chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	30939735	30939736	A	G	24	GENIC	homozygous	109679067
19	30940194	30940195	C	A	32	GENIC	homozygous	109679069
19	30942301	30942302	G	A	23	GENIC	homozygous	109679071
19	30943973	30943974	G	A	21	GENIC	homozygous	109679073
19	30945853	30945854	A	G	16	GENIC	homozygous	109679075
19	30946107	30946108	G	A	15	GENIC	homozygous	109679077
19	30946850	30946851	A	T	29	GENIC	homozygous	109679079
19	30948517	30948518	G	A	14	GENIC	homozygous	109679083
19	30950431	30950432	G	A	14	GENIC	homozygous	109679085
19	30951631	30951632	T	C	45	GENIC	homozygous	109805781
19	30954046	30954047	C	T	17	GENIC	homozygous	109679087
19	30954288	30954289	G	T	18	GENIC	homozygous	109679089
19	30955390	30955391	G	A	34	GENIC	homozygous	109679091
19	30956266	30956267	C	T	33	GENIC	homozygous	109679093
19	30958346	30958347	A	G	24	GENIC	homozygous	109679095
19	30959119	30959120	T	C	24	GENIC	homozygous	109679097
19	30960984	30960985	T	A	26	GENIC	homozygous	109679099
19	30961427	30961428	G	T	23	GENIC	homozygous	109679101
19	30961547	30961548	G	C	36	GENIC	homozygous	109679103
19	30963831	30963832	G	A	25	GENIC	homozygous	109679105
19	30967399	30967400	G	A	49	GENIC	homozygous	109679107
19	30953766	30953767	G	A	23	GENIC	homozygous	119624170
19	30967439	30967440	A	G	53	GENIC	homozygous	109679109
19	30968174	30968175	G	A	26	GENIC	homozygous	109679111
19	30961338	30961339	C	T	25	GENIC	possibly homozygous	119624172
19	30961313	30961314	G	T	23	GENIC	homozygous	109919070
19	30961320	30961321	G	T	22	GENIC	homozygous	109919072
19	30967820	30967821	G	A	26	GENIC	possibly homozygous	109919074