| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112086716-112086916 | Rare:86; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:114400444-114400755 | Common:2; Rare:124 | ||||
| chr11:116787899-116788379 | Rare:140 | ||||
| chr11:117144166-117144377 | Common:2; Rare:106 | ||||
| chr11:117232525-117232752 | Common:2; Rare:77 | ||||
| chr11:118565051-118565286 | Common:1; Rare:35 | ||||
| chr11:118790913-118791259 | Rare:98 | ||||
| chr11:118997977-118998193 | Common:4; Rare:68 | ||||
| chr11:119018281-119018599 | Common:8; Rare:123 | ||||
| chr11:119018616-119018801 | Common:5; Rare:74 | ||||
| chr11:119057070-119057481 | Common:3; Rare:160 | ||||
| chr11:119067659-119067826 | Common:2; Rare:60 | ||||
| chr11:119101377-119101454 | Rare:15 | ||||
| chr11:119206211-119206367 | Common:4; Rare:68; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:124673712-124673969 | Common:5; Rare:73 |