chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108666399586663996TC33GENICpossibly homozygous51528452
108666409886664099AG25GENIChomozygous51528453
108666459286664593TC24GENIChomozygous51528454
108666522486665225TC18GENIChomozygous51528455
108666546686665467TG20GENIChomozygous51528456
108666579586665796GA36GENIChomozygous51528457
108666709986667100TC22GENIChomozygous51528458
108666790186667902AG16GENIChomozygous51528459
108666828986668290GA32GENIChomozygous51528460
108666911886669119TC29GENIChomozygous51528461
108666914186669155TCTCTCTCTCTCTC--------------8GENIChomozygous52808352
108666977486669775TC35GENIChomozygous51528463
108667014686670147TC32GENIChomozygous51528464
108667146286671463CT37GENIChomozygous51528465
108667378086673781TC37GENICpossibly homozygous51528466
108667398086673981AATGTGTGTGTGTG19GENICpossibly homozygous52392428
108667784886677849GGC10GENIChomozygous51528467
108667814086678141GC27GENIChomozygous51528468
108667818386678184GA30GENIChomozygous51528469
108667820286678206TGTG----25GENICpossibly homozygous52444612
108667933686679337GA33GENIChomozygous51528471
108667957986679580CG27GENIChomozygous51528472
108668084286680844TG--29GENICheterozygous52683351
108668096586680966TA33GENIChomozygous51528473
108668105086681051TC25GENIChomozygous51528474
108668181086681811T-26GENICpossibly homozygous51528475