chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3883225	3883226	A	G	30	GENIC	homozygous	109294717
20	3883741	3883742	C	T	12	GENIC	homozygous	109370837
20	3883756	3883757	T	C	13	GENIC	homozygous	109070185
20	3884223	3884224	C	G	26	GENIC	homozygous	109070191
20	3884297	3884298	G	A	28	GENIC	homozygous	109070193
20	3884304	3884305	T	C	28	GENIC	homozygous	109070195
20	3884342	3884343	A	G	30	GENIC	homozygous	109070197
20	3884388	3884389	A	G	30	GENIC	homozygous	109070199
20	3884394	3884395	A	G	29	GENIC	homozygous	109070201
20	3884411	3884412	T	C	32	GENIC	homozygous	109070203
20	3884423	3884424	A	G	28	GENIC	homozygous	109070205
20	3884541	3884542	A	T	25	GENIC	homozygous	109070207
20	3884550	3884551	A	G	25	GENIC	homozygous	109070209
20	3884575	3884576	T	C	23	GENIC	homozygous	109070211
20	3884590	3884591	G	C	21	GENIC	homozygous	109070213
20	3884595	3884596	T	C	22	GENIC	homozygous	109070215
20	3884990	3884991	T	C	23	GENIC	homozygous	109070223
20	3885004	3885005	T	C	24	GENIC	homozygous	109070227
20	3884988	3884989	T	C	22	GENIC	homozygous	109231925
20	3884204	3884205	G	A	22	GENIC	homozygous	109231923