chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205635050205635051CCAA25GENICheterozygous61963946
1205635051205635053AA--25GENICheterozygous61065164
1205635052205635053A-25GENICheterozygous61065165
1205636671205636756TACCTAGACAGAGACATGGGAGCCAGAGTATAGACCTGTGTGGGAATGGGCTTAATCAGGTCAGGGTGTGCTGAGGCTTGTGGCC-------------------------------------------------------------------------------------71GENICheterozygous62095843
1205637156205637157TC17GENIChomozygous61065166
1205637350205637351AG34GENIChomozygous61065167
1205637473205637474AT31GENIChomozygous61065168
1205638359205638360AT33GENIChomozygous61065169
1205638415205638416TC33GENIChomozygous61065170
1205638518205638519AG19GENIChomozygous62236233
1205638542205638543AATG16GENIChomozygous61065173
1205638546205638547TG19GENIChomozygous61065174
1205638548205638549AT19GENIChomozygous61065175
1205638873205638874AT31GENIChomozygous61065176
1205638875205638876TC31GENIChomozygous61065177
1205639593205639594AG30GENIChomozygous61065178
1205639988205639989AG36GENIChomozygous61065179
1205640945205640949AATA----27GENIChomozygous61065180
1205641066205641067GGA26GENIChomozygous61065181
1205641556205641557GGA21GENIChomozygous62030344
1205642568205642570TG--28GENIChomozygous61065182
1205642788205642789CCAA15GENICpossibly homozygous61065183
1205642788205642789CCAAA15GENICheterozygous62330909
1205642966205642967AG25GENIChomozygous61065184
1205643155205643156GA27GENIChomozygous61065185
1205643333205643334AAAAG21GENIChomozygous61065186
1205643942205643943GA41GENIChomozygous61065187
1205645251205645252GA30GENIChomozygous61065188