chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4220863861220863862GT6GENIChomozygous598126012
4220865950220865951TC26GENICpossibly homozygous598126013
4220866308220866309CT13GENICpossibly homozygous598126014
4220867182220867183CT27GENIChomozygous598126015
4220867457220867458GT22GENICpossibly homozygous598126016
4220867545220867546AT7GENIChomozygous598126017
4220870021220870022TC24GENIChomozygous598126018
4220870972220870973AATTTT1GENIChomozygous727019298
4220873146220873147TC21GENIChomozygous598126019
4220873953220873954TC19GENIChomozygous598126020
4220875728220875729TTA7GENICpossibly homozygous727019299
4220877136220877137GGTCTCTC1GENIChomozygous727019300
4220877271220877272CG4GENIChomozygous598126021
4220879291220879292GA12GENICpossibly homozygous598126022
4220880183220880184CT18GENICpossibly homozygous598126023
4220880485220880486GA29GENIChomozygous598126024
4220880567220880568AG10GENIChomozygous598126025
4220880591220880592AC11GENIChomozygous598126026