chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18511306685113067CG25GENIChomozygous120522187
18511306885113068G26GENIChomozygous127399743
18511306985113069T27GENIChomozygous127399744
18511307485113074A28GENIChomozygous127399745
18511308185113081G27GENIChomozygous127399746
18511310785113107C28GENIChomozygous127399747
18511313585113135G27GENIChomozygous127399748
18511314385113144C28GENIChomozygous127399749
18511314985113149G28GENIChomozygous127399750
18511315585113155G28GENIChomozygous127399751
18511316185113161GG32GENIChomozygous127399752
18511316985113169G39GENIChomozygous127399753
18511319385113194C52GENIChomozygous127399754
18511332485113326CC36GENIChomozygous127399755
18511333285113333CG39GENIChomozygous120472192
18511333285113332G37GENIChomozygous127399756
18511336185113361C36GENIChomozygous127399757
18511337485113374G34GENIChomozygous127399758
18511340685113408CC35GENIChomozygous127399759
18511342285113422G36GENIChomozygous127399760
18511342985113429G35GENIChomozygous127399761
18511343385113433G35GENIChomozygous127399762
18511344185113441C32GENIChomozygous127399763
18511350885113509C27GENIChomozygous127399764
18511357285113572G35GENIChomozygous127399765
18511358185113582G39GENIChomozygous127399766
18511362785113627C46GENIChomozygous127399767
18511364985113650C46GENIChomozygous127399768
18512003485120034AGCT55GENIChomozygous127399769