chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155574176155574177GA17GENIChomozygous113183226
4155574905155574906GA26GENIChomozygous112896256
4155576361155576362CG22GENIChomozygous112896260
4155576795155576796TC23GENIChomozygous112896262
4155577017155577018AG17GENIChomozygous112896264
4155579352155579353CT20GENIChomozygous113398997
4155583294155583295TC22GENIChomozygous112896268
4155583482155583483AT15GENIChomozygous112896270
4155584526155584527TG5GENIChomozygous113398999
4155584977155584978GT23GENIChomozygous112896274
4155584995155584996GC20GENIChomozygous112896276
4155584996155584997GC20GENIChomozygous112896278
4155585314155585315CA13GENIChomozygous113183230
4155586643155586644GC3GENIChomozygous119282344
4155602528155602529AT6GENIChomozygous112896290
4155603147155603148AG22GENICpossibly homozygous113183232
4155603468155603469TC28GENIChomozygous112896294
4155604538155604539TG9GENIChomozygous112896302
4155605173155605174TA10GENIChomozygous113061873
4155605211155605212GT10GENIChomozygous113399001
4155605646155605647TC22GENIChomozygous112896310
4155607982155607983AG18GENIChomozygous112896312
4155608281155608282AG36GENIChomozygous112896314
4155609026155609027AG21GENIChomozygous112896316
4155609433155609434GA26GENIChomozygous113399003
4155609805155609806AG22GENICpossibly homozygous113183235
4155611223155611224CA25GENIChomozygous113183236
4155612544155612545TA8GENIChomozygous113399005
4155612836155612837AG15GENIChomozygous112896326
4155615080155615081TC21GENIChomozygous112896340
4155616314155616315CT13GENIChomozygous113183241
4155616559155616560GA23GENIChomozygous113183242
4155617234155617235AG29GENIChomozygous113183243
4155618064155618065AG17GENIChomozygous112896350
4155622066155622067TA25GENIChomozygous113399007