| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:16612910-16613141 | Rare:33 | ||||
| chr11:16738432-16738857 | Common:3; Rare:105 | ||||
| chr11:17014211-17014321 | Rare:36 | ||||
| chr11:17077595-17077899 | Common:2; Rare:127 | ||||
| chr11:17207916-17208078 | Common:2; Rare:61 | ||||
| chr11:17276580-17276828 | Common:3; Rare:64; Clinvar:3 | ||||
| chr11:17351686-17351827 | Rare:26 | ||||
| chr11:17351882-17352020 | Common:2; Rare:29 | ||||
| chr11:17352272-17352326 | Common:1; Rare:11 | ||||
| chr11:18012903-18013185 | Common:6; Rare:101 | ||||
| chr11:18106050-18106179 | Common:1; Rare:48 | ||||
| chr11:18322131-18322312 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322521-18322623 | Common:1; Rare:46 | ||||
| chr11:18394401-18394645 | Common:1; Rare:96; Clinvar (benign):1 | ||||
| chr11:18396203-18396410 | Rare:76 |