chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11193567	11193568	T	C	22	GENIC	homozygous	115361392
12	11194336	11194337	A	G	35	GENIC	homozygous	115254756
12	11194568	11194569	A	G	22	GENIC	homozygous	115445082
12	11194596	11194597	G	T	22	GENIC	homozygous	115632303
12	11194883	11194884	T	C	19	GENIC	heterozygous	118244389
12	11195668	11195669	T	C	44	GENIC	homozygous	115254758
12	11195810	11195811	A	G	38	GENIC	homozygous	115254760
12	11195825	11195826	A	G	41	GENIC	homozygous	115254762
12	11196273	11196274	C	A	40	GENIC	homozygous	115415254
12	11196487	11196488	C	T	32	GENIC	homozygous	115415256
12	11196798	11196799	G	A	23	GENIC	homozygous	115254766
12	11197080	11197081	T	C	30	GENIC	homozygous	115254770
12	11197286	11197287	C	T	44	GENIC	homozygous	115415258
12	11198000	11198001	G	A	45	GENIC	homozygous	115254772
12	11198165	11198166	T	C	38	GENIC	homozygous	115254774
12	11198182	11198183	T	C	38	GENIC	homozygous	115254776
12	11194934	11194935	G	A	14	GENIC	possibly homozygous	118335672
12	11194944	11194945	C	T	17	GENIC	possibly homozygous	118335673