chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2173984080173984080CTCCA16GENIChomozygous127706719
2173984081173984082CT14GENIChomozygous120172086
2173984082173984083GC14GENIChomozygous120172087
2173984086173984086AAAAAA14GENIChomozygous127706720
2173989999173990000GT15GENIChomozygous110134975
2173990001173990002AG15GENIChomozygous110134976
2173990006173990007GT14GENIChomozygous110134977
2173990138173990139TC19GENIChomozygous110612138
2173990140173990141A19GENIChomozygous127706725
2173994189173994190A18GENIChomozygous127706727
2173994194173994195A18GENIChomozygous127706728
2173994264173994268AAAT12GENIChomozygous127706729
2173994293173994294C12GENIChomozygous127706730
2173994315173994316A12GENIChomozygous127706731
2173994329173994330T12GENIChomozygous127706732
2173994372173994373TG8GENIChomozygous121531264
2173994374173994375GT8GENIChomozygous121531265
2173994408173994408G3GENIChomozygous127706733
2173997066173997067G3GENIChomozygous129868735
2173997119173997119T3GENIChomozygous127706734
2173997151173997152C4GENIChomozygous127706735
2173997174173997174T4GENIChomozygous127706736
2173997194173997195CA6GENIChomozygous121531270
2173997195173997196TC6GENIChomozygous121531271
2173997205173997205T4GENIChomozygous127706737
2173997314173997314T3GENIChomozygous127706738
2173998188173998189CG27GENIChomozygous110134985
2173998225173998225G27GENIChomozygous127706740
2173997046173997047A2GENIChomozygous131295812
2173997041173997041C1GENIChomozygous131295811