chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	11693775	11693776	C	T	58	GENIC	homozygous	142035403
8	11693968	11693969	C	T	48	GENIC	homozygous	142035404
8	11694302	11694303	T	C	56	GENIC	homozygous	142035405
8	11695172	11695176	CACT		23	GENIC	homozygous	142017194
8	11696436	11696437	T	C	52	GENIC	homozygous	142035406
8	11696449	11696450	G	A	52	GENIC	homozygous	142035407
8	11698395	11698396	G	A	51	GENIC	homozygous	142035408
8	11698605	11698606	C	T	48	GENIC	homozygous	142035409
8	11698965	11698966	A	G	46	GENIC	homozygous	142035410
8	11699578	11699579	T	G	49	GENIC	homozygous	142035411
8	11699582	11699583	T	C	48	GENIC	homozygous	142035412
8	11699711	11699731	CTTGGAACTTCTAGGAGGCA		50	GENIC	homozygous	142017196
8	11699764	11699765	G	A	61	GENIC	homozygous	142035413
8	11700266	11700267	T	C	47	GENIC	homozygous	142035414
8	11700602	11700602		CACT	36	GENIC	homozygous	142017197
8	11700782	11700783	G	C	42	GENIC	homozygous	142035415
8	11701031	11701032	G	A	46	GENIC	homozygous	142035416
8	11701432	11701433	T	C	57	GENIC	homozygous	142035417
8	11701708	11701709	C	T	56	GENIC	homozygous	142035418
8	11702426	11702427	C	T	53	GENIC	homozygous	142035419
8	11697255	11697255		C	13	GENIC	heterozygous	146840645
8	11702760	11702761	G	C	29	GENIC	heterozygous	403896803
8	11695175	11695176	T		23	GENIC	homozygous	403896800
8	11695175	11695176	T	C	23	GENIC	heterozygous	403896801
8	11702760	11702761	G		29	GENIC	homozygous	403896802
8	11703082	11703083	T	A	54	GENIC	homozygous	142035420
8	11703134	11703135	T	A	49	GENIC	homozygous	142035421
8	11703219	11703220	T	C	43	GENIC	homozygous	142035422