chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	144103342	144103343	C	G	16	GENIC	homozygous	115945007
7	144103528	144103529	T	C	11	GENIC	homozygous	115945008
7	144103747	144103748	C	T	8	GENIC	homozygous	115945009
7	144105165	144105166	T	G	20	GENIC	homozygous	115945010
7	144107661	144107662	A	G	21	GENIC	homozygous	115945011
7	144107952	144107953	C	T	20	GENIC	homozygous	115945012
7	144109385	144109386	T	C	24	GENIC	homozygous	115945013
7	144109598	144109599	C	G	19	GENIC	homozygous	115945014
7	144109629	144109630	C	T	17	GENIC	homozygous	115945015
7	144109681	144109682	A	C	24	GENIC	homozygous	115945016
7	144110529	144110530	C	T	21	GENIC	homozygous	115945018
7	144110726	144110727	G	A	20	GENIC	homozygous	116100910
7	144110901	144110902	A	C	10	GENIC	homozygous	115945019
7	144111438	144111439	T	C	22	GENIC	homozygous	115945020
7	144112053	144112054	G	A	30	GENIC	homozygous	115945021
7	144112570	144112571	T	C	22	GENIC	homozygous	115945022
7	144113830	144113831	A	G	12	GENIC	homozygous	116100912
7	144115195	144115196	C	T	13	GENIC	homozygous	115945023
7	144115606	144115607	A	G	22	GENIC	homozygous	115945024
7	144115720	144115721	G	A	17	GENIC	homozygous	115945025
7	144115776	144115777	G	A	16	GENIC	homozygous	115945026
7	144116204	144116205	G	A	28	GENIC	homozygous	115945027
7	144116838	144116839	G	A	16	GENIC	homozygous	115945028
7	144116920	144116921	T	C	25	GENIC	homozygous	115945029