| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67443419-67443643 | Common:2; Rare:81 | ||||
| chr11:67443748-67443986 | Rare:56 | ||||
| chr11:67464629-67464904 | Rare:155 | ||||
| chr11:67469128-67469478 | Common:4; Rare:118 | ||||
| chr11:67482891-67483238 | Rare:87; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):4 | ||||
| chr11:67483360-67483550 | Rare:44 | ||||
| chr11:67505322-67505452 | Rare:32 | ||||
| chr11:67508071-67508686 | Common:2; Rare:139 | ||||
| chr11:67508689-67508818 | Common:1; Rare:57 | ||||
| chr11:67583450-67583707 | Common:7; Rare:48 | ||||
| chr11:67583709-67583933 | Common:1; Rare:80 | ||||
| chr11:67584081-67584189 | Common:1; Rare:34 | ||||
| chr11:67584294-67584467 | Common:2; Rare:44 | ||||
| chr11:67606700-67607017 | Common:1; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:67629365-67629522 | Common:1; Rare:39 |