chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7133630931133630932CG25GENIChomozygous138229242
7133631117133631118TC28GENIChomozygous138229243
7133631336133631337CT5GENIChomozygous138229244
7133632719133632719A21GENIChomozygous137985253
7133632754133632755TG29GENIChomozygous138229245
7133632762133632762C28GENIChomozygous137985254
7133635250133635251AG28GENIChomozygous138229246
7133635541133635542CT39GENIChomozygous138229247
7133636974133636975TC25GENIChomozygous138229248
7133637187133637188CG27GENIChomozygous138229249
7133637218133637219CT22GENIChomozygous138229250
7133637270133637271AC28GENIChomozygous138229251
7133638118133638119CT18GENIChomozygous138229252
7133638315133638316GA39GENIChomozygous142016218
7133638490133638491AC28GENIChomozygous138229253
7133638908133638909CA18GENIChomozygous138229254
7133639027133639028TC38GENIChomozygous138229255
7133639642133639643GA32GENIChomozygous138229256
7133640159133640160TC41GENIChomozygous138229257
7133641419133641420AG18GENIChomozygous142016219
7133642119133642120A14GENIChomozygous137985255
7133642784133642785CT40GENIChomozygous138229258
7133643196133643197AG33GENIChomozygous138229259
7133643310133643311GA39GENIChomozygous138229260
7133643366133643367GA43GENIChomozygous138229261
7133643794133643795GA33GENIChomozygous138229262
7133644100133644119GCTAAGACCGCCTGCAAAC50GENIChomozygous137985256
7133644428133644429GA34GENIChomozygous138229263
7133644510133644511TC33GENIChomozygous138229264
7133647044133647045CA40GENIChomozygous138229265
7133647262133647263TA27GENIChomozygous138229266
7133647587133647598CCTCCTCCTCC30GENIChomozygous141924529