chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	31816833	31816834	G	T	21	GENIC	homozygous	115637673
7	31817399	31817400	G	A	31	GENIC	homozygous	115637674
7	31817426	31817427	T	C	28	GENIC	homozygous	115637675
7	31817416	31817416		G	31	GENIC	homozygous	128449977
7	31817418	31817418		T	31	GENIC	homozygous	128449978
7	31817419	31817419		GT	32	GENIC	homozygous	128449979
7	31818852	31818855	GTG		29	GENIC	homozygous	128449980
7	31818856	31818856		GC	29	GENIC	homozygous	128449981
7	31819599	31819600	A	C	31	GENIC	homozygous	115637676
7	31821381	31821382	G	A	30	GENIC	homozygous	115637677
7	31821452	31821453	T	C	24	GENIC	homozygous	115637678
7	31821489	31821608	AAGAAATGAAGCGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGATCCCCAGCTCCGAAAAAAAGAACCAAAAAAAAAAAAAAAAAAAA		18	GENIC	heterozygous	128449982
7	31822694	31822695	C	T	21	GENIC	homozygous	115637679
7	31822887	31822897	TGTGTGTGTC		35	GENIC	homozygous	128449983
7	31823307	31823307		GGGTTGGTGGGG	30	GENIC	homozygous	128449984