Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71819463-71819902 | Common:1; Rare:173; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71851151-71851514 | Common:5; Rare:137; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:71964302-71964556 | Common:4; Rare:67; Clinvar:1; Clinvar (benign):3 | ||||
chr10:72216215-72216374 | Rare:67 | ||||
chr10:72273571-72273643 | Rare:19 | ||||
chr10:72273693-72274041 | Rare:106 | ||||
chr10:72354841-72355176 | Common:2; Rare:120 | ||||
chr10:72626026-72626279 | Common:1; Rare:63 | ||||
chr10:73096751-73097028 | Common:4; Rare:83 | ||||
chr10:73097054-73097153 | Common:1; Rare:22 | ||||
chr10:73167907-73168270 | Rare:95 | ||||
chr10:73252552-73252791 | Common:2; Rare:69; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73358728-73358882 | Common:2; Rare:39 | ||||
chr10:73495606-73495776 | Rare:39 | ||||
chr10:73495824-73496050 | Common:2; Rare:70 |