chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3164999453164999454GA37GENIChomozygous73776912
3165000855165000856AG30GENIChomozygous73105248
3165002265165002266AG17GENIChomozygous72551090
3165002272165002273TA13GENIChomozygous72551093
3165002275165002276AC14GENIChomozygous72551096
3165002301165002302GT20GENIChomozygous72551099
3165002374165002375CG25GENICheterozygous79705880
3165002413165002414CG12GENICheterozygous72551129
3165002485165002486AC1GENIChomozygous72551141
3165002525165002526CG2GENIChomozygous73247101
3165002521165002522TG2GENIChomozygous72795507
3165002626165002627CG4GENICheterozygous79705881
3165002737165002738CA10GENIChomozygous72551149
3165003101165003102TA22GENICpossibly homozygous79705882
3165003110165003111TA23GENIChomozygous74071945
3165005150165005151CG18GENIChomozygous73776919
3165007517165007518GA27GENIChomozygous73776923
3165007625165007626AG34GENIChomozygous73776927
3165007647165007648TC41GENIChomozygous72551213
3165008213165008214AG24GENIChomozygous74071948
3165009154165009155TG26GENIChomozygous73776931
3165009230165009231TA36GENIChomozygous72551216
3165009630165009631TG14GENICpossibly homozygous79705883
3165009715165009716TC12GENIChomozygous79705884
3165013142165013143CT26GENIChomozygous72551231
3165013641165013642AT10GENIChomozygous79705885
3165014479165014480TC23GENIChomozygous73776939
3165014739165014740GA23GENIChomozygous72551236
3165015017165015018CT24GENIChomozygous73776943
3165015164165015165CT28GENIChomozygous73776946
3165015356165015357CT22GENIChomozygous73776950
3165015395165015396GA14GENIChomozygous73776954
3165017674165017675AG17GENIChomozygous72551241
3165017752165017753AC18GENIChomozygous72551243
3165021123165021124TC21GENIChomozygous72551246
3165021711165021712TC27GENIChomozygous73776958
3165022190165022191GA28GENIChomozygous73776962
3165022310165022311CT36GENIChomozygous73776965
3165017376165017377GT12GENIChomozygous79661887