chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166031252166031272GCCTTGCGCTCGCTAGGCAA12GENIChomozygous127453278
1166031601166031602CT20GENIChomozygous108355978
1166031659166031660AG15GENIChomozygous108355980
1166032837166032838TG20GENIChomozygous108355981
1166032986166032987GT19GENIChomozygous109436485
1166033099166033099CAT18GENIChomozygous127453279
1166033538166033539CT23GENIChomozygous108355982
1166033544166033545C24GENIChomozygous127453280
1166033844166033847TTC21GENIChomozygous133801090
1166033956166033957TC24GENIChomozygous108355983
1166034463166034464AG10GENIChomozygous108355984
1166034474166034475GA11GENIChomozygous108355985
1166034506166034507C13GENIChomozygous127453281
1166034841166034842GA14GENIChomozygous108355986
1166035030166035031A9GENIChomozygous127453282
1166035059166035059T5GENIChomozygous127453283
1166035967166035968CT17GENIChomozygous109436487
1166036567166036576CTCTGTACC19GENIChomozygous130826569
1166036577166036578AC19GENIChomozygous109522598
1166036771166036772TC24GENIChomozygous108355987
1166036918166036919CT18GENIChomozygous109163065
1166037242166037243G15GENIChomozygous130826570
1166037244166037244GCAGGTGCTGCAGCAGGTGCTCTT15GENIChomozygous130826571
1166038099166038100TC26GENIChomozygous108355988
1166038102166038103AG26GENIChomozygous108355989
1166038508166038509CT27GENIChomozygous108751544
1166038566166038567CT25GENIChomozygous108355990
1166039394166039395TC17GENIChomozygous108355991
1166040885166040886AG27GENIChomozygous108355992
1166041051166041051GTGTGTGTGA20GENIChomozygous127453284
1166041095166041096AG20GENIChomozygous108355994
1166043101166043101CTCT23GENIChomozygous127453285
1166043557166043557CACCCAAA17GENIChomozygous127453286
1166043558166043558GCA16GENIChomozygous127453287
1166043950166043951AG18GENIChomozygous108355998
1166044573166044574AT25GENIChomozygous109436489
1166044972166044973GA16GENIChomozygous108355999