| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112086729-112086905 | Rare:71; Clinvar:1 | ||||
| chr11:112226298-112226677 | Common:1; Rare:156; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961102-112961187 | Common:1; Rare:18 | ||||
| chr11:112961203-112961654 | Common:5; Rare:200 | ||||
| chr11:113875503-113875799 | Common:4; Rare:115 | ||||
| chr11:114059417-114059740 | Rare:69 | ||||
| chr11:114400427-114400747 | Common:2; Rare:128 | ||||
| chr11:115504372-115504673 | Common:2; Rare:91 | ||||
| chr11:116773029-116773349 | Common:1; Rare:93 | ||||
| chr11:116787976-116788060 | Rare:29 | ||||
| chr11:117144183-117144418 | Common:2; Rare:106 | ||||
| chr11:117232049-117232177 | Rare:31 | ||||
| chr11:117232525-117232719 | Common:2; Rare:66 | ||||
| chr11:117316247-117316432 | Common:1; Rare:41 | ||||
| chr11:117797137-117797285 | Common:1; Rare:58 |