chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2188745904188745905CT40GENIChomozygous110993892
2188746796188746797TC42GENIChomozygous110804688
2188747628188747629CT30GENIChomozygous110804689
2188748716188748717GC30GENIChomozygous110804692
2188749427188749428CT38GENIChomozygous110169788
2188749939188749940AG28GENIChomozygous110804693
2188750224188750225GA34GENIChomozygous110804694
2188750226188750227TC34GENIChomozygous110169794
2188750503188750504CA26GENIChomozygous111278572
2188751316188751317TC36GENIChomozygous110804695
2188751589188751590GA34GENIChomozygous111278574
2188751685188751686TG44GENIChomozygous110169797
2188751785188751785T38GENIChomozygous130873853
2188751848188751849CT26GENIChomozygous110906280
2188752166188752167TG26GENIChomozygous110169799
2188752398188752399A26GENIChomozygous130873854
2188752438188752439AG30GENIChomozygous110169803
2188752485188752486GA36GENIChomozygous111278576
2188753583188753584T33GENICpossibly homozygous127717514
2188754271188754272AG39GENIChomozygous110169807
2188754333188754334AG36GENIChomozygous110169809
2188754548188754549A27GENICheterozygous127717515
2188754793188754793GTT26GENIChomozygous131811105
2188754899188754900CT6GENIChomozygous111278580
2188755052188755053CT27GENIChomozygous110993902
2188755203188755203TCCTTCACCG23GENIChomozygous127717517
2188755356188755357GA33GENIChomozygous111278582
2188756530188756536CGCTCG28GENIChomozygous127717518
2188756727188756728T17GENIChomozygous127717519