chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5176256133176256134CT29GENIChomozygous55847943
5176256549176256558GAGACAGGG---------29GENIChomozygous55847945
5176257361176257362TC32GENIChomozygous55847947
5176257662176257663TC34GENIChomozygous55847949
5176258200176258201AG30GENIChomozygous55847951
5176258697176258698AAC14GENICpossibly homozygous55847953
5176258806176258807AG20GENIChomozygous55847955
5176259833176259834AG29GENIChomozygous55847957
5176259861176259862TC26GENIChomozygous55847959
5176260486176260487C-7GENIChomozygous55847961
5176260694176260695TC15GENIChomozygous55847963
5176261112176261113AG13GENIChomozygous55847965
5176261495176261496GA18GENIChomozygous55847967
5176261601176261602TA32GENIChomozygous55847969
5176262538176262539TTC19GENIChomozygous55847971
5176262539176262540TTGTCTGTC19GENIChomozygous55847974
5176262978176262979AG45GENIChomozygous55847976
5176263658176263659CT18GENIChomozygous55847978
5176263833176263834TTC4GENICheterozygous55847980
5176264088176264089AG26GENIChomozygous55847982
5176264644176264645TC25GENIChomozygous55847984
5176264947176264948TC35GENIChomozygous55847986
5176265006176265007TTC13GENIChomozygous55847987
5176265531176265543CAGACAGACAGG------------25GENIChomozygous56366113
5176265904176265905TG14GENIChomozygous55847993
5176265906176265908CC--14GENIChomozygous55847995
5176265961176265962AG8GENIChomozygous55847997
5176265979176265984TTTTT-----4GENICheterozygous55847999
5176266192176266193CA22GENIChomozygous55848000
5176267503176267504CA11GENIChomozygous55848002