Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:73385647-73386076 | Common:4; Rare:201; Clinvar:16; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr2:74147862-74148150 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74178784-74179066 | Common:4; Rare:85 | ||||
chr2:74440425-74440679 | Rare:69 | ||||
chr2:74459691-74459974 | Rare:102 | ||||
chr2:74465350-74465440 | Rare:25; Clinvar:1 | ||||
chr2:74482897-74483129 | Common:1; Rare:84 | ||||
chr2:74529668-74530036 | Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74554662-74554769 | Common:1; Rare:50 | ||||
chr2:74958497-74958677 | Common:3; Rare:64 | ||||
chr2:74958876-74959011 | Rare:53 | ||||
chr2:75199513-75199696 | Rare:33 | ||||
chr2:84459185-84459574 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:85327915-85328056 | Common:1; Rare:65 | ||||
chr2:85354518-85354790 | Common:1; Rare:90 |