chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4147089313147089314AT25GENICheterozygous112873944
4147089365147089367CC22GENICheterozygous128088700
4147089371147089372CT28GENICheterozygous122138216
4147089487147089488CT57GENICheterozygous112873949
4147089690147089691CT61GENICheterozygous122138221
4147089691147089692TC63GENICheterozygous122138222
4147089692147089693GA65GENICheterozygous122138223
4147089782147089783AC60GENICheterozygous112873952
4147089802147089803GT60GENICheterozygous112873953
4147089821147089822GA59GENICheterozygous112873954
4147089824147089825TC58GENICheterozygous112873955
4147089882147089883TG58GENICheterozygous112873956
4147089957147089958AT59GENICheterozygous112873957
4147089978147089979AC51GENICheterozygous112873958
4147089995147089996GC44GENICheterozygous112873959
4147090107147090108T39GENICheterozygous128088701
4147090108147090109GA40GENICheterozygous128136191
4147090186147090187TC31GENICheterozygous130306323
4147090227147090228GA34GENICheterozygous128136192
4147090284147090285AC32GENICheterozygous128136193
4147112834147112835GT5GENICheterozygous130306324
4147113209147113210GC7GENICheterozygous130306327
4147113466147113467GT2GENIChomozygous128136199
4147113503147113504GT3GENIChomozygous128136200
4147114739147114740TA6GENICheterozygous128136201
4147115168147115169AG17GENICheterozygous130652823
4147113670147113671TC2GENIChomozygous130652820
4147115070147115071CT15GENICheterozygous130652821
4147115078147115079TC15GENICheterozygous130652822
4147115645147115646GA4GENICheterozygous130652824
4147115711147115712CT3GENICheterozygous130652825
4147115942147115943AT6GENICheterozygous130652826
4147116898147116899GC44GENICheterozygous130652827
4147167478147167480AG19GENICheterozygous130298645