| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74254352-74254505 | Rare:69 | ||||
| chr7:75914911-75915164 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994493-75994779 | Common:4; Rare:141 | ||||
| chr7:76047939-76048200 | Common:2; Rare:91 | ||||
| chr7:76302440-76302700 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:76302866-76303075 | Rare:87; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:76303659-76303864 | Common:1; Rare:92; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:77199701-77199760 | Rare:15 | ||||
| chr7:77199765-77199911 | Rare:37 | ||||
| chr7:77696236-77696520 | Rare:125 | ||||
| chr7:77697064-77697173 | Common:1; Rare:35 | ||||
| chr7:77798387-77798971 | Common:1; Rare:139 | ||||
| chr7:79453581-79453698 | Rare:32 | ||||
| chr7:79453795-79454150 | Common:2; Rare:84 | ||||
| chr7:80638576-80638680 | Common:3; Rare:21 |