chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1198934586198934587CA38GENIChomozygous61043189
1198934600198934601TC39GENIChomozygous61043190
1198936137198936138CCGT8GENICheterozygous62353846
1198936138198936146GTGTGTGT--------8GENICheterozygous62189741
1198936140198936146GTGTGT------8GENICheterozygous62189743
1198938049198938050GGATAA25GENIChomozygous61043191
1198938239198938240TTA4GENIChomozygous61043192
1198939331198939333CC--5GENICheterozygous62095468
1198939561198939562CCT13GENICheterozygous61043193
1198939775198939776CT21GENIChomozygous61043197
1198941710198941711CCAAA19GENIChomozygous61043201
1198943453198943454CT32GENIChomozygous61043203
1198943517198943518CCT13GENICheterozygous61043204
1198943517198943518CCTT13GENICheterozygous61043205
1198943518198943519T-13GENICheterozygous62353847
1198944160198944161AG30GENIChomozygous61043206
1198944231198944232TC26GENIChomozygous61043207
1198945040198945041GA35GENIChomozygous61043208
1198945086198945087TC26GENIChomozygous61043209
1198947500198947501CCAT12GENICheterozygous61043210
1198948038198948039TC21GENIChomozygous61043211
1198948128198948131CCC---34GENIChomozygous61043212
1198949016198949017AAG20GENIChomozygous61043213
1198949118198949119TC21GENIChomozygous61043214
1198949171198949172AAC25GENIChomozygous61043215
1198949578198949579TC37GENIChomozygous61043216
1198949580198949581AG37GENIChomozygous61043217
1198949617198949618AG33GENIChomozygous61043218
1198949705198949706CA30GENIChomozygous61043219
1198949758198949759CT20GENIChomozygous61043220
1198949879198949880CT34GENIChomozygous61043221
1198949985198949986AG35GENIChomozygous61043222
1198950475198950476CT21GENIChomozygous61043223
1198951657198951658TC16GENIChomozygous61043224
1198951754198951755AG27GENIChomozygous61043225
1198952293198952295AA--28GENIChomozygous61043226