| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111557834-111558200 | Common:1; Rare:55 | ||||
| chr11:111559220-111559270 | Rare:8 | ||||
| chr11:111559352-111559433 | Rare:13 | ||||
| chr11:111563407-111563672 | Common:4; Rare:48 | ||||
| chr11:114294838-114295083 | Common:1; Rare:52 | ||||
| chr11:116521067-116521181 | Rare:27 | ||||
| chr11:117293110-117293286 | Rare:44 | ||||
| chr11:118399157-118399368 | Rare:38 | ||||
| chr11:118791687-118791863 | Common:1; Rare:51 | ||||
| chr11:119090020-119090266 | Rare:64; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:119335357-119335671 | Common:2; Rare:83 | ||||
| chr11:121829148-121829324 | Common:1; Rare:31 | ||||
| chr11:122090242-122090383 | Common:1; Rare:24 | ||||
| chr11:122091187-122091507 | Rare:49 | ||||
| chr11:122092362-122092411 | Rare:6 |