chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
179003406590034066TC39GENIChomozygous980726335
179003920690039207AG37GENIChomozygous980726336
179004155290041553CT55GENIChomozygous980726337
179004613490046135AG41GENIChomozygous980726338
179005005790050058AT34GENIChomozygous980726339
179005264290052643GT31GENIChomozygous980726340
179005273690052737AC41GENIChomozygous980726341
179006082390060824AT32GENIChomozygous980726342
179006124690061247AG29GENIChomozygous980726343
179006129790061298CG25GENIChomozygous980726344
179006154190061542TG20GENIChomozygous980726345
179006155990061560AC18GENIChomozygous980726346
179006199290061993TG7GENIChomozygous980726347
179006210290062103AG18GENIChomozygous980726348
179006234790062348AT19GENIChomozygous980726349
179006234890062349TA21GENIChomozygous980726350
179006358690063587GA34GENIChomozygous980726351