| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74254288-74254586 | Rare:136 | ||||
| chr7:74453709-74454100 | Common:1; Rare:99 | ||||
| chr7:74727865-74728068 | Common:1; Rare:41 | ||||
| chr7:75486220-75486348 | Common:1; Rare:55 | ||||
| chr7:75878847-75879101 | Common:12; Rare:95 | ||||
| chr7:75914908-75915179 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994507-75994772 | Common:4; Rare:133 | ||||
| chr7:76047798-76048220 | Common:3; Rare:133 | ||||
| chr7:76302792-76303048 | Rare:120; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):4 | ||||
| chr7:76358738-76358815 | Rare:17 | ||||
| chr7:76358856-76359095 | Common:1; Rare:92 | ||||
| chr7:76397405-76397666 | Rare:103 | ||||
| chr7:76627251-76627389 | Common:5; Rare:39 | ||||
| chr7:77122302-77122601 | Common:1; Rare:63 | ||||
| chr7:77326226-77326458 | Common:3; Rare:50 |