Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179081962-179082070 | Common:1; Rare:32 | ||||
chr1:179882023-179882311 | Common:3; Rare:66 | ||||
chr1:179882537-179882834 | Rare:148; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179954755-179954817 | Rare:18 | ||||
chr1:181088494-181088733 | Rare:88 | ||||
chr1:182391269-182391480 | Rare:45 | ||||
chr1:182789642-182789778 | Common:2; Rare:44 | ||||
chr1:183590650-183591064 | Common:5; Rare:68 | ||||
chr1:183635659-183635850 | Common:1; Rare:59 | ||||
chr1:184387228-184387368 | Rare:24 | ||||
chr1:185156923-185157303 | Common:1; Rare:105 | ||||
chr1:185301135-185301446 | Common:1; Rare:67 | ||||
chr1:186375104-186375488 | Rare:111 | ||||
chr1:186375557-186375899 | Common:1; Rare:100 | ||||
chr1:193059328-193059732 | Rare:190 |