chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1198934586198934587CA17GENIChomozygous61043189
1198934600198934601TC16GENIChomozygous61043190
1198938049198938050GGATAA14GENIChomozygous61043191
1198939775198939776CT19GENIChomozygous61043197
1198943453198943454CT15GENIChomozygous61043203
1198944160198944161AG14GENIChomozygous61043206
1198944231198944232TC22GENIChomozygous61043207
1198945040198945041GA16GENIChomozygous61043208
1198945086198945087TC22GENIChomozygous61043209
1198948038198948039TC27GENIChomozygous61043211
1198948128198948131CCC---8GENIChomozygous61043212
1198949016198949017AAG11GENIChomozygous61043213
1198949118198949119TC11GENIChomozygous61043214
1198949171198949172AAC9GENIChomozygous61043215
1198949578198949579TC14GENIChomozygous61043216
1198949580198949581AG14GENIChomozygous61043217
1198949617198949618AG9GENIChomozygous61043218
1198949705198949706CA16GENICpossibly homozygous61043219
1198949758198949759CT22GENIChomozygous61043220
1198949879198949880CT15GENIChomozygous61043221
1198949985198949986AG24GENIChomozygous61043222
1198950475198950476CT27GENIChomozygous61043223
1198951657198951658TC17GENIChomozygous61043224
1198951754198951755AG16GENIChomozygous61043225
1198952293198952295AA--12GENIChomozygous61043226
1198948800198948801A-15GENICheterozygous62801390
1198942253198942254GA24GENICheterozygous62801389