chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48596302685963027A15GENIChomozygous141114890
48596306585963066CA15GENIChomozygous137110650
48596496685964967AG16GENIChomozygous137110653
48596581285965813GT14GENICpossibly homozygous145474934
48596691685966917C9GENICheterozygous403106395
48596691285966913C9GENICheterozygous403106391
48596691285966913CT9GENICheterozygous403106392
48596691485966915C9GENICheterozygous403106393
48596691485966915CT9GENICheterozygous403106394
48596691685966917CT9GENICheterozygous403106396
48596691885966919C9GENICheterozygous403106397
48596691885966919CT9GENICheterozygous403106398
48596692085966921CT9GENICheterozygous403106399
48596692085966921C9GENICheterozygous403106400
48596903885969039GA28GENIChomozygous137110655
48596976285969763GA22GENIChomozygous137110656
48597002585970026CG30GENIChomozygous137110657
48597076285970763CT31GENIChomozygous137110660
48596692285966923CT9GENICheterozygous404431691
48596692285966923C9GENICheterozygous404431692
48596954585969546GT22GENIChomozygous143101929
48596956585969566CT22GENIChomozygous149325711
48596957385969574CT22GENIChomozygous149325712
48597678385976784GT22GENIChomozygous141637637
48597695585976956GA22GENIChomozygous149325713
48597721785977218CT17GENICpossibly homozygous149325714
48597925285979253C5GENIChomozygous136897122
48597992785979928GA26GENIChomozygous149325715
48598577485985775CT26GENIChomozygous145474943
48598797685987977GA16GENIChomozygous149325716
48598826585988266AG26GENIChomozygous137110679
48599099985991000GA14GENIChomozygous137110684
48599390385993904TC20GENIChomozygous137110688
48599406685994067GA15GENIChomozygous137110689
48599994585999946CT11GENIChomozygous137110695
48599653485996535T12GENICheterozygous403583268
48599653485996535TA12GENICheterozygous403583269