chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6136682825136682826CT65GENIChomozygous114995409
6136683051136683052TC67GENIChomozygous114995410
6136684824136684835TCCCTGGAGGA60GENIChomozygous128400220
6136685398136685399TC71GENIChomozygous114995411
6136685529136685530TC69GENIChomozygous114995412
6136685867136685868GC70GENIChomozygous114995413
6136685887136685888CT66GENIChomozygous114995414
6136689073136689074CG51GENIChomozygous114995415
6136689103136689104TC49GENIChomozygous114995416
6136689283136689284CA58GENIChomozygous114995417
6136690374136690375AG81GENIChomozygous114995418
6136691528136691529TA54GENIChomozygous114995419
6136691818136691819GA67GENICpossibly homozygous114995420
6136692058136692059CG69GENIChomozygous114995421
6136693143136693144G63GENIChomozygous128400221
6136693289136693290CA73GENIChomozygous114995422
6136693298136693299TC72GENIChomozygous114995423
6136694093136694093CCCCACCCCCT20GENIChomozygous128400222
6136695041136695042AC53GENIChomozygous114995424
6136695736136695737CT74GENIChomozygous114995425
6136698626136698627TC66GENIChomozygous114995426
6136701294136701295CG61GENIChomozygous114995427
6136693733136693733G38GENICpossibly homozygous133741588