chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84731952847319529TC29GENIChomozygous53181713
84731972547319726CT34GENIChomozygous53109389
84731989147319892CT23GENIChomozygous53181714
84731992347319924TC20GENIChomozygous53181715
84731993147319932TC17GENIChomozygous53109390
84732061447320615GA18GENIChomozygous53181716
84732076047320761GT41GENIChomozygous53181717
84732151947321526GTGATAG-------24GENIChomozygous53181718
84732202847322029GT28GENICheterozygous53181719
84732203047322031AT28GENICheterozygous53181720
84732203247322033GA28GENICheterozygous53181721
84732227447322275CT29GENIChomozygous53181722
84732309247323093TC25GENIChomozygous53181723
84732357247323573GA32GENIChomozygous53181724
84732358447323585CT30GENIChomozygous53181725
84732446147324462CT33GENIChomozygous53181726
84732629547326296CT34GENIChomozygous53181727
84732697547326976AG33GENIChomozygous53181728
84732839547328396AG29GENIChomozygous53181729
84732867747328678AG18GENIChomozygous53181730
84732948947329490TC21GENIChomozygous53181731
84732993547329936GA22GENIChomozygous53181732
84733015047330151TA23GENIChomozygous53181733
84733029447330295AG27GENIChomozygous53181734