| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:90346583-90346728 | Common:3; Rare:59 | ||||
| chr7:91880656-91880815 | Common:1; Rare:46 | ||||
| chr7:92528475-92528816 | Common:3; Rare:106; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:96709812-96709920 | Rare:30 | ||||
| chr7:97117495-97117711 | Rare:77 | ||||
| chr7:99325801-99325963 | Common:1; Rare:64 | ||||
| chr7:99408545-99409032 | Common:3; Rare:139 | ||||
| chr7:99438755-99438996 | Common:1; Rare:69 | ||||
| chr7:99466137-99466254 | Rare:41 | ||||
| chr7:99558541-99558701 | Common:2; Rare:54 | ||||
| chr7:99616833-99616970 | Common:2; Rare:43 | ||||
| chr7:100088905-100089015 | Common:1; Rare:39 | ||||
| chr7:100101335-100101677 | Common:1; Rare:129 | ||||
| chr7:100119352-100119667 | Rare:91 | ||||
| chr7:100852622-100852709 | Rare:26 |