| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107891034-107891283 | Rare:112; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:107929063-107929496 | Common:3; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:107937123-107937404 | Rare:74; Clinvar (benign):1 | ||||
| chr7:108001705-108001806 | Common:1; Rare:49; Clinvar:1 | ||||
| chr7:108002886-108003289 | Common:1; Rare:126; Clinvar (benign):1 | ||||
| chr7:108526039-108526475 | Common:5; Rare:130 | ||||
| chr7:108569592-108570019 | Common:2; Rare:150 | ||||
| chr7:112206339-112206765 | Common:2; Rare:142 | ||||
| chr7:112450205-112450526 | Common:6; Rare:99 | ||||
| chr7:112939705-112940216 | Common:5; Rare:160 | ||||
| chr7:114086165-114086568 | Common:2; Rare:145 | ||||
| chr7:114087544-114087728 | Rare:52 | ||||
| chr7:114922238-114922530 | Common:2; Rare:90 | ||||
| chr7:116210193-116210731 | Common:4; Rare:133 | ||||
| chr7:116222835-116223018 | Common:2; Rare:33 |