Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70816468-70816725 | Rare:47 | ||||
chr10:70888526-70888825 | Common:2; Rare:79; Clinvar:5; Clinvar (benign):2 | ||||
chr10:71851170-71851453 | Common:5; Rare:120; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216215-72216508 | Common:2; Rare:89 | ||||
chr10:72273901-72274460 | Common:3; Rare:189 | ||||
chr10:72354848-72355056 | Common:2; Rare:94 | ||||
chr10:72355127-72355337 | Common:1; Rare:43 | ||||
chr10:72626019-72626286 | Common:1; Rare:67 | ||||
chr10:73096761-73097033 | Common:3; Rare:81 | ||||
chr10:73167935-73168183 | Rare:72 | ||||
chr10:73252383-73252450 | Rare:25 | ||||
chr10:73252550-73252808 | Common:2; Rare:75; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73495595-73495771 | Rare:38 | ||||
chr10:73495800-73496052 | Common:2; Rare:75 | ||||
chr10:73576335-73576379 | Rare:6 |