| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:104991759-104991984 | Common:1; Rare:32 | ||||
| chr7:104993210-104993216 | Rare:1 | ||||
| chr7:105000958-105000985 | Rare:5 | ||||
| chr7:105008829-105008932 | Common:1; Rare:21 | ||||
| chr7:105012666-105012776 | Rare:34 | ||||
| chr7:105013000-105013207 | Common:1; Rare:72 | ||||
| chr7:105106927-105107220 | Common:2; Rare:71 | ||||
| chr7:107192677-107192793 | Rare:23 | ||||
| chr7:107763984-107764265 | Common:3; Rare:46 | ||||
| chr7:107766916-107767219 | Rare:44 | ||||
| chr7:107770505-107770882 | Rare:72 | ||||
| chr7:107773918-107774444 | Common:1; Rare:131; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:107778040-107778360 | Common:1; Rare:77 | ||||
| chr7:107782668-107782884 | Common:1; Rare:58; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:107782961-107783360 | Common:1; Rare:110; Clinvar (benign):1; Clinvar (pathogenic):2 |