chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206135837206135838AAGAG14GENIChomozygous61066210
1206152393206152394TTA10GENICheterozygous62236387
1206154626206154627AG16GENICpossibly homozygous61066251
1206156900206156901G-7GENICheterozygous62483448
1206159917206159918TTA2GENICheterozygous61066272
1206162185206162186CCTT5GENICheterozygous62192758
1206164883206164884T-5GENIChomozygous62274811
1206166947206166948TTGGGGATTTAG6GENIChomozygous62192762
1206166950206166951CCAGTGGTAGAG6GENIChomozygous62192764
1206166952206166953GGCCTGCCTAGCA6GENIChomozygous62192766
1206170437206170438T-8GENICheterozygous62192768
1206177129206177131AC--22GENICheterozygous62248628