| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:160697893-160698183 | Rare:57 | ||||
| chr6:160718266-160718835 | Common:3; Rare:148; Clinvar (pathogenic):1 | ||||
| chr6:160722542-160722585 | Common:1; Rare:13 | ||||
| chr6:167268816-167269053 | Common:2; Rare:39 | ||||
| chr6:167308767-167308980 | Common:5; Rare:43 | ||||
| chr6:167373452-167373626 | Common:3; Rare:11 | ||||
| chr6:167494482-167494606 | Common:1; Rare:32 | ||||
| chr6:167791201-167791408 | Common:2; Rare:31 | ||||
| chr6:167796819-167796892 | Common:1; Rare:16 | ||||
| chr6:169702772-169702801 | Rare:15 | ||||
| chr7:149153-149274 | Common:2; Rare:43 | ||||
| chr7:149412-149758 | Common:8; Rare:122 | ||||
| chr7:194355-194535 | Common:3; Rare:39 | ||||
| chr7:711467-711571 | Rare:38 | ||||
| chr7:1101985-1102264 | Common:2; Rare:61 |