| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16645690-16646208 | Common:3; Rare:184 | ||||
| chr7:17298444-17298734 | Common:3; Rare:78 | ||||
| chr7:17940390-17940595 | Common:2; Rare:98 | ||||
| chr7:20330706-20330885 | Rare:56 | ||||
| chr7:20330898-20331081 | Common:2; Rare:47 | ||||
| chr7:20331714-20331887 | Common:1; Rare:65 | ||||
| chr7:21542635-21542824 | Common:3; Rare:37 | ||||
| chr7:21542916-21543101 | Rare:64 | ||||
| chr7:22220154-22220484 | Common:3; Rare:56 | ||||
| chr7:22822704-22822954 | Common:3; Rare:94 | ||||
| chr7:23105666-23105871 | Common:4; Rare:108; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181779-23181861 | Rare:25 | ||||
| chr7:23181951-23182179 | Rare:100 | ||||
| chr7:23299193-23299490 | Common:2; Rare:151 | ||||
| chr7:23531932-23532083 | Common:2; Rare:62 |