Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:93893630-93894366 | Common:6; Rare:443 | ||||
chr10:94362690-94363220 | Common:25; Rare:534 | ||||
chr10:94402101-94402620 | Rare:564 | ||||
chr10:94402700-94402831 | Common:2; Rare:54 | ||||
chr10:94402808-94403208 | Common:1; Rare:123 | ||||
chr10:94545097-94545966 | Common:22; Rare:581 | ||||
chr10:95290524-95290808 | Common:2; Rare:65 | ||||
chr10:95290865-95291186 | Common:8; Rare:401 | ||||
chr10:95493339-95493740 | Common:6; Rare:164 | ||||
chr10:95561289-95561706 | Common:22; Rare:515 | ||||
chr10:95656610-95657080 | Common:3; Rare:401; Clinvar:23; Clinvar (benign):6 | ||||
chr10:95693790-95694252 | Common:15; Rare:350; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr10:95755440-95755710 | Common:1; Rare:43 | ||||
chr10:95907042-95907822 | Common:9; Rare:252 | ||||
chr10:95907813-95907927 | Common:2; Rare:60 |