chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104560246345602464AG49GENIChomozygous116584029
104560386545603865G20GENIChomozygous128813997
104560541345605414AT37GENIChomozygous116877265
104560581145605812AC52GENIChomozygous116584043
104560971045609711AG47GENIChomozygous116584073
104561879945618800GA32GENIChomozygous117008483
104561975745619758AG30GENIChomozygous116584091
104560400445604004AAACACACACACACATACACACAAACAC19GENICpossibly homozygous133680090
104561465945614660TG63GENIChomozygous117252470
104561483245614833CT41GENIChomozygous117252473
104562105545621056AG35GENIChomozygous116771850
104562188145621882TC30GENIChomozygous116771852
104562244045622441GC42GENIChomozygous117252475
104562270745622708TG43GENIChomozygous118036333
104562374945623750AT47GENIChomozygous116584093
104562569245625693TC45GENIChomozygous116584095
104562686045626861TC41GENIChomozygous116771854
104562770545627706GA44GENICpossibly homozygous117252477
104562772945627730GA40GENICpossibly homozygous116771856
104562971145629712CT48GENIChomozygous116771858
104562976845629769AG42GENIChomozygous117252479
104563089845630899CT42GENIChomozygous117252481
104563538045635381TC54GENIChomozygous116584099
104563687345636874G31GENIChomozygous133680091
104563886945638870GA34GENIChomozygous116584101
104563964745639648CT54GENIChomozygous117252483
104564006945640070GA58GENIChomozygous116877273
104564183145641832CT38GENIChomozygous116877277
104564196945641970AG41GENIChomozygous116584103
104564285645642857GA33GENIChomozygous116584105
104564298445642985AG37GENIChomozygous116584107
104564314945643150G7GENIChomozygous128814007