chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1216161450216161451AT35GENICheterozygous61082086
1216165204216165205CT26GENICheterozygous61082100
1216189660216189661CT27GENICheterozygous61082140
1216229539216229540CA22GENICheterozygous61082227
1216229639216229640AG38GENICheterozygous61082228
1216233831216233832AG31GENICheterozygous61082237
1216235418216235419GA21GENICheterozygous61082246
1216235700216235701GA17GENICheterozygous61082247
1216237784216237785GA17GENICheterozygous61082255
1216237797216237798GC10GENICheterozygous61082256
1216245906216245907CA20GENICheterozygous61082264
1216245921216245922AG21GENICheterozygous61082265
1216252738216252739CT17GENICheterozygous61082292
1216253047216253048GA38GENICheterozygous61082293
1216268064216268065AG36GENICheterozygous61082374
1216276498216276499GA10GENICheterozygous61082383
1216306588216306593AAAAT-----17GENICheterozygous61082426
1216314068216314069AG31GENICheterozygous61082443
1216327358216327359CT28GENICheterozygous61082467
1216327856216327857TC21GENICheterozygous61082468
1216344201216344202GA41GENICheterozygous61082483
1216347751216347752GA15GENICheterozygous61082484
1216354474216354475CT12GENICheterozygous61082497
1216365786216365787AG37GENICheterozygous61082533