| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:157010632-157010926 | Common:5; Rare:89 | ||||
| chr7:157138660-157138966 | Common:1; Rare:88 | ||||
| chr7:157336918-157337083 | Common:1; Rare:78; Clinvar:2 | ||||
| chr7:158704732-158704986 | Common:1; Rare:89 | ||||
| chr7:158856423-158856765 | Common:7; Rare:127 | ||||
| chr8:232196-232448 | Common:2; Rare:101 | ||||
| chr8:406707-406999 | Common:4; Rare:139 | ||||
| chr8:1973561-1973923 | Common:4; Rare:155 | ||||
| chr8:6406527-6406668 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6563216-6563307 | Common:1; Rare:20 | ||||
| chr8:6708179-6708373 | Common:3; Rare:78 | ||||
| chr8:6925849-6925973 | Common:4; Rare:67 | ||||
| chr8:8386420-8386552 | Common:2; Rare:57 | ||||
| chr8:8701881-8702197 | Common:6; Rare:104 | ||||
| chr8:9150349-9150734 | Common:2; Rare:122 |