chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159639681159639682GT34GENIChomozygous114073074
5159639794159639795CT50GENICpossibly homozygous114073075
5159641223159641224GA38GENIChomozygous114073076
5159642805159642806CT36GENIChomozygous114073077
5159648206159648207CT56GENIChomozygous114073078
5159648732159648733CT51GENIChomozygous114073079
5159648780159648781GA40GENIChomozygous114073080
5159649309159649310AG34GENIChomozygous114073081
5159650383159650384GA41GENIChomozygous114073082
5159650944159650945TA56GENIChomozygous114073083
5159651012159651013TC46GENIChomozygous114073084
5159651791159651792AG52GENIChomozygous114073085
5159653029159653030TC32GENIChomozygous114073086
5159655029159655030CT54GENIChomozygous114073087
5159656888159656889GA41GENICpossibly homozygous114073088
5159661740159661741AT42GENIChomozygous114073089