chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1198934586198934587CA17GENIChomozygous61043189
1198934600198934601TC16GENIChomozygous61043190
1198936138198936146GTGTGTGT--------5GENICheterozygous62189741
1198936140198936146GTGTGT------5GENICheterozygous62189743
1198938049198938050GGATAA16GENIChomozygous61043191
1198938239198938240TTA19GENICpossibly homozygous61043192
1198939561198939562CCT10GENICheterozygous61043193
1198939775198939776CT21GENIChomozygous61043197
1198941710198941711CCAAA16GENIChomozygous61043201
1198942822198942823CCATAAATAAATAAATAA7GENIChomozygous62189745
1198943453198943454CT19GENIChomozygous61043203
1198943517198943518CCT8GENICheterozygous61043204
1198943517198943518CCTT8GENICheterozygous61043205
1198944160198944161AG24GENIChomozygous61043206
1198944231198944232TC21GENIChomozygous61043207
1198945040198945041GA21GENIChomozygous61043208
1198945086198945087TC23GENIChomozygous61043209
1198947500198947501CCAT12GENICheterozygous61043210
1198948038198948039TC22GENIChomozygous61043211
1198948128198948131CCC---21GENIChomozygous61043212
1198949016198949017AAG21GENIChomozygous61043213
1198949118198949119TC19GENIChomozygous61043214
1198949171198949172AAC21GENIChomozygous61043215
1198949578198949579TC18GENIChomozygous61043216
1198949580198949581AG18GENIChomozygous61043217
1198949617198949618AG27GENIChomozygous61043218
1198949705198949706CA19GENIChomozygous61043219
1198949758198949759CT21GENIChomozygous61043220
1198949879198949880CT15GENIChomozygous61043221
1198949985198949986AG16GENIChomozygous61043222
1198950475198950476CT17GENIChomozygous61043223
1198951657198951658TC15GENIChomozygous61043224
1198951754198951755AG30GENIChomozygous61043225
1198952293198952295AA--29GENIChomozygous61043226