chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191064436510644366TC18GENICheterozygous46059620
191064446910644470GA14GENICheterozygous46279896
191064451610644517CT13GENICheterozygous46059621
191064470510644706GA7GENICheterozygous46059625
191064497310644974CT6GENICheterozygous46059626
191064511110645112TC10GENICheterozygous46059628
191064512910645130GA10GENICheterozygous46059629
191064519710645198AG11GENICheterozygous46059630
191064520210645203TA10GENICheterozygous46279897
191064528010645281GA11GENICheterozygous46279898
191064567010645671CT14GENICheterozygous46059631
191064604110646042CG16GENICheterozygous46279899
191064605710646058CT16GENICheterozygous46059632
191064621610646217TC13GENIChomozygous46059633
191064637710646378GA13GENICheterozygous46059638
191064673710646738TC12GENIChomozygous46059639
191064674510646746TA13GENIChomozygous46059640
191064767110647672TC7GENICheterozygous46059644
191064768010647681TC8GENICheterozygous46059645
191064782310647824CT15GENICheterozygous46279901
191065019110650192AT14INTERGENICheterozygous46279902
191065067210650673CCT8INTERGENICheterozygous46279904
191065129610651297AC8INTERGENIChomozygous46059650
191065216110652162AG16INTERGENICheterozygous46279907
191065223210652233TG12INTERGENICheterozygous46059658
191065257810652579CA23INTERGENICheterozygous46059659
191065306210653063GA12INTERGENICheterozygous46059660
191065337710653378CA12INTERGENICheterozygous46059662
191065453910654540GA26INTERGENICheterozygous46279908
191065193610651960CTTGCTTGCTTTCTTTCTTTCTTT------------------------10INTERGENICheterozygous46458626