chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3152929849152929850AG40GENIChomozygous136842018
3152929884152929885GA40GENIChomozygous136842019
3152929897152929898AG38GENIChomozygous136842020
3152930226152930227T34GENIChomozygous136596266
3152930232152930233GT35GENIChomozygous136842021
3152930311152930312T39GENIChomozygous136596267
3152930361152930362TG41GENIChomozygous136842022
3152930577152930578AG41GENIChomozygous136842023
3152930638152930639CT44GENIChomozygous136842024
3152930737152930738AG41GENICpossibly homozygous136842025
3152930796152930797AG34GENIChomozygous136842026
3152931129152931130CT50GENIChomozygous136842027
3152931168152931169GA53GENIChomozygous136842028
3152932409152932410AG53GENIChomozygous136842029
3152932429152932430CT46GENIChomozygous136842030
3152933541152933542TG52GENIChomozygous136842031
3152933976152933977CG49GENIChomozygous136842032
3152934230152934231TC42GENIChomozygous136842033
3152934617152934618GA37GENIChomozygous136842034
3152934796152934797GC46GENIChomozygous136842035
3152934797152934798CA46GENIChomozygous136842036
3152934862152934863TC45GENIChomozygous136842037
3152935837152935838CT45GENIChomozygous136842038
3152936234152936235CT44GENIChomozygous136842039
3152932151152932152TG44GENIChomozygous154148259
3152932141152932142GC40GENIChomozygous154148258