chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142829642142829643CA18GENIChomozygous54161844
7142830072142830076TTTT----4GENICheterozygous55017779
7142830073142830076TTT---4GENICheterozygous55100893
7142830302142830305TTT---15GENICpossibly homozygous54161845
7142830303142830305TT--15GENICheterozygous55180769
7142830730142830731GGT15GENIChomozygous54161846
7142830788142830789GA15GENIChomozygous54802992
7142831435142831444AAACTTATT---------12GENIChomozygous54161848
7142831476142831482ACACAC------9GENICheterozygous55017783
7142831478142831482ACAC----9GENICpossibly homozygous55017785
7142832252142832253AG27GENIChomozygous54802993
7142833374142833376AG--11GENICheterozygous54161850
7142833374142833375A-11GENICpossibly homozygous54802994
7142833477142833478G-25GENIChomozygous54161851
7142834259142834260GGA6GENIChomozygous54161853
7142834261142834264GTG---7GENICpossibly homozygous54591487
7142835986142835987TTCTTCCCCAAGACTTGGAGCTGTTAGGATGCTTATCA18GENICheterozygous55017787
7142836128142836129TTC13GENIChomozygous54161856
7142836993142836994CCT1GENIChomozygous54161857
7142838609142838610TA21GENIChomozygous54161860
7142839049142839050TA22GENIChomozygous54161861
7142839542142839543TG19GENIChomozygous54161862
7142840013142840209CTAGAAGGAATAATTCTTGTTAGGTTTCGCCTGTGTTCCATTTCTGAAAACCTCTGAAGCGATATTGTATCTCAACTTTAAGAACAGTTAGTTTCTAACTGTGATCAGAAGCAAAGAGCAAAACCAAAGAACTATCCTTTTATACTCTGAAAAAATTTCCCTCTTGTAATTTACAGTTATTGTTGGGGGAACTTAC----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------105GENICheterozygous55017791
7142844789142844790TC20GENIChomozygous54161865
7142845261142845262CT20GENIChomozygous54802995