chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8110604182110604183CA23GENIChomozygous52802111
8110604922110604923AC26GENIChomozygous52802117
8110605180110605181CT18GENIChomozygous52802121
8110605702110605703TC22GENIChomozygous52802123
8110606000110606001CT33GENIChomozygous52802125
8110606135110606136CT11GENIChomozygous53327967
8110606279110606280GA13GENIChomozygous53327968
8110606443110606444GGCACA20GENICpossibly homozygous52802127
8110606913110606914CG27GENIChomozygous53327969
8110607573110607574TC20GENIChomozygous53034413
8110607598110607700AATCTACTCTCTTTTTTTTTTTTCCTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC------------------------------------------------------------------------------------------------------30GENIChomozygous53367571
8110607987110607988TC21GENIChomozygous53327970
8110608270110608271GGT16GENIChomozygous53409054
8110608377110608378TTGTGTGC18GENICheterozygous53409056
8110608377110608378TTGTGTGTGC18GENICpossibly homozygous53409058
8110608578110608579AG31GENIChomozygous53034431
8110608653110608654TC28GENIChomozygous53034433
8110609114110609115GA29GENIChomozygous53327972
8110609559110609560TG28GENIChomozygous53034439
8110609667110609668GA34GENIChomozygous53327973
8110609725110609726TA34GENIChomozygous53034441
8110610099110610100CT32GENICpossibly homozygous53327974
8110610614110610616CA--7GENIChomozygous53034445
8110610787110610788AG40GENIChomozygous53034447
8110611165110611166GA24GENIChomozygous53327975
8110611717110611718GA19GENIChomozygous53327976
8110612227110612228GT24GENIChomozygous53034451
8110612746110612747AG35GENIChomozygous53034453
8110613298110613299TC20GENIChomozygous53034455
8110613487110613488TC16GENIChomozygous53034457
8110613563110613564TG26GENIChomozygous53034459
8110615410110615411GGC27GENIChomozygous52802156
8110616082110616083CT47GENIChomozygous53034465
8110616432110616433TC37GENIChomozygous53327977