chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	30818264	30818265	A	T	41	GENIC	homozygous	109163309
20	30818266	30818272	AAAGAA		43	GENIC	homozygous	129678903
20	30818281	30818281		C	46	GENIC	homozygous	129678904
20	30818291	30818292	A		47	GENIC	homozygous	129678905
20	30829888	30829888		A	21	GENIC	homozygous	129678917
20	30829893	30829894	C		19	GENIC	homozygous	129678918
20	30829901	30829902	G		13	GENIC	homozygous	129678919
20	30829906	30829907	G		12	GENIC	homozygous	129678920
20	30830170	30830171	A	C	10	GENIC	homozygous	109253038
20	30830171	30830172	C	A	10	GENIC	homozygous	109253040
20	30830181	30830182	A		11	GENIC	homozygous	129678921
20	30830190	30830190		A	11	GENIC	homozygous	129678922
20	30830196	30830196		CTA	11	GENIC	homozygous	129678923
20	30830199	30830200	C		11	GENIC	homozygous	129678924
20	30830212	30830213	C		13	GENIC	homozygous	129678925
20	30830225	30830225		G	13	GENIC	homozygous	129678926
20	30830258	30830258		G	20	GENIC	homozygous	129678927
20	30830261	30830262	C		21	GENIC	homozygous	129678928
20	30830271	30830272	T		22	GENIC	homozygous	129678929
20	30830455	30830456	C	G	27	GENIC	homozygous	109163323
20	30830456	30830457	C	G	29	GENIC	homozygous	109163325
20	30830457	30830458	C	G	29	GENIC	homozygous	109163327
20	30830459	30830460	C		31	GENIC	homozygous	129678930