| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118264290-118264593 | Common:1; Rare:48 | ||||
| chr11:118401340-118401720 | Rare:129 | ||||
| chr11:118790904-118791263 | Rare:103 | ||||
| chr11:118997980-118998189 | Common:4; Rare:63 | ||||
| chr11:119018280-119018452 | Common:6; Rare:71 | ||||
| chr11:119018622-119018793 | Common:5; Rare:71 | ||||
| chr11:119057132-119057437 | Common:3; Rare:121 | ||||
| chr11:119067626-119067821 | Common:3; Rare:65 | ||||
| chr11:119206187-119206369 | Common:5; Rare:80; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119317110-119317284 | Rare:60 | ||||
| chr11:119381602-119381721 | Rare:33 | ||||
| chr11:123062403-123062663 | Common:4; Rare:120 | ||||
| chr11:124673686-124673920 | Common:4; Rare:76 | ||||
| chr11:124762197-124762441 | Rare:67 | ||||
| chr11:124800406-124800454 | Rare:16 |