chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	12031134	12031135	C	T	23	GENIC	homozygous	45684581
20	12031895	12031896	C	CTG	30	GENIC	possibly homozygous	45429986
20	12033417	12033418	G	GCTTTGGAGACGGTGGTGAGTTGCCACCGT	17	GENIC	homozygous	45429991
20	12033515	12033516	T	TATGATCAACTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC	7	GENIC	possibly homozygous	45842587
20	12033647	12033648	T	TTTG	37	GENIC	homozygous	45684583
20	12034140	12034141	A	G	12	GENIC	homozygous	45429993
20	12034147	12034148	G	A	11	GENIC	homozygous	45429994
20	12034353	12034354	C	T	19	GENIC	homozygous	45684586
20	12034536	12034537	T	C	27	GENIC	homozygous	45684587
20	12034801	12034802	T	-	13	GENIC	homozygous	45684588
20	12035289	12035290	A	G	29	GENIC	homozygous	45684589