chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15975903259759033CG20GENIChomozygous108116355
15975942359759424GA28GENIChomozygous108116356
15975974859759749TC11GENIChomozygous108116358
15976006859760069AG11GENIChomozygous108116359
15976017059760171AG15GENIChomozygous108116360
15976018859760189TC13GENIChomozygous108116361
15976026659760267CT11GENIChomozygous108116362
15976039759760398GA15GENIChomozygous108116363
15976078159760782AG22GENIChomozygous108116364
15976197559761976AT15GENIChomozygous108116373
15976242759762428CG14GENIChomozygous108116374
15976266959762670GA12GENIChomozygous108116375
15976272459762725GA19GENIChomozygous108116376
15976306559763066CT11GENIChomozygous108116377
15976366859763669GT18GENIChomozygous108116379
15976445959764460CT19GENIChomozygous108116380
15976457959764580GA20GENIChomozygous108116381
15976463759764638CG19GENIChomozygous108116382
15976484159764842CA21GENIChomozygous108116383
15976504359765044GA23GENIChomozygous108116384
15976583859765839AG20GENIChomozygous108116385
15976691159766912AC21GENIChomozygous108116386
15976713159767132CT18GENIChomozygous108116387