chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4214698797214698800AAA---1GENIChomozygous58371837
4214698799214698800AATT2GENICheterozygous58371839
4214701530214701531CT19GENIChomozygous57081082
4214701658214701659CT22GENICpossibly homozygous57081083
4214701781214701782CA29GENIChomozygous57081084
4214702040214702041CT4GENIChomozygous57081085
4214702048214702049AT1GENIChomozygous57081086
4214702388214702389TC22GENICpossibly homozygous57081090
4214702438214702439TC6GENIChomozygous57081091
4214702442214702443TA5GENIChomozygous57081092
4214702448214702449AG9GENIChomozygous57081093
4214702531214702532TTAGGCATGTCTGC3GENIChomozygous57081095
4214702654214702655TC21GENICpossibly homozygous57081096
4214702796214702797T-20GENIChomozygous57081097
4214702982214702983TC17GENIChomozygous57081098