chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	30301466	30301467	G	A	19	GENIC	homozygous	118341799
12	30301604	30301605	T	C	13	GENIC	homozygous	115562171
12	30301835	30301836	A	T	17	GENIC	possibly homozygous	115562173
12	30302623	30302624	T	C	28	GENIC	homozygous	115703742
12	30302735	30302736	A	G	19	GENIC	heterozygous	118341800
12	30302751	30302752	A	G	14	GENIC	heterozygous	118341801
12	30303296	30303297	T	C	2	GENIC	homozygous	118341802
12	30303299	30303300	G	A	2	GENIC	homozygous	118341803
12	30303308	30303309	G	T	4	GENIC	homozygous	118341804
12	30303313	30303314	T	A	4	GENIC	heterozygous	118341805
12	30303315	30303316	G	A	4	GENIC	homozygous	115703746
12	30303466	30303467	A	G	28	GENIC	homozygous	115562179
12	30303489	30303490	T	G	24	GENIC	homozygous	115562181
12	30303551	30303552	G	A	24	GENIC	homozygous	115562183
12	30303695	30303696	C	T	21	GENIC	homozygous	115562185
12	30301628	30301629	G	A	18	GENIC	homozygous	115582437