| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151028170-151028487 | Rare:114 | ||||
| chr7:151057856-151058154 | Common:3; Rare:88 | ||||
| chr7:151080785-151080962 | Rare:51 | ||||
| chr7:151227158-151227402 | Common:1; Rare:68 | ||||
| chr7:151232396-151232525 | Rare:41 | ||||
| chr7:152025567-152025802 | Rare:92 | ||||
| chr7:152676135-152676295 | Common:2; Rare:63 | ||||
| chr7:155644377-155644719 | Common:2; Rare:117 | ||||
| chr7:156640543-156640791 | Common:3; Rare:118 | ||||
| chr7:157336778-157337101 | Common:3; Rare:154; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158856424-158856710 | Common:7; Rare:102 | ||||
| chr8:232081-232162 | Rare:24 | ||||
| chr8:232176-232452 | Common:3; Rare:114 | ||||
| chr8:2127579-2127827 | Common:7; Rare:52 | ||||
| chr8:6406521-6406677 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):1 |