chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	103990132	103990133	T	C	28	GENIC	homozygous	61733184
1	103990688	103990689	A	G	19	GENIC	homozygous	61733186
1	103991733	103991734	T	A	23	GENIC	homozygous	61733188
1	103992100	103992110	CGCGCGCGCG	----------	16	GENIC	homozygous	61670982
1	103992615	103992616	G	A	24	GENIC	homozygous	61733190
1	103992728	103992729	G	GTT	8	GENIC	homozygous	61733192
1	103992773	103992774	C	-	15	GENIC	possibly homozygous	61733194
1	103992779	103992783	TTTC	----	13	GENIC	heterozygous	61733196
1	103993052	103993053	G	A	22	GENIC	homozygous	61733198
1	103994790	103994791	T	G	25	GENIC	possibly homozygous	61733200
1	103996312	103996313	C	T	26	GENIC	homozygous	61733202
1	103996752	103996753	T	C	19	GENIC	homozygous	61733204
1	103997380	103997381	A	C	39	GENIC	homozygous	61733206
1	103998103	103998104	C	T	12	GENIC	homozygous	61733208
1	103998230	103998231	G	A	13	GENIC	homozygous	61733210
1	103999820	103999821	C	T	25	GENIC	possibly homozygous	61733212
1	103999825	103999826	A	G	21	GENIC	homozygous	61733214
1	104000288	104000289	G	A	30	GENIC	homozygous	61733216
1	104000442	104000443	T	C	22	GENIC	homozygous	61733218
1	104000937	104000939	TT	--	24	GENIC	homozygous	61733220
1	104001396	104001397	A	G	39	GENIC	homozygous	61733222
1	104001444	104001445	T	C	46	GENIC	homozygous	61733224
1	104001587	104001588	T	C	20	GENIC	homozygous	61733226
1	104001616	104001617	C	T	20	GENIC	homozygous	61733228
1	104002346	104002347	G	T	26	GENIC	heterozygous	61733230
1	104002349	104002350	G	GATGC	23	GENIC	heterozygous	61733232
1	104002433	104002434	G	A	19	GENIC	homozygous	61733234
1	104002880	104002882	AT	--	16	GENIC	homozygous	61299650
1	104002926	104002927	G	T	23	GENIC	homozygous	61733236
1	104004001	104004002	G	A	18	GENIC	possibly homozygous	61733238
1	104004693	104004694	G	A	17	GENIC	heterozygous	61299651
1	104006232	104006233	A	-	19	GENIC	homozygous	60780366