Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:71130215-71130680 | Common:6; Rare:133; Clinvar:1; Clinvar (benign):2 | ||||
chr2:71453466-71453907 | Common:3; Rare:82 | ||||
chr2:72144416-72144710 | Common:4; Rare:65 | ||||
chr2:73828916-73829024 | Rare:30 | ||||
chr2:74147866-74148149 | Common:1; Rare:71; Clinvar:2 | ||||
chr2:74421629-74421756 | Rare:42 | ||||
chr2:74465352-74465439 | Rare:22 | ||||
chr2:74482928-74483098 | Common:1; Rare:58 | ||||
chr2:74507664-74507775 | Rare:23 | ||||
chr2:74529607-74530036 | Rare:141; Clinvar:4; Clinvar (benign):1 | ||||
chr2:74530433-74530616 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74554406-74554761 | Common:2; Rare:107 | ||||
chr2:74958877-74959024 | Rare:55 | ||||
chr2:75710669-75710778 | Common:2; Rare:42 | ||||
chr2:75710872-75710990 | Common:1; Rare:42 |