| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151059537-151059690 | Rare:43 | ||||
| chr7:151080793-151081122 | Common:2; Rare:101 | ||||
| chr7:151227158-151227446 | Common:1; Rare:79 | ||||
| chr7:151232419-151232528 | Rare:35 | ||||
| chr7:151876715-151876849 | Rare:39 | ||||
| chr7:151876884-151877835 | Common:6; Rare:235; Clinvar:7; Clinvar (benign):1 | ||||
| chr7:152025583-152025802 | Rare:87 | ||||
| chr7:152435718-152435798 | Common:1; Rare:27 | ||||
| chr7:155644359-155644836 | Common:4; Rare:158 | ||||
| chr7:156640541-156640685 | Common:3; Rare:76 | ||||
| chr7:157336749-157337108 | Common:3; Rare:171; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158704784-158704965 | Common:1; Rare:62 | ||||
| chr7:158856423-158856696 | Common:7; Rare:97 | ||||
| chr8:232174-232480 | Common:3; Rare:128 | ||||
| chr8:406717-407018 | Common:4; Rare:143 |