chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9105178438105178439CT51GENIChomozygous138647714
9105180655105180656AG47GENIChomozygous138647715
9105180972105180973TC54GENIChomozygous138647716
9105181950105181951AG49GENIChomozygous138647717
9105182386105182387AC57GENIChomozygous138647718
9105182460105182461AG41GENIChomozygous138647719
9105183179105183183TTAG49GENIChomozygous138478187
9105185241105185242A50GENIChomozygous138478188
9105186297105186298GA39GENIChomozygous138647720
9105186597105186598AG46GENIChomozygous138647721
9105187289105187290AG22GENIChomozygous138647722
9105187305105187306AG18GENICheterozygous145214887
9105190001105190002GA49GENIChomozygous138647723
9105190056105190057GA53GENIChomozygous138647724
9105190713105190713GT42GENIChomozygous138478189
9105193177105193178AG51GENIChomozygous138647725
9105195403105195404CA50GENIChomozygous138647726
9105197286105197391AGAAATTGAAACTCGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCAAAAAAAAAAAAAAAAA25GENIChomozygous138478190
9105198674105198674T35GENIChomozygous138478191
9105201342105201343AG52GENIChomozygous138647727
9105201891105201891G39GENIChomozygous138478192
9105201989105201990CG48GENIChomozygous138647728
9105202590105202591AG51GENIChomozygous138647729
9105204452105204453TA48GENICpossibly homozygous138647730
9105205033105205034TG41GENIChomozygous138647731
9105207101105207102AG27GENIChomozygous138647732
9105207256105207256GCGG16GENIChomozygous138478193
9105207883105207884CA44GENIChomozygous138647733
9105208255105208256AC65GENICpossibly homozygous138647734
9105208364105208365CT44GENIChomozygous138647735
9105187274105187275GA26GENICheterozygous145726990
9105187284105187285GC23GENICheterozygous145726991