chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1146032760146032761AG32GENIChomozygous108275324
1146033565146033566GA26GENIChomozygous108275326
1146034211146034212CT24GENIChomozygous108275328
1146035397146035398GA27GENIChomozygous108275332
1146035407146035408TA34GENIChomozygous108275334
1146035474146035475TC23GENIChomozygous108275336
1146035881146035882AG31GENIChomozygous108275338
1146036645146036646GA23GENIChomozygous120486607
1146037516146037517AT6GENIChomozygous108275340
1146037953146037954TA14GENIChomozygous108275342
1146038212146038213TC19GENIChomozygous108275344
1146038829146038830GA23GENIChomozygous108275346
1146039125146039126AG27GENIChomozygous108275348
1146039429146039430TC33GENIChomozygous108275350
1146039434146039435CT31GENIChomozygous108275352
1146039801146039802GA30GENIChomozygous108275354
1146042048146042049CT13GENIChomozygous108275358
1146042577146042578GA29GENIChomozygous108275360
1146042758146042759GA34GENIChomozygous108275362
1146042906146042907GC28GENIChomozygous108275364