| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:12687396-12687643 | Common:5; Rare:75 | ||||
| chr7:16645725-16646217 | Common:4; Rare:173 | ||||
| chr7:17940438-17940569 | Common:1; Rare:65 | ||||
| chr7:18495649-18495771 | Rare:29 | ||||
| chr7:20217335-20217585 | Common:1; Rare:53 | ||||
| chr7:20331714-20331756 | Rare:10 | ||||
| chr7:20331760-20331786 | Common:1; Rare:10 | ||||
| chr7:21427836-21428146 | Common:1; Rare:114 | ||||
| chr7:21945827-21946199 | Common:3; Rare:122 | ||||
| chr7:22500136-22500245 | Common:1; Rare:40 | ||||
| chr7:23105626-23105972 | Common:4; Rare:157; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23106436-23106666 | Common:2; Rare:39 | ||||
| chr7:23181840-23182128 | Common:2; Rare:118 | ||||
| chr7:23470282-23470580 | Common:1; Rare:92 | ||||
| chr7:23531923-23532083 | Common:2; Rare:68 |