| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:88337733-88337845 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:93741369-93741695 | Common:7; Rare:134 | ||||
| chr11:94493842-94494005 | Common:3; Rare:43; Clinvar (benign):1 | ||||
| chr11:94973542-94973705 | Rare:48 | ||||
| chr11:106077348-106077676 | Common:2; Rare:88 | ||||
| chr11:112086728-112086899 | Rare:69 | ||||
| chr11:112226257-112226446 | Rare:75 | ||||
| chr11:112961444-112961557 | Rare:47 | ||||
| chr11:119018292-119018538 | Common:8; Rare:104 | ||||
| chr11:119018659-119018793 | Common:4; Rare:62 | ||||
| chr11:126211661-126211782 | Rare:51 | ||||
| chr11:126268867-126269049 | Rare:64; Clinvar:1 | ||||
| chr11:126355552-126355742 | Rare:46 | ||||
| chr11:134253306-134253561 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chr12:4649049-4649149 | Common:1; Rare:42; Clinvar (benign):1 |