Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:68157478-68157976 | Common:3; Rare:259 | ||||
chr2:68252491-68252804 | Common:3; Rare:97 | ||||
chr2:68467292-68467609 | Common:1; Rare:81 | ||||
chr2:71068538-71068675 | Rare:60 | ||||
chr2:71130220-71130367 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
chr2:74147821-74148141 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
chr2:74362650-74362994 | Common:3; Rare:95; Clinvar:5; Clinvar (benign):4 | ||||
chr2:74421639-74421768 | Rare:42 | ||||
chr2:74458097-74458528 | Common:1; Rare:131 | ||||
chr2:74503334-74503475 | Rare:36 | ||||
chr2:74529662-74530036 | Rare:110; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74554643-74554801 | Common:1; Rare:70 | ||||
chr2:74833922-74834133 | Rare:62 | ||||
chr2:74958726-74959073 | Common:1; Rare:132 | ||||
chr2:84905464-84905666 | Common:2; Rare:66 |