chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144264423144264424GA70GENIChomozygous115945192
7144264533144264534GA58GENIChomozygous115945193
7144264639144264640G58GENIChomozygous128531691
7144264722144264726TGGC54GENIChomozygous128531692
7144264873144264874T43GENICpossibly homozygous128531693
7144265166144265172GAGTAC62GENIChomozygous128531694
7144265280144265281CT54GENIChomozygous115945194
7144265440144265441GA42GENIChomozygous115945195
7144265488144265489AG51GENIChomozygous115945196
7144265682144265683AG54GENIChomozygous115945197
7144265720144265721TC42GENIChomozygous115945198
7144265799144265800AG21GENIChomozygous115945199
7144265805144265806CT21GENICpossibly homozygous115945200
7144265813144265814GA23GENICheterozygous132120722
7144265916144265917TC42GENIChomozygous115945201
7144266009144266010C57GENIChomozygous128531695
7144266105144266106TC57GENIChomozygous115945202
7144266144144266144A49GENICheterozygous132659079
7144266678144266679GA65GENIChomozygous115945203
7144266911144266912AT44GENIChomozygous115945204
7144267203144267204TC62GENIChomozygous115945205
7144267423144267424AG61GENIChomozygous115945206
7144267802144267803GA75GENIChomozygous115945207
7144267818144267819CT73GENIChomozygous115945208
7144269016144269017C49GENIChomozygous128531696
7144269102144269103CT58GENIChomozygous115945209
7144269744144269745TC39GENIChomozygous115945210
7144269962144269963C64GENIChomozygous128531697
7144269967144269967T64GENIChomozygous128531698
7144270111144270111CAAGACCTTAAGCATACTAGT30GENIChomozygous128531699
7144270498144270499AG34GENIChomozygous115945211
7144270615144270616TC42GENIChomozygous115945212
7144271140144271140AT43GENIChomozygous128531700
7144271284144271285CT74GENIChomozygous115945213
7144271376144271377TC57GENIChomozygous115945214
7144271487144271488AG57GENIChomozygous115945215
7144271910144271911GA46GENIChomozygous115945216