chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2267240985267240986CA14GENIChomozygous59557814
2267243729267243730GA21GENIChomozygous59557817
2267244205267244206GA29GENIChomozygous59557818
2267245025267245026AG12GENIChomozygous59557819
2267245351267245352AG15GENIChomozygous59557820
2267245472267245473AAGCTGGCG6GENIChomozygous60529588
2267245473267245474AAC6GENIChomozygous60529589
2267245476267245479ATA---5GENIChomozygous60529590
2267245480267245481AATCTGTCCCG3GENIChomozygous60529591
2267245482267245483AATGCGGCC3GENIChomozygous60529592
2267245485267245486AG3GENIChomozygous60529593
2267245487267245488TTGTAGGTGAGTAGTGGTGGGG3GENIChomozygous60529594
2267245493267245494AATTT3GENIChomozygous60529595
2267245495267245496TA3GENIChomozygous60529596
2267245498267245499CCG3GENIChomozygous60529597
2267245516267245517AT2GENIChomozygous60529598
2267245531267245532AACTTTTC3GENIChomozygous60529599
2267245534267245535AAGTTTT4GENIChomozygous60529600
2267245538267245539AG4GENIChomozygous60529601
2267245540267245541AATGGGTGGGAGT4GENIChomozygous60529602
2267245566267245567AG8GENIChomozygous60529603
2267245622267245623C-15GENIChomozygous59557821
2267245712267245713CT16GENIChomozygous59557822
2267246189267246190GA14GENIChomozygous59557823
2267251822267251823AAGTCTAAGGGCAAGAGTACAC24GENIChomozygous59557824
2267255349267255350GT31GENICpossibly homozygous59557826
2267256202267256212AAAATACAGT----------18GENIChomozygous59557827