| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99504837-99504990 | Rare:45 | ||||
| chr7:99505082-99505313 | Common:6; Rare:77 | ||||
| chr7:99551996-99552246 | Rare:78 | ||||
| chr7:99558490-99558736 | Common:2; Rare:81 | ||||
| chr7:99616502-99616658 | Common:1; Rare:42 | ||||
| chr7:99616786-99617032 | Common:2; Rare:82 | ||||
| chr7:99919487-99919737 | Rare:83 | ||||
| chr7:100015489-100015652 | Common:1; Rare:45 | ||||
| chr7:100049627-100050062 | Rare:132 | ||||
| chr7:100081692-100081991 | Common:2; Rare:79 | ||||
| chr7:100082576-100083050 | Rare:139 | ||||
| chr7:100088701-100089023 | Common:2; Rare:93 | ||||
| chr7:100100647-100100914 | Common:2; Rare:109 | ||||
| chr7:100101327-100101714 | Common:1; Rare:149; Clinvar (benign):1 | ||||
| chr7:100101855-100102074 | Common:1; Rare:94; Clinvar:1 |