chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105495827854958279AT28GENIChomozygous142248624
105495867854958679GA37GENIChomozygous142248626
105495869554958696TC40GENIChomozygous142248627
105495884554958846GC36GENIChomozygous142248628
105495913654959137GA24GENIChomozygous142248629
105495956254959563TG28GENIChomozygous142248630
105495966354959664GA31GENIChomozygous145741548
105495970954959710TG30GENIChomozygous142248631
105495974054959741TC31GENIChomozygous142248632
105495977854959779GA31GENIChomozygous142248633
105496001654960016A31GENICheterozygous142203588
105496003854960039T31GENIChomozygous142203589
105496068554960686GA21GENIChomozygous142248634
105496151754961518AT33GENIChomozygous142248635
105496174454961745AG29GENIChomozygous142248636
105496221454962215GC27GENIChomozygous142248637
105496250554962506AG25GENIChomozygous142248638
105496274054962741GA36GENIChomozygous142248639
105496317054963171TC33GENIChomozygous142248640
105496319154963192TA34GENIChomozygous145741549
105496328954963290GA32GENIChomozygous145741550
105496349154963492AG29GENIChomozygous142248641
105496372754963728GA39GENIChomozygous145741551
105496386554963866TG24GENIChomozygous142248642
105496411854964119AG29GENIChomozygous142248643
105496500554965006AG30GENIChomozygous142248645
105496535154965352CT29GENIChomozygous142248646
105496973754969738AG17GENIChomozygous142248650
105496611754966118TC22GENIChomozygous142248647
105496687454966875CT25GENIChomozygous142248648
105496879554968796TA28GENIChomozygous142248649
105497011554970116AG28GENIChomozygous142248652