chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15975903259759033CG20GENIChomozygous108116355
15975942359759424GA24GENIChomozygous108116356
15975956059759561TC18GENIChomozygous108116357
15975974859759749TC13GENIChomozygous108116358
15976006859760069AG31GENIChomozygous108116359
15976017059760171AG25GENIChomozygous108116360
15976018859760189TC20GENIChomozygous108116361
15976026659760267CT23GENIChomozygous108116362
15976039759760398GA26GENIChomozygous108116363
15976078159760782AG21GENIChomozygous108116364
15976242759762428CG17GENIChomozygous108116374
15976266959762670GA16GENIChomozygous108116375
15976272459762725GA17GENIChomozygous108116376
15976306559763066CT15GENIChomozygous108116377
15976366859763669GT19GENIChomozygous108116379
15976445959764460CT14GENIChomozygous108116380
15976457959764580GA19GENIChomozygous108116381
15976463759764638CG23GENIChomozygous108116382
15976484159764842CA21GENIChomozygous108116383
15976504359765044GA25GENIChomozygous108116384
15976583859765839AG19GENIChomozygous108116385
15976691159766912AC24GENIChomozygous108116386
15976713159767132CT23GENIChomozygous108116387