chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	21756111	21756112	T	G	12	GENIC	homozygous	109136959
20	21758053	21758054	G	T	25	GENIC	homozygous	109136961
20	21758054	21758055	C	G	24	GENIC	homozygous	109136963
20	21758097	21758098	A	C	27	GENIC	homozygous	109136965
20	21758287	21758288	C	G	23	GENIC	homozygous	109136967
20	21758328	21758329	C	A	34	GENIC	homozygous	109136969
20	21758902	21758903	G	T	33	GENIC	homozygous	109136979
20	21759181	21759182	G	T	29	GENIC	homozygous	109136982
20	21773125	21773126	G	A	27	GENIC	homozygous	109136986
20	21773146	21773147	C	T	25	GENIC	homozygous	109136988
20	21810740	21810741	A	G	29	GENIC	possibly homozygous	109136998
20	21810996	21810997	G	T	13	GENIC	homozygous	109137000
20	21831675	21831676	T	C	20	GENIC	homozygous	109137002
20	21839728	21839729	T	A	10	GENIC	homozygous	109137004
20	21839757	21839758	A	G	11	GENIC	homozygous	109137006
20	21846389	21846390	A	T	16	GENIC	homozygous	109137049
20	21846854	21846855	G	A	19	GENIC	homozygous	109137053
20	21846905	21846906	T	C	20	GENIC	homozygous	109137055
20	21810985	21810986	G	T	14	GENIC	homozygous	109309935
20	21879302	21879303	A	C	18	GENIC	heterozygous	109309937