Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:72354287-72354783 | Common:2; Rare:116 | ||||
chr10:72354873-72355226 | Common:2; Rare:124 | ||||
chr10:72625993-72626276 | Common:1; Rare:63 | ||||
chr10:72691970-72692367 | Common:1; Rare:126 | ||||
chr10:72692417-72692574 | Rare:34 | ||||
chr10:73096102-73096390 | Common:1; Rare:80 | ||||
chr10:73096470-73096640 | Rare:58 | ||||
chr10:73096662-73096715 | Rare:8 | ||||
chr10:73096718-73096916 | Common:3; Rare:59 | ||||
chr10:73096932-73097219 | Common:2; Rare:79 | ||||
chr10:73110420-73110586 | Rare:37 | ||||
chr10:73110934-73111112 | Common:3; Rare:24 | ||||
chr10:73167556-73167755 | Common:1; Rare:26 | ||||
chr10:73167821-73168418 | Common:1; Rare:156 | ||||
chr10:73252346-73252498 | Common:2; Rare:50; Clinvar (benign):2 |