chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218481172218481173CA38GENIChomozygous108538284
1218482114218482115TC46GENIChomozygous108538285
1218482833218482834CG15GENICheterozygous127577972
1218482835218482836CG11GENIChomozygous127577973
1218482837218482838CG11GENIChomozygous127577974
1218484419218484420AG40GENIChomozygous108538288
1218484796218484797CT69GENIChomozygous108538289
1218486498218486499GA47GENIChomozygous108538290
1218486683218486684GA38GENIChomozygous108538291
1218487396218487397TC39GENIChomozygous108538292
1218487988218487989GT57GENIChomozygous108538293
1218491188218491189TC38GENIChomozygous108538294
1218491505218491506TC36GENIChomozygous108538295
1218491583218491584GA33GENIChomozygous108538296
1218491679218491680TA55GENIChomozygous108538297
1218491892218491893TC40GENIChomozygous108538298
1218491904218491905TC42GENIChomozygous108538299
1218482877218482877CAGAGACAGAGG38GENIChomozygous127484011
1218483659218483659AT22GENICpossibly homozygous127484012
1218486616218486617AC49GENIChomozygous120475918