chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18511306685113067CG8GENIChomozygous120522187
18511306885113068G8GENIChomozygous127399743
18511306985113069T8GENIChomozygous127399744
18511307485113074A8GENIChomozygous127399745
18511308185113081G9GENIChomozygous127399746
18511310785113107C10GENIChomozygous127399747
18511313585113135G15GENIChomozygous127399748
18511314385113144C15GENIChomozygous127399749
18511314985113149G15GENIChomozygous127399750
18511315585113155G18GENIChomozygous127399751
18511316185113161GG18GENIChomozygous127399752
18511316985113169G23GENIChomozygous127399753
18511319385113194C29GENIChomozygous127399754
18511332485113326CC23GENIChomozygous127399755
18511333285113332G23GENIChomozygous127399756
18511336185113361C19GENIChomozygous127399757
18511337485113374G17GENIChomozygous127399758
18511340685113408CC17GENIChomozygous127399759
18511342285113422G17GENIChomozygous127399760
18511342985113429G17GENIChomozygous127399761
18511358185113582G3GENIChomozygous127399766
18511343385113433G15GENIChomozygous127399762
18511344185113441C12GENIChomozygous127399763
18511350885113509C6GENIChomozygous127399764
18511357285113572G2GENIChomozygous127399765
18511333285113333CG22GENIChomozygous120472192
18511362785113627C9GENIChomozygous127399767
18511364985113650C11GENIChomozygous127399768
18512003485120034AGCT22GENIChomozygous127399769