chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145758962145758963AG23GENIChomozygous143258998
5145759017145759018CT16GENIChomozygous143258999
5145759023145759024GA15GENIChomozygous143259000
5145759081145759081AC14GENIChomozygous143186870
5145759259145759260CA22GENIChomozygous143259001
5145759438145759439AG16GENIChomozygous143259002
5145759690145759691TC20GENIChomozygous143259003
5145760368145760369TC13GENIChomozygous143259004
5145760398145760399CG9GENIChomozygous143259005
5145763213145763214C15GENIChomozygous403996114
5145763213145763214CG15GENICheterozygous403996115
5145763217145763218C15GENIChomozygous403996116
5145763217145763218CG15GENICheterozygous403996117
5145765735145765736GC10GENIChomozygous143968145
5145767214145767215GA9GENIChomozygous143259006
5145767831145767832TC21GENIChomozygous143259007
5145768628145768629AG20GENIChomozygous143259008
5145769278145769279AG18GENIChomozygous143259009
5145770359145770360GA18GENIChomozygous143259010
5145770590145770591CT15GENIChomozygous143259011
5145771125145771126TG14GENIChomozygous143259012