chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5176256133176256134CT20GENIChomozygous55847943
5176256549176256558GAGACAGGG---------11GENIChomozygous55847945
5176257361176257362TC20GENIChomozygous55847947
5176257662176257663TC18GENIChomozygous55847949
5176258200176258201AG22GENIChomozygous55847951
5176258697176258698AAC10GENIChomozygous55847953
5176258806176258807AG15GENIChomozygous55847955
5176259833176259834AG11GENIChomozygous55847957
5176259861176259862TC11GENIChomozygous55847959
5176260486176260487C-4GENIChomozygous55847961
5176260694176260695TC27GENIChomozygous55847963
5176261112176261113AG23GENIChomozygous55847965
5176261495176261496GA17GENIChomozygous55847967
5176261601176261602TA25GENIChomozygous55847969
5176262538176262539TTC22GENIChomozygous55847971
5176262539176262540TTGTCTGTC23GENIChomozygous55847974
5176262978176262979AG25GENICpossibly homozygous55847976
5176263658176263659CT9GENIChomozygous55847978
5176263833176263834TTC3GENICheterozygous55847980
5176264088176264089AG24GENIChomozygous55847982
5176264644176264645TC33GENIChomozygous55847984
5176264947176264948TC23GENIChomozygous55847986
5176265006176265007TTC9GENICheterozygous55847987
5176265531176265543CAGACAGACAGG------------16GENIChomozygous56366113
5176265904176265905TG8GENIChomozygous55847993
5176265906176265908CC--8GENIChomozygous55847995
5176265961176265962AG23GENIChomozygous55847997
5176265979176265984TTTTT-----5GENICheterozygous55847999
5176266192176266193CA29GENIChomozygous55848000
5176267503176267504CA12GENIChomozygous55848002