chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142817523142817524GA18GENIChomozygous54161823
7142818199142818200GA19GENIChomozygous54161824
7142818509142818510TTA5GENICheterozygous54161826
7142818857142818858CT5GENICheterozygous54161827
7142819680142819681TC17GENIChomozygous54161828
7142819708142819709CT11GENIChomozygous54161829
7142822069142822070CT10GENICpossibly homozygous54161834
7142823027142823028CT1GENIChomozygous54161835
7142823513142823514GA3GENIChomozygous54161836
7142824481142824482GA12GENIChomozygous54161837
7142825224142825225TC9GENIChomozygous54161839
7142827305142827306TC15GENIChomozygous54161840
7142827976142827977CCA3GENICheterozygous54161843
7142829642142829643CA14GENIChomozygous54161844
7142830073142830076TTT---1GENIChomozygous55100893
7142831435142831444AAACTTATT---------2GENIChomozygous54161848
7142833477142833478G-1GENIChomozygous54161851
7142835947142835948GA4GENIChomozygous54161855
7142836128142836129TTC6GENIChomozygous54161856
7142836998142836999A-7GENICheterozygous55132997
7142838609142838610TA12GENIChomozygous54161860
7142839542142839543TG11GENIChomozygous54161862
7142841407142841411GGAG----9GENIChomozygous54161863
7142844789142844790TC19GENICpossibly homozygous54161865
7142845745142845746AC14INTERGENIChomozygous54161866
7142847522142847523CT15INTERGENICpossibly homozygous54161868
7142847931142847932AAG5INTERGENICheterozygous55680549
7142850014142850015GC3GENIChomozygous54161882
7142852569142852570GA6GENICheterozygous54161883
7142854129142854132TTG---1GENIChomozygous54161887
7142855475142855476GA35GENICpossibly homozygous54161890
7142857159142857160AT6GENIChomozygous54161894
7142857987142857988GA7GENIChomozygous54161896
7142858109142858110T-3GENICheterozygous54161897