chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17254576872545769AG29GENIChomozygous108866032
17254667172546672AG34GENIChomozygous109106503
17254728672547287CG49GENIChomozygous109106505
17254890872548909TC32GENIChomozygous108866033
17254935672549357CT32GENIChomozygous109106507
17254943972549440AG25GENIChomozygous109106509
17254960272549603AT20GENIChomozygous109292211
17255016072550161TC19GENIChomozygous109106511
17255058072550581AG18GENIChomozygous108866034
17255068972550690AG19GENIChomozygous109106513
17255075672550757TA34GENIChomozygous109106515
17255099972551000GA40GENIChomozygous109106517
17255184572551846CT35GENIChomozygous109106519
17255194972551950TC43GENIChomozygous108866035
17255292972552930TC16GENICheterozygous109106521
17255314472553145AC31GENIChomozygous109106523
17255382572553826GA4GENIChomozygous109106527
17255468172554682GA24GENIChomozygous109106529
17255523372555234AG22GENIChomozygous109106533
17255580872555809CG41GENIChomozygous109106535
17255596872555969TG26GENIChomozygous109106537
17255601972556020GA26GENIChomozygous109106539
17255605672556057GA27GENIChomozygous109106541
17255627272556273TG36GENIChomozygous109106543
17255675572556756AG34GENIChomozygous109106545
17255696272556963AG14GENIChomozygous109292212
17255702472557025CT22GENIChomozygous109106547
17255768672557687TA16GENICpossibly homozygous109106549
17255900872559009GA29GENIChomozygous109106555
17255918872559189GT31GENIChomozygous109106557
17255941472559415GA15GENIChomozygous109106559
17255959272559593CT32GENIChomozygous109106561
17255994972559950GC47GENIChomozygous109106563
17256238372562384CT17GENIChomozygous109292213
17256249872562499TC23GENIChomozygous109106567
17256307672563077TC39GENIChomozygous109106569
17256365772563658GT50GENIChomozygous109292214