chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135415991354159914GGTTT11GENIChomozygous50042483
135416110854161109CT3GENIChomozygous50042485
135416323454163235GT25GENIChomozygous49952164
135416386354163864GC24GENIChomozygous49952165
135416409454164095AG15GENIChomozygous50042487
135416451454164515AC25GENIChomozygous50042489
135416507754165078GA30GENIChomozygous50042491
135416566254165663CT15GENIChomozygous50042493
135416594654165947GA24GENIChomozygous50042495
135416610054166102CG--16GENIChomozygous50042497
135416614554166147AT--13GENIChomozygous50042499
135416642154166422AG21GENIChomozygous49952167
135416682154166822CT28GENIChomozygous50042501
135416700154167002TC26GENIChomozygous49952170
135416783954167840GA17GENIChomozygous49952171
135416887254168873CCAG30GENIChomozygous49952173
135416898854168989CT27GENIChomozygous49952174
135416956454169565GA22GENIChomozygous49952175
135417027754170278GT26GENIChomozygous49952176
135417076754170768TC17GENIChomozygous49952177
135417100054171010TGTGTGTGTG----------10GENIChomozygous49952178
135417104054171041TC16GENIChomozygous49952180
135417119154171193GT--12GENICheterozygous50518449
135417282554172826CT33GENIChomozygous49952183
135417122954171230CG17GENIChomozygous49952181
135417249554172496AG15GENIChomozygous49952182
135417304554173046TC35GENIChomozygous49952184
135417369054173691AG18GENIChomozygous49952185
135417394754173948CCG17GENIChomozygous49952186
135417404754174048CT23GENIChomozygous49952187
135417498654174990TCCC----11GENIChomozygous49952188
135417640754176408AG7GENIChomozygous49952189
135417675254176753TC18GENIChomozygous50042505
135417686054176861AG23GENIChomozygous50042507
135417747554177476TTTTTGTTTG18GENIChomozygous50042511
135417743854177439CT23GENIChomozygous50889901