| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76302538-76303069 | Common:3; Rare:225; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76303751-76303999 | Common:2; Rare:127; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr7:77696133-77696467 | Common:1; Rare:124 | ||||
| chr7:77798261-77798756 | Common:2; Rare:91 | ||||
| chr7:79453781-79454070 | Common:2; Rare:73 | ||||
| chr7:80919008-80919111 | Rare:29 | ||||
| chr7:87059621-87059818 | Common:1; Rare:69 | ||||
| chr7:87345461-87345730 | Common:5; Rare:86 | ||||
| chr7:87876305-87876495 | Common:1; Rare:89 | ||||
| chr7:90211677-90211886 | Common:3; Rare:64 | ||||
| chr7:90595855-90596034 | Common:6; Rare:62 | ||||
| chr7:91880664-91880811 | Common:1; Rare:42 | ||||
| chr7:92528451-92528831 | Common:4; Rare:123; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:94394532-94395102 | Common:1; Rare:108; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:94656092-94656372 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):2 |