chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145758962145758963AG44GENIChomozygous143258998
5145759017145759018CT42GENIChomozygous143258999
5145759023145759024GA40GENIChomozygous143259000
5145759081145759081AC48GENIChomozygous143186870
5145759259145759260CA62GENIChomozygous143259001
5145759438145759439AG43GENIChomozygous143259002
5145759690145759691TC44GENIChomozygous143259003
5145760368145760369TC22GENIChomozygous143259004
5145760398145760399CG19GENIChomozygous143259005
5145763217145763218C25GENICpossibly homozygous403996116
5145763217145763218CG25GENICheterozygous403996117
5145763213145763214C25GENICpossibly homozygous403996114
5145763213145763214CG25GENICheterozygous403996115
5145767214145767215GA28GENIChomozygous143259006
5145767831145767832TC29GENICpossibly homozygous143259007
5145768628145768629AG38GENIChomozygous143259008
5145769278145769279AG31GENIChomozygous143259009
5145765735145765736GC15GENIChomozygous143968145
5145770359145770360GA22GENIChomozygous143259010
5145770590145770591CT31GENIChomozygous143259011
5145771125145771126TG37GENIChomozygous143259012