chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149413648149413649GA19GENICpossibly homozygous589142478
4149413834149413835TG12GENICpossibly homozygous589142479
4149414184149414185TC8GENICpossibly homozygous589142480
4149415196149415197CT5GENIChomozygous589142481
4149415245149415246T-3GENIChomozygous723870482
4149415868149415869AG5GENIChomozygous589142482
4149415940149415945AAAGG-----1GENIChomozygous723870483
4149415964149415965GGT1GENIChomozygous723870484
4149416020149416021TC12GENICpossibly homozygous589142483
4149418788149418789AG4GENIChomozygous589142484
4149419103149419104GA10GENIChomozygous589142485
4149420199149420200GA15GENICpossibly homozygous589142486
4149420394149420395C-4GENICheterozygous723870485
4149420398149420419AACAAAAAACAAAAAAAAACC---------------------4GENICheterozygous723870486
4149420584149420585CCT3GENIChomozygous723870487
4149421912149421913TG17GENIChomozygous589142487
4149422042149422043CT21GENIChomozygous589142488
4149422253149422254AT19GENICpossibly homozygous589142489
4149422497149422498AG10GENIChomozygous589142490
4149425096149425097TG11GENICpossibly homozygous589142491
4149425174149425175A-3GENIChomozygous723870488
4149425945149425946GA15GENICpossibly homozygous589142492
4149426129149426134TTTTG-----3GENIChomozygous723870489
4149426288149426289AG8GENIChomozygous589142493
4149427447149427448CA9GENIChomozygous589142494