chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT13GENIChomozygous739911749
99073349690733497GGT18GENIChomozygous739911750
99073383290733846GTGTGTGTGTGTGT--------------9GENIChomozygous739911751
99073573190735732AAGT43GENIChomozygous739911754
99073588290735884GT--15GENIChomozygous739911755
99073603090736031TTGGGA26GENIChomozygous739911759
99073603290736033TG25GENIChomozygous622488219
99073639590736396TG31GENIChomozygous622488220
99073687890736879TG20GENIChomozygous622488221
99073692190736922TG27GENIChomozygous622488222
99073693290736933TG27GENIChomozygous622488223
99073694690736947AG26GENIChomozygous622488224
99073695490736955TG26GENIChomozygous622488225
99073697190736972TA27GENIChomozygous622488226
99073856290738563TC8GENIChomozygous622488227
99073982890739830AA--29GENIChomozygous739911760
99074145590741456AAAGG20GENIChomozygous739911761
99074242690742428AA--12GENIChomozygous739911762
99074258390742584CT5GENIChomozygous622488228
99074258590742586TC4GENIChomozygous622488229
99074259990742600CA2GENIChomozygous622488230
99074260190742602GT2GENIChomozygous622488231
99074260490742606CC--1GENIChomozygous739911763
99074261090742611CT2GENIChomozygous622488232
99074261190742612CA3GENIChomozygous622488233
99074280890742809AAG2GENIChomozygous739911764
99074517990745180AT22GENIChomozygous622488234
99074558690745587TG32GENIChomozygous622488235
99074575390745754TA24GENIChomozygous622488236
99074741590747416CT23GENIChomozygous622488237
99074743390747434GA20GENIChomozygous622488238
99074751590747518GTA---19GENICpossibly homozygous739911765
99074761790747618GC18GENICheterozygous622488239
99074781790747820TTG---4GENIChomozygous739911766
99074813190748137GTTGTT------9GENICheterozygous739911767
99074813490748137GTT---9GENICheterozygous739911768
99074863090748631TG14GENIChomozygous622488240
99074869490748696GT--2GENIChomozygous739911770
99074879190748792GGT17GENIChomozygous739911772
99074898990748990CT28GENIChomozygous622488241
99074956390749564GGT5GENICheterozygous739911773