| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66257559-66257777 | Rare:54 | ||||
| chr11:66345077-66345227 | Common:1; Rare:34 | ||||
| chr11:66347605-66347841 | Common:5; Rare:57 | ||||
| chr11:66480222-66480459 | Common:2; Rare:64 | ||||
| chr11:66510551-66510687 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:66593036-66593205 | Common:1; Rare:59 | ||||
| chr11:66616396-66616649 | Common:1; Rare:69 | ||||
| chr11:66638360-66638728 | Common:3; Rare:165 | ||||
| chr11:66677810-66678024 | Common:1; Rare:87 | ||||
| chr11:66744656-66744771 | Common:1; Rare:40 | ||||
| chr11:67353517-67353870 | Common:2; Rare:90 | ||||
| chr11:67401783-67402071 | Common:3; Rare:108 | ||||
| chr11:67428287-67428531 | Rare:83 | ||||
| chr11:67469225-67469407 | Common:1; Rare:52 | ||||
| chr11:67482901-67483154 | Rare:57; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |