chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5167110393167110394TC23GENIChomozygous114282302
5167110641167110642GA19GENIChomozygous114454978
5167110643167110644AG19GENIChomozygous114454979
5167110791167110792GA18GENIChomozygous114454980
5167111339167111340CT9GENIChomozygous114454981
5167112185167112186GA25GENIChomozygous114454982
5167112311167112312CT19GENIChomozygous114454983
5167112849167112850AG23GENIChomozygous114454984
5167112901167112902AT22GENIChomozygous114454985
5167112979167112980GA12GENIChomozygous114454986
5167113081167113082AG18GENIChomozygous114454987
5167113335167113336AC19GENIChomozygous114282308
5167113869167113870TC23GENIChomozygous114454988
5167114059167114060AG17GENIChomozygous114454989
5167114253167114254CA13GENIChomozygous114454990
5167114504167114505TC14GENIChomozygous114454991
5167114556167114557GA19GENIChomozygous114454992
5167115420167115421TC19GENIChomozygous114282312
5167115849167115850CT9GENIChomozygous114282316
5167117579167117580CT8GENIChomozygous114454995
5167117587167117588GT4GENIChomozygous118859038
5167118541167118542GA17GENIChomozygous114454996
5167118589167118590GA20GENIChomozygous114454997
5167119261167119262GA22GENIChomozygous114454998
5167119874167119875TC18GENIChomozygous114454999
5167120398167120399GA20GENIChomozygous114282330
5167120907167120908TC29GENIChomozygous114282332
5167121153167121154TC22GENIChomozygous114282334
5167121173167121174CT18GENIChomozygous114282336
5167121374167121375CA13GENIChomozygous114282338
5167122485167122486GA18GENIChomozygous114455000
5167122623167122624GA13GENIChomozygous114455001
5167122654167122655TC14GENIChomozygous114282346
5167122901167122902GA14GENIChomozygous114455002
5167123847167123848GA16GENIChomozygous114282374
5167124056167124057AG15GENIChomozygous114282378
5167124168167124169CT16GENIChomozygous114455004
5167124381167124382GC21GENIChomozygous114455005
5167124654167124655GA19GENIChomozygous114455006
5167125373167125374GA23GENIChomozygous114455007