chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77046885470468855GA36GENIChomozygous54445201
77046964870469649AG30GENIChomozygous54445203
77047149370471494CA38GENIChomozygous54445205
77047161570471616TC29GENIChomozygous54445207
77047200070472001AG35GENIChomozygous54445209
77047212870472129GA37GENIChomozygous54445210
77047219270472193AG46GENIChomozygous54445212
77047257670472577CT35GENIChomozygous54445214
77047284870472862AGGCAGGAAGCTGG--------------19GENIChomozygous54445216
77047330370473313TTTTGTTTTG----------12GENIChomozygous54445218
77047406270474063TC43GENIChomozygous54445221
77047412870474129CT35GENIChomozygous54445223
77047617770476178AG32GENIChomozygous54445225
77047635270476353TC32GENIChomozygous54445227
77047723770477238CT35GENIChomozygous54445229
77047738670477387CT42GENIChomozygous54445231
77047774970477750GA22GENIChomozygous54445233
77047776470477765AG25GENIChomozygous54445235
77047832870478329TC20GENIChomozygous54445237
77047854970478550TA30GENIChomozygous54445239
77047909970479119ACACACACACACACACACAC--------------------11GENIChomozygous54906947
77047935470479355CT15GENIChomozygous54445241
77047980570479806GA23GENIChomozygous54445243
77047998470479985TC25GENIChomozygous54445245
77048061470480615CT28GENIChomozygous54445247
77048074170480742GGACAC5GENICheterozygous53956631
77048086470480865TC19GENIChomozygous53956633
77048153270481533AG28GENIChomozygous54445251
77048201370482014CA30GENIChomozygous54445253
77048204270482043TC29GENIChomozygous54445255
77048271070482711GGT16GENICpossibly homozygous53956635
77048299570482996GA22GENIChomozygous54445257
77048306970483077CCGCAAGG--------31GENIChomozygous54445259
77048492170484922CT14GENIChomozygous53956637
77048521570485216CT20GENIChomozygous54445261
77048599870485999CT23GENIChomozygous54445263