| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:155003409-155003474 | Common:3; Rare:40 | ||||
| chr7:155644357-155644724 | Common:2; Rare:129 | ||||
| chr7:156640556-156640816 | Common:3; Rare:118 | ||||
| chr7:157336776-157337085 | Common:2; Rare:149; Clinvar:2 | ||||
| chr7:158704737-158704961 | Common:1; Rare:77 | ||||
| chr7:158856423-158856695 | Common:7; Rare:97 | ||||
| chr8:232181-232377 | Common:3; Rare:74 | ||||
| chr8:406704-406992 | Common:4; Rare:139 | ||||
| chr8:6406485-6406679 | Common:4; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:9150626-9150806 | Common:1; Rare:61 | ||||
| chr8:10839783-10840094 | Common:2; Rare:106 | ||||
| chr8:11284719-11284861 | Common:2; Rare:59 | ||||
| chr8:11769569-11769728 | Common:4; Rare:64 | ||||
| chr8:11802429-11802835 | Common:6; Rare:226 | ||||
| chr8:11849097-11849262 | Common:1; Rare:79 |