| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107743579-107743806 | Common:3; Rare:89 | ||||
| chr7:107744053-107744233 | Rare:70 | ||||
| chr7:107929525-107929782 | Common:1; Rare:53; Clinvar:1 | ||||
| chr7:108001559-108001906 | Common:3; Rare:125; Clinvar:1 | ||||
| chr7:108526039-108526442 | Common:5; Rare:122 | ||||
| chr7:108569503-108570058 | Common:3; Rare:198 | ||||
| chr7:111090934-111091175 | Rare:46 | ||||
| chr7:112206375-112206817 | Common:1; Rare:166 | ||||
| chr7:112450287-112450616 | Common:4; Rare:98 | ||||
| chr7:112790282-112790460 | Rare:54 | ||||
| chr7:113086718-113086861 | Rare:28 | ||||
| chr7:116499417-116499827 | Common:3; Rare:137 | ||||
| chr7:116524413-116524751 | Rare:70 | ||||
| chr7:116524822-116525280 | Common:5; Rare:143; Clinvar (benign):2 | ||||
| chr7:116526181-116526684 | Common:3; Rare:139; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |