| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73683419-73683622 | Common:3; Rare:81 | ||||
| chr7:74174080-74174423 | Common:1; Rare:163 | ||||
| chr7:74254385-74254528 | Rare:66 | ||||
| chr7:76047964-76048180 | Common:1; Rare:68 | ||||
| chr7:76302873-76303075 | Rare:84; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr7:77696236-77696465 | Rare:91 | ||||
| chr7:79453839-79454130 | Common:1; Rare:73 | ||||
| chr7:80134691-80134888 | Common:2; Rare:84 | ||||
| chr7:87152329-87152474 | Common:1; Rare:50 | ||||
| chr7:87345452-87345706 | Common:4; Rare:85 | ||||
| chr7:87876314-87876634 | Common:2; Rare:139 | ||||
| chr7:90211606-90211890 | Common:3; Rare:83 | ||||
| chr7:90346571-90346733 | Common:3; Rare:71 | ||||
| chr7:91880674-91880823 | Common:2; Rare:40 | ||||
| chr7:92134741-92134852 | Common:2; Rare:25 |