chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1207085383207085384CG1GENIChomozygous61068682
1207085927207085930GCA---1GENIChomozygous61068683
1207136949207136950CCGG13GENIChomozygous61068686
1207137563207137564TTA2GENIChomozygous61068687
1207138313207138317TATT----3GENICheterozygous61068688
1207138629207138630CT22GENICheterozygous61068689
1207138973207138974CT16GENIChomozygous61068690
1207139873207139874TC31GENIChomozygous61068691
1207145017207145023GTGTGT------1GENIChomozygous61068695
1207146320207146321CA17GENIChomozygous61068696
1207148204207148208TTTG----9GENICheterozygous61068699
1207149420207149421TA1GENIChomozygous61068700
1207150305207150306AG19GENICpossibly homozygous61068708
1207150796207150797AG13GENICheterozygous61068709
1207150810207150811AAGGCCTT8GENICpossibly homozygous61068710
1207150824207150825AG13GENIChomozygous61068711
1207151271207151272CA22GENICheterozygous61068712
1207151602207151603A-10GENICpossibly homozygous61068713
1207152829207152830GA9GENIChomozygous61068714
1207155232207155233TC16GENIChomozygous61068717
1207156087207156088GA9GENICpossibly homozygous61068718
1207156771207156772T-17GENICheterozygous61068719
1207157282207157283CCT23GENICpossibly homozygous61068720
1207158393207158394T-9GENIChomozygous61068722
1207158658207158659CT13GENICheterozygous61068723
1207158817207158818GA16GENIChomozygous61068724
1207159278207159282AGAA----5GENICheterozygous61068725
1207159465207159466TC19GENIChomozygous61068726
1207159986207159987AG19GENICpossibly homozygous61068727
1207160366207160367AG16GENICpossibly homozygous61068728
1207162359207162360GA27GENICpossibly homozygous61068730
1207162632207162633GC20GENICpossibly homozygous61068731
1207163015207163016TC24GENIChomozygous61068732
1207163615207163616GA21GENICpossibly homozygous61068733
1207163910207163911GA25GENICpossibly homozygous61068734