| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:88220003-88220131 | Rare:67 | ||||
| chr7:90211614-90211920 | Common:4; Rare:93 | ||||
| chr7:90245083-90245253 | Common:1; Rare:55 | ||||
| chr7:90346603-90346733 | Common:3; Rare:58 | ||||
| chr7:91880668-91880801 | Common:1; Rare:36 | ||||
| chr7:92134442-92134558 | Rare:31 | ||||
| chr7:92245849-92245970 | Rare:35; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528371-92528816 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93232201-93232394 | Common:2; Rare:34 | ||||
| chr7:94394550-94394995 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:94425748-94426043 | Rare:91; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:94656118-94656380 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95434924-95435097 | Common:1; Rare:84; Clinvar (benign):1 | ||||
| chr7:95596507-95596699 | Common:2; Rare:38 | ||||
| chr7:96321994-96322379 | Rare:137; Clinvar:4 |