chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118161056118161057TA65GENIChomozygous116673189
8118161319118161320CT9GENIChomozygous116673191
8118166915118166916CT47GENIChomozygous116673193
8118167052118167053TC44GENICpossibly homozygous116673195
8118167649118167650TC38GENIChomozygous116673197
8118170343118170344GA47GENIChomozygous116673199
8118171107118171108AG40GENIChomozygous116673201
8118171420118171421GA26GENIChomozygous116673203
8118175426118175427CT44GENIChomozygous116673205
8118177667118177668GA44GENIChomozygous116673207
8118178403118178404AG42GENIChomozygous116673209
8118179554118179555GA33GENIChomozygous116673211
8118179605118179606AC38GENIChomozygous116673213
8118179766118179767GA36GENIChomozygous116673215
8118182231118182232CT49GENIChomozygous116673217
8118185764118185765GA55GENIChomozygous116673219
8118186299118186300GT36GENIChomozygous116673221
8118190683118190684TC51GENIChomozygous116673225
8118190891118190892AG45GENIChomozygous116673227
8118190968118190969CG48GENIChomozygous116673229
8118191706118191707CG52GENIChomozygous116673231
8118193950118193951AC13GENIChomozygous116673233
8118193953118193954AC13GENIChomozygous116673235
8118194344118194345TG38GENICheterozygous116673237
8118194412118194413AG46GENICpossibly homozygous116673239