| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:26170304-26170348 | Rare:4 | ||||
| chr1:26233911-26234281 | Common:3; Rare:111 | ||||
| chr1:26234383-26234551 | Common:2; Rare:57 | ||||
| chr1:26279588-26279770 | Common:1; Rare:51 | ||||
| chr1:26279910-26280177 | Rare:150 | ||||
| chr1:26306550-26306864 | Common:13; Rare:95 | ||||
| chr1:26336870-26336923 | Rare:15 | ||||
| chr1:26431853-26431995 | Rare:30 | ||||
| chr1:26432050-26432449 | Common:5; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:26471957-26472640 | Common:6; Rare:212 | ||||
| chr1:26472735-26473244 | Common:2; Rare:208 | ||||
| chr1:26529561-26529815 | Common:3; Rare:85 | ||||
| chr1:26695567-26696057 | Common:1; Rare:160 | ||||
| chr1:26696060-26696170 | Rare:25 | ||||
| chr1:26696439-26696650 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):4 |