chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103635731536357316A-1GENIChomozygous52139319
103635885236358853AG7GENIChomozygous51413782
103635903436359035T-1GENIChomozygous52040293
103636096336360964AG16GENIChomozygous51413790
103636117136361172GA5GENIChomozygous51413792
103636342436363425CG18GENICpossibly homozygous51413794
103636411136364112AT15GENIChomozygous51413796
103636440836364409TC13GENIChomozygous51413798
103636497036364971CT27GENICpossibly homozygous52139321
103636513436365135AC12GENIChomozygous52139323
103636545336365454CT18GENICpossibly homozygous52139325
103636635536366356GA20GENIChomozygous52139329
103636660936366610GA27GENICpossibly homozygous51413802
103636687936366880GA21GENICheterozygous52139331
103636727936367280T-3GENIChomozygous51413812
103636750636367507CT13GENICheterozygous51413825
103637063936370640A-10GENICpossibly homozygous51413829