chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2188745904188745905CT65GENIChomozygous110993892
2188746796188746797TC71GENIChomozygous110804688
2188747628188747629CT61GENIChomozygous110804689
2188748716188748717GC78GENIChomozygous110804692
2188749427188749428CT66GENIChomozygous110169788
2188749939188749940AG66GENIChomozygous110804693
2188750224188750225GA67GENIChomozygous110804694
2188750226188750227TC67GENIChomozygous110169794
2188751316188751317TC85GENIChomozygous110804695
2188751685188751686TG69GENICpossibly homozygous110169797
2188751785188751785T64GENICpossibly homozygous130873853
2188752166188752167TG78GENIChomozygous110169799
2188752398188752399A54GENICpossibly homozygous130873854
2188752438188752439AG52GENIChomozygous110169803
2188754271188754272AG58GENIChomozygous110169807
2188754333188754334AG71GENIChomozygous110169809
2188754793188754793GTT13GENICheterozygous131811105
2188753583188753584T58GENIChomozygous127717514
2188754548188754549A40GENICheterozygous127717515
2188750503188750504CA57GENIChomozygous111278572
2188751589188751590GA67GENIChomozygous111278574
2188752485188752486GA62GENIChomozygous111278576
2188754899188754900CT41GENIChomozygous111278580
2188751848188751849CT63GENIChomozygous110906280
2188754949188754950AG46GENIChomozygous110169815
2188755052188755053CT56GENIChomozygous110993902
2188755203188755203TCCTTCACCG80GENIChomozygous127717517
2188755356188755357GA60GENIChomozygous111278582
2188756530188756536CGCTCG42GENIChomozygous127717518
2188756727188756728T50GENIChomozygous127717519