chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120950457120950458TC59GENIChomozygous115857546
7120950613120950614GA35GENIChomozygous115857548
7120951346120951347CT32GENIChomozygous115857550
7120953218120953219AG48GENIChomozygous115857552
7120953358120953359GA45GENIChomozygous115857554
7120953370120953371TG48GENIChomozygous115857556
7120954698120954699CG52GENIChomozygous115857558
7120954749120954750TC49GENIChomozygous115857560
7120955571120955572CT53GENIChomozygous115857562
7120956111120956112TG49GENIChomozygous115857564
7120956295120956296TC43GENIChomozygous115857566
7120956401120956402GA38GENIChomozygous115857568
7120956503120956504GA44GENIChomozygous115857570
7120956673120956674GC49GENIChomozygous115857572
7120956918120956919CT59GENICpossibly homozygous115857574
7120957744120957745TC68GENIChomozygous115857576
7120957943120957944CT55GENIChomozygous115857578
7120959317120959318CT54GENIChomozygous115857580
7120959595120959596AG54GENICheterozygous115857582
7120959599120959600AG54GENICheterozygous115857584
7120959649120959650TC57GENICpossibly homozygous115857586
7120960257120960258AT49GENIChomozygous115857588
7120960461120960462AG45GENIChomozygous115857590
7120960482120960483AG64GENICheterozygous115857592
7120960616120960617GA59GENIChomozygous115857594
7120960771120960772TC57GENIChomozygous115857596
7120961204120961205AG43GENIChomozygous115857598
7120961270120961271CA47GENIChomozygous115857600
7120961572120961573CT54GENIChomozygous115857602
7120961842120961843TA56GENIChomozygous115857604
7120962172120962173TC56GENIChomozygous115857606
7120962772120962773CT61GENIChomozygous115857608
7120963341120963342CT34GENICpossibly homozygous115857610
7120963451120963452GA43GENIChomozygous115857612
7120963534120963535GT53GENIChomozygous115857614
7120963644120963645AG58GENIChomozygous115857617
7120964005120964006GT54GENIChomozygous115857619
7120964006120964007GT54GENIChomozygous115857621
7120964740120964741CT59GENIChomozygous115857623
7120967335120967336CG29GENIChomozygous115857625