chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189829747189829748TC32GENIChomozygous797658326
2189829929189829930TC30GENIChomozygous797658327
2189829990189829991CT22GENIChomozygous797658328
2189830468189830469TA21GENIChomozygous797658329
2189830476189830477AC22GENIChomozygous797658330
2189830617189830618CG33GENICpossibly homozygous797658331
2189830864189830865AG37GENICheterozygous797658332
2189831061189831062CT32GENIChomozygous797658333
2189831619189831620CT21GENIChomozygous797658334
2189831649189831650GA22GENIChomozygous797658335
2189832252189832253GA44GENIChomozygous797658336
2189832513189832514GA38GENICpossibly homozygous797658337
2189832825189832826CG19GENICheterozygous797658338
2189832888189832889GA39GENICheterozygous797658339
2189832938189832939TC66GENICheterozygous797658340
2189833106189833107TA249GENICheterozygous797658341
2189833110189833111GT250GENICheterozygous797658342
2189833762189833763GA11GENIChomozygous797658343
2189833886189833887CT28GENIChomozygous797658344
2189833916189833917AC27GENIChomozygous797658345
2189834736189834737AG31GENICpossibly homozygous797658346