chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 110140024 110140025 C T 24 GENIC homozygous 51958641 10 110140154 110140155 A G 25 GENIC homozygous 51601062 10 110140346 110140347 A - 13 GENIC homozygous 51601063 10 110140427 110140428 G - 3 GENIC homozygous 51958644 10 110140631 110140632 G C 19 GENIC homozygous 51958647 10 110140635 110140636 A G 20 GENIC homozygous 51601064 10 110141328 110141342 GTCGTCAGTGCTGC -------------- 8 GENIC homozygous 52331909 10 110142102 110142103 A C 13 INTERGENIC homozygous 51958653 10 110142724 110142725 A - 20 INTERGENIC homozygous 51774840 10 110142859 110142860 T C 24 INTERGENIC homozygous 51601068 10 110145666 110145667 T C 21 GENIC homozygous 51601069 10 110147057 110147058 C CTTTT 6 GENIC homozygous 51958658 10 110147376 110147377 T A 21 GENIC homozygous 51958661 10 110147657 110147658 C A 20 GENIC homozygous 51601074 10 110147827 110147828 A C 24 GENIC homozygous 51601075 10 110147935 110147936 G A 31 GENIC homozygous 51958664