| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17013010-17013169 | Common:4; Rare:24 | ||||
| chr11:17013850-17013962 | Common:4; Rare:47 | ||||
| chr11:17013977-17014012 | Rare:13 | ||||
| chr11:17014355-17014653 | Common:5; Rare:115 | ||||
| chr11:17077614-17078119 | Common:4; Rare:184 | ||||
| chr11:17078156-17078302 | Rare:44 | ||||
| chr11:17207622-17207728 | Rare:26 | ||||
| chr11:17207853-17208210 | Common:2; Rare:126 | ||||
| chr11:17208311-17208646 | Rare:64 | ||||
| chr11:17276223-17276396 | Common:1; Rare:43 | ||||
| chr11:17276401-17277042 | Common:6; Rare:166; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:17351719-17351851 | Rare:18 | ||||
| chr11:17351863-17352099 | Common:2; Rare:65 | ||||
| chr11:17352128-17352299 | Rare:20 | ||||
| chr11:17389255-17389506 | Common:2; Rare:44 |