:119018280-119018421 | Common:5; Rare:58 | ||||
| chr11:119018626-119018789 | Common:5; Rare:68 | ||||
| chr11:119057127-119057446 | Common:3; Rare:128 | ||||
| chr11:119067756-119067817 | Rare:20 | ||||
| chr11:119084792-119084932 | Common:1; Rare:41; Clinvar (benign):1 | ||||
| chr11:119095408-119095777 | Common:3; Rare:123 | ||||
| chr11:119121284-119121639 | Common:1; Rare:81 | ||||
| chr11:119423154-119423325 | Common:3; Rare:50 | ||||
| chr11:119729414-119729590 | Rare:44 | ||||
| chr11:121292569-121292793 | Rare:76; Clinvar:3 |