chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14103451255103451256TA16GENIChomozygous139612754
14103453323103453324AG32GENIChomozygous139612755
14103463027103463028GA26GENIChomozygous139612756
14103464842103464843CG9GENIChomozygous139612757
14103464904103464905CT11GENIChomozygous139612758
14103471442103471443TC17GENIChomozygous139612759
14103471575103471576CT10GENIChomozygous139612760
14103472208103472209GC19GENIChomozygous139612761
14103472971103472972TG26GENIChomozygous139612762
14103473021103473022CA30GENICpossibly homozygous139612763
14103480016103480017AT9GENIChomozygous139612764
14103480314103480315AG20GENIChomozygous139612765
14103480591103480592CA11GENIChomozygous139612766
14103482584103482585AT23GENIChomozygous139612767
14103482716103482717CT21GENIChomozygous139612768
14103483251103483252TC14GENICpossibly homozygous139612769
14103484148103484148T27GENIChomozygous139414710
14103458335103458335TATT33GENIChomozygous139414705
14103470366103470367G9GENICheterozygous139414707
14103478019103478019AGAGTGATGGG11GENIChomozygous139414708
14103483552103483675CTTATTACTAGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCC4GENICheterozygous139414709
14103486245103486246GT16GENIChomozygous139612770
14103486793103486793A23GENIChomozygous139414711
14103486794103486794AAACA24GENIChomozygous139414712
14103486796103486797TA23GENIChomozygous139612771
14103487264103487265GA13GENIChomozygous139612772
14103487506103487507AG18GENIChomozygous139612773
14103493316103493317TC8GENIChomozygous403368503
14103493316103493317T8GENICheterozygous403368504
14103493314103493315TC8GENICheterozygous403368501
14103493314103493315T8GENICheterozygous403368502
14103493318103493319TC8GENIChomozygous403368505
14103493318103493319T8GENICheterozygous403368506
14103495955103495956TC23GENIChomozygous139612774
14103496135103496161TAGGTATGATGCTCACTCTTAGACGG17GENIChomozygous139414713