chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2188745904188745905CT79GENIChomozygous110993892
2188746796188746797TC79GENIChomozygous110804688
2188747628188747629CT67GENIChomozygous110804689
2188748716188748717GC92GENIChomozygous110804692
2188749427188749428CT71GENIChomozygous110169788
2188749939188749940AG88GENIChomozygous110804693
2188750224188750225GA78GENIChomozygous110804694
2188750226188750227TC79GENIChomozygous110169794
2188751316188751317TC59GENIChomozygous110804695
2188751685188751686TG61GENICpossibly homozygous110169797
2188751785188751785T59GENICpossibly homozygous130873853
2188751848188751849CT63GENIChomozygous110906280
2188752166188752167TG50GENIChomozygous110169799
2188752398188752399A66GENIChomozygous130873854
2188752438188752439AG72GENIChomozygous110169803
2188754271188754272AG75GENIChomozygous110169807
2188754333188754334AG67GENIChomozygous110169809
2188754793188754793GTT45GENIChomozygous131811105
2188753583188753584T66GENIChomozygous127717514
2188750503188750504CA80GENIChomozygous111278572
2188751589188751590GA71GENICpossibly homozygous111278574
2188752485188752486GA86GENIChomozygous111278576
2188754899188754900CT45GENIChomozygous111278580
2188754949188754950AG59GENIChomozygous110169815
2188755052188755053CT65GENIChomozygous110993902
2188755203188755203TCCTTCACCG57GENIChomozygous127717517
2188755356188755357GA77GENIChomozygous111278582
2188756530188756536CGCTCG44GENIChomozygous127717518
2188756554188756589CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC36GENICheterozygous131298087
2188756727188756728T45GENICpossibly homozygous127717519
2188754875188754876C40GENIChomozygous133942183