chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14103451255103451256TA39GENIChomozygous139612754
14103453323103453324AG49GENIChomozygous139612755
14103463027103463028GA48GENIChomozygous139612756
14103464842103464843CG49GENIChomozygous139612757
14103464904103464905CT49GENIChomozygous139612758
14103471442103471443TC53GENIChomozygous139612759
14103471575103471576CT19GENIChomozygous139612760
14103472208103472209GC60GENIChomozygous139612761
14103472971103472972TG56GENICpossibly homozygous139612762
14103473021103473022CA45GENIChomozygous139612763
14103480016103480017AT33GENIChomozygous139612764
14103480314103480315AG43GENIChomozygous139612765
14103480591103480592CA45GENIChomozygous139612766
14103482584103482585AT63GENIChomozygous139612767
14103482716103482717CT45GENIChomozygous139612768
14103483251103483252TC52GENIChomozygous139612769
14103484148103484148T36GENICpossibly homozygous139414710
14103458335103458335TATT57GENIChomozygous139414705
14103466163103466164T27GENICheterozygous139414706
14103478019103478019AGAGTGATGGG25GENICpossibly homozygous139414708
14103483552103483675CTTATTACTAGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCC15GENICheterozygous139414709
14103486245103486246GT52GENIChomozygous139612770
14103486793103486793A52GENIChomozygous139414711
14103486794103486794AAACA53GENIChomozygous139414712
14103486796103486797TA50GENIChomozygous139612771
14103487264103487265GA27GENIChomozygous139612772
14103487506103487507AG48GENIChomozygous139612773
14103495955103495956TC54GENIChomozygous139612774
14103496135103496161TAGGTATGATGCTCACTCTTAGACGG46GENIChomozygous139414713