chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1192525069192525070TTA21GENIChomozygous61026503
1192525360192525361GA48GENIChomozygous61026504
1192525532192525533TTG28GENIChomozygous61026505
1192525587192525588CCAA35GENICheterozygous62094977
1192525627192525628TG32GENICheterozygous61026506
1192525627192525628TA32GENICheterozygous61316455
1192526833192526834AG33GENIChomozygous61026507
1192528897192528898GA18GENIChomozygous61026509
1192528922192528923CCAAAAT18GENIChomozygous61026511
1192530783192530784AG31GENIChomozygous61026512
1192530834192530835TC46GENIChomozygous61026513
1192530919192530920GA37GENIChomozygous61026514
1192530984192531070CCAAGTAGTGTACCATGCGGCCCTGGGTTCGGTCCCCAGCTCTGGAAAAAAAAAAAGAACCAAAACAAAACAAAACAAAACAAAAA--------------------------------------------------------------------------------------25GENIChomozygous62185933
1192531131192531132AC26GENIChomozygous61026515
1192531287192531288GGA14GENICpossibly homozygous61026516
1192531480192531481GA19GENIChomozygous61026517
1192532399192532400A-18GENIChomozygous61026518
1192532859192532860CT20GENIChomozygous61026519
1192533130192533131TG43GENIChomozygous61026520
1192533205192533206GA38GENIChomozygous61026521
1192533227192533228CT36GENIChomozygous61026522
1192533616192533617GGTGGCATATCAGATGTTTACAGTATGGTTCATAA40GENIChomozygous62094978
1192534282192534283AC18GENIChomozygous61026523
1192534303192534304AC18GENIChomozygous61026524
1192535461192535462AACCAG21GENIChomozygous61026525
1192535792192535793GT15GENIChomozygous61026526