| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151341578-151341874 | Common:5; Rare:94 | ||||
| chr7:151409948-151410141 | Rare:52 | ||||
| chr7:152676081-152676270 | Common:2; Rare:77; Clinvar (benign):12 | ||||
| chr7:155644377-155644719 | Common:2; Rare:117 | ||||
| chr7:156640554-156640791 | Common:2; Rare:111 | ||||
| chr7:157336749-157337093 | Common:3; Rare:165; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158704729-158704943 | Common:1; Rare:76 | ||||
| chr7:158856401-158856676 | Common:6; Rare:96 | ||||
| chr8:232223-232377 | Common:2; Rare:61 | ||||
| chr8:731159-731444 | Common:3; Rare:112 | ||||
| chr8:6406507-6406688 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708165-6708347 | Common:2; Rare:70 | ||||
| chr8:6835501-6835552 | Rare:26 | ||||
| chr8:10839824-10839966 | Rare:56 | ||||
| chr8:11284746-11284861 | Common:2; Rare:53 |