chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5116994663116994664CT17GENIChomozygous113975358
5116994764116994765TC16GENIChomozygous113975359
5116997832116997833AG30GENIChomozygous113975360
5116998098116998099CT18GENIChomozygous113975361
5116999504116999505AT17GENIChomozygous113975362
5117002278117002279TC17GENIChomozygous113975363
5117002434117002435CT26GENIChomozygous113975364
5117003025117003026AG14GENIChomozygous113975365
5117004916117004917AG25GENICheterozygous113975366
5117005572117005573TC19GENIChomozygous113975367
5117012118117012119GA18GENIChomozygous113975368
5117013067117013068GA29GENIChomozygous113975369
5117016315117016316GA13GENICheterozygous113975371
5117018423117018424CT22GENIChomozygous113975372
5117019429117019430TC22GENIChomozygous113975373
5117020533117020534TA14GENIChomozygous113975374
5117021766117021767GT9GENIChomozygous113975375
5117021903117021904AG25GENIChomozygous113975376
5117022216117022217GA16GENIChomozygous113975377
5117022335117022336CG23GENICpossibly homozygous113975378
5117023440117023441AG24GENIChomozygous113975379
5117024967117024968GC15GENIChomozygous113975380
5117025707117025708AC15GENIChomozygous113975381
5117026027117026028AG9GENIChomozygous113975382
5117027173117027174AG22GENIChomozygous113975383
5117027368117027369CT23GENICheterozygous113975384
5117029471117029472GT13GENIChomozygous113975385
5117030657117030658AG17GENIChomozygous113975386
5117031236117031237CT32GENICheterozygous114134211
5117031450117031451TA16GENIChomozygous113975387
5117035055117035056AT23GENIChomozygous113975388
5117035745117035746AG13GENICpossibly homozygous113975389
5117036750117036751TC18GENIChomozygous113975390
5117037359117037360CT19GENIChomozygous113975391
5117037603117037604CT12GENIChomozygous113975392