chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3881941	3881942	T	C	3	GENIC	homozygous	131235617
20	3881959	3881960	C	T	3	GENIC	homozygous	132244286
20	3882093	3882094	G	A	4	GENIC	homozygous	131559179
20	3883183	3883183		A	28	GENIC	homozygous	129651578
20	3883491	3883492	C	T	26	GENIC	homozygous	119756756
20	3883131	3883132	T	C	19	GENIC	homozygous	109552228
20	3883225	3883226	A	G	31	GENIC	homozygous	109294717
20	3883503	3883504	C	T	27	GENIC	homozygous	131559180
20	3883537	3883538	T	C	36	GENIC	homozygous	119756759
20	3884342	3884343	A	G	39	GENIC	homozygous	109070197
20	3884061	3884062	T	C	35	GENIC	homozygous	109070189
20	3884297	3884298	G	A	40	GENIC	homozygous	109070193
20	3884304	3884305	T	C	35	GENIC	homozygous	109070195
20	3883852	3883853	A		21	GENIC	homozygous	131554628
20	3883853	3883854	A	G	21	GENIC	homozygous	109547311
20	3883867	3883868	G	A	18	GENIC	homozygous	109389159
20	3884388	3884389	A	G	33	GENIC	homozygous	109070199
20	3884394	3884395	A	G	34	GENIC	homozygous	109070201
20	3884411	3884412	T	C	36	GENIC	homozygous	109070203
20	3884423	3884424	A	G	34	GENIC	homozygous	109070205
20	3884471	3884473	TT		37	GENIC	possibly homozygous	129651579
20	3884474	3884490	CATCCTGACCCCGAGG		37	GENIC	possibly homozygous	129651580
20	3884495	3884496	A	G	36	GENIC	possibly homozygous	109389160
20	3884514	3884515	G	A	41	GENIC	possibly homozygous	109231924
20	3884541	3884542	A	T	39	GENIC	possibly homozygous	109070207
20	3884550	3884551	A	G	47	GENIC	possibly homozygous	109070209
20	3884575	3884576	T	C	51	GENIC	possibly homozygous	109070211
20	3884590	3884591	G	C	52	GENIC	homozygous	109070213
20	3884595	3884596	T	C	53	GENIC	homozygous	109070215
20	3884663	3884664	G	A	51	GENIC	homozygous	109389162
20	3884816	3884817	G	C	47	GENIC	possibly homozygous	109389163
20	3884833	3884834	G	T	51	GENIC	possibly homozygous	109070217
20	3884988	3884989	T	C	42	GENIC	homozygous	109231925
20	3884990	3884991	T	C	42	GENIC	homozygous	109070223
20	3885129	3885130	C	T	42	GENIC	homozygous	109547312