| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100015474-100015641 | Common:1; Rare:48 | ||||
| chr7:100081692-100081991 | Common:2; Rare:79 | ||||
| chr7:100088867-100089186 | Common:1; Rare:90 | ||||
| chr7:100101316-100101722 | Common:1; Rare:159; Clinvar (benign):1 | ||||
| chr7:100119312-100119717 | Rare:121 | ||||
| chr7:100148716-100149017 | Common:1; Rare:131 | ||||
| chr7:100428665-100428793 | Common:3; Rare:45 | ||||
| chr7:100429137-100429447 | Common:4; Rare:142 | ||||
| chr7:100436442-100436574 | Rare:48 | ||||
| chr7:100586116-100586456 | Common:3; Rare:109 | ||||
| chr7:100603096-100603263 | Common:1; Rare:23 | ||||
| chr7:100604836-100605116 | Rare:71 | ||||
| chr7:100611936-100612192 | Common:4; Rare:50 | ||||
| chr7:100705828-100706174 | Common:4; Rare:118 | ||||
| chr7:100852623-100852786 | Common:1; Rare:42 |