chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4214696690214696691TTAA2GENIChomozygous57081080
4214698797214698798A-10GENICpossibly homozygous57081081
4214698989214698991AC--6GENICheterozygous57365691
4214701530214701531CT20GENIChomozygous57081082
4214701658214701659CT24GENIChomozygous57081083
4214701781214701782CA21GENIChomozygous57081084
4214702040214702041CT20GENICheterozygous57081085
4214702048214702049AT22GENICheterozygous57081086
4214702055214702056AG22GENICheterozygous57081087
4214702059214702060CT27GENICheterozygous57081088
4214702142214702143GA32GENICheterozygous57081089
4214702388214702389TC21GENIChomozygous57081090
4214702438214702439TC22GENIChomozygous57081091
4214702442214702443TA22GENIChomozygous57081092
4214702448214702449AG22GENIChomozygous57081093
4214702531214702532TC19GENICheterozygous57081094
4214702531214702532TTAGGCATGTCTGC18GENIChomozygous57081095
4214702654214702655TC16GENIChomozygous57081096
4214702796214702797T-27GENIChomozygous57081097
4214702982214702983TC28GENIChomozygous57081098