| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100429137-100429430 | Common:4; Rare:136 | ||||
| chr7:100436466-100436650 | Rare:53 | ||||
| chr7:100479159-100479307 | Common:1; Rare:40 | ||||
| chr7:100586100-100586456 | Common:3; Rare:116 | ||||
| chr7:100611992-100612192 | Common:2; Rare:39 | ||||
| chr7:100612368-100612591 | Rare:50 | ||||
| chr7:100633356-100633474 | Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:100656346-100656573 | Rare:59 | ||||
| chr7:100676048-100676287 | Rare:78 | ||||
| chr7:100705918-100706213 | Common:4; Rare:113 | ||||
| chr7:100852629-100852769 | Rare:32 | ||||
| chr7:100867277-100867425 | Rare:42 | ||||
| chr7:100874955-100875210 | Common:2; Rare:86 | ||||
| chr7:100896079-100896181 | Common:1; Rare:24 | ||||
| chr7:101017511-101017685 | Rare:64 |