| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:94656055-94656587 | Common:2; Rare:87; Clinvar:4; Clinvar (benign):3 | ||||
| chr7:94908384-94908551 | Rare:30 | ||||
| chr7:94908590-94908774 | Common:2; Rare:44 | ||||
| chr7:95434899-95435088 | Common:1; Rare:86; Clinvar (benign):1 | ||||
| chr7:97005064-97005160 | Common:1; Rare:12 | ||||
| chr7:97005350-97005919 | Common:1; Rare:146 | ||||
| chr7:97006119-97006227 | Common:1; Rare:56 | ||||
| chr7:97024354-97024532 | Rare:62 | ||||
| chr7:97024543-97025001 | Common:1; Rare:107 | ||||
| chr7:97117441-97117824 | Common:2; Rare:169 | ||||
| chr7:97731880-97732752 | Common:3; Rare:175 | ||||
| chr7:97733482-97733677 | Common:2; Rare:46 | ||||
| chr7:97733684-97734077 | Rare:102 | ||||
| chr7:97872106-97872224 | Rare:40 | ||||
| chr7:97872391-97872605 | Common:2; Rare:66 |