| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112024957-112025185 | Rare:55; Clinvar:3 | ||||
| chr11:112025284-112025560 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:112073995-112074367 | Common:1; Rare:78 | ||||
| chr11:112086692-112086881 | Rare:81 | ||||
| chr11:113314379-113314684 | Common:1; Rare:99 | ||||
| chr11:113875475-113875768 | Common:4; Rare:105 | ||||
| chr11:114400434-114400755 | Common:2; Rare:126 | ||||
| chr11:114439290-114439708 | Common:3; Rare:136 | ||||
| chr11:115504386-115504673 | Common:1; Rare:85 | ||||
| chr11:116772954-116773069 | Rare:42 | ||||
| chr11:116787988-116788095 | Rare:33 | ||||
| chr11:117098392-117098581 | Rare:70 | ||||
| chr11:117144191-117144418 | Common:2; Rare:104 | ||||
| chr11:117191169-117191355 | Common:4; Rare:51 | ||||
| chr11:117199008-117199455 | Common:6; Rare:136 |