| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65890437-65890730 | Common:5; Rare:92 | ||||
| chr11:65900384-65900669 | Common:3; Rare:64 | ||||
| chr11:65961532-65961764 | Rare:81 | ||||
| chr11:66002127-66002818 | Common:4; Rare:192; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:66257578-66257845 | Rare:75 | ||||
| chr11:66258397-66258615 | Rare:59 | ||||
| chr11:66268409-66268677 | Common:3; Rare:79 | ||||
| chr11:66347562-66347869 | Common:5; Rare:73 | ||||
| chr11:66348041-66348119 | Rare:34 | ||||
| chr11:66466706-66466972 | Rare:81 | ||||
| chr11:66480212-66480450 | Common:3; Rare:63 | ||||
| chr11:66593095-66593209 | Common:1; Rare:40 | ||||
| chr11:66616422-66616646 | Common:1; Rare:59 | ||||
| chr11:66638410-66638747 | Common:4; Rare:146 | ||||
| chr11:66677765-66678024 | Common:1; Rare:103 |