| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118910487-118910777 | Common:7; Rare:246 | ||||
| chr11:118911010-118911967 | Common:8; Rare:448 | ||||
| chr11:118924976-118925173 | Rare:55 | ||||
| chr11:118925276-118925676 | Common:11; Rare:79 | ||||
| chr11:118925849-118926151 | Common:7; Rare:223 | ||||
| chr11:118956053-118956377 | Common:2; Rare:115 | ||||
| chr11:118997870-118998262 | Common:12; Rare:315 | ||||
| chr11:119018228-119018869 | Common:39; Rare:635 | ||||
| chr11:119030735-119030989 | Common:3; Rare:74; Clinvar (benign):3 | ||||
| chr11:119056099-119056879 | Common:8; Rare:576 | ||||
| chr11:119056997-119057600 | Common:13; Rare:550 | ||||
| chr11:119067508-119067927 | Common:8; Rare:201 | ||||
| chr11:119084782-119084999 | Common:5; Rare:176; Clinvar (benign):5 | ||||
| chr11:119085000-119085300 | Common:9; Rare:262; Clinvar (benign):6 | ||||
| chr11:119094810-119095160 | Rare:193 |