chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	12031895	12031896	C	CTGTGTG	18	GENIC	possibly homozygous	46020973
20	12032398	12032399	T	C	44	GENIC	homozygous	46020974
20	12032401	12032402	T	A	46	GENIC	homozygous	46020975
20	12033417	12033418	G	GCTTTGGAGACGGTGGTGAGTTGCCACCGT	33	GENIC	homozygous	45429991
20	12033515	12033516	T	TATGATCAACTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC	19	GENIC	homozygous	45842587
20	12033630	12033631	T	TTTTG	11	GENIC	homozygous	46020976
20	12034353	12034354	C	T	19	GENIC	homozygous	45684586
20	12034633	12034634	T	-	25	GENIC	homozygous	45975893
20	12034635	12034640	CGTAG	-----	25	GENIC	homozygous	45975894
20	12034914	12034915	G	T	19	GENIC	homozygous	45975899
20	12035289	12035290	A	G	15	GENIC	homozygous	45684589