chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12408950524089506AG21GENIChomozygous609931631
12408956824089569TC24GENIChomozygous609931632
12409122124091222GC23GENIChomozygous612213303
12409244224092443GA23GENIChomozygous612213304
12409596824095969CA9GENIChomozygous612213305
12409648724096488GC19GENIChomozygous612213306
12409666424096665TG31GENIChomozygous612213307
12409680024096801AG20GENIChomozygous612213308
12409697924096980AG26GENIChomozygous609931633
12409728724097288AC25GENIChomozygous609931634
12409775424097755C-14GENIChomozygous733835732
12409798424097985CT21GENIChomozygous612213309
12409800824098009AC22GENIChomozygous609931635
12409842024098421TC23GENIChomozygous612213310
12409864224098643GC24GENIChomozygous609931636
12409896324098964CG26GENIChomozygous609931637
12409896424098965AG25GENIChomozygous612213311
12409897424098975AT21GENIChomozygous612213312
12409897524098976AG21GENIChomozygous612213313
12409898024098983GAC---23GENIChomozygous733835733
12409898424098985AATTT22GENIChomozygous733835734
12409898524098986GT22GENIChomozygous612213314
12409959024099591TTA15GENICheterozygous733835735