| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:117876612-117876964 | Common:3; Rare:96 | ||||
| chr11:117986080-117986510 | Common:5; Rare:126; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:118152781-118152988 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:118251810-118252570 | Common:3; Rare:195 | ||||
| chr11:118359383-118359662 | Common:3; Rare:109 | ||||
| chr11:118401257-118401644 | Rare:112 | ||||
| chr11:118437232-118437364 | Rare:21 | ||||
| chr11:118531011-118531206 | Rare:54 | ||||
| chr11:118565860-118566280 | Common:1; Rare:87 | ||||
| chr11:118572274-118572445 | Common:3; Rare:54 | ||||
| chr11:118615415-118615587 | Common:1; Rare:31 | ||||
| chr11:118621190-118621433 | Rare:49 | ||||
| chr11:118621540-118622000 | Common:2; Rare:70 | ||||
| chr11:118790130-118790732 | Common:9; Rare:203 | ||||
| chr11:118791083-118791310 | Rare:93 |