| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126268787-126269198 | Common:1; Rare:157; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:126283002-126283134 | Common:1; Rare:51 | ||||
| chr11:126303974-126304083 | Rare:63 | ||||
| chr11:126355545-126355771 | Rare:60 | ||||
| chr11:128693803-128694106 | Common:2; Rare:54 | ||||
| chr11:129024092-129024234 | Common:2; Rare:23 | ||||
| chr11:129279491-129279760 | Common:3; Rare:116 | ||||
| chr11:129436614-129436911 | Common:2; Rare:94 | ||||
| chr11:129815748-129815885 | Common:1; Rare:34 | ||||
| chr11:129895535-129895666 | Common:2; Rare:48 | ||||
| chr11:130069644-130070080 | Common:2; Rare:153 | ||||
| chr11:130314395-130314509 | Common:1; Rare:37 | ||||
| chr11:131911209-131911502 | Common:1; Rare:93 | ||||
| chr11:134253306-134253592 | Common:2; Rare:93; Clinvar (benign):1 | ||||
| chr12:389249-389364 | Rare:40 |