chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2142503629142503630AG20GENICpossibly homozygous60450976
2142504139142504140GA21GENIChomozygous60450977
2142505369142505370CG17GENIChomozygous59870382
2142506048142506049GT12GENIChomozygous60450978
2142506503142506504TC11GENIChomozygous59870383
2142507146142507147TA4GENICheterozygous59870386
2142507395142507396GGGACTGATGGGGGAGGTGGGCGA5GENIChomozygous60450979
2142507445142507446CG24GENICpossibly homozygous60450980
2142508985142508986CG3GENICheterozygous59870389
2142509082142509083TC6GENICheterozygous59870390