| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:4775478-4775634 | Common:6; Rare:65 | ||||
| chr7:6009030-6009313 | Common:3; Rare:116; Clinvar:3; Clinvar (benign):13 | ||||
| chr7:7182369-7182683 | Common:3; Rare:113 | ||||
| chr7:10940074-10940210 | Rare:68 | ||||
| chr7:16645819-16646140 | Common:2; Rare:102 | ||||
| chr7:19709017-19709212 | Common:4; Rare:62 | ||||
| chr7:20331738-20331771 | Rare:10 | ||||
| chr7:21945852-21946174 | Common:3; Rare:94 | ||||
| chr7:22500153-22500241 | Common:1; Rare:38 | ||||
| chr7:22822766-22822954 | Common:3; Rare:69 | ||||
| chr7:23105673-23105785 | Common:1; Rare:53; Clinvar:1 | ||||
| chr7:23347731-23347927 | Rare:50 | ||||
| chr7:24980157-24980446 | Common:8; Rare:118 | ||||
| chr7:25125230-25125469 | Rare:105; Clinvar:3 | ||||
| chr7:26864570-26864866 | Common:3; Rare:95 |