chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85685881356858814AATGTTTT1GENIChomozygous52980265
85685929856859299AG30GENIChomozygous52651615
85685951156859512CT20GENIChomozygous53341693
85685976256859763GA32GENIChomozygous52651618
85686154156861542TC27GENIChomozygous52651630
85686361656863617G-22GENIChomozygous52651636
85686438356864384AAG26GENIChomozygous52651639
85686449756864498GT20GENICpossibly homozygous52651649
85686474156864745TGAA----14GENIChomozygous52651651
85686912456869129AAAAA-----1GENIChomozygous52651655
85686929456869296AA--16GENIChomozygous52980276
85686944256869443CG32GENICheterozygous52651661
85686963856869639CCA26GENICheterozygous53341695
85686964056869641CA33GENICheterozygous53341697
85686964056869641CCAA26GENICheterozygous53341699
85686976256869763AG42GENIChomozygous52651667
85687029456870295A-14GENICpossibly homozygous53121242
85686610956866115CTCCCT------13GENIChomozygous53121241
85687075756870758AG24GENIChomozygous53341701
85687194356871944TG18GENIChomozygous53341703
85687344856873450TT--7GENICheterozygous52651684
85687344956873450T-7GENICheterozygous52651687