| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:88220022-88220103 | Rare:47 | ||||
| chr7:88306886-88306997 | Rare:18 | ||||
| chr7:90346501-90346750 | Common:4; Rare:102 | ||||
| chr7:91880675-91880801 | Common:1; Rare:34 | ||||
| chr7:92134372-92134580 | Rare:68 | ||||
| chr7:92134709-92134900 | Common:3; Rare:57 | ||||
| chr7:92245849-92246516 | Common:6; Rare:221; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528402-92528816 | Common:3; Rare:130; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590046-92590123 | Rare:31 | ||||
| chr7:92836445-92836498 | Rare:9 | ||||
| chr7:93232201-93232389 | Common:2; Rare:34 | ||||
| chr7:93890730-93890944 | Common:2; Rare:49 | ||||
| chr7:93921841-93922112 | Common:4; Rare:66 | ||||
| chr7:94425713-94426070 | Rare:103; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr7:94656118-94656387 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 |