chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103635728936357290GA7GENIChomozygous51413770
103635738636357387AG12GENICheterozygous51413772
103635757136357572CT12GENICheterozygous51413774
103635901036359018CTGGGCTA--------8GENICheterozygous51413784
103635934136359342GA11GENICheterozygous51413786
103636008236360083AATG17GENICheterozygous51413788
103636096336360964AG17GENIChomozygous51413790
103636117136361172GA20GENIChomozygous51413792
103636342436363425CG12GENIChomozygous51413794
103636411136364112AT14GENIChomozygous51413796
103636440836364409TC11GENIChomozygous51413798
103636497036364971CT17GENICheterozygous52139321
103636513436365135AC14GENICheterozygous52139323
103636584636365847GA16GENICheterozygous52139327
103636635536366356GA11GENICheterozygous52139329
103636660936366610GA16GENIChomozygous51413802
103636687936366880GA11GENICheterozygous52139331
103636723236367233CT7GENIChomozygous51413810
103635903436359035T-8GENICheterozygous52040293
103637063936370640A-13GENIChomozygous51413829