chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	261834061	261834062	G	A	22	GENIC	homozygous	109026343
1	261834697	261834698	T	C	31	GENIC	homozygous	109026344
1	261835631	261835632	T	C	21	GENIC	homozygous	109026345
1	261836446	261836447	C	T	22	GENIC	homozygous	109026346
1	261836712	261836713	C	T	23	GENIC	homozygous	109026347
1	261836805	261836806	A	G	21	GENIC	homozygous	109026348
1	261837425	261837426	A	G	19	GENIC	homozygous	108630096
1	261837610	261837611	T	C	16	GENIC	homozygous	109026349
1	261837740	261837741	T	C	25	GENIC	homozygous	109026350
1	261839521	261839522	C	T	22	GENIC	homozygous	109026351
1	261840222	261840223	A	G	23	GENIC	homozygous	109026352
1	261841118	261841119	C	T	24	GENIC	homozygous	109026353
1	261842757	261842758	T	C	24	GENIC	homozygous	108630099
1	261846422	261846423	T	C	21	GENIC	homozygous	109026354
1	261846581	261846582	G	A	17	GENIC	homozygous	109026355
1	261847007	261847008	C	T	24	GENIC	homozygous	109026356
1	261847296	261847297	C	T	30	GENIC	homozygous	109026357
1	261848172	261848173	C	G	24	GENIC	homozygous	109026358
1	261850759	261850760	T	A	26	GENIC	homozygous	109026359
1	261852986	261852987	C	A	23	GENIC	homozygous	109026360