| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119087762-119088013 | Rare:38 | ||||
| chr11:119101788-119102198 | Rare:102; Clinvar:4 | ||||
| chr11:119121273-119121635 | Common:1; Rare:87 | ||||
| chr11:119206178-119206392 | Common:5; Rare:97; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119317097-119317250 | Rare:54 | ||||
| chr11:119334287-119334561 | Rare:75 | ||||
| chr11:120336120-120336578 | Rare:172 | ||||
| chr11:121292456-121292808 | Rare:106; Clinvar:3 | ||||
| chr11:121452050-121452615 | Common:2; Rare:151 | ||||
| chr11:121452663-121452769 | Common:1; Rare:25 | ||||
| chr11:121452842-121453083 | Rare:47 | ||||
| chr11:122655377-122655823 | Common:2; Rare:96 | ||||
| chr11:122655849-122656034 | Common:1; Rare:42 | ||||
| chr11:122656113-122656172 | Rare:18 | ||||
| chr11:122779252-122779414 | Rare:19 |