| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166627950-166628073 | Rare:27 | ||||
| chr6:166956544-166956769 | Common:5; Rare:77; Clinvar:3 | ||||
| chr6:166999088-166999406 | Common:1; Rare:110 | ||||
| chr6:167826759-167827161 | Common:2; Rare:224 | ||||
| chr6:169702004-169702149 | Common:1; Rare:64 | ||||
| chr6:169725527-169725646 | Common:1; Rare:30 | ||||
| chr6:169751507-169751644 | Rare:49; Clinvar (benign):1 | ||||
| chr6:170306559-170306809 | Common:1; Rare:82 | ||||
| chr6:170554195-170554416 | Common:1; Rare:69 | ||||
| chr7:519103-519304 | Rare:51 | ||||
| chr7:520015-520197 | Rare:49 | ||||
| chr7:727252-727317 | Rare:20; Clinvar:1 | ||||
| chr7:975513-975674 | Common:1; Rare:64 | ||||
| chr7:1028315-1028465 | Rare:52 | ||||
| chr7:1138196-1138433 | Common:2; Rare:73 |