Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70888531-70888649 | Common:1; Rare:41; Clinvar:5; Clinvar (benign):1 | ||||
chr10:71319156-71319291 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
chr10:71819463-71819801 | Common:1; Rare:128; Clinvar:4; Clinvar (benign):2 | ||||
chr10:71851204-71851464 | Common:5; Rare:110; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216244-72216408 | Rare:64 | ||||
chr10:72273680-72273942 | Rare:71 | ||||
chr10:72354556-72354730 | Rare:54 | ||||
chr10:72354881-72355217 | Common:2; Rare:119 | ||||
chr10:72626041-72626279 | Common:1; Rare:58 | ||||
chr10:73096764-73097024 | Common:3; Rare:80 | ||||
chr10:73097039-73097194 | Common:1; Rare:46 | ||||
chr10:73110473-73110524 | Rare:12 | ||||
chr10:73167921-73168270 | Rare:91 | ||||
chr10:73252552-73252829 | Common:2; Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73358728-73358897 | Common:2; Rare:45 |