Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10032763-10032965 | Rare:53 | ||||
chr1:11099819-11100006 | Common:2; Rare:67 | ||||
chr1:11858848-11859139 | Rare:93 | ||||
chr1:12019215-12019532 | Common:5; Rare:110 | ||||
chr1:13749175-13749455 | Common:2; Rare:101 | ||||
chr1:15526578-15526905 | Common:2; Rare:104 | ||||
chr1:16352420-16352593 | Common:3; Rare:91 | ||||
chr1:16440557-16440757 | Common:1; Rare:54 | ||||
chr1:17053976-17054320 | Common:3; Rare:108; Clinvar:12; Clinvar (benign):10 | ||||
chr1:19210254-19210422 | Rare:66 | ||||
chr1:19251505-19251838 | Common:6; Rare:109 | ||||
chr1:19311982-19312333 | Common:8; Rare:163 | ||||
chr1:19485451-19485762 | Rare:116 | ||||
chr1:19596730-19597081 | Common:3; Rare:128 | ||||
chr1:20486201-20486360 | Rare:33 |