| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99325784-99325963 | Common:1; Rare:71 | ||||
| chr7:99408545-99408753 | Common:2; Rare:58 | ||||
| chr7:99408811-99409032 | Common:1; Rare:69 | ||||
| chr7:99438691-99439002 | Common:1; Rare:101 | ||||
| chr7:99472669-99472967 | Common:4; Rare:92 | ||||
| chr7:99500241-99500435 | Common:2; Rare:52 | ||||
| chr7:99552021-99552184 | Rare:56 | ||||
| chr7:99558440-99558880 | Common:3; Rare:129 | ||||
| chr7:99616892-99616985 | Common:2; Rare:29 | ||||
| chr7:99919490-99919657 | Rare:55 | ||||
| chr7:100015504-100015635 | Common:1; Rare:34 | ||||
| chr7:100049687-100049823 | Rare:49 | ||||
| chr7:100088729-100089023 | Common:2; Rare:89 | ||||
| chr7:100101329-100101706 | Common:1; Rare:146; Clinvar (benign):1 | ||||
| chr7:100119308-100119717 | Rare:122 |