| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66372470-66372565 | Rare:13 | ||||
| chr11:66438989-66439317 | Common:1; Rare:72 | ||||
| chr11:66480239-66480450 | Common:1; Rare:56 | ||||
| chr11:66510551-66510674 | Common:1; Rare:54; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:66616389-66616646 | Common:1; Rare:72 | ||||
| chr11:66638393-66638728 | Common:3; Rare:147 | ||||
| chr11:66677769-66678125 | Common:1; Rare:126 | ||||
| chr11:66744632-66744881 | Common:3; Rare:102 | ||||
| chr11:66958368-66958634 | Common:2; Rare:74; Clinvar:1 | ||||
| chr11:67239875-67240134 | Rare:54 | ||||
| chr11:67353294-67353390 | Rare:28 | ||||
| chr11:67353434-67353785 | Common:2; Rare:88 | ||||
| chr11:67401783-67402078 | Common:3; Rare:110 | ||||
| chr11:67403754-67403992 | Rare:40 | ||||
| chr11:67409286-67409433 | Common:1; Rare:38 |