chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116821548116821561TTTTTTTTTTTTT-------------11GENICheterozygous684176882
7116823142116823143TC53GENIChomozygous503564151
7116823521116823522TC47GENIChomozygous503564152
7116824211116824212TC42GENIChomozygous503564153
7116825093116825094GA57GENIChomozygous503564154
7116825103116825104GA57GENIChomozygous503564155
7116825628116825629AT49GENIChomozygous503564156
7116825978116825979GGAA25GENICheterozygous684176883
7116825978116825979GGA25GENICpossibly homozygous684176884
7116826221116826222GGA18GENICpossibly homozygous684176885
7116826222116826223A-18GENICheterozygous684176886
7116826543116826544AG43GENIChomozygous503564157
7116826982116826983GA48GENIChomozygous503564158
7116828351116828352GT36GENIChomozygous503564159
7116828897116828898GT35GENICheterozygous504463769
7116829856116829857GT56GENIChomozygous503564160
7116832075116832076CCCTG74GENIChomozygous684176887
7116832310116832311TG50GENIChomozygous503564161
7116832609116832611AA--25GENIChomozygous684176888
7116833888116833889TC62GENICpossibly homozygous503564162
7116834093116834094AG64GENIChomozygous503564163
7116834099116834100TA61GENIChomozygous504463770
7116834100116834101CA61GENIChomozygous504463771
7116834256116834257A-33GENIChomozygous684176890
7116834291116834292CA47GENIChomozygous503564164
7116834292116834293TG46GENIChomozygous503564165