chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	31493371	31493372	C	A	39	INTERGENIC	homozygous	47082185
17	31493421	31493422	T	C	46	INTERGENIC	homozygous	47082186
17	31493735	31493736	G	T	38	INTERGENIC	homozygous	47082187
17	31494235	31494236	T	C	33	INTERGENIC	homozygous	47082188
17	31494253	31494254	T	TTCC	29	INTERGENIC	homozygous	47082189
17	31494884	31494885	A	ATGTTTGTTTGTT	20	INTERGENIC	homozygous	47082190
17	31495121	31495122	C	T	34	INTERGENIC	homozygous	47082191
17	31495235	31495236	A	G	46	INTERGENIC	homozygous	47082192
17	31495734	31495735	T	C	27	INTERGENIC	homozygous	47082193
17	31496029	31496030	T	C	33	INTERGENIC	homozygous	47082194
17	31496349	31496350	C	T	50	INTERGENIC	homozygous	47082195
17	31496541	31496542	C	T	26	INTERGENIC	homozygous	47082196
17	31496801	31496802	G	A	39	INTERGENIC	homozygous	47082197