chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1198934586198934587CA28GENIChomozygous61043189
1198934600198934601TC24GENIChomozygous61043190
1198936138198936146GTGTGTGT--------1GENIChomozygous62189741
1198938049198938050GGATAA12GENIChomozygous61043191
1198938239198938240TTA6GENIChomozygous61043192
1198939561198939562CCT5GENIChomozygous61043193
1198939775198939776CT20GENIChomozygous61043197
1198941710198941711CCAAA16GENIChomozygous61043201
1198942822198942823CCATAAATAAATAAATAA3GENIChomozygous62189745
1198943453198943454CT19GENIChomozygous61043203
1198943517198943518CCT6GENICheterozygous61043204
1198943517198943518CCTT6GENICheterozygous61043205
1198943518198943519T-6GENICheterozygous62353847
1198944160198944161AG34GENIChomozygous61043206
1198944231198944232TC32GENIChomozygous61043207
1198945040198945041GA20GENIChomozygous61043208
1198945086198945087TC16GENIChomozygous61043209
1198947500198947501CCAT14GENICpossibly homozygous61043210
1198948038198948039TC13GENIChomozygous61043211
1198948128198948131CCC---21GENIChomozygous61043212
1198948799198948800CCA13GENICheterozygous62330733
1198948801198948802A-13GENICheterozygous61799469
1198949016198949017AAG24GENIChomozygous61043213
1198949118198949119TC25GENIChomozygous61043214
1198949171198949172AAC26GENIChomozygous61043215
1198949578198949579TC17GENIChomozygous61043216
1198949580198949581AG16GENIChomozygous61043217
1198949617198949618AG27GENIChomozygous61043218
1198949705198949706CA27GENIChomozygous61043219
1198949758198949759CT30GENIChomozygous61043220
1198951754198951755AG31GENIChomozygous61043225
1198949879198949880CT30GENIChomozygous61043221
1198949985198949986AG31GENIChomozygous61043222
1198950475198950476CT49GENIChomozygous61043223
1198951657198951658TC15GENIChomozygous61043224
1198952293198952295AA--29GENIChomozygous61043226