chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119222816119222817T-7GENIChomozygous54080711
7119223731119223732CCTCTT6GENIChomozygous55000970
7119230413119230414TTAC4GENICheterozygous55059644
7119255702119255703TTA12GENICheterozygous54080772
7119262352119262353AG12GENIChomozygous54080777
7119290154119290156TG--11GENICheterozygous55059645
7119296826119296827CCCA2GENICheterozygous54080828
7119297859119297860CCTT4GENICheterozygous55000976
7119298148119298150GT--9GENICheterozygous55000980
7119313744119313747TAG---4GENIChomozygous55000984
7119325182119325184TC--2GENICheterozygous55000988
7119332717119332718AG24GENIChomozygous54080901
7119303124119303126TG--6GENICheterozygous55179693
7119339357119339358GT22GENIChomozygous54672292
7119340150119340151AG8GENIChomozygous54672294
7119340229119340231CT--5GENIChomozygous54080928
7119341210119341211GC12GENIChomozygous54080931
7119341414119341415A-16GENIChomozygous54232982
7119341429119341430CA19GENIChomozygous54080932
7119341860119341861AG17GENIChomozygous54080933
7119342264119342265AG29GENIChomozygous54859213
7119339623119339624GA16GENIChomozygous54859210
7119341468119341469AC13GENIChomozygous54859211
7119342105119342106GA11GENIChomozygous54859212
7119342296119342297A-14GENIChomozygous54859214
7119343019119343020CT21GENIChomozygous54859215
7119343504119343505CT18GENIChomozygous54859216
7119344170119344171CA20GENIChomozygous54859217