chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	15287913	15287919	GCACCA	------	23	GENIC	homozygous	45780422
20	15288238	15288239	G	A	34	GENIC	homozygous	45790945
20	15288817	15288818	C	CTT	7	GENIC	homozygous	45444936
20	15289010	15289011	G	A	20	GENIC	homozygous	45790946
20	15289639	15289640	G	T	38	GENIC	homozygous	45780426
20	15290225	15290226	C	A	33	GENIC	homozygous	45790947
20	15290237	15290238	T	-	31	GENIC	homozygous	45444951
20	15290406	15290407	T	C	33	GENIC	homozygous	45444955
20	15290667	15290668	A	AG	26	GENIC	homozygous	45790948
20	15290938	15290939	A	AAGT	25	GENIC	homozygous	45790949
20	15291003	15291004	A	G	15	GENIC	homozygous	45790950
20	15291199	15291207	GTGTGTGT	--------	8	GENIC	heterozygous	45864195
20	15291637	15291638	T	C	18	GENIC	homozygous	45790951
20	15292177	15292178	T	C	27	GENIC	homozygous	45790952
20	15292990	15292991	A	G	25	GENIC	homozygous	45790953
20	15293196	15293197	G	A	11	GENIC	homozygous	45790954
20	15293230	15293231	G	A	8	GENIC	homozygous	45790955
20	15293297	15293298	C	CAAA	1	GENIC	homozygous	45864196
20	15293573	15293574	A	G	36	GENIC	homozygous	45780435
20	15293654	15293655	C	T	20	GENIC	homozygous	45790956
20	15293732	15293733	A	G	25	GENIC	homozygous	45790957
20	15293758	15293759	A	T	27	GENIC	homozygous	45444978
20	15293966	15293967	G	A	12	GENIC	homozygous	45790958
20	15294021	15294022	T	C	13	GENIC	homozygous	45444982
20	15294108	15294109	A	AAAGAAG	7	GENIC	heterozygous	45843613
20	15294190	15294191	G	T	11	GENIC	homozygous	45780437
20	15294349	15294350	C	CGT	7	GENIC	heterozygous	45444984
20	15294349	15294350	C	CG	7	GENIC	heterozygous	45864197
20	15294378	15294379	T	C	10	GENIC	possibly homozygous	45780439
20	15295728	15295729	C	T	29	GENIC	homozygous	45790961
20	15295854	15295855	A	ATT	24	GENIC	heterozygous	45780441
20	15295854	15295855	A	AT	24	GENIC	possibly homozygous	45790962
20	15296364	15296365	C	T	28	GENIC	homozygous	45790963