| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118252288-118252375 | Rare:31 | ||||
| chr11:118264283-118264593 | Common:1; Rare:50 | ||||
| chr11:118790893-118791258 | Rare:106 | ||||
| chr11:118997980-118998191 | Common:4; Rare:64 | ||||
| chr11:119018280-119018795 | Common:13; Rare:199 | ||||
| chr11:119057120-119057437 | Common:3; Rare:123 | ||||
| chr11:119067730-119067826 | Rare:35 | ||||
| chr11:119121273-119121621 | Common:1; Rare:81 | ||||
| chr11:119206180-119206367 | Common:5; Rare:84; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119423142-119423302 | Common:2; Rare:52 | ||||
| chr11:121292586-121292793 | Rare:69; Clinvar:3 | ||||
| chr11:123062393-123062662 | Common:4; Rare:126 | ||||
| chr11:123560165-123560340 | Common:1; Rare:36 | ||||
| chr11:123654564-123654742 | Common:2; Rare:46 | ||||
| chr11:124673837-124673935 | Common:4; Rare:20 |