chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7133630931133630932CG42GENIChomozygous138229242
7133631117133631118TC39GENIChomozygous138229243
7133631336133631337CT18GENIChomozygous138229244
7133632754133632755TG46GENIChomozygous138229245
7133635250133635251AG60GENIChomozygous138229246
7133635541133635542CT70GENIChomozygous138229247
7133636974133636975TC53GENIChomozygous138229248
7133637187133637188CG49GENIChomozygous138229249
7133637218133637219CT48GENIChomozygous138229250
7133637270133637271AC43GENIChomozygous138229251
7133638118133638119CT54GENIChomozygous138229252
7133638490133638491AC59GENIChomozygous138229253
7133638908133638909CA17GENIChomozygous138229254
7133639027133639028TC59GENIChomozygous138229255
7133639642133639643GA66GENIChomozygous138229256
7133640159133640160TC58GENIChomozygous138229257
7133642784133642785CT77GENIChomozygous138229258
7133643196133643197AG54GENIChomozygous138229259
7133643310133643311GA67GENIChomozygous138229260
7133643366133643367GA62GENIChomozygous138229261
7133643794133643795GA49GENIChomozygous138229262
7133642119133642120A26GENICpossibly homozygous137985255
7133644100133644119GCTAAGACCGCCTGCAAAC52GENIChomozygous137985256
7133632719133632719A40GENICpossibly homozygous137985253
7133632762133632762C42GENICpossibly homozygous137985254
7133644428133644429GA48GENIChomozygous138229263
7133644510133644511TC56GENIChomozygous138229264
7133647044133647045CA52GENICpossibly homozygous138229265
7133647262133647263TA44GENIChomozygous138229266
7133647587133647598CCTCCTCCTCC53GENIChomozygous141924529
7133638315133638316GA59GENIChomozygous142016218
7133641419133641420AG57GENIChomozygous142016219