chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5143260604143260606AA--16GENICheterozygous55759106
5143260605143260606A-16GENICheterozygous55759107
5143261105143261106CT23GENIChomozygous55759108
5143261652143261654GT--15GENIChomozygous56355253
5143261655143261669TGCAGGTATACAGG--------------18GENIChomozygous56355254
5143262275143262276AG25GENIChomozygous55759111
5143262438143262439GA27GENIChomozygous55759112
5143263473143263474GGGGGC10GENIChomozygous56355255
5143263477143263484TAGTACA-------8GENIChomozygous56355256
5143263545143263546GT28GENIChomozygous55759117
5143264377143264378GC24GENIChomozygous55759118
5143266675143266676CG30GENIChomozygous55759119
5143267749143267752AAA---7GENICpossibly homozygous55759120
5143273181143273182AG17GENIChomozygous55759124
5143273354143273355CCCT14GENIChomozygous55759125
5143275031143275032GA14GENIChomozygous55759126
5143276060143276062AA--15GENIChomozygous55759127
5143276647143276654AAAAAAA-------7GENIChomozygous55759129
5143277873143277874AG15GENIChomozygous55759130
5143278412143278413CT8GENIChomozygous55759132
5143278583143278584AAT11GENIChomozygous55759133
5143279644143279645TC13GENIChomozygous55759134
5143279950143279951TA3GENIChomozygous55759135
5143283394143283401TTCAACC-------33GENIChomozygous55759136
5143284462143284463GGA17GENICpossibly homozygous55759140
5143284856143284857CCT7GENICheterozygous55759141
5143285526143285527TG24GENIChomozygous55759142
5143286150143286151TC23GENIChomozygous55759143
5143286394143286395A-12GENIChomozygous55759144
5143286739143286747TTTCTCTC--------3GENIChomozygous56458328
5143286793143286813CCTCTCCCTCTCCCTCTCTG--------------------2GENIChomozygous56458329
5143286826143286827GT17GENIChomozygous55759150
5143287079143287080GT24GENIChomozygous55759151
5143287158143287159AG18GENIChomozygous55759152
5143287295143287296CT21GENIChomozygous55759153
5143287513143287514GGCCCC1GENIChomozygous56458330
5143287865143287866AG3GENIChomozygous55759157
5143287910143287911TC1GENIChomozygous55759158