chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7108301687108301688TC55GENIChomozygous138177686
7108302002108302003CT58GENIChomozygous138177687
7108302141108302142GA57GENIChomozygous138177688
7108303510108303511AG54GENIChomozygous138177689
7108304764108304765GA43GENIChomozygous138177690
7108305330108305331CT48GENIChomozygous138177691
7108305407108305408AG37GENIChomozygous138177692
7108305558108305559GA36GENIChomozygous138177693
7108305755108305756TC41GENIChomozygous138177694
7108307703108307704GC20GENIChomozygous143365095
7108308454108308455AT52GENIChomozygous138177695
7108308469108308470TA49GENIChomozygous138177696
7108309283108309283T32GENICheterozygous137973304
7108311534108311535G42GENIChomozygous137973305
7108311927108311928GC48GENIChomozygous138177697
7108312093108312094AG51GENIChomozygous138177698
7108312844108312844CCTTGGGTAGGAGCAGCA58GENIChomozygous137973306
7108312850108312851CG56GENIChomozygous138177699
7108313484108313485GA48GENIChomozygous138177700
7108313546108313547AT57GENIChomozygous138177701
7108316041108316042CT50GENIChomozygous138177702
7108317309108317309G44GENIChomozygous137973307
7108317738108317739CA48GENIChomozygous138177703
7108317862108317863TC50GENIChomozygous138177704
7108317974108317975CT57GENIChomozygous138177705
7108318304108318305TG72GENIChomozygous138177706
7108319088108319089GA61GENIChomozygous138177707
7108319239108319240GA49GENIChomozygous138177708