chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108802681488026815AG72GENIChomozygous144081129
108802721288027213GA68GENIChomozygous146972129
108802906788029068AG61GENIChomozygous146972130
108803042988030430CT67GENIChomozygous145748678
108803060688030607AT49GENIChomozygous144416694
108803093688030937TC37GENICheterozygous154657641
108803120288031203CT57GENIChomozygous146972131
108803232488032325CT68GENIChomozygous144416697
108803264788032648AG65GENIChomozygous144081138
108803560188035602TC80GENIChomozygous138843337
108803696888036969GA86GENIChomozygous146972132
108803721488037215TG76GENIChomozygous146972133
108803899888038999GA34GENIChomozygous146972134
108803093688030937T37GENIChomozygous403294246
108803276388032763A55GENIChomozygous144077776
108803996488039966CA18GENIChomozygous146939644
108803091988030937ACCACCACCACCACCACT37GENIChomozygous146939642
108803905288039052TCTCTCTCTCTCTCTCTCTT15GENIChomozygous146939643
108803282988032829GAG66GENIChomozygous144077777
108804000088040002CA21GENIChomozygous146939645
108804079988040800TA35GENICheterozygous154657647
108804079988040800T35GENICheterozygous403294249
108804079988040800TC35GENIChomozygous403294250
108804080188040802TC35GENIChomozygous146972135
108804083088040831TC40GENIChomozygous146972136
108804320288043203AG57GENIChomozygous144081150
108804553088045531CT74GENIChomozygous146972137
108804650288046503TC42GENIChomozygous144081152
108804651988046519G39GENICpossibly homozygous146939646