| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74053589-74053844 | Rare:43 | ||||
| chr7:74059718-74059939 | Rare:59; Clinvar (benign):1 | ||||
| chr7:74060169-74060468 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:74062219-74062330 | Rare:19 | ||||
| chr7:74700308-74700652 | Common:1; Rare:72 | ||||
| chr7:74890513-74890836 | Common:3; Rare:108 | ||||
| chr7:75358976-75359274 | Common:1; Rare:13 | ||||
| chr7:75415882-75416325 | Common:1; Rare:183 | ||||
| chr7:75639158-75639359 | Common:1; Rare:46 | ||||
| chr7:75979278-75979475 | Common:1; Rare:57 | ||||
| chr7:76304181-76304425 | Common:3; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:76549663-76549748 | Rare:33 | ||||
| chr7:76595962-76596238 | Common:4; Rare:39 | ||||
| chr7:77312159-77312245 | Common:2; Rare:26 | ||||
| chr7:77404559-77404709 | Common:2; Rare:32 |