chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124989068949890690AAC2GENIChomozygous50235075
124989171849891728ACACACACAC----------5GENIChomozygous50235077
124989195249891953TC21GENIChomozygous50235079
124989251549892516AG24GENIChomozygous50235081
124989256449892565CCG23GENIChomozygous50235083
124989299449892995AG22GENIChomozygous50235085
124989300649893007CT22GENIChomozygous50235087
124989366649893667GA26GENIChomozygous50235089
124989590749895908AC20GENIChomozygous50235091
124989670249896703TG26GENICheterozygous50387995
124989702849897029GT17GENIChomozygous50235093
124989710549897106GC16GENIChomozygous50235095
124989904349899044TC30GENIChomozygous50235097
124990069149900692GA24GENIChomozygous50235101
124990257749902578GA6GENIChomozygous50235103
124990313049903131CA14GENIChomozygous50235105
124990330949903310CA32GENICheterozygous50235107
124990332549903326CCG9GENICheterozygous50235109
124990343449903435GA22GENICheterozygous50235111
124990348149903482CA23GENICheterozygous50235113
124990369949903700CCTT3GENIChomozygous50235115
124990372149903722CCT12GENICheterozygous50235117
124990487949904883AAAA----14GENIChomozygous50235119
124990516749905168GA20GENIChomozygous50235121
124990714049907141AT19GENIChomozygous50235123