chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7133630931133630932CG23GENIChomozygous138229242
7133631117133631118TC19GENIChomozygous138229243
7133631336133631337CT10GENIChomozygous138229244
7133632719133632719A22GENIChomozygous137985253
7133632754133632755TG27GENIChomozygous138229245
7133632762133632762C25GENIChomozygous137985254
7133635250133635251AG31GENIChomozygous138229246
7133635541133635542CT31GENIChomozygous138229247
7133636974133636975TC20GENIChomozygous138229248
7133637187133637188CG29GENIChomozygous138229249
7133637218133637219CT29GENIChomozygous138229250
7133637270133637271AC27GENIChomozygous138229251
7133638118133638119CT24GENIChomozygous138229252
7133638490133638491AC21GENIChomozygous138229253
7133638908133638909CA16GENIChomozygous138229254
7133639027133639028TC31GENIChomozygous138229255
7133639642133639643GA21GENIChomozygous138229256
7133640159133640160TC31GENIChomozygous138229257
7133642119133642120A20GENIChomozygous137985255
7133642784133642785CT16GENIChomozygous138229258
7133643196133643197AG19GENIChomozygous138229259
7133643310133643311GA29GENIChomozygous138229260
7133643366133643367GA27GENIChomozygous138229261
7133643794133643795GA35GENIChomozygous138229262
7133644100133644119GCTAAGACCGCCTGCAAAC20GENIChomozygous137985256
7133644428133644429GA25GENIChomozygous138229263
7133644510133644511TC27GENIChomozygous138229264
7133647044133647045CA23GENIChomozygous138229265
7133647262133647263TA20GENIChomozygous138229266