| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112226319-112226657 | Common:1; Rare:141; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961237-112961654 | Common:4; Rare:192 | ||||
| chr11:113314454-113314603 | Rare:52 | ||||
| chr11:113875493-113875787 | Common:4; Rare:110 | ||||
| chr11:114059410-114059734 | Rare:71 | ||||
| chr11:114400455-114400755 | Common:2; Rare:119 | ||||
| chr11:115504376-115504673 | Common:2; Rare:89 | ||||
| chr11:116772960-116773054 | Rare:34 | ||||
| chr11:117144188-117144385 | Common:2; Rare:98 | ||||
| chr11:117199040-117199424 | Common:6; Rare:120 | ||||
| chr11:117232533-117232717 | Common:2; Rare:64 | ||||
| chr11:117316354-117316432 | Rare:22 | ||||
| chr11:117327656-117327915 | Common:1; Rare:46 | ||||
| chr11:117797141-117797361 | Common:2; Rare:84 | ||||
| chr11:117876593-117876813 | Rare:63 |