| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:149239464-149239685 | Common:1; Rare:49 | ||||
| chr7:151008828-151008951 | Common:1; Rare:46 | ||||
| chr7:151057856-151058137 | Common:3; Rare:80 | ||||
| chr7:151080793-151080920 | Rare:41 | ||||
| chr7:151232382-151232499 | Common:1; Rare:29 | ||||
| chr7:155644377-155644724 | Common:2; Rare:120 | ||||
| chr7:157336770-157337073 | Common:2; Rare:147; Clinvar:1 | ||||
| chr7:158856299-158856701 | Common:9; Rare:130 | ||||
| chr8:232223-232403 | Common:2; Rare:69 | ||||
| chr8:731156-731464 | Common:3; Rare:121 | ||||
| chr8:2127633-2127804 | Common:7; Rare:37 | ||||
| chr8:6406529-6406680 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:8822057-8822288 | Common:4; Rare:65 | ||||
| chr8:9555660-9555928 | Common:6; Rare:100 | ||||
| chr8:10839819-10839972 | Rare:61 |