chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4100760829100760830TG20GENIChomozygous113284634
4100763329100763330CT12GENIChomozygous113537959
4100764153100764154AT26GENIChomozygous113284635
4100764723100764724TC29GENIChomozygous113284636
4100766148100766149AG14GENIChomozygous113284637
4100766188100766189GC17GENIChomozygous113284638
4100766335100766336AC16GENIChomozygous113537963
4100766482100766483AT21GENIChomozygous113284639
4100768836100768837CA17GENIChomozygous113537965
4100769942100769943CA18GENIChomozygous113537967
4100771125100771126GA23GENIChomozygous113284642
4100771206100771207AG24GENIChomozygous113284643
4100772101100772102T12GENICheterozygous132058626
4100766311100766319ACAAAAAC12GENIChomozygous134199006
4100768830100768830A16GENIChomozygous134199007
4100774701100774701A16GENIChomozygous134199008
4100775567100775568A23GENIChomozygous128063798
4100775603100775603T22GENIChomozygous128063799
4100775613100775613G22GENIChomozygous128063800
4100775675100775676A19GENIChomozygous128063801
4100775697100775698CG21GENIChomozygous112798864
4100775717100775717G21GENIChomozygous128063802
4100775723100775724G21GENIChomozygous128063803
4100775727100775730CTC21GENIChomozygous128063804
4100775756100775756T30GENIChomozygous128063805
4100775807100775807AG24GENIChomozygous128063806
4100776161100776162CT28GENIChomozygous113537975
4100778471100778472TC23GENIChomozygous113284649
4100778570100778572CA26GENIChomozygous134199009
4100780020100780021AC8GENIChomozygous113537979
4100780640100780641GA16GENIChomozygous112798866
4100780799100780800TC14GENIChomozygous113284650
4100782302100782303TA21GENIChomozygous113284651
4100781672100781673A20GENICpossibly homozygous130935606
4100778680100778681C11GENIChomozygous130935604