chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3164995629164995629G4GENIChomozygous73776909
3164999453164999454GA26GENIChomozygous73776912
3165002265165002266AG7GENIChomozygous72551090
3165002272165002273TA11GENIChomozygous72551093
3165002301165002302GT7GENIChomozygous72551099
3165000855165000856AG18GENIChomozygous73105248
3164998242164998243AT20GENIChomozygous72286667
3165002791165002792CT4GENIChomozygous73776916
3165005150165005151CG27GENIChomozygous73776919
3165007517165007518GA23GENIChomozygous73776923
3165007625165007626AG18GENIChomozygous73776927
3165007647165007648TC19GENIChomozygous72551213
3165009154165009155TG20GENIChomozygous73776931
3165009230165009231TA19GENIChomozygous72551216
3165013136165013136TAT8GENICheterozygous73776935
3165013142165013143CT5GENIChomozygous72551231
3165014479165014480TC13GENIChomozygous73776939
3165014739165014740GA20GENIChomozygous72551236
3165015017165015018CT16GENIChomozygous73776943
3165015164165015165CT15GENIChomozygous73776946
3165015356165015357CT25GENIChomozygous73776950
3165015395165015396GA12GENIChomozygous73776954
3165017674165017675AG18GENIChomozygous72551241
3165017752165017753AC10GENIChomozygous72551243
3165021123165021124TC18GENIChomozygous72551246
3165021711165021712TC20GENIChomozygous73776958
3165022190165022191GA16GENICheterozygous73776962
3165022310165022311CT15GENIChomozygous73776965