chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4100181646100181647TG35GENIChomozygous112798282
4100181681100181682AG27GENIChomozygous112798284
4100182202100182203CT29GENIChomozygous112798286
4100183655100183656CT25GENIChomozygous112798287
4100185787100185788AG40GENIChomozygous112798289
4100186813100186814CA28GENIChomozygous112798291
4100187611100187612AT33GENIChomozygous112798293
4100188139100188140GA30GENIChomozygous112798295
4100189896100189897CT20GENIChomozygous112798301
4100189937100189938AG22GENIChomozygous112798303
4100189990100189991AG21GENIChomozygous112798305
4100190298100190299TC26GENIChomozygous112798307
4100190318100190319TC40GENIChomozygous112798309
4100190628100190629TA35GENIChomozygous112798311
4100191591100191592GA26GENIChomozygous112798313
4100192567100192568GC31GENIChomozygous112798315
4100193002100193003GT24GENIChomozygous112798316
4100195290100195291GA36GENIChomozygous112798318
4100195344100195345TC39GENIChomozygous112798320
4100199169100199170AG26GENIChomozygous112798322
4100199941100199942GA42GENIChomozygous112798324
4100199969100199970CT30GENIChomozygous112798326
4100200101100200102AG30GENIChomozygous112798328
4100200452100200453CT24GENIChomozygous112798330
4100201486100201487AC37GENIChomozygous112798334
4100206538100206539TG26GENIChomozygous112798353
4100207304100207305TC42GENIChomozygous112798355
4100207361100207362TC32GENIChomozygous112798357
4100208662100208663TG34GENIChomozygous112798360
4100209553100209554CT25GENIChomozygous112798362
4100209815100209816GA40GENIChomozygous112798364