| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:17940359-17940603 | Common:2; Rare:111 | ||||
| chr7:20217330-20217594 | Common:1; Rare:56 | ||||
| chr7:20330463-20330735 | Common:2; Rare:64 | ||||
| chr7:20331001-20331193 | Rare:40 | ||||
| chr7:20331733-20331870 | Common:1; Rare:50 | ||||
| chr7:21946130-21946336 | Rare:60 | ||||
| chr7:22726986-22727205 | Common:1; Rare:24 | ||||
| chr7:22822676-22822985 | Common:3; Rare:116 | ||||
| chr7:23105667-23105942 | Common:4; Rare:129; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23181906-23182128 | Rare:95 | ||||
| chr7:23299216-23299482 | Common:2; Rare:142 | ||||
| chr7:24980108-24980333 | Common:6; Rare:92 | ||||
| chr7:25125201-25125426 | Rare:94; Clinvar:3 | ||||
| chr7:26200536-26201013 | Common:2; Rare:231 | ||||
| chr7:26201180-26201550 | Rare:143 |