chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138560203285602033GA13GENIChomozygous126070434
138560207185602072CT13GENIChomozygous126070435
138560211085602111TC12GENIChomozygous118464993
138560229485602295GA28GENIChomozygous118464994
138560229785602298CA29GENIChomozygous114422428
138560263485602635AG15GENIChomozygous118502587
138560271085602711TC16GENIChomozygous114645908
138560276385602763ATAT25GENIChomozygous129082596
138560272385602723AC16GENIChomozygous129082595
138560269785602701ATAC13GENIChomozygous129082594
138560317785603178TC28GENIChomozygous114422430
138560380485603805AT20GENIChomozygous114422432
138560395085603957CTGGGTG11GENIChomozygous129082597
138560463985604640TC22GENIChomozygous114422434
138560539685605397AG29GENIChomozygous114422436
138560624885606249TC22GENIChomozygous114422438
138560697185606971TATT32GENIChomozygous129082598
138560264785602647TA14GENIChomozygous129082593
138560722785607228CT30GENIChomozygous114422440
138560777185607772GC18GENIChomozygous114422442
138560785685607857CA23GENIChomozygous114422444
138560961385609614GA23GENIChomozygous114422446
138561008485610085TA23GENIChomozygous114422452
138561010185610102CG23GENIChomozygous114422454
138561012685610127CT23GENIChomozygous114422456
138561013585610136CA26GENIChomozygous114422458
138561108985611090GA26GENIChomozygous114422460
138561222185612222TC22GENIChomozygous114422462
138561326685613272GGTCTT16GENIChomozygous129082599
138561335985613360TG16GENIChomozygous114422464
138561358885613589CG19GENIChomozygous114422466
138561513385615134GA28GENICpossibly homozygous114422470
138561524685615251GGGAT26GENIChomozygous129082600
138561568785615688AG29GENIChomozygous114422472
138561572285615723AG25GENIChomozygous114422474
138561553685615537CG9GENIChomozygous114830687
138561823185618232CT28GENIChomozygous114422476
138562174285621743CA2GENIChomozygous118464996