chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	103990132	103990133	T	C	36	GENIC	homozygous	61733184
1	103990688	103990689	A	G	25	GENIC	homozygous	61733186
1	103991733	103991734	T	A	35	GENIC	homozygous	61733188
1	103992100	103992110	CGCGCGCGCG	----------	6	GENIC	homozygous	61670982
1	103992144	103992152	CACACACG	--------	10	GENIC	heterozygous	62245752
1	103992146	103992152	CACACG	------	7	GENIC	heterozygous	62147697
1	103992615	103992616	G	A	10	GENIC	homozygous	61733190
1	103992728	103992729	G	GTT	8	GENIC	homozygous	61733192
1	103992771	103992774	TTC	---	7	GENIC	homozygous	62147699
1	103992781	103992783	TC	--	6	GENIC	homozygous	62147701
1	103993052	103993053	G	A	33	GENIC	homozygous	61733198
1	103994790	103994791	T	G	29	GENIC	homozygous	61733200
1	103996312	103996313	C	T	21	GENIC	homozygous	61733202
1	103996751	103996752	A	AC	5	GENIC	homozygous	62147703
1	103997380	103997381	A	C	14	GENIC	homozygous	61733206
1	103998103	103998104	C	T	24	GENIC	homozygous	61733208
1	103998230	103998231	G	A	18	GENIC	homozygous	61733210
1	103999820	103999821	C	T	26	GENIC	homozygous	61733212
1	103999825	103999826	A	G	31	GENIC	homozygous	61733214
1	104000288	104000289	G	A	29	GENIC	homozygous	61733216
1	104000442	104000443	T	C	35	GENIC	homozygous	61733218
1	104000937	104000939	TT	--	16	GENIC	homozygous	61733220
1	104001396	104001397	A	G	27	GENIC	homozygous	61733222
1	104001444	104001445	T	C	29	GENIC	homozygous	61733224
1	104001587	104001588	T	C	26	GENIC	homozygous	61733226
1	104001616	104001617	C	T	31	GENIC	homozygous	61733228
1	104002880	104002882	AT	--	4	GENIC	homozygous	61299650
1	104002926	104002927	G	T	9	GENIC	homozygous	61733236
1	104004001	104004002	G	A	24	GENIC	homozygous	61733238
1	104004671	104004672	C	CA	1	GENIC	homozygous	62147705
1	104006232	104006233	A	-	36	GENIC	homozygous	60780366