Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:72996709-72997030 | Common:2; Rare:120 | ||||
chr3:87227186-87227373 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
chr3:88058932-88059279 | Common:3; Rare:118 | ||||
chr3:88149591-88149999 | Common:1; Rare:106 | ||||
chr3:94062920-94063040 | Rare:33 | ||||
chr3:97764448-97764755 | Rare:70 | ||||
chr3:98522855-98523120 | Common:1; Rare:78 | ||||
chr3:99638395-99638661 | Common:1; Rare:66 | ||||
chr3:99817777-99817925 | Rare:49 | ||||
chr3:99876126-99876254 | Rare:32 | ||||
chr3:100260688-100261021 | Rare:89 | ||||
chr3:100401402-100401580 | Common:1; Rare:33 | ||||
chr3:100492434-100492619 | Common:2; Rare:64 | ||||
chr3:100709203-100709718 | Common:9; Rare:155; Clinvar (benign):1 | ||||
chr3:101686666-101686870 | Common:2; Rare:84 |