chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97674306776743068CT63GENIChomozygous143409414
97674325476743255AG44GENIChomozygous143409415
97674331276743313TA32GENIChomozygous143409416
97674336576743365CT36GENIChomozygous143397942
97674398376743984TC55GENIChomozygous143409417
97674493976744940CT11GENIChomozygous143409418
97674541676745417AG27GENICpossibly homozygous143409419
97674604876746049GA40GENIChomozygous143409420
97674753876747539TC57GENIChomozygous143409421
97674876076748761CT42GENIChomozygous143409422
97674906876749069GC55GENIChomozygous143409423
97674912676749127CA47GENIChomozygous143409424
97674943476749435CG26GENIChomozygous143409425
97674977276749773CT60GENIChomozygous143409426
97675114676751147TC36GENIChomozygous143409427
97675147176751471GA8GENIChomozygous143397943
97675151176751521GAGAGGGAGA6GENIChomozygous143397944
97675202676752027GA22GENIChomozygous143409428
97675232376752324AG57GENIChomozygous143409429
97675410976754110CT47GENIChomozygous143409430
97675507976755080TC44GENIChomozygous143409431