chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1177448704177448705CCTTTCT15GENICpossibly homozygous61961690
1177448784177448785CT15GENIChomozygous60968905
1177448837177448838GA16GENIChomozygous60968907
1177448861177448862TC16GENIChomozygous60968909
1177448873177448874TC15GENIChomozygous61788375
1177450079177450080TC33GENIChomozygous60968912
1177454699177454700TG29GENIChomozygous60968914
1177455652177455653GT42GENIChomozygous60968916
1177460604177460605CCTTCCCATGGTT11GENIChomozygous60968928
1177460608177460609AC16GENICheterozygous60968930
1177461184177461185TC25GENIChomozygous61788381
1177463068177463069CT14GENIChomozygous61788383
1177464863177464864GA32GENIChomozygous61788385
1177464998177464999TC17GENIChomozygous60968939
1177465707177465708TC26GENIChomozygous60968941
1177466215177466216GC12GENIChomozygous60968943
1177466237177466238G-6GENIChomozygous60968945
1177466998177466999AG25GENIChomozygous60968949
1177468213177468215AC--6GENICheterozygous61561596
1177468260177468261TTACAC9GENIChomozygous61788387
1177468486177468487TC23GENIChomozygous61788389
1177469286177469293TTTTCTT-------19GENIChomozygous61788391
1177469291177469293TT--12GENIChomozygous61788392
1177469979177469980AG34GENIChomozygous60968959
1177468210177468211TTAC6GENICheterozygous61312631