chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91021647810216479CA21GENIChomozygous929672123
91022251410222515CT58GENIChomozygous929672124
91022284210222843CT35GENIChomozygous929672125
91022439010224391CA49GENIChomozygous929672126
91022637410226375AC38GENIChomozygous929672127
91023050210230503AG33GENIChomozygous929672128
91023361210233613TG36GENIChomozygous929672129
91023446010234461AC37GENIChomozygous929672130
91023561510235616GC40GENIChomozygous929672131
91023912110239122AG43GENIChomozygous929672132
91023982010239821TC34GENIChomozygous929672133
91023983310239834GC34GENIChomozygous929672134
91023983510239836GC30GENIChomozygous929672135
91023984210239843AC28GENIChomozygous929672136
91023984510239846AC30GENIChomozygous929672137
91024266110242662AC36GENIChomozygous929672138
91024309810243099TC45GENIChomozygous929672139
91024486110244862AG49GENIChomozygous929672140
91024592410245925TC33GENIChomozygous929672141
91024610910246110GT58GENICpossibly homozygous929672142
91024859510248596CT37GENIChomozygous929672143
91024872610248727CT40GENIChomozygous929672144
91024964710249648TC54GENIChomozygous929672145
91024999610249997CT39GENIChomozygous929672146
91025113810251139CT33GENIChomozygous929672147
91025343810253439GA32GENIChomozygous929672148
91025374710253748AG31GENIChomozygous929672149
91025415110254152CG25GENICpossibly homozygous929672150
91025571910255720CT39GENIChomozygous929672151
91026048710260488CT40GENIChomozygous929672152
91026162810261629GC45GENIChomozygous929672153
91026706410267065AG39GENIChomozygous929672154
91026819110268192GA54GENIChomozygous929672155
91027007010270071GA36GENIChomozygous929672156
91027011610270117TC35GENIChomozygous929672157
91027011810270119GA35GENIChomozygous929672158
91027091810270919CT53GENIChomozygous929672159
91027117910271180TC37GENIChomozygous929672160
91027947210279473TC51GENIChomozygous929672161