| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100088916-100089005 | Rare:30 | ||||
| chr7:100100719-100100800 | Rare:33 | ||||
| chr7:100101336-100101711 | Common:1; Rare:144; Clinvar (benign):1 | ||||
| chr7:100119328-100119717 | Rare:112 | ||||
| chr7:100148716-100149033 | Common:1; Rare:140 | ||||
| chr7:100428264-100428420 | Common:1; Rare:42 | ||||
| chr7:100428633-100428804 | Common:4; Rare:66 | ||||
| chr7:100429137-100429420 | Common:4; Rare:133 | ||||
| chr7:100436157-100436217 | Common:1; Rare:14 | ||||
| chr7:100436455-100436510 | Rare:19 | ||||
| chr7:100586100-100586288 | Common:1; Rare:68 | ||||
| chr7:100612376-100612588 | Rare:48 | ||||
| chr7:100687568-100687879 | Common:1; Rare:98 | ||||
| chr7:100852604-100852786 | Common:1; Rare:48 | ||||
| chr7:100874951-100875243 | Common:2; Rare:100 |