chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3148386566148386567TC18GENIChomozygous111769454
3148386925148386926CT12GENIChomozygous111769456
3148387631148387632TC14GENIChomozygous111769460
3148387704148387704T18GENIChomozygous127940912
3148388465148388466TG20GENIChomozygous111769464
3148388739148388740CT20GENIChomozygous111769466
3148389287148389288TC25GENIChomozygous111769468
3148389288148389289GA25GENIChomozygous111769470
3148389480148389481AC18GENIChomozygous111769472
3148390539148390539AA19GENIChomozygous127940913
3148390912148390914TT16GENIChomozygous127940915
3148390972148390973TC11GENIChomozygous111769474
3148391069148391070TG15GENIChomozygous111769476
3148391178148391179AG15GENIChomozygous111769478
3148391264148391265GA18GENIChomozygous111769480
3148392039148392040A6GENIChomozygous127940916
3148392649148392650TC17GENIChomozygous111769482
3148393023148393024TC14GENIChomozygous111769486
3148393230148393231TC18GENIChomozygous111769490
3148395342148395343TC21GENIChomozygous111769494
3148395704148395705AT21GENIChomozygous111769496
3148397137148397138CT17GENIChomozygous111769498
3148397156148397157CT19GENIChomozygous111769500
3148397315148397315T15GENICpossibly homozygous131330196
3148388773148388774GT26GENIChomozygous112365400