chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12408950524089506AG18GENIChomozygous60639373
12408956824089569TC25GENIChomozygous60639374
12409122124091222GC28GENIChomozygous60639375
12409244224092443GA26GENIChomozygous60639377
12409596824095969CA32GENIChomozygous60639378
12409648724096488GC32GENIChomozygous60639379
12409666424096665TG24GENIChomozygous60639380
12409680024096801AG26GENIChomozygous60639381
12409697924096980AG28GENIChomozygous60639382
12409728724097288AC24GENIChomozygous60639383
12409775424097755C-22GENIChomozygous60639384
12409798424097985CT21GENIChomozygous60639385
12409800824098009AC24GENIChomozygous60639386
12409842024098421TC15GENIChomozygous60639387
12409864224098643GC26GENIChomozygous60639388
12409896324098964CG34GENIChomozygous60639389
12409896424098965AG34GENIChomozygous60639390
12409897424098975AT33GENIChomozygous60639391
12409897524098976AG33GENIChomozygous60639392
12409898024098983GAC---37GENIChomozygous62072829
12409898424098985AATTT35GENIChomozygous62363661
12409898524098986GT35GENIChomozygous62363662
12409959024099591TTA16GENICheterozygous60639393