Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74147821-74148039 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
chr2:74362656-74363002 | Common:3; Rare:96; Clinvar:5; Clinvar (benign):4 | ||||
chr2:74421629-74421762 | Rare:43 | ||||
chr2:74465353-74465439 | Rare:22 | ||||
chr2:74503340-74503481 | Rare:34 | ||||
chr2:74529649-74530037 | Rare:121; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74553941-74554160 | Rare:47 | ||||
chr2:74833795-74834147 | Common:1; Rare:107 | ||||
chr2:74958721-74959079 | Common:1; Rare:135 | ||||
chr2:75710689-75710802 | Common:1; Rare:51 | ||||
chr2:84459179-84459572 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:84905482-84905697 | Common:2; Rare:69 | ||||
chr2:85354550-85354799 | Common:1; Rare:75 | ||||
chr2:85561421-85561571 | Rare:55; Clinvar:4 | ||||
chr2:85595565-85595760 | Common:1; Rare:60 |