chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102246613102246614TC24GENIChomozygous619255598
1102246702102246703GA15GENIChomozygous619255599
1102246870102246871TC21GENIChomozygous619255600
1102247122102247123TC27GENIChomozygous619255601
1102249405102249406GT30GENIChomozygous619255602
1102249813102249814TC28GENIChomozygous619255603
1102249910102249911TA19GENIChomozygous619255604
1102250282102250283TC25GENIChomozygous619255605
1102250452102250453GA31GENIChomozygous619255606
1102250667102250668AG24GENIChomozygous619255607
1102251416102251417TC30GENIChomozygous619255608
1102251536102251537TC20GENIChomozygous619255609
1102252161102252162CT22GENIChomozygous619255610
1102252732102252733CT19GENIChomozygous619255611
1102252869102252870GA31GENIChomozygous619255612
1102254276102254277AATGTGTGTG22GENIChomozygous737969163
1102254379102254380AG23GENIChomozygous619255613
1102254904102254905GA15GENIChomozygous619255614
1102255276102255277AG27GENIChomozygous619255615
1102258743102258744TC19GENIChomozygous619255616
1102259056102259057GA17GENIChomozygous619255617
1102259876102259877AG20GENIChomozygous619255618
1102260060102260061TC33GENIChomozygous619255619
1102260070102260071GA36GENIChomozygous619255620
1102260942102260943GA34GENICpossibly homozygous619255621
1102261023102261024CT38GENICpossibly homozygous619255622
1102261337102261338TC14GENIChomozygous619255623
1102262027102262028TC28GENIChomozygous619255624
1102263052102263053AG13GENIChomozygous619255625
1102263080102263081TC10GENIChomozygous619255626
1102265280102265281AG19GENIChomozygous619255627
1102265366102265367GA20GENIChomozygous619255628
1102266625102266626TTA12GENIChomozygous737969167
1102267108102267109AT11GENIChomozygous619255629
1102267119102267120CG12GENIChomozygous619255630
1102267270102267271CA18GENIChomozygous619255631