chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181197240211972403CG52GENIChomozygous110270578
181197241711972418TA53GENIChomozygous110270580
181197246011972461CT50GENIChomozygous110270582
181197249011972491AT49GENIChomozygous110270584
181197255911972560AG48GENIChomozygous110270586
181197283311972833TTTG47GENIChomozygous129514925
181197285111972852GC46GENIChomozygous110270588
181197286611972867CT44GENIChomozygous110270590
181197316811973169CT47GENIChomozygous110270592
181197333411973335TC56GENIChomozygous110270594
181197346411973465GA49GENIChomozygous110574970
181197348511973486TC49GENICpossibly homozygous110574972
181197349711973498AG49GENICpossibly homozygous110270596
181197353811973539TA53GENICpossibly homozygous110270598
181197376611973767CT63GENIChomozygous110270600
181197393911973940GA48GENIChomozygous110270602
181197418411974185GA49GENIChomozygous110270604
181197454811974549TC47GENIChomozygous110270606
181197591911975920AC52GENIChomozygous110270608
181197518211975183AG54GENIChomozygous110449782