chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14114128031114128032TA13GENIChomozygous113558457
14114130099114130100AG20GENIChomozygous113558459
14114139803114139804GA18GENIChomozygous113558461
14114141618114141619CG15GENIChomozygous113558463
14114141680114141681CT19GENIChomozygous113558465
14114135111114135111TATT25GENIChomozygous129198926
14114143926114143926A22GENICheterozygous129198928
14114143954114143955AG20GENICheterozygous113558467
14114143988114143989AT21GENICheterozygous113558469
14114143995114143996TG23GENICheterozygous113558471
14114144024114144025AG22GENICheterozygous113558473
14114148216114148217TC18GENIChomozygous113558475
14114148349114148350CT10GENIChomozygous118727286
14114149745114149746TG15GENIChomozygous113558477
14114149795114149796CA15GENIChomozygous113558479
14114143872114143873TC21GENICheterozygous113699777
14114148982114148983GC10GENIChomozygous113699779
14114154793114154793AGAGTGATGGG9GENIChomozygous129198930
14114157086114157087AG14GENIChomozygous113558481
14114157363114157364CA9GENIChomozygous113558483
14114159356114159357AT11GENICpossibly homozygous113558485
14114159488114159489CT11GENIChomozygous113558487
14114160023114160024TC13GENIChomozygous113558489
14114160324114160445CTTATTACTAGTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCC14GENICheterozygous129198931
14114160918114160918T14GENIChomozygous129198932
14114163015114163016GT18GENIChomozygous113558491
14114163563114163563A25GENIChomozygous129198933
14114163564114163564AAACA26GENIChomozygous129198934
14114163566114163567TA24GENIChomozygous113558493
14114164034114164035GA11GENIChomozygous113831531
14114164276114164277AG17GENIChomozygous113558495
14114172727114172728TC25GENIChomozygous113558497
14114172907114172933TAGGTATGATGCTCACTCTTAGACGG16GENIChomozygous129198935