chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4807228	4807229	C	T	30	GENIC	homozygous	109075297
20	4807596	4807597	T	C	22	GENIC	homozygous	109075299
20	4807873	4807874	C	T	32	GENIC	homozygous	109075301
20	4809544	4809545	T	C	21	GENIC	homozygous	109075307
20	4809993	4809994	T	C	13	GENIC	homozygous	109075309
20	4810957	4810958	A	G	21	GENIC	homozygous	109075311
20	4810962	4810963	A	G	21	GENIC	homozygous	109075313
20	4811126	4811127	G	A	24	GENIC	homozygous	109075315
20	4812040	4812041	G	A	19	GENIC	homozygous	109075317
20	4812112	4812113	C	T	31	GENIC	homozygous	109075319
20	4812117	4812118	G	A	31	GENIC	homozygous	109075321
20	4812321	4812322	C	A	20	GENIC	homozygous	109075323
20	4812472	4812473	C	T	25	GENIC	homozygous	109075325
20	4813327	4813328	G	A	28	GENIC	homozygous	109075327
20	4813759	4813760	C	T	28	GENIC	homozygous	109075329
20	4814252	4814253	G	A	21	GENIC	homozygous	109075331
20	4816238	4816239	A	G	30	GENIC	homozygous	109075333
20	4816327	4816328	G	A	37	GENIC	homozygous	109075335
20	4816587	4816588	G	C	28	GENIC	homozygous	109075337
20	4817334	4817335	C	G	21	GENIC	homozygous	109233630
20	4817344	4817345	G	C	18	GENIC	homozygous	109233631
20	4817510	4817511	G	A	22	GENIC	homozygous	109075339