| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118997973-118998199 | Common:4; Rare:72 | ||||
| chr11:119018280-119018798 | Common:13; Rare:201 | ||||
| chr11:119030776-119030972 | Common:3; Rare:57; Clinvar (benign):3 | ||||
| chr11:119057073-119057481 | Common:3; Rare:160 | ||||
| chr11:119067645-119067821 | Common:3; Rare:63 | ||||
| chr11:119095230-119095498 | Common:1; Rare:103 | ||||
| chr11:119101380-119101473 | Rare:21 | ||||
| chr11:119101750-119101961 | Rare:56; Clinvar:3 | ||||
| chr11:119121284-119121626 | Common:1; Rare:77 | ||||
| chr11:119206180-119206424 | Common:5; Rare:105; Clinvar:8; Clinvar (benign):5 | ||||
| chr11:119317114-119317420 | Rare:85 | ||||
| chr11:119334264-119334536 | Rare:71 | ||||
| chr11:119381607-119381807 | Common:1; Rare:41 | ||||
| chr11:119423127-119423387 | Common:3; Rare:67 | ||||
| chr11:121292569-121292883 | Rare:106; Clinvar:3 |