chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154330124243301242AAT21GENIChomozygous129251017
154330817443308175C14GENIChomozygous129251020
154333542043335420TC7GENIChomozygous129251031
154333893543338936G11GENIChomozygous129251032
154333896643338967G14GENIChomozygous129251033
154333896943338970A14GENIChomozygous129251034
154333900143339002C17GENIChomozygous129251035
154333901243339013A16GENIChomozygous129251036
154333917043339170CC2GENIChomozygous129251037
154333917543339175C2GENIChomozygous129251038
154337421943374220AG3GENIChomozygous119024426
154337423243374233TC3GENIChomozygous119059748
154337423343374234GT3GENIChomozygous124069863
154337426843374269TA3GENIChomozygous124069865
154337427143374272CT3GENIChomozygous124069866
154337427943374280TC2GENIChomozygous129315510
154337469343374694GT20GENICheterozygous130701423
154337470343374704CT21GENICheterozygous130790967
154337496543374966AG10GENICheterozygous129315518
154337541443375415GA15GENICheterozygous130595119
154337475743374758AG21GENICheterozygous131168713
154337496343374964CT12GENICheterozygous134496076
154337543843375439AC15GENICheterozygous130595120
154337812543378126GA19GENICheterozygous131939683
154337859743378598TC19GENICheterozygous118915734
154337885543378856TC14GENICheterozygous119070353
154338487743384878GC18GENIChomozygous112496177
154337846343378464CT17GENICheterozygous134457855
154337846143378461TATT17GENICheterozygous134456332