chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12408950524089506AG30GENIChomozygous60639373
12408956824089569TC17GENIChomozygous60639374
12409026924090270AAC5GENIChomozygous61276321
12409298124092982GA23GENIChomozygous61276322
12409315824093159TC25GENIChomozygous61276323
12409320524093206GA22GENIChomozygous61276324
12409430224094303AG21GENIChomozygous61276325
12409434124094342AT26GENIChomozygous61276326
12409454724094548CCAAA13GENIChomozygous61276327
12409455124094552CA14GENIChomozygous61276328
12409455224094553TG14GENIChomozygous61276329
12409486724094868TTTTTA17GENICpossibly homozygous61276330
12409642524096426AT23GENICpossibly homozygous61276331
12409697324096974GA26GENIChomozygous61276332
12409697924096980AG23GENIChomozygous60639382
12409728724097288AC10GENIChomozygous60639383
12409800824098009AC25GENIChomozygous60639386
12409864224098643GC16GENIChomozygous60639388
12409878024098781GA23GENIChomozygous61276333
12409896324098964CG24GENIChomozygous60639389
12409896424098965AG23GENIChomozygous60639390
12409897424098975AT22GENIChomozygous60639391
12409897524098976AG20GENIChomozygous60639392
12409898024098983GAC---21GENIChomozygous62072829
12409898424098985AATTT16GENIChomozygous62363661
12409898524098986GT16GENIChomozygous62363662
12409932824099329AC19GENIChomozygous61276334
12409959024099591TTAAAAAAAAAAA5GENIChomozygous62363663