chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	28113542	28113544	TT	--	19	GENIC	heterozygous	46659162
18	28113546	28113547	T	TTTG	20	GENIC	homozygous	46659163
18	28115277	28115278	C	CT	21	GENIC	possibly homozygous	46659164
18	28115277	28115278	C	CTT	21	GENIC	heterozygous	46659165
18	28115382	28115383	C	CTTTTT	9	GENIC	heterozygous	46659166
18	28115382	28115383	C	CTTT	9	GENIC	heterozygous	46659167
18	28115403	28115404	C	T	25	GENIC	heterozygous	46659168
18	28115911	28115912	A	AAC	9	GENIC	homozygous	46407334
18	28116893	28116894	C	T	15	GENIC	homozygous	46659169
18	28117173	28117174	T	A	13	GENIC	heterozygous	46659170
18	28117175	28117176	T	A	12	GENIC	heterozygous	46659171
18	28117177	28117178	T	A	12	GENIC	heterozygous	46659172
18	28117179	28117180	T	A	13	GENIC	heterozygous	46659173
18	28117790	28117791	A	T	26	GENIC	homozygous	46659174
18	28118013	28118014	C	CA	8	GENIC	possibly homozygous	46659175
18	28118183	28118184	C	CT	6	GENIC	homozygous	46659176
18	28118202	28118203	C	CT	8	GENIC	homozygous	46659177
18	28119984	28119988	TTTA	----	14	GENIC	heterozygous	46659178
18	28120003	28120004	A	G	18	GENIC	homozygous	46659179
18	28120674	28120675	G	T	17	GENIC	possibly homozygous	46659180
18	28121164	28121165	A	G	23	GENIC	homozygous	46659181
18	28121296	28121297	A	G	24	GENIC	homozygous	46659182
18	28124582	28124583	C	CT	11	GENIC	possibly homozygous	46659183
18	28127966	28127967	G	A	14	GENIC	homozygous	46659184
18	28127979	28127980	T	-	2	GENIC	homozygous	46585964
18	28128294	28128295	G	A	29	GENIC	heterozygous	46585965
18	28128348	28128349	C	A	29	GENIC	heterozygous	46407338
18	28128457	28128458	A	G	38	GENIC	heterozygous	46407340
18	28128466	28128467	T	G	42	GENIC	heterozygous	46407342
18	28128947	28128948	G	A	17	GENIC	heterozygous	46585967