chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7133630931133630932CG42GENICpossibly homozygous138229242
7133631117133631118TC48GENICpossibly homozygous138229243
7133631336133631337CT16GENIChomozygous138229244
7133632719133632719A42GENICpossibly homozygous137985253
7133632754133632755TG43GENIChomozygous138229245
7133632762133632762C39GENICpossibly homozygous137985254
7133635250133635251AG53GENIChomozygous138229246
7133635541133635542CT51GENIChomozygous138229247
7133636974133636975TC54GENIChomozygous138229248
7133637187133637188CG58GENIChomozygous138229249
7133637218133637219CT60GENIChomozygous138229250
7133637270133637271AC66GENIChomozygous138229251
7133638118133638119CT52GENIChomozygous138229252
7133638490133638491AC48GENIChomozygous138229253
7133638908133638909CA17GENIChomozygous138229254
7133639027133639028TC47GENIChomozygous138229255
7133639642133639643GA64GENIChomozygous138229256
7133640159133640160TC60GENIChomozygous138229257
7133642119133642120A29GENICpossibly homozygous137985255
7133642784133642785CT47GENIChomozygous138229258
7133643196133643197AG35GENIChomozygous138229259
7133643310133643311GA54GENIChomozygous138229260
7133643366133643367GA61GENIChomozygous138229261
7133643794133643795GA75GENIChomozygous138229262
7133644100133644119GCTAAGACCGCCTGCAAAC55GENIChomozygous137985256
7133644428133644429GA45GENIChomozygous138229263
7133644510133644511TC46GENIChomozygous138229264
7133647044133647045CA61GENIChomozygous138229265
7133647262133647263TA56GENIChomozygous138229266