Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73247128-73247478 | Rare:178 | ||||
chr10:73413124-73413440 | Common:4; Rare:69 | ||||
chr10:73647460-73647821 | Common:1; Rare:130 | ||||
chr10:73729943-73730044 | Common:1; Rare:23 | ||||
chr10:73730205-73730314 | Rare:19 | ||||
chr10:73730384-73730813 | Common:3; Rare:88 | ||||
chr10:73786233-73786499 | Common:1; Rare:71 | ||||
chr10:73804034-73804177 | Rare:43 | ||||
chr10:73810597-73810822 | Rare:46 | ||||
chr10:73865770-73866117 | Common:1; Rare:56 | ||||
chr10:73875179-73875392 | Rare:52 | ||||
chr10:73940682-73940786 | Common:1; Rare:31 | ||||
chr10:73956637-73956860 | Common:1; Rare:25 | ||||
chr10:73960097-73960142 | Rare:8 | ||||
chr10:74117786-74118059 | Rare:54; Clinvar:1; Clinvar (benign):1 |