| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151080776-151080959 | Rare:54 | ||||
| chr7:151227158-151227425 | Common:1; Rare:73 | ||||
| chr7:151232385-151232537 | Common:1; Rare:52 | ||||
| chr7:151877158-151877535 | Common:2; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:152025579-152025798 | Rare:86 | ||||
| chr7:152435970-152436323 | Rare:123 | ||||
| chr7:152676083-152676280 | Common:2; Rare:81; Clinvar (benign):12 | ||||
| chr7:155644377-155644724 | Common:2; Rare:120 | ||||
| chr7:157336776-157337083 | Common:2; Rare:148; Clinvar:2 | ||||
| chr7:158704732-158704986 | Common:1; Rare:89 | ||||
| chr7:158856403-158856677 | Common:6; Rare:96 | ||||
| chr8:232181-232397 | Common:3; Rare:80 | ||||
| chr8:6406486-6406680 | Common:4; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708179-6708341 | Common:2; Rare:62 | ||||
| chr8:6708530-6708709 | Common:1; Rare:78 |