chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116821548116821562TTTTTTTTTTTTTT--------------12GENICheterozygous751954040
7116821549116821562TTTTTTTTTTTTT-------------12GENICheterozygous751954041
7116823142116823143TC14GENIChomozygous641519085
7116823343116823344T-23GENIChomozygous751954042
7116823521116823522TC22GENIChomozygous641519086
7116824211116824212TC28GENIChomozygous641519087
7116825093116825094GA25GENIChomozygous641519088
7116825103116825104GA27GENIChomozygous641519089
7116825628116825629AT29GENICpossibly homozygous641519090
7116825974116825975TTA20GENICheterozygous751954043
7116826213116826214CCA14GENICheterozygous751954044
7116826543116826544AG25GENIChomozygous641519091
7116826982116826983GA25GENIChomozygous641519092
7116828351116828352GT22GENIChomozygous641519093
7116829856116829857GT27GENIChomozygous641519094
7116832075116832076CCCTG13GENIChomozygous751954045
7116832310116832311TG32GENIChomozygous641519095
7116832608116832611AAA---19GENIChomozygous751954046
7116833888116833889TC32GENIChomozygous641519096
7116834093116834094AG24GENIChomozygous641519097
7116834099116834100TA24GENICpossibly homozygous641519098
7116834100116834101CA24GENICpossibly homozygous641519099
7116834256116834257A-29GENIChomozygous751954048
7116834291116834292CA26GENIChomozygous641519100
7116834292116834293TG26GENIChomozygous641519101