chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	26118804	26118805	G	A	18	GENIC	homozygous	111407367
2	26118819	26118820	A	G	18	GENIC	homozygous	111407368
2	26118915	26118916	A	C	25	GENIC	homozygous	110494107
2	26119727	26119728	T	C	53	GENIC	homozygous	109653221
2	26119919	26119920	T	C	31	GENIC	homozygous	110494109
2	26123100	26123101	T	C	25	GENIC	homozygous	109653225
2	26123228	26123229	C	T	8	GENIC	homozygous	110494111
2	26123784	26123785	C	A	33	GENIC	homozygous	111407369
2	26125110	26125111	G	A	36	GENIC	homozygous	111407370
2	26125496	26125497	C	T	12	GENIC	homozygous	110928106
2	26127073	26127074	A	G	7	GENIC	homozygous	110928108
2	26128997	26128998	A	G	14	GENIC	homozygous	109653231
2	26129107	26129108	T	G	22	GENIC	homozygous	109653233
2	26129981	26129982	A	G	42	GENIC	homozygous	109653235
2	26130987	26130988	C	A	20	GENIC	homozygous	111407371
2	26131400	26131401	T	A	37	GENIC	homozygous	109653237
2	26133006	26133007	C	T	42	GENIC	homozygous	111407372
2	26133069	26133070	T	C	38	GENIC	homozygous	109653239
2	26133531	26133532	A	G	32	GENIC	homozygous	109653241
2	26134340	26134341	A	T	25	GENIC	homozygous	120122476
2	26134341	26134342	T	C	26	GENIC	homozygous	120122478
2	26134358	26134359	T	A	19	GENIC	homozygous	109653243
2	26135262	26135263	G	C	20	GENIC	homozygous	120122480
2	26135264	26135265	C	G	20	GENIC	homozygous	120122482
2	26135064	26135065	A	G	28	GENIC	homozygous	109653247