chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	52465808	52465809	T	C	11	GENIC	homozygous	109825013
19	52466735	52466736	C	T	14	GENIC	homozygous	109825015
19	52467363	52467364	G	A	14	GENIC	homozygous	109825017
19	52474413	52474414	T	C	22	GENIC	homozygous	109825019
19	52475657	52475658	A	G	10	GENIC	homozygous	109825021
19	52481416	52481417	T	C	19	GENIC	homozygous	109825023
19	52482379	52482380	C	T	23	GENIC	homozygous	109825025
19	52482393	52482394	T	C	26	GENIC	homozygous	109825027
19	52482893	52482894	T	C	15	GENIC	homozygous	109825029
19	52483528	52483529	G	T	22	GENIC	homozygous	109825031
19	52483529	52483530	T	C	22	GENIC	homozygous	109825033
19	52484945	52484946	G	T	19	GENIC	possibly homozygous	109825035
19	52485590	52485591	C	T	10	GENIC	homozygous	109825037
19	52486091	52486092	G	C	26	GENIC	homozygous	109825039
19	52490477	52490478	A	G	16	GENIC	homozygous	109825041
19	52491456	52491457	C	G	14	GENIC	homozygous	109825043
19	52491877	52491878	G	A	9	GENIC	homozygous	125320102
19	52493124	52493125	G	A	8	GENIC	homozygous	109825045
19	52493453	52493454	G	A	16	GENIC	homozygous	109825047
19	52495223	52495224	G	A	14	GENIC	homozygous	109825049
19	52495226	52495227	C	T	13	GENIC	homozygous	109825051
19	52495253	52495254	G	A	15	GENIC	homozygous	109825053
19	52496581	52496582	T	G	11	GENIC	homozygous	109825055
19	52497198	52497199	C	T	18	GENIC	homozygous	109825057
19	52481917	52481918	G	A	14	GENIC	possibly homozygous	125267000
19	52484229	52484230	C	T	14	GENIC	homozygous	125267001
19	52477355	52477358	ATA		13	GENIC	heterozygous	130481478
19	52473287	52473288	G		18	GENIC	homozygous	132236376
19	52486791	52486791		TTTTTTTCTTTTTTTCTT	9	GENIC	homozygous	132236377
19	52486934	52486934		T	17	GENIC	homozygous	132236378
19	52478735	52478736	T	A	22	GENIC	homozygous	132239817
19	52486879	52486880	T	C	18	GENIC	homozygous	132239818