chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	126434653	126434654	T	C	54	GENIC	homozygous	118734360
6	126435353	126435354	A	G	42	GENIC	homozygous	118734361
6	126435436	126435437	A	T	37	GENIC	homozygous	118734362
6	126435862	126435862		CG	15	GENIC	homozygous	131662399
6	126435863	126435863		CCGTCC	15	GENIC	homozygous	131662400
6	126435871	126435872	G	A	13	GENIC	homozygous	131668500
6	126435874	126435875	C	T	12	GENIC	homozygous	131668501
6	126436303	126436304	T	C	47	GENIC	homozygous	118734363
6	126436397	126436398	T	G	41	GENIC	homozygous	118734364
6	126436410	126436411	G	A	42	GENIC	homozygous	118734365
6	126436867	126436868	C	T	53	GENIC	homozygous	118734366
6	126436942	126436943	C	T	48	GENIC	homozygous	118734367
6	126436979	126436980	G	T	47	GENIC	homozygous	118734368
6	126437097	126437098	G	C	45	GENIC	homozygous	118734369
6	126437098	126437099	G	A	45	GENIC	homozygous	118734370
6	126437142	126437143	G	C	45	GENIC	homozygous	118734371
6	126437408	126437409	C	T	47	GENIC	homozygous	118734373
6	126437623	126437624	C		39	GENIC	homozygous	131662403
6	126438103	126438104	C	T	44	GENIC	homozygous	118734374
6	126438201	126438202	T	C	48	GENIC	homozygous	118734375
6	126438724	126438725	T	C	52	GENIC	homozygous	118734376
6	126438779	126438780	G	A	61	GENIC	homozygous	118734377
6	126438968	126438972	AAAG		30	GENIC	possibly homozygous	131662404
6	126439003	126439003		GGAA	29	GENIC	possibly homozygous	131662405
6	126439879	126439880	G	A	29	GENIC	homozygous	131668502
6	126440821	126440822	C	T	50	GENIC	homozygous	118734378
6	126442321	126442324	GAG		45	GENIC	homozygous	131662406
6	126442622	126442623	A	G	46	GENIC	homozygous	118734379
6	126443655	126443656	G	A	55	GENIC	homozygous	118734380
6	126443680	126443681	A	G	56	GENIC	homozygous	118734381
6	126443757	126443758	C	T	58	GENIC	homozygous	118734382
6	126444397	126444397		AGA	32	GENIC	homozygous	131662407
6	126445114	126445115	G	A	40	GENIC	homozygous	118734383
6	126445409	126445410	G	T	50	GENIC	homozygous	118734384