chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4207838508207838509GGGTGTGT3GENIChomozygous58368794
4207839663207839664AACTCTCTCTCTCT10GENIChomozygous58368796
4207842088207842089CCAAAAAAAAAAAAA4GENIChomozygous58368799
4207842148207842149TC13GENIChomozygous57065515
4207849666207849667AAT17GENICpossibly homozygous57065516
4207850115207850116CA7GENIChomozygous58368801
4207850117207850118CCAAAAA5GENIChomozygous58368804
4207850140207850141CA7GENIChomozygous58302074
4207860178207860179TC10GENIChomozygous57065519
4207861783207861784TTTTA3GENICheterozygous57065520
4207861783207861784TTTTATTA3GENICheterozygous58486698
4207862450207862454ATGT----15GENIChomozygous57065522
4207862553207862554AG20GENIChomozygous57065524
4207866548207866549C-17GENICheterozygous58447402
4207853958207853960TG--11GENIChomozygous57607705
4207869291207869292C-12GENICheterozygous57607709
4207874144207874145AC17GENIChomozygous57065547
4207876099207876113GCGTGCGTGCGTGC--------------7GENIChomozygous58368809
4207883992207883993A-9GENICpossibly homozygous57065552
4207886230207886231GGGGT11GENIChomozygous57065553
4207891327207891328TC18GENIChomozygous57065554
4207893216207893218TA--25GENIChomozygous57065555
4207895099207895100TTG2GENICheterozygous57065556
4207896328207896329CCTCTCTCTG16GENIChomozygous57065557
4207900338207900339A-29GENIChomozygous57065559
4207901591207901592AAAATTCCCTCTAACTAAGT29GENIChomozygous57065560
4207906614207906615TC17GENIChomozygous57065561
4207906616207906617GGTT17GENIChomozygous57065562
4207906617207906618AACGTAAT17GENIChomozygous57065563
4207906948207906949GA34GENIChomozygous57065564
4207907201207907202CA25GENIChomozygous57065565
4207911235207911236TC25GENIChomozygous57065566
4207911290207911291AAC11GENIChomozygous57065567
4207913348207913349A-7GENICpossibly homozygous57065568
4207918860207918861CA14GENIChomozygous58368820
4207918866207918867CA14GENIChomozygous58368822
4207918874207918875CA12GENIChomozygous58368824
4207919395207919396CG21GENIChomozygous57065570