chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1211249164211249165AG20GENIChomozygous984241010
1211250496211250497TC14GENIChomozygous984241011
1211250622211250623CG18GENIChomozygous984241012
1211250971211250972AC16GENIChomozygous984241013
1211251987211251988GA19GENIChomozygous984241014
1211252068211252069CT11GENIChomozygous984241015
1211252076211252077AC11GENIChomozygous984241016
1211252203211252204AG28GENIChomozygous984241017
1211254118211254119AT24GENIChomozygous984241018
1211254143211254144CT16GENIChomozygous984241019
1211254145211254146CT16GENIChomozygous984241020
1211254496211254497CT14GENIChomozygous984241021
1211254854211254855CG22GENIChomozygous984241022
1211255440211255441GT33GENIChomozygous984241023
1211255616211255617AT14GENIChomozygous984241024
1211256722211256723TC26GENIChomozygous984241025
1211257074211257075AG22GENIChomozygous984241026
1211258803211258804TC28GENIChomozygous984241027
1211259421211259422AG7GENIChomozygous984241028
1211259737211259738AG19GENIChomozygous984241029
1211260475211260476CG28GENIChomozygous984241030
1211261278211261279AG29GENIChomozygous984241031
1211261430211261431CT38GENIChomozygous984241032
1211262513211262514GA17GENIChomozygous984241033
1211262865211262866AG19GENIChomozygous984241034
1211264098211264099TG17GENIChomozygous984241035