| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67353269-67353365 | Rare:36 | ||||
| chr11:67353443-67353853 | Common:2; Rare:98 | ||||
| chr11:67372931-67373205 | Common:1; Rare:56 | ||||
| chr11:67373576-67373927 | Rare:65 | ||||
| chr11:67374054-67374292 | Rare:30 | ||||
| chr11:67401773-67402076 | Common:3; Rare:113 | ||||
| chr11:67415206-67415327 | Rare:25 | ||||
| chr11:67428349-67428531 | Rare:65 | ||||
| chr11:67443421-67443628 | Common:1; Rare:78 | ||||
| chr11:67469213-67469410 | Common:1; Rare:63 | ||||
| chr11:67482957-67483154 | Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:67507789-67508143 | Rare:108 | ||||
| chr11:67508145-67508440 | Common:1; Rare:57 | ||||
| chr11:67508615-67508768 | Common:3; Rare:53 | ||||
| chr11:67586551-67586777 | Rare:53 |