chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	2183246	2183247	T	G	29	GENIC	homozygous	109370227
20	2183363	2183364	T	C	28	GENIC	homozygous	109370229
20	2183385	2183386	A	T	28	GENIC	homozygous	109370232
20	2183582	2183583	A	G	23	GENIC	homozygous	109370234
20	2185260	2185261	G	A	22	GENIC	homozygous	109370236
20	2185292	2185293	C	T	23	GENIC	homozygous	109370238
20	2185428	2185429	A	G	8	GENIC	homozygous	109370240
20	2185455	2185456	G	A	15	GENIC	homozygous	109370242
20	2185963	2185964	G	A	27	GENIC	homozygous	109370244
20	2186020	2186021	A	C	26	GENIC	homozygous	109370246
20	2186596	2186597	A	T	34	GENIC	homozygous	109370248
20	2186671	2186672	G	A	22	GENIC	homozygous	109370251
20	2186811	2186812	T	C	25	GENIC	homozygous	109370253
20	2187174	2187175	T	C	9	GENIC	homozygous	109370255
20	2188054	2188055	C	T	24	GENIC	homozygous	109370257
20	2188237	2188238	C	T	23	GENIC	homozygous	109370259
20	2188624	2188625	G	C	34	GENIC	homozygous	109370261
20	2188949	2188950	A	G	27	GENIC	possibly homozygous	109370263
20	2189659	2189660	C	T	34	GENIC	homozygous	109370265
20	2189752	2189753	G	T	33	GENIC	homozygous	109370267
20	2189765	2189766	T	C	33	GENIC	homozygous	109370269
20	2190288	2190289	C	T	14	GENIC	homozygous	109370271
20	2190345	2190346	T	A	27	GENIC	homozygous	109370273
20	2190532	2190533	G	A	35	GENIC	heterozygous	119843120