chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	245974544	245974545	G	A	14	GENIC	homozygous	135855539
1	245974900	245974901	G	A	6	GENIC	homozygous	135855540
1	245975343	245975344	G	A	18	GENIC	homozygous	135855541
1	245975519	245975520	C	T	12	GENIC	homozygous	135855542
1	245975878	245975895	AGCGCTCTACCACTGAG		10	GENIC	homozygous	135470964
1	245976193	245976197	AGTC		12	GENIC	homozygous	135470965
1	245977068	245977069	A	G	15	GENIC	homozygous	135855547
1	245975947	245975948	G	A	9	GENIC	homozygous	135855543
1	245976216	245976217	T	C	12	GENIC	homozygous	135855544
1	245976976	245976977	C	T	24	GENIC	homozygous	135855545
1	245977016	245977017	A	G	19	GENIC	homozygous	135855546
1	245978415	245978416	C	A	19	GENIC	homozygous	135855548
1	245978535	245978536	G	C	11	GENIC	homozygous	135855549
1	245979116	245979119	CAC		15	GENIC	homozygous	135470966
1	245979125	245979131	CACCAC		15	GENIC	homozygous	135470967
1	245979142	245979143	C	T	15	GENIC	homozygous	135855550
1	245979151	245979152	C	T	15	GENIC	homozygous	135855551
1	245979154	245979155	C	T	15	GENIC	homozygous	135855552
1	245979170	245979176	CACCAT		14	GENIC	homozygous	135470968
1	245979193	245979208	TCATCACCACCACCG		10	GENIC	homozygous	135470969
1	245979193	245979194	T		10	GENIC	homozygous	402984199
1	245979193	245979194	T	C	10	GENIC	heterozygous	402984200
1	245979127	245979128	C		15	GENIC	homozygous	402984197
1	245979127	245979128	C	T	15	GENIC	heterozygous	402984198
1	245979196	245979197	T		10	GENIC	homozygous	402984201
1	245979196	245979197	T	C	10	GENIC	heterozygous	402984202
1	245979207	245979208	G		10	GENIC	homozygous	402984203
1	245979207	245979208	G	A	10	GENIC	heterozygous	402984204
1	245979324	245979324		GT	13	GENIC	possibly homozygous	135470970
1	245979455	245979456	C	T	13	GENIC	homozygous	135855553