chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104690272104690273CT32GENIChomozygous51951077
10104690382104690383CT37GENIChomozygous51951080
10104690434104690435GC30GENIChomozygous51951083
10104690694104690695AG34GENIChomozygous51951086
10104690707104690708AT35GENIChomozygous51951089
10104690806104690807GA42GENIChomozygous51951092
10104690958104690959AG24GENIChomozygous51951095
10104691059104691060TC43GENIChomozygous51951097
10104691156104691158CA--28GENIChomozygous51951100
10104691189104691190CCCA25GENIChomozygous51951104
10104691308104691309TC32GENIChomozygous51951107
10104691319104691321CA--23GENIChomozygous51951110
10104691681104691682CA24GENIChomozygous51951113
10104691775104691776AT28GENIChomozygous51951116
10104691980104691981GA19GENIChomozygous51951119
10104692126104692127GA22GENIChomozygous51951122
10104692195104692196TC23GENIChomozygous51951125