chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110460688110460689TC26GENIChomozygous502126540
3110461280110461281C-19GENICpossibly homozygous683734474
3110461294110461295C-19GENICheterozygous683734475
3110462040110462041AG31GENIChomozygous502126541
3110462258110462259CT23GENIChomozygous504632690
3110464154110464156TT--20GENICpossibly homozygous683734476
3110467189110467190A-28GENIChomozygous683734477
3110467412110467413TC20GENIChomozygous502126542
3110469546110469547GGTTTTTTT10GENIChomozygous683734478
3110469912110469913CCTT13GENIChomozygous683734480
3110470427110470428AG21GENIChomozygous502126543
3110470474110470475CT21GENIChomozygous504632691
3110470635110470636CT43GENIChomozygous504632692
3110471064110471065TTCA18GENIChomozygous683734481
3110473760110473761T-15GENIChomozygous683734482
3110474759110474760CT37GENIChomozygous504632693
3110479033110479034CT37GENIChomozygous504632694
3110479922110479923AAAGG52GENIChomozygous683734483
3110480051110480052AG40GENIChomozygous502126544
3110481610110481611TTTC18GENIChomozygous683734484
3110481732110481733CT32GENIChomozygous504632695
3110482159110482160CT32GENICpossibly homozygous504632696
3110482553110482554CT39GENICpossibly homozygous502126545
3110484146110484147AC29GENIChomozygous502126546
3110485277110485278GA39GENIChomozygous504632697
3110486948110486949GGC19GENIChomozygous683734485
3110487973110487974CCTT16GENICheterozygous683734486
3110487983110487984CG15GENICheterozygous504632698
3110489247110489248GGTTGTT18GENICpossibly homozygous683734487
3110489247110489248GGTT18GENICheterozygous683734488
3110490793110490800AAAAAAA-------4GENIChomozygous683734489
3110496412110496413AG35GENIChomozygous502126547
3110497509110497510AAT19GENICheterozygous683734490