chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1233127354233127354A61GENIChomozygous127491174
1233141153233141154AG23GENIChomozygous108563601
1233141253233141254CG9GENIChomozygous121193428
1233141253233141253TTGGGGATTTA7GENIChomozygous127491175
1233141255233141256CT9GENIChomozygous121193429
1233141259233141260AT9GENIChomozygous121193430
1233144371233144372AG29GENICheterozygous132557455
1233144387233144388A34GENICheterozygous127491176
1233144417233144418T43GENICheterozygous130521149
1233144593233144594AG43GENICheterozygous121193441
1233144473233144474GT56GENICheterozygous108563603
1233144562233144563GA44GENICheterozygous108563605
1233144569233144570GC44GENICheterozygous108563607
1233144594233144595GT43GENICheterozygous121193442
1233144599233144600GA43GENICheterozygous108563616
1233144624233144625GT45GENICheterozygous108563618
1233144626233144627CT44GENICheterozygous108563620
1233144646233144647TG36GENICheterozygous108563622
1233144676233144683CCTAAGC40GENICheterozygous127491178
1233144700233144701TG38GENICheterozygous108563624
1233144716233144717C42GENICheterozygous127491179
1233144730233144730C41GENIChomozygous127491180
1233144756233144757TC43GENICheterozygous108563626
1233144771233144771TGATAA43GENICheterozygous127491181
1233144790233144791G48GENICheterozygous127491182
1233144799233144800AT47GENICheterozygous108563628
1233144810233144810C47GENIChomozygous127491183
1233144838233144839CT49GENICheterozygous108563630
1233144858233144859TG49GENICheterozygous108563631