chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76076530260765303AG14GENIChomozygous116332219
76076556860765569GA11GENIChomozygous116332220
76076560760765608GA11GENIChomozygous116332221
76076606960766070GA33GENICpossibly homozygous116370253
76076607060766071CT34GENIChomozygous116370254
76076608960766090AT26GENIChomozygous116177890
76076609060766091GC26GENIChomozygous116177892
76076669560766696AG28GENIChomozygous116370255
76076713460767135GA15GENIChomozygous116370256
76076749360767494CT30GENIChomozygous116370257
76076916360769164GA19GENIChomozygous116332223
76076942860769429GA18GENIChomozygous116332224
76076949960769500AG35GENIChomozygous116332225
76076973660769737TC25GENIChomozygous116332227
76076973960769740AG25GENIChomozygous116332228
76077002160770022CT26GENIChomozygous116332229
76077006760770068GA24GENIChomozygous116332231
76077009360770094AG24GENIChomozygous116332232
76077098160770982AG25GENIChomozygous116332233
76077137160771372TC23GENIChomozygous116177896
76077233760772338CT19GENIChomozygous116332235
76077276660772767TC26GENIChomozygous116332236
76077291960772920TC21GENIChomozygous116332237
76077426560774266GA19GENIChomozygous116370258
76077426660774267CA19GENIChomozygous116370259
76077434960774350TA40GENIChomozygous116370260
76077582660775827GT18GENIChomozygous116177906
76077586460775865GA20GENIChomozygous116370261
76077615460776155CT23GENICpossibly homozygous116370262
76077708060777081AC23GENIChomozygous116177908