chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84094415740944158A-5GENICheterozygous754279384
84094417940944183TCGT----20GENICheterozygous754279385
84094446340944464AAT225GENICheterozygous754279386
84094471540944716G-136GENICheterozygous754279387
84094483540944836C-72GENICheterozygous754279388
84094537740945378TTG112GENICheterozygous754279389
84094773140947732C-95GENICheterozygous754279390
84094826440948265T-131GENICheterozygous754279391
84094976740949769AG--57GENICheterozygous754279392
84094984940949851AA--20GENICheterozygous754279393
84094985040949851A-20GENICheterozygous754279394
84095043640950437A-21GENICheterozygous754279395
84095794940957950GGCTT25GENICheterozygous754279396
84095844140958442T-48GENICpossibly homozygous754279397
84095852440958525C-18GENICheterozygous754279398
84096328240963283T-21GENICheterozygous754279399
84096347740963478CCT26GENICheterozygous754279400
84096380540963806CCTTT12GENICheterozygous754279403
84096380640963808TT--12GENICheterozygous754279401
84096533940965340A-7GENICheterozygous754279404
84096539740965398CCA8GENICheterozygous754279406
84096539840965400AA--8GENICheterozygous754279405
84096629840966301CTT---57GENICheterozygous754279407
84096840440968405A-20GENIChomozygous754279408
84096867240968673C-35GENICheterozygous754279409
84096955640969557T-161GENICheterozygous754279410
84096998540969986G-80GENICheterozygous754279411
84097026040970261GGCAAGGA11GENICheterozygous754279412
84097608440976085T-101GENICheterozygous754279413
84098080840980809CCAT16GENICheterozygous754279414
84098213240982136TGAT----40GENICheterozygous754279415
84098246840982471AAC---8GENICheterozygous754279416