| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107744021-107744159 | Rare:44 | ||||
| chr7:108569590-108569958 | Common:1; Rare:134 | ||||
| chr7:116499458-116499802 | Common:3; Rare:109 | ||||
| chr7:134646582-134646856 | Common:6; Rare:77 | ||||
| chr7:135170689-135170973 | Common:5; Rare:91 | ||||
| chr7:155644398-155644667 | Common:2; Rare:82 | ||||
| chr8:6406552-6406661 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:17246841-17246982 | Common:1; Rare:56 | ||||
| chr8:23457626-23457806 | Common:2; Rare:62 | ||||
| chr8:26382942-26383108 | Rare:75 | ||||
| chr8:30095330-30095459 | Common:1; Rare:37 | ||||
| chr8:38176449-38176860 | Common:5; Rare:108 | ||||
| chr8:38996473-38996826 | Common:2; Rare:110 | ||||
| chr8:42541559-42541608 | Rare:14 | ||||
| chr8:42843311-42843527 | Common:3; Rare:61; Clinvar (benign):3 |