| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143380905-143381021 | Rare:28 | ||||
| chr7:148698602-148698934 | Common:1; Rare:118 | ||||
| chr7:151028149-151028469 | Rare:104 | ||||
| chr7:151080792-151080964 | Rare:52 | ||||
| chr7:155644384-155644691 | Common:2; Rare:98 | ||||
| chr7:157336938-157337075 | Common:1; Rare:65; Clinvar:1 | ||||
| chr7:158704774-158705125 | Common:1; Rare:117 | ||||
| chr8:6406543-6406661 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:11802440-11802782 | Common:6; Rare:183 | ||||
| chr8:17246826-17246982 | Common:1; Rare:63 | ||||
| chr8:22245026-22245183 | Common:1; Rare:76 | ||||
| chr8:22604547-22604802 | Common:1; Rare:90 | ||||
| chr8:23457632-23457782 | Common:2; Rare:55 | ||||
| chr8:23528562-23528903 | Rare:88 | ||||
| chr8:24956085-24956187 | Rare:32; Clinvar (benign):1; Clinvar (pathogenic):1 |