chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X122728408122728408TTT32GENIChomozygous129785755
X122729683122729683TGTGCTTGCTAGGCAAGCGCTCTACCAC12GENIChomozygous129785757
X122729687122729688TC8GENIChomozygous129827062
X122777634122777635TA11GENIChomozygous129827064
X122777635122777636AT11GENIChomozygous129827065
X122777641122777641G12GENIChomozygous129785768
X122777643122777645CT12GENIChomozygous129785769
X122777647122777648C12GENIChomozygous129785770
X122777656122777657C13GENIChomozygous129785771
X122777661122777662CT14GENIChomozygous129827066
X122777662122777663TA14GENIChomozygous129827067
X122777664122777665GA14GENIChomozygous129827068
X122777670122777671TC14GENIChomozygous129827069
X122777674122777675A14GENIChomozygous129785772
X122777678122777679A14GENIChomozygous129785773
X122777688122777689T14GENIChomozygous129785774
X122777717122777720TGT20GENIChomozygous129785775
X122777744122777745C23GENIChomozygous129785776
X122777758122777759T24GENIChomozygous129785777
X122777783122777784T23GENIChomozygous129785778
X122777796122777797T22GENIChomozygous129785779
X122777804122777805A24GENIChomozygous129785780
X122777816122777817GC27GENIChomozygous119951025
X122777820122777820C27GENIChomozygous129785781
X122777827122777828C28GENIChomozygous129785782
X122777854122777855TA27GENIChomozygous120731647
X122777861122777862GC25GENIChomozygous108599391
X122777901122777902GA22GENIChomozygous108323150
X122777931122777932C19GENIChomozygous129785783
X122777946122777947T23GENIChomozygous129785784
X122777959122777959A20GENIChomozygous129785785
X122777970122777971TA20GENIChomozygous108323152
X122778018122778019A25GENIChomozygous129785786
X122778033122778034T24GENIChomozygous129785787
X122783800122783801A23GENIChomozygous129785791
X122770268122770268TGTATGGGCCACATG9GENIChomozygous130502002
X122777713122777714GT19GENIChomozygous120060954
X122777853122777854AT28GENIChomozygous108688498