chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	38368031	38368033	AC		13	GENIC	heterozygous	129246646
15	38369012	38369012		AGA	10	GENIC	homozygous	129246647
15	38369016	38369017	T	G	9	GENIC	homozygous	129314868
15	38369017	38369018	T	G	9	GENIC	homozygous	129314869
15	38369021	38369021		GG	9	GENIC	homozygous	129246648
15	38369023	38369024	T		8	GENIC	homozygous	129246649
15	38369037	38369038	C		8	GENIC	homozygous	129246650
15	38369042	38369042		G	7	GENIC	homozygous	129246651
15	38369045	38369045		C	7	GENIC	homozygous	129246652
15	38369052	38369052		GG	6	GENIC	homozygous	129246653
15	38369057	38369060	AGA		4	GENIC	homozygous	129246654
15	38374496	38374498	TC		7	GENIC	homozygous	130440427
15	38374507	38374509	AA		9	GENIC	homozygous	129246655
15	38374511	38374512	A		9	GENIC	homozygous	129246656
15	38374516	38374517	G	A	10	GENIC	homozygous	124065062
15	38374518	38374519	A		10	GENIC	homozygous	129246657
15	38374521	38374522	C		10	GENIC	homozygous	129246658
15	38374534	38374536	TT		12	GENIC	homozygous	129246659
15	38374540	38374542	AA		12	GENIC	homozygous	129246660
15	38374542	38374543	A	G	13	GENIC	homozygous	124065067
15	38374558	38374560	AC		15	GENIC	homozygous	129246661
15	38374571	38374572	G	A	16	GENIC	homozygous	118913913
15	38374578	38374579	T	G	17	GENIC	homozygous	118913915
15	38374586	38374587	A		18	GENIC	homozygous	129246662
15	38374597	38374598	T	G	19	GENIC	homozygous	112480803
15	38374599	38374601	AC		19	GENIC	homozygous	129246663
15	38383774	38383775	C		40	GENIC	homozygous	129246665
15	38383779	38383779		A	41	GENIC	homozygous	129246666
15	38383782	38383782		A	42	GENIC	homozygous	129246667
15	38383775	38383776	C	A	42	GENIC	homozygous	112672713
15	38374581	38374582	T	G	17	GENIC	homozygous	118955830