| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75994489-75994772 | Common:4; Rare:139 | ||||
| chr7:76047932-76048210 | Common:2; Rare:96 | ||||
| chr7:76302466-76303075 | Common:3; Rare:246; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76397472-76397558 | Rare:40 | ||||
| chr7:76478906-76479035 | Rare:10 | ||||
| chr7:76541524-76541602 | Common:1; Rare:13 | ||||
| chr7:76627197-76627361 | Common:8; Rare:58 | ||||
| chr7:77122265-77122680 | Common:2; Rare:87 | ||||
| chr7:77199719-77199745 | Rare:5 | ||||
| chr7:77199789-77199886 | Rare:24 | ||||
| chr7:77416360-77416566 | Common:4; Rare:51 | ||||
| chr7:77536880-77537174 | Common:3; Rare:79 | ||||
| chr7:77696195-77696500 | Common:1; Rare:131 | ||||
| chr7:77696801-77696972 | Rare:74 | ||||
| chr7:77697007-77697164 | Common:1; Rare:55 |