chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4100181681100181682AG18GENIChomozygous112798284
4100183655100183656CT21GENIChomozygous112798287
4100185098100185099CT17GENIChomozygous113537197
4100185538100185539CT24GENIChomozygous113537199
4100186813100186814CA15GENIChomozygous112798291
4100187211100187212CT25GENIChomozygous113537201
4100188487100188488AG18GENIChomozygous113537203
4100189019100189020AG32GENIChomozygous113537205
4100189103100189104GA18GENIChomozygous113537207
4100189332100189333TC23GENIChomozygous113537209
4100189514100189515CG12GENIChomozygous113537211
4100189937100189938AG17GENIChomozygous112798303
4100191591100191592GA27GENIChomozygous112798313
4100192567100192568GC18GENIChomozygous112798315
4100193950100193951CG15GENIChomozygous113537215
4100195344100195345TC21GENIChomozygous112798320
4100199550100199551GT33GENIChomozygous113537217
4100199941100199942GA31GENIChomozygous112798324
4100199969100199970CT35GENIChomozygous112798326
4100200661100200662CT27GENIChomozygous113537219
4100201445100201446CA20GENIChomozygous113537221
4100206538100206539TG24GENIChomozygous112798353