chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185708102857081029AG20GENIChomozygous63900965
185708455057084551AG28GENIChomozygous63900969
185708500357085004AG23GENIChomozygous63900970
185708795357087954TC26GENIChomozygous63900987
185708450857084509CT42GENIChomozygous64043308
185708468557084686CT25GENIChomozygous64043311
185708554357085544GA37GENIChomozygous64043314
185709247457092475AG36GENIChomozygous63900995
185709520857095209GA39GENIChomozygous64043317
185709598757095988AG8GENICpossibly homozygous63901000
185709721157097212GA29GENIChomozygous63901003
185709793857097939TC17GENIChomozygous64043320
185709799057097991TA27GENIChomozygous63901004
185709822057098221GA50GENIChomozygous64043323
185709865657098657CT27GENIChomozygous63901006
185709919057099191CA37GENIChomozygous63901007
185709922757099228CT43GENIChomozygous64043325
185709978357099784TC27GENIChomozygous63901009
185709986157099862TG30GENIChomozygous63901010
185710022057100221CA21GENIChomozygous64043328
185710124257101243TC32GENIChomozygous64043331
185710161357101614TC33GENIChomozygous63901013
185710182257101823GT23GENIChomozygous64043334
185710225257102253GC34GENIChomozygous64043337
185710308357103084GA28GENIChomozygous64043340
185710337757103378TC31GENIChomozygous63901016
185710348857103489TC19GENICpossibly homozygous63901017
185710370457103705GA34GENIChomozygous64043343
185710454757104548GA37GENIChomozygous63901018
185710461557104616GA25GENIChomozygous64043346
185710511057105111TC19GENIChomozygous64043348
185710551257105513CA25GENIChomozygous64043351
185710566757105668GA29GENIChomozygous64043354
185710623057106231CT27GENIChomozygous64043357
185710626757106268AT36GENIChomozygous64043360
185710647157106472TC36GENIChomozygous64043363
185710670257106703CA18GENIChomozygous64043366
185710718257107183GA32GENIChomozygous64043369
185709931957099320GA24GENIChomozygous84639154
185710491757104918TG31GENIChomozygous84639155