chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132746643927466440TC39GENIChomozygous114517695
132746781627467817CG33GENIChomozygous114304196
132746798827467989TC35GENIChomozygous114517697
132746853927468540CT32GENIChomozygous114304197
132746889827468899GA35GENIChomozygous114517699
132746986327469864AG42GENIChomozygous114517701
132747199227471993CA37GENIChomozygous114304199
132747202927472030CT44GENIChomozygous114304200
132747283227472833AT30GENIChomozygous114304201
132747300327473004AC31GENIChomozygous114304202
132747449527474496GA31GENIChomozygous114304203
132747646827476469TC30GENIChomozygous114304205
132747734127477342CT40GENIChomozygous114304206
132747772927477730GA32GENIChomozygous114304207
132747786427477865AT36GENIChomozygous114304208
132747811727478118TC27GENIChomozygous114304209
132747885827478859CT24GENIChomozygous114304210
132748049427480495CA32GENIChomozygous114304212
132748110027481101GA21GENIChomozygous114304213
132748213027482131GA39GENIChomozygous114304214
132748260427482605TC23GENIChomozygous114517703
132748278327482784TC33GENIChomozygous114517705
132748290027482901AG36GENIChomozygous114517707
132748305627483057CT31GENIChomozygous114517709
132748320527483206GA29GENIChomozygous114517711
132748343127483432TC22GENIChomozygous114304215