chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2192973776192973777CT16GENIChomozygous59918972
2192973779192973780TC16GENIChomozygous59918973
2192975004192975005AG15GENIChomozygous59311598
2192975477192975478CT14GENIChomozygous59918974
2192975577192975578AC14GENIChomozygous59918975
2192976031192976032GA10GENIChomozygous59311601
2192976257192976258CA11GENIChomozygous59918976
2192976539192976540AT10GENIChomozygous59311603
2192976557192976558TC8GENIChomozygous59918977
2192982395192982396GA22GENIChomozygous59311608
2192982649192982650CG14GENIChomozygous59311610
2192984280192984281GC20GENIChomozygous59918978
2192987561192987562A-21GENIChomozygous59918979
2192988535192988536TC10GENIChomozygous59311622
2192989427192989428AG9GENIChomozygous59311627
2192991937192991938GA15GENIChomozygous59918981
2192992344192992345CCACAAAACAAA11GENIChomozygous59311635
2192993737192993738GA9GENIChomozygous59918982
2192993995192993996A-18GENIChomozygous59918983
2192994494192994495TG17GENIChomozygous59311640
2192995789192995790CT16GENIChomozygous59311643
2192998594192998595AC15GENIChomozygous59918984
2192999796192999797CCCT17GENIChomozygous59311654
2193001058193001059GA19GENIChomozygous59918987