chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5116994663116994664CT33GENIChomozygous113975358
5116994764116994765TC24GENIChomozygous113975359
5116997832116997833AG25GENIChomozygous113975360
5116998098116998099CT29GENIChomozygous113975361
5116999504116999505AT21GENIChomozygous113975362
5117002278117002279TC25GENICpossibly homozygous113975363
5117002434117002435CT26GENICpossibly homozygous113975364
5117003025117003026AG22GENIChomozygous113975365
5117005572117005573TC28GENIChomozygous113975367
5117010300117010301TA26GENIChomozygous118845044
5117010301117010302AC26GENIChomozygous118845045
5117012118117012119GA34GENICpossibly homozygous113975368
5117018423117018424CT31GENIChomozygous113975372
5117018993117018994CA11GENIChomozygous118936602
5117019032117019033CA12GENIChomozygous114134208
5117019429117019430TC33GENIChomozygous113975373
5117020533117020534TA25GENIChomozygous113975374
5117021766117021767GT19GENIChomozygous113975375
5117022216117022217GA20GENIChomozygous113975377
5117022335117022336CG12GENIChomozygous113975378
5117023440117023441AG20GENIChomozygous113975379
5117024967117024968GC20GENIChomozygous113975380
5117025707117025708AC28GENIChomozygous113975381
5117026027117026028AG22GENIChomozygous113975382
5117029471117029472GT33GENIChomozygous113975385
5117030657117030658AG12GENIChomozygous113975386
5117031450117031451TA22GENIChomozygous113975387
5117035055117035056AT25GENIChomozygous113975388
5117035745117035746AG24GENIChomozygous113975389
5117036750117036751TC19GENIChomozygous113975390
5117037359117037360CT13GENIChomozygous113975391