| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87039826-87039994 | Common:3; Rare:54 | ||||
| chr7:87040211-87040355 | Common:1; Rare:44 | ||||
| chr7:91267685-91267915 | Rare:38 | ||||
| chr7:91365068-91365306 | Common:1; Rare:40 | ||||
| chr7:94183412-94183744 | Common:4; Rare:61 | ||||
| chr7:94374201-94374464 | Common:2; Rare:40 | ||||
| chr7:94392160-94392316 | Common:2; Rare:20 | ||||
| chr7:94404552-94404893 | Rare:86; Clinvar:7; Clinvar (pathogenic):1 | ||||
| chr7:94409318-94409822 | Common:4; Rare:136; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr7:94410207-94410526 | Common:1; Rare:72; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr7:94420194-94420665 | Rare:131; Clinvar:4; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr7:96321327-96321549 | Common:2; Rare:56 | ||||
| chr7:100335862-100336146 | Common:1; Rare:94 | ||||
| chr7:100344909-100345026 | Rare:29 | ||||
| chr7:101121970-101122219 | Rare:35 |