chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159979749159979750GGT24GENIChomozygous55814946
5159991081159991094CGCCACCCCCCCA-------------3GENIChomozygous55814966
5159991083159991093CCACCCCCCC----------3GENIChomozygous55814967
5159991112159991113TG11GENICpossibly homozygous55814969
5159991117159991118TG11GENIChomozygous55814970
5159991122159991123TG12GENIChomozygous55814971
5159991127159991128TG13GENICpossibly homozygous55814972
5160005781160005782CCT21GENIChomozygous55815009
5160006118160006119C-9GENIChomozygous55815010
5160012065160012067CA--42GENICheterozygous55815030
5160017781160017782AG6GENIChomozygous55815037
5160017796160017797AG5GENIChomozygous55815039
5160018434160018435TTAC23GENICheterozygous55815042
5160037732160037733T-4GENICheterozygous55815082
5160042547160042549GT--19GENICheterozygous55815087
5160047060160047062TG--27GENIChomozygous55815094
5160049553160049554CCGT23GENICpossibly homozygous55815106
5160050742160050743TG39GENICheterozygous55815108
5160050764160050765GT34GENICheterozygous55815109