chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 96551769 96551770 C G 21 GENIC homozygous 116589658 8 96551885 96551886 G A 24 GENIC homozygous 116589660 8 96551899 96551899 TTTG 25 GENIC homozygous 128618139 8 96551911 96551911 TTTTTG 28 GENIC homozygous 128618140 8 96552087 96552088 T 10 GENIC homozygous 128618141 8 96553852 96553853 T C 19 GENIC homozygous 116589674 8 96552201 96552202 T C 10 GENIC homozygous 116589664 8 96552421 96552422 G C 19 GENIC homozygous 116589666 8 96552966 96552967 T G 26 GENIC homozygous 116589668 8 96553528 96553529 T C 20 GENIC homozygous 116589670 8 96553566 96553567 G A 19 GENIC homozygous 116589672 8 96554077 96554077 T 10 GENIC homozygous 128618142 8 96554544 96554545 A G 19 GENIC homozygous 116589676 8 96554915 96554915 TCACGGAAA 13 GENIC homozygous 128618143 8 96555336 96555337 T G 19 GENIC homozygous 116589678 8 96555760 96555761 C T 20 GENIC homozygous 116589680 8 96556018 96556019 C T 30 GENIC homozygous 116589682 8 96556678 96556679 T C 20 GENIC homozygous 116589684 8 96557635 96557636 G A 19 GENIC homozygous 116589686 8 96558132 96558133 T C 12 GENIC homozygous 116589688