| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112025267-112025690 | Common:4; Rare:139; Clinvar:3; Clinvar (benign):9 | ||||
| chr11:112074179-112074345 | Rare:40 | ||||
| chr11:112086709-112086944 | Common:1; Rare:102; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr11:112961263-112961654 | Common:4; Rare:178 | ||||
| chr11:113246363-113246371 | |||||
| chr11:113314458-113314616 | Rare:55 | ||||
| chr11:113875461-113875781 | Common:4; Rare:117 | ||||
| chr11:114059410-114059793 | Rare:80 | ||||
| chr11:114059801-114059891 | Common:1; Rare:15 | ||||
| chr11:114400445-114400747 | Common:2; Rare:122 | ||||
| chr11:117144203-117144365 | Common:2; Rare:83 | ||||
| chr11:117199018-117199385 | Common:6; Rare:121 | ||||
| chr11:117232036-117232177 | Rare:36 | ||||
| chr11:117232542-117232717 | Common:2; Rare:61 | ||||
| chr11:117986225-117986415 | Common:4; Rare:61; Clinvar:2 |