Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74147874-74148150 | Common:2; Rare:65; Clinvar:2 | ||||
chr2:74178834-74179066 | Common:3; Rare:72 | ||||
chr2:74421571-74421768 | Rare:67 | ||||
chr2:74454792-74455123 | Rare:81 | ||||
chr2:74483019-74483098 | Rare:33 | ||||
chr2:74507672-74507795 | Rare:25 | ||||
chr2:74529665-74529964 | Rare:87; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74553941-74554142 | Rare:43 | ||||
chr2:74958448-74958656 | Common:2; Rare:66 | ||||
chr2:75710669-75710990 | Common:3; Rare:137 | ||||
chr2:85327945-85328066 | Common:1; Rare:57 | ||||
chr2:85354526-85354775 | Common:1; Rare:81 | ||||
chr2:85595555-85595762 | Common:2; Rare:64 | ||||
chr2:85612030-85612098 | Rare:18 | ||||
chr2:86105866-86105942 | Common:1; Rare:17 |