chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9110017927110017928TC12GENIChomozygous117642040
9110018627110018628GC10GENICheterozygous117423309
9110019155110019156GA8GENIChomozygous117642042
9110020106110020107CG18GENIChomozygous126532340
9110020278110020279GT7GENIChomozygous117642044
9110021884110021885CG14GENIChomozygous126532342
9110022708110022709CT4GENICheterozygous126641343
9110023054110023055TA13GENIChomozygous117642046
9110023615110023616CT12GENIChomozygous117642048
9110023750110023751CT21GENIChomozygous117642050
9110024555110024556GA23GENIChomozygous117423319
9110027460110027461AG12GENIChomozygous117642054
9110027473110027474CT17GENIChomozygous117642056
9110027505110027506GA20GENIChomozygous117642058
9110027970110027971TC20GENIChomozygous117642060
9110028719110028720CG26GENIChomozygous117642062
9110030654110030655CG5GENIChomozygous117642066
9110022723110022724TG11GENICheterozygous117776634