chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	44186514	44186515	C	T	21	GENIC	homozygous	47114239
17	44187170	44187171	T	C	31	GENIC	homozygous	47114240
17	44187379	44187383	GTGT	----	9	GENIC	homozygous	47114241
17	44187485	44187486	T	A	26	GENIC	homozygous	47114245
17	44188172	44188173	C	T	16	GENIC	homozygous	47114247
17	44188182	44188183	T	C	20	GENIC	homozygous	47114249
17	44188662	44188663	T	C	21	GENIC	homozygous	47114250
17	44189112	44189113	G	-	33	GENIC	homozygous	47114252
17	44189133	44189134	T	A	35	GENIC	possibly homozygous	47114253
17	44189186	44189187	T	C	29	GENIC	possibly homozygous	47114255
17	44189506	44189507	G	A	19	GENIC	homozygous	47114257
17	44189544	44189548	ACTT	----	14	GENIC	homozygous	47114259
17	44189566	44189567	C	T	18	GENIC	homozygous	47114261
17	44189759	44189763	AAAC	----	10	GENIC	homozygous	47114263
17	44189794	44189797	TGA	---	16	GENIC	homozygous	47114265
17	44191229	44191230	C	G	16	GENIC	heterozygous	47114267
17	44191373	44191374	C	CT	18	GENIC	possibly homozygous	47114269
17	44192019	44192020	T	TC	30	GENIC	homozygous	47114271
17	44192086	44192087	C	T	39	GENIC	possibly homozygous	47114273
17	44192614	44192615	A	G	26	GENIC	homozygous	47114275
17	44192707	44192708	G	A	38	GENIC	heterozygous	47590818