chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99402465394024654TG35GENIChomozygous52051628
99402514394025144GA26GENIChomozygous52280094
99402586894025869GT36GENIChomozygous52051630
99402618294026183GA48GENICpossibly homozygous52051632
99402635194026352AAG8GENIChomozygous52051634
99402669994026700CT38GENIChomozygous52051636
99402695094026951GA29GENIChomozygous52280095
99402729594027296GA22GENIChomozygous52280097
99402810894028109GGA31GENIChomozygous52280098
99402960094029601GC39GENIChomozygous52280100
99402970594029706A-24GENIChomozygous52051640
99402971594029716A-27GENIChomozygous52051642
99402973294029733TC28GENIChomozygous52280101
99403065094030651AG24GENIChomozygous52051645
99403138894031389GA27GENIChomozygous52280103
99402698094027099AACAAAAAGAGAGCAGGGGGGCTGGGGATTTAGCTCAGTGGTAGAACGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAGAACCAAAAAAAAAACAAA-----------------------------------------------------------------------------------------------------------------------21GENIChomozygous52861447
99402971794029718AG27GENIChomozygous52861449
99402973094029731CA29GENIChomozygous52861451
99402905494029056AC--16GENICheterozygous52955357