| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:65750910-65751133 | Common:3; Rare:100 | ||||
| chr7:65770719-65770938 | Common:6; Rare:70 | ||||
| chr7:66493506-66493777 | Common:4; Rare:110 | ||||
| chr7:66592308-66592420 | Common:2; Rare:42 | ||||
| chr7:66654441-66654571 | Rare:50 | ||||
| chr7:66844872-66845087 | Common:2; Rare:88 | ||||
| chr7:67302400-67302812 | Common:5; Rare:127 | ||||
| chr7:67302872-67302924 | Rare:18 | ||||
| chr7:72829318-72829598 | Rare:84 | ||||
| chr7:72836707-72836863 | Common:1; Rare:28 | ||||
| chr7:72954713-72954811 | Rare:16 | ||||
| chr7:73005862-73006172 | Rare:29 | ||||
| chr7:73769064-73769101 | Rare:11 | ||||
| chr7:74059716-74060043 | Common:1; Rare:115; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:74060111-74060414 | Common:1; Rare:74; Clinvar (benign):2; Clinvar (pathogenic):1 |