chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154330124243301242AAT60GENIChomozygous129251017
154330817443308175C51GENIChomozygous129251020
154330742343307424G5GENIChomozygous130698670
154333509643335097TA3GENICheterozygous112674275
154333509843335099TA4GENICheterozygous112495994
154333542043335420TC22GENIChomozygous129251031
154333893543338936G16GENIChomozygous129251032
154333896643338967G26GENIChomozygous129251033
154333896943338970A26GENIChomozygous129251034
154333900143339002C32GENIChomozygous129251035
154333901243339013A33GENIChomozygous129251036
154333917043339170CC4GENIChomozygous129251037
154333917543339175C4GENIChomozygous129251038
154337421943374220AG27GENIChomozygous119024426
154337423243374233TC23GENIChomozygous119059748
154337423343374234GT23GENIChomozygous124069863
154337426843374269TA10GENIChomozygous124069865
154337427143374272CT8GENIChomozygous124069866
154337427943374280TC5GENIChomozygous129315510
154337429443374295CA2GENIChomozygous129315511
154337496543374966AG25GENICheterozygous129315518
154337543843375439AC44GENICheterozygous130595120
154337541443375415GA40GENICheterozygous130595119
154337846143378462TC64GENICheterozygous118915733
154337846143378461TATT65GENICheterozygous134456332
154337846343378464CT64GENICheterozygous134457855
154337871643378717CT62GENICheterozygous129315521
154337885543378856TC52GENICheterozygous119070353
154338487743384878GC59GENIChomozygous112496177