chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2203667873203667874AG17GENIChomozygous111157386
2203669202203669203CT9GENIChomozygous111157388
2203669347203669348CT18GENIChomozygous111157390
2203669483203669484TC22GENIChomozygous111157392
2203670101203670102GA14GENIChomozygous111157394
2203670435203670436AG14GENIChomozygous111157396
2203670566203670567CT10GENICheterozygous111157398
2203670630203670631TG14GENIChomozygous111157400
2203670703203670704TC22GENIChomozygous111157402
2203671031203671032GC15GENIChomozygous111157408
2203671286203671287CT11GENIChomozygous111157410
2203671316203671317GA11GENIChomozygous111157412
2203671326203671327GC9GENIChomozygous111157414
2203671374203671375GA8GENIChomozygous120447762
2203671668203671669AG4GENIChomozygous111157416
2203671733203671734GA22GENIChomozygous111157418
2203671934203671935AG23GENICpossibly homozygous110210705
2203671985203671986AG17GENIChomozygous111157420
2203672013203672014AG15GENIChomozygous110210706
2203672337203672338CA6GENIChomozygous110210709
2203674025203674026AG20GENIChomozygous110210711
2203674070203674071TC19GENIChomozygous111157422
2203675365203675366CT18GENIChomozygous111157424
2203675391203675392CT14GENIChomozygous111157426
2203675451203675452CT16GENIChomozygous111157429
2203678222203678223AG29GENIChomozygous110210733
2203678836203678837GA11GENIChomozygous120447764
2203678846203678847TG9GENIChomozygous110210740
2203678908203678909GA8GENIChomozygous110210741
2203678989203678990TC7GENIChomozygous110210742
2203679005203679006CT8GENIChomozygous111157433