chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	22738545	22738546	G	T	14	GENIC	homozygous	115484256
12	22738811	22738812	G	A	18	GENIC	homozygous	115597777
12	22738911	22738912	G	A	12	GENIC	homozygous	115484259
12	22738960	22738961	G	A	19	GENIC	homozygous	115484260
12	22739727	22739728	A	G	14	GENIC	homozygous	115484261
12	22739768	22739769	A	G	10	GENIC	homozygous	115484262
12	22739903	22739904	C	T	8	GENIC	homozygous	115484263
12	22739929	22739930	G	A	8	GENIC	homozygous	115597779
12	22740143	22740144	C	T	11	GENIC	homozygous	115597781
12	22740422	22740423	C	T	14	GENIC	homozygous	115484264
12	22740471	22740472	A	G	10	GENIC	homozygous	115484266
12	22744698	22744699	G	A	16	GENIC	homozygous	115484269
12	22744910	22744911	C	T	15	GENIC	homozygous	115597783
12	22745587	22745588	G	A	28	GENIC	homozygous	115484270
12	22745621	22745622	C	T	19	GENIC	homozygous	115597785
12	22746477	22746478	A	G	23	GENIC	homozygous	115282680
12	22747001	22747002	G	T	6	GENIC	homozygous	115597787
12	22750329	22750330	A	G	10	GENIC	homozygous	115282684