chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	120344891	120344892	A	G	6	GENIC	homozygous	115855997
7	120345137	120345138	G	A	9	GENIC	homozygous	135189396
7	120347270	120347271	G	T	21	GENIC	homozygous	116081517
7	120347375	120347376	G	A	21	GENIC	homozygous	115856001
7	120347874	120347875	T	G	30	GENIC	homozygous	116081520
7	120348268	120348274	TGTCAT		13	GENIC	homozygous	131433544
7	120348459	120348460	A	G	16	GENIC	homozygous	116081522
7	120354774	120354775	T	C	19	GENIC	homozygous	116081529
7	120359186	120359187	A	G	26	GENIC	homozygous	115856009
7	120367697	120367698	G	T	18	GENIC	homozygous	118512406
7	120363812	120363813	A	G	21	GENIC	homozygous	116081545
7	120364323	120364324	T	C	21	GENIC	homozygous	115856013
7	120348875	120348876	A	G	15	GENIC	homozygous	118512396
7	120353416	120353417	C	T	9	GENIC	homozygous	118512397
7	120353760	120353761	G	C	19	GENIC	homozygous	118512398
7	120355006	120355007	A	T	22	GENIC	homozygous	118512399
7	120356100	120356101	T	C	24	GENIC	homozygous	118512400
7	120361049	120361050	C	T	14	GENIC	homozygous	118512401
7	120361343	120361344	G	A	20	GENIC	homozygous	118512402
7	120362546	120362547	G	C	20	GENIC	homozygous	118512403
7	120362701	120362702	G	T	20	GENIC	homozygous	118512404
7	120367524	120367525	G	A	22	GENIC	homozygous	118512405
7	120349414	120349414		AAAC	21	GENIC	possibly homozygous	135186184
7	120366132	120366188	CCTCTCTGCCTCTCTGCCCCTCTCCCCCTCTGCCCCTCTCCCCCTCTGCCCCTCTC		17	GENIC	homozygous	135186185
7	120357903	120357903		A	15	GENIC	homozygous	128512201
7	120368016	120368017	C	T	20	GENIC	homozygous	118512407
7	120370549	120370550	A	G	25	GENIC	homozygous	116081560
7	120370653	120370654	T	C	24	GENIC	homozygous	115856021
7	120371463	120371464	G	A	22	GENIC	homozygous	118512408
7	120373293	120373294	A	G	16	GENIC	homozygous	116081564
7	120374099	120374100	T	G	15	GENIC	homozygous	115856023