chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183571097435710975AG43GENIChomozygous110324744
183571277235712773GA22GENIChomozygous110324746
183571484135714842CT30GENIChomozygous110324748
183571513235715133TG4GENIChomozygous110324750
183571513435715135CG3GENIChomozygous110324752
183571819835718199AC31GENIChomozygous110324754
183571863635718637CA26GENIChomozygous110324756
183571902235719023AG48GENIChomozygous110324758
183572204935722050TC51GENIChomozygous110324760
183572380735723808AG57GENIChomozygous110324762
183572558135725582GA30GENIChomozygous110324764
183572641935726420CG63GENIChomozygous110324766
183572659135726592GA31GENIChomozygous110324768
183572667135726672CT28GENIChomozygous110324770
183572669035726691CT24GENIChomozygous110324772
183572692135726922AT37GENIChomozygous110324774
183572827635728277AC45GENIChomozygous110324776
183572867335728674TC59GENIChomozygous110324778
183572882335728824GA38GENIChomozygous110324780
183572979935729800CT40GENIChomozygous110324782
183573192635731927GA51GENIChomozygous110324784
183573216235732163AT31GENIChomozygous110324786
183579264735792648TC16GENIChomozygous110324788