chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91022251410222515CT35GENIChomozygous952912221
91022284210222843CT43GENIChomozygous952912222
91022439010224391CA26GENIChomozygous952912223
91022472910224730GA27GENIChomozygous952912224
91022755610227557TC39GENIChomozygous952912225
91023050210230503AG28GENIChomozygous952912226
91023361210233613TG18GENIChomozygous952912227
91023446010234461AC22GENIChomozygous952912228
91023561510235616GC23GENIChomozygous952912229
91023912110239122AG22GENIChomozygous952912230
91023941710239418AG24GENIChomozygous952912231
91023982010239821TC24GENIChomozygous952912232
91023983310239834GC28GENIChomozygous952912233
91023983510239836GC28GENIChomozygous952912234
91023984210239843AC27GENIChomozygous952912235
91023984510239846AC27GENIChomozygous952912236
91024266110242662AC24GENIChomozygous952912237
91024309810243099TC18GENIChomozygous952912238
91024486110244862AG39GENIChomozygous952912239
91024592410245925TC13GENIChomozygous952912240
91024610910246110GT25GENIChomozygous952912241
91024872610248727CT9GENIChomozygous952912242
91024957910249580AG16GENIChomozygous952912243
91024964710249648TC30GENIChomozygous952912244
91024999610249997CT14GENIChomozygous952912245
91025113810251139CT23GENIChomozygous952912246
91025343810253439GA17GENIChomozygous952912247
91025374710253748AG25GENIChomozygous952912248
91025859510258596GT42GENIChomozygous952912249
91026048710260488CT27GENIChomozygous952912250
91026162810261629GC22GENIChomozygous952912251
91026708910267090TA14GENIChomozygous952912252
91026819110268192GA32GENIChomozygous952912253
91026852410268525AG17GENIChomozygous952912254
91026854210268543AC21GENICheterozygous952912255
91027011610270117TC9GENIChomozygous952912256
91027011810270119GA8GENIChomozygous952912257
91027117910271180TC20GENIChomozygous952912258
91027947210279473TC32GENIChomozygous952912259