chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1229879584229879585GA25GENIChomozygous61604949
1229879905229879909GTGT----5GENIChomozygous61604950
1229880995229880996TC17GENIChomozygous61109473
1229881497229881503GTGTGT------4GENIChomozygous61604951
1229881929229881930TC33GENIChomozygous61109475
1229883588229883589CT26GENIChomozygous61109479
1229884531229884532TC25GENIChomozygous61109481
1229885422229885423CCCAGCAG14GENICheterozygous62561695
1229885422229885423CCCAGCAGCAG14GENICpossibly homozygous62561696
1229885803229885804CA18GENIChomozygous61604952
1229886876229886877CCT18GENICpossibly homozygous61109485
1229887033229887034TTGCCATGGTGGA16GENIChomozygous62556525
1229887345229887347GC--33GENIChomozygous61604953
1229887624229887625TC27GENIChomozygous61604954
1229888078229888079CT21GENIChomozygous61604955
1229889494229889495TC25GENIChomozygous61109492