| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:116772667-116773211 | Common:3; Rare:176 | ||||
| chr11:116787892-116788160 | Rare:100 | ||||
| chr11:117098416-117098737 | Common:5; Rare:92 | ||||
| chr11:117144140-117144377 | Common:5; Rare:112 | ||||
| chr11:117144694-117144793 | Common:3; Rare:33 | ||||
| chr11:117178629-117178878 | Common:1; Rare:90 | ||||
| chr11:117179619-117179876 | Common:1; Rare:47 | ||||
| chr11:117232028-117232239 | Rare:56 | ||||
| chr11:117328040-117328217 | Common:1; Rare:45 | ||||
| chr11:117817458-117817490 | Common:1; Rare:6 | ||||
| chr11:117817493-117817711 | Common:4; Rare:38 | ||||
| chr11:117817827-117817949 | Rare:23 | ||||
| chr11:117824698-117824744 | Rare:10 | ||||
| chr11:117985945-117986086 | Common:1; Rare:31 | ||||
| chr11:117986169-117986549 | Common:5; Rare:126; Clinvar:5; Clinvar (benign):2 |