| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:7969131-7969346 | Common:4; Rare:129 | ||||
| chr7:7969840-7970330 | Common:1; Rare:126 | ||||
| chr7:8262021-8262259 | Rare:131 | ||||
| chr7:10940046-10940465 | Common:4; Rare:231; Clinvar (benign):3 | ||||
| chr7:10973593-10973953 | Common:2; Rare:281 | ||||
| chr7:12211145-12211400 | Common:6; Rare:225 | ||||
| chr7:12403420-12403790 | Common:5; Rare:150 | ||||
| chr7:12403810-12404240 | Common:5; Rare:126 | ||||
| chr7:12686704-12686913 | Common:4; Rare:117 | ||||
| chr7:12687389-12687661 | Common:10; Rare:157 | ||||
| chr7:16645590-16646205 | Common:6; Rare:416 | ||||
| chr7:16753532-16753800 | Rare:146 | ||||
| chr7:17298413-17298728 | Common:7; Rare:160 | ||||
| chr7:17940301-17940631 | Common:4; Rare:264 | ||||
| chr7:19708994-19709206 | Common:8; Rare:140 |