| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:10940117-10940418 | Common:3; Rare:101 | ||||
| chr7:16645593-16646192 | Common:3; Rare:205 | ||||
| chr7:19116864-19116905 | Rare:9 | ||||
| chr7:19117634-19117773 | Common:1; Rare:26 | ||||
| chr7:20330755-20330918 | Rare:46 | ||||
| chr7:20331278-20331387 | Rare:35 | ||||
| chr7:22822765-22822985 | Common:3; Rare:81 | ||||
| chr7:23105681-23105828 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181921-23182146 | Rare:98 | ||||
| chr7:23467919-23468091 | Common:2; Rare:42 | ||||
| chr7:23470284-23470563 | Rare:86 | ||||
| chr7:23531786-23532083 | Common:2; Rare:116 | ||||
| chr7:24980107-24980409 | Common:8; Rare:130 | ||||
| chr7:25125245-25125409 | Rare:66; Clinvar:3 | ||||
| chr7:26196557-26197019 | Common:2; Rare:156; Clinvar (benign):3 |