chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8131995314131995315GA28GENICheterozygous53066628
8131996359131996360GA48GENICheterozygous53066630
8131996489131996490CT34GENICheterozygous53066632
8131996654131996655GA21GENICheterozygous53066633
8131996749131996750CG25GENICheterozygous53066634
8131996877131996878CT31GENICheterozygous53066635
8131997169131997170TC27GENICheterozygous52900450
8131997409131997410GT16GENICheterozygous53066636
8131997461131997462CT19GENICheterozygous53066637
8131997633131997634A-21GENICheterozygous52900456
8131997936131997937A-23GENICheterozygous52900458
8131997939131997940AG22GENICheterozygous53369847
8131997962131997963AG20GENICheterozygous52900460
8132000104132000105TC13GENICheterozygous53066643
8132006021132006022GA26GENICheterozygous53066662
8132006160132006161AG36GENICheterozygous53066663
8132006179132006180CA38GENICheterozygous53066664
8132006183132006184AG37GENICheterozygous53066665
8132006231132006232TG16GENICheterozygous54475389
8132006232132006233TG14GENICheterozygous54475392
8132006233132006234TG14GENICheterozygous54475395
8132006235132006236AG15GENICheterozygous54475398
8132006252132006253CT32GENICheterozygous53066669
8132006283132006285AG--39GENICheterozygous53066670
8132006404132006405CA44GENICheterozygous53066671
8132006591132006592AG34GENICheterozygous53066672
8132006849132006850TC40GENICheterozygous53066673
8132007383132007384CT74GENICheterozygous53066675
8132007429132007430AT75GENICheterozygous53066676
8132035526132035527GA33GENICheterozygous53066762
8132038781132038782AC15GENICheterozygous53066770
8132039173132039174GA11GENICheterozygous54757144
8132040014132040015TC16GENICheterozygous52900557
8132041253132041254GA25GENICheterozygous53066772
8132042100132042101CT11GENICheterozygous53066776
8132049541132049542CT16GENICheterozygous53066789
8132052247132052248AT16GENICheterozygous53066792
8132053844132053845TG18GENICheterozygous53066796
8132061852132061853GA10GENICheterozygous53066808