| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100049693-100049816 | Rare:42 | ||||
| chr7:100081641-100082043 | Common:3; Rare:110 | ||||
| chr7:100088905-100089023 | Common:1; Rare:41 | ||||
| chr7:100101343-100101711 | Common:1; Rare:140; Clinvar (benign):1 | ||||
| chr7:100119308-100119742 | Rare:133; Clinvar:1 | ||||
| chr7:100148716-100149017 | Common:1; Rare:131 | ||||
| chr7:100428652-100428797 | Common:3; Rare:53 | ||||
| chr7:100429137-100429454 | Common:4; Rare:145 | ||||
| chr7:100429662-100429718 | Common:1; Rare:20 | ||||
| chr7:100436442-100436642 | Rare:62 | ||||
| chr7:100479104-100479341 | Common:2; Rare:61 | ||||
| chr7:100586140-100586453 | Common:2; Rare:92 | ||||
| chr7:100602448-100602477 | Rare:13 | ||||
| chr7:100611989-100612192 | Common:2; Rare:40 | ||||
| chr7:100705917-100706184 | Common:3; Rare:103 |