chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4163753181163753182GA29GENIChomozygous556005435
4163754047163754048GA26GENIChomozygous556005436
4163755295163755296CCT10GENIChomozygous704848862
4163755619163755620CCT1GENIChomozygous704848863
4163755662163755663CCT1GENIChomozygous704848864
4163755756163755757CCT8GENIChomozygous704848865
4163755764163755765TTATC6GENIChomozygous704848866
4163755799163755807CTACCTGT--------10GENIChomozygous704848867
4163759248163759249CT27GENIChomozygous558609853
4163760224163760225TC14GENIChomozygous556005437
4163761367163761368A-22GENIChomozygous704848868
4163761723163761724GA23GENIChomozygous556005438
4163761910163761911TC25GENIChomozygous556005439
4163764382163764383GT16GENIChomozygous556005440
4163765473163765474AG21GENIChomozygous556005441
4163765474163765475GA22GENIChomozygous556005442
4163766022163766023AACTTCTTTTTTTTTTGGTT3GENIChomozygous704848869
4163766147163766148GT7GENIChomozygous558609854
4163766163163766164GT7GENIChomozygous558609855
4163766184163766185AT5GENIChomozygous556005443
4163766712163766713TC20GENIChomozygous556005444
4163767563163767564AC20GENIChomozygous556005445
4163769001163769002GA21GENIChomozygous556005446
4163771058163771059CCT4GENICheterozygous704848871
4163771291163771292CT22GENICpossibly homozygous556005447
4163771602163771603G-14GENIChomozygous704848872