chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3119583959119583960TC28GENIChomozygous112024604
3119584367119584368GC18GENIChomozygous112142598
3119584728119584729CT20GENIChomozygous112142599
3119585155119585156AG20GENIChomozygous112142600
3119585873119585874GC20GENIChomozygous112024610
3119585901119585902TC21GENIChomozygous112024614
3119585902119585903GA20GENIChomozygous112024616
3119585983119585984C30GENIChomozygous132587620
3119585029119585030G16GENIChomozygous132587617
3119585288119585289C13GENIChomozygous132587618
3119585907119585910AGT20GENIChomozygous132587619
3119589167119589168GA19GENIChomozygous112142601
3119589274119589275AG12GENIChomozygous111688073
3119590626119590627AG17GENIChomozygous111688074
3119590777119590778CT25GENIChomozygous112142602
3119591292119591293CT26GENIChomozygous112142603
3119591471119591472GA8GENIChomozygous111688075
3119591729119591730A11GENIChomozygous132587621
3119593436119593437AG16GENIChomozygous111688076
3119593764119593765GA15GENIChomozygous112142604
3119596365119596366CT17GENIChomozygous112142605
3119596575119596576CT11GENIChomozygous112142606
3119596683119596684GA17GENIChomozygous111688077
3119596893119596893C11GENIChomozygous127923949
3119598083119598084TC22GENIChomozygous111688078
3119598754119598755AT25GENICpossibly homozygous112142607
3119601382119601382CTGGCCCTCCTGGGAGGGTGTGATCTTGCTGTCCTCACAGCCCCAGGGCAGCACCCTGGGTCCCAGAAAGGGACACGCTCTATACCCCCGGCCTCTCAGCTGTTCCCATCCAGGCAGCTTCACAGTGCCCGCCATGAG18GENICpossibly homozygous127923950
3119601848119601849CT22GENIChomozygous111688082
3119603037119603038GT25GENIChomozygous112142608
3119604536119604537GC18GENIChomozygous112024658
3119605020119605021G29GENIChomozygous127923952
3119605505119605506C24GENIChomozygous132587622
3119605613119605614AG18GENIChomozygous111688085
3119606729119606730CT16GENIChomozygous112142609
3119608783119608783G9GENIChomozygous127923954
3119609451119609452AG18GENIChomozygous111688088