chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110369262110369263TC23GENIChomozygous111672755
3110372441110372442GA25GENIChomozygous111672757
3110373623110373624TC28GENIChomozygous111672759
3110373894110373895CT34GENIChomozygous111672761
3110374580110374581CT28GENIChomozygous112003569
3110377945110377946TC37GENIChomozygous111672765
3110380099110380100AG34GENIChomozygous111672767
3110383290110383291CT32GENIChomozygous111672769
3110384199110384200GA30GENIChomozygous111672771
3110385311110385312GA30GENIChomozygous111672772
3110388385110388386GA39GENIChomozygous111672774
3110388893110388894AG28GENIChomozygous111672776
3110390055110390056AG37GENIChomozygous111672777
3110391724110391725AG31GENIChomozygous111672779
3110395365110395366CG26GENIChomozygous111672781
3110397181110397182TC30GENIChomozygous111672785
3110398517110398518TC36GENIChomozygous111672788
3110399798110399799GA29GENIChomozygous111672791
3110402686110402687CT29GENIChomozygous111672794
3110402849110402850TG31GENIChomozygous111672796
3110404607110404608CA24GENIChomozygous111672798
3110404739110404740GA24GENIChomozygous111672799
3110404853110404854CT18GENIChomozygous111672801
3110405179110405180GA25GENIChomozygous111672803
3110407838110407839CG23GENIChomozygous111672805
3110412256110412257CT19GENIChomozygous111672809
3110415663110415664CG29GENIChomozygous112003585
3110415668110415669CT30GENIChomozygous111672820
3110416029110416030GT25GENIChomozygous112255707
3110419387110419388GA26GENIChomozygous111672825
3110414970110414971AT5GENIChomozygous119684721
3110415333110415334GA10GENIChomozygous119739757
3110415634110415635TA23GENIChomozygous119651105