chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91021647810216479CA22GENIChomozygous988578124
91022251410222515CT41GENIChomozygous988578125
91022284210222843CT26GENIChomozygous988578126
91022439010224391CA47GENIChomozygous988578127
91022472910224730GA24GENIChomozygous988578128
91022755610227557TC30GENIChomozygous988578129
91023050210230503AG15GENIChomozygous988578130
91023361210233613TG23GENIChomozygous988578131
91023446010234461AC28GENIChomozygous988578132
91023561510235616GC28GENIChomozygous988578133
91023912110239122AG35GENIChomozygous988578134
91023941710239418AG22GENIChomozygous988578135
91023982010239821TC32GENIChomozygous988578136
91023983310239834GC33GENIChomozygous988578137
91023983510239836GC32GENIChomozygous988578138
91023984210239843AC31GENIChomozygous988578139
91023984510239846AC33GENIChomozygous988578140
91024197610241977TC2GENIChomozygous988578141
91024266110242662AC33GENIChomozygous988578142
91024309810243099TC48GENIChomozygous988578143
91024486110244862AG26GENIChomozygous988578144
91024592410245925TC41GENIChomozygous988578145
91024610910246110GT36GENIChomozygous988578146
91024872610248727CT48GENIChomozygous988578147
91024957910249580AG34GENIChomozygous988578148
91024964710249648TC41GENIChomozygous988578149
91024999610249997CT34GENIChomozygous988578150
91025113810251139CT39GENIChomozygous988578151
91025343810253439GA43GENIChomozygous988578152
91025374710253748AG20GENIChomozygous988578153
91025415110254152CG21GENIChomozygous988578154
91025571910255720CT21GENIChomozygous988578155
91026048710260488CT12GENIChomozygous988578156
91026162810261629GC36GENIChomozygous988578157
91026708910267090TA40GENIChomozygous988578158
91026819110268192GA28GENIChomozygous988578159
91026852410268525AG28GENIChomozygous988578160
91027011610270117TC35GENIChomozygous988578161
91027011810270119GA35GENIChomozygous988578162
91027947210279473TC31GENIChomozygous988578163
91028057010280571AT26GENIChomozygous988578164