chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	2202915	2202916	C	T	16	GENIC	homozygous	109370283
20	2203651	2203652	T	A	29	GENIC	homozygous	109370285
20	2203671	2203672	G	A	29	GENIC	homozygous	109370287
20	2206150	2206151	T	C	28	GENIC	homozygous	109066435
20	2207415	2207416	A	T	25	GENIC	homozygous	109370289
20	2207512	2207513	C	T	21	GENIC	homozygous	109370291
20	2207780	2207781	G	A	25	GENIC	homozygous	109370293
20	2213572	2213573	C	A	11	GENIC	homozygous	109066449
20	2215328	2215329	C	T	26	GENIC	homozygous	109066459
20	2216410	2216411	G	A	38	GENIC	homozygous	109370295
20	2220049	2220050	A	G	28	GENIC	homozygous	109066471
20	2221434	2221435	T	C	27	GENIC	homozygous	109066479
20	2222276	2222277	T	C	22	GENIC	homozygous	109066481
20	2223926	2223927	G	T	23	GENIC	homozygous	109066487
20	2223927	2223928	T	G	22	GENIC	homozygous	109066489
20	2224102	2224103	C	A	17	GENIC	homozygous	109066491
20	2224142	2224143	G	T	15	GENIC	homozygous	109066493
20	2224465	2224466	A	C	7	GENIC	homozygous	109231341
20	2223230	2223231	G	A	12	GENIC	homozygous	109416706