chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107652550107652552TG--9GENICheterozygous58618579
3107656723107656724GGT16GENICheterozygous57588019
3107673478107673480TC--2GENIChomozygous58618580
3107706053107706054TTA6GENICheterozygous57588025
3107707773107707774CCTTT21GENICheterozygous58558093
3107710231107710232GGGTGT3GENICheterozygous58618582
3107710284107710285GC12GENIChomozygous57588031
3107710296107710297GC19GENIChomozygous57588033
3107710303107710304AC18GENIChomozygous57588035
3107710369107710370TA27GENIChomozygous57588037
3107711509107711510TG24GENIChomozygous57588039
3107714520107714522TG--33GENICheterozygous57588044
3107716110107716111A-29GENIChomozygous58618586
3107716118107716119AAT27GENIChomozygous58618587
3107716141107716142GGT32GENIChomozygous57588050
3107716180107716181C-44GENIChomozygous57588052
3107718681107718682TTCTGCC33GENIChomozygous57588054
3107718682107718683AG43GENIChomozygous58558095
3107725888107725902TGTGTGTGTGTGTG--------------13GENICheterozygous57588056
3107725890107725902TGTGTGTGTGTG------------13GENICpossibly homozygous59044906
3107748655107748656GC43GENIChomozygous57588058
3107749266107749269CTG---30GENICheterozygous59044908
3107749272107749275CCA---29GENICheterozygous59044910