chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14103451255103451256TA39GENICpossibly homozygous139612754
14103453323103453324AG72GENIChomozygous139612755
14103463027103463028GA63GENIChomozygous139612756
14103458335103458335TATT60GENIChomozygous139414705
14103464842103464843CG67GENIChomozygous139612757
14103464904103464905CT72GENIChomozygous139612758
14103466163103466164T26GENICheterozygous139414706
14103470366103470367G22GENICheterozygous139414707
14103471442103471443TC56GENIChomozygous139612759
14103471575103471576CT44GENIChomozygous139612760
14103472208103472209GC69GENIChomozygous139612761
14103472971103472972TG75GENIChomozygous139612762
14103473021103473022CA58GENIChomozygous139612763
14103478019103478019AGAGTGATGGG18GENIChomozygous139414708
14103480016103480017AT27GENIChomozygous139612764
14103480314103480315AG49GENIChomozygous139612765
14103480591103480592CA42GENIChomozygous139612766
14103482584103482585AT45GENIChomozygous139612767
14103482716103482717CT50GENIChomozygous139612768
14103483251103483252TC55GENIChomozygous139612769
14103483552103483675CTTATTACTAGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCC18GENICheterozygous139414709
14103484148103484148T54GENIChomozygous139414710
14103486245103486246GT49GENIChomozygous139612770
14103486793103486793A48GENIChomozygous139414711
14103486794103486794AAACA48GENIChomozygous139414712
14103486796103486797TA45GENIChomozygous139612771
14103487264103487265GA33GENIChomozygous139612772
14103487506103487507AG63GENIChomozygous139612773
14103493316103493317TC11GENIChomozygous403368503
14103493318103493319TC11GENIChomozygous403368505
14103493314103493315TC11GENIChomozygous403368501
14103493314103493315T11GENICheterozygous403368502
14103493316103493317T11GENICheterozygous403368504
14103493318103493319T11GENICheterozygous403368506
14103495955103495956TC54GENIChomozygous139612774
14103496135103496161TAGGTATGATGCTCACTCTTAGACGG46GENIChomozygous139414713