Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71319203-71319288 | Common:2; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
chr10:71773474-71773666 | Common:2; Rare:60 | ||||
chr10:71851181-71851454 | Common:5; Rare:117; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216214-72216496 | Common:2; Rare:88 | ||||
chr10:72273575-72274047 | Rare:134 | ||||
chr10:72354886-72355217 | Common:2; Rare:119 | ||||
chr10:72626041-72626313 | Common:1; Rare:66 | ||||
chr10:72691960-72692154 | Rare:51 | ||||
chr10:73096754-73097131 | Common:5; Rare:108 | ||||
chr10:73110394-73110531 | Rare:28 | ||||
chr10:73167955-73168150 | Rare:49 | ||||
chr10:73252552-73252837 | Common:2; Rare:82; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73358739-73358888 | Common:2; Rare:37 | ||||
chr10:73414011-73414157 | Common:2; Rare:42 | ||||
chr10:73495565-73495790 | Rare:53 |