| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91880655-91880834 | Common:2; Rare:49 | ||||
| chr7:91940771-91941091 | Common:4; Rare:102; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134346-92134603 | Rare:78 | ||||
| chr7:92134721-92134891 | Common:3; Rare:51 | ||||
| chr7:92447251-92447516 | Common:3; Rare:80 | ||||
| chr7:92528305-92528826 | Common:4; Rare:156; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833902-92834074 | Rare:43 | ||||
| chr7:93148333-93148418 | Rare:11 | ||||
| chr7:93232186-93232417 | Common:2; Rare:50 | ||||
| chr7:93890725-93890864 | Common:2; Rare:40 | ||||
| chr7:93921656-93922188 | Common:7; Rare:127 | ||||
| chr7:94394545-94395050 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:94425748-94426060 | Rare:93; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:94656049-94656387 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:94908384-94908559 | Rare:34 |