chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4163753181163753182GA11GENIChomozygous565778997
4163754047163754048GA28GENIChomozygous565778998
4163755295163755296CCT17GENIChomozygous709933387
4163755619163755620CCT6GENIChomozygous709933388
4163755662163755663CCT7GENIChomozygous709933389
4163755670163755671T-7GENIChomozygous709933390
4163755688163755700TCTGTCTGTCTA------------2GENIChomozygous709933391
4163755756163755757CCT25GENIChomozygous709933392
4163755764163755765TTATC15GENIChomozygous709933393
4163755799163755807CTACCTGT--------18GENIChomozygous709933394
4163759248163759249CT27GENIChomozygous568409763
4163760224163760225TC14GENIChomozygous565778999
4163761367163761368A-20GENIChomozygous709933395
4163761723163761724GA19GENIChomozygous565779000
4163761910163761911TC19GENIChomozygous565779001
4163764382163764383GT38GENIChomozygous565779002
4163765473163765474AG27GENIChomozygous565779003
4163765474163765475GA27GENIChomozygous565779004
4163766022163766023AACTTCTTTTTTTTTTGGTT1GENIChomozygous709933396
4163766147163766148GT4GENIChomozygous568409764
4163766163163766164GT3GENIChomozygous568409765
4163766184163766185AT3GENIChomozygous565779005
4163766712163766713TC33GENIChomozygous565779006
4163767563163767564AC28GENIChomozygous565779007
4163769001163769002GA24GENIChomozygous565779008
4163771058163771059CCT11GENICheterozygous709933398
4163771291163771292CT9GENIChomozygous565779009
4163771602163771603G-4GENIChomozygous709933399