chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104632606346326064TTA7GENICheterozygous734068719
104632631846326319GA26GENIChomozygous610350886
104632646146326462CCAG19GENIChomozygous734068721
104632725246327253TC36GENIChomozygous610350887
104632934046329341CT34GENIChomozygous612375170
104632979046329791AAGGTGGCTCAGC29GENIChomozygous734068722
104632994746329948A-13GENIChomozygous734068723
104633297346332974TG27GENIChomozygous610350888
104633378546333786AG48GENIChomozygous610350889
104633479346334794TTTCAC10GENIChomozygous734068724
104633507346335074GA44GENIChomozygous612375171
104633540246335403AATG11GENICheterozygous734068726
104633540246335403AATGTG11GENICheterozygous734068727
104633540246335403AATGTGTG11GENICheterozygous734068728
104633576946335770TC29GENIChomozygous610350890
104633619746336198TTATATCC12GENIChomozygous734068729
104633627246336273CT27GENIChomozygous612375172
104633736546337366CT20GENIChomozygous612375173
104633878746338788AACACACACACT23GENICpossibly homozygous734068730
104633948946339490AG35GENIChomozygous610350891
104633980546339806AT27GENIChomozygous610350892
104634143546341436TC24GENIChomozygous610350893
104634251746342518AG25GENIChomozygous612375174
104634374846343749GA26GENIChomozygous612375175
104634430646344307TC32GENIChomozygous612375176
104634465246344653TG23GENIChomozygous612375177