chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90809917	90809918	T	A	15	GENIC	homozygous	126104378
13	90810722	90810723	C	T	16	GENIC	homozygous	126104380
13	90811628	90811629	T	C	14	GENIC	homozygous	126104382
13	90814815	90814816	T	C	16	GENIC	homozygous	126104384
13	90815762	90815763	G	A	14	GENIC	homozygous	126104386
13	90816548	90816549	T	C	12	GENIC	homozygous	126104388
13	90819678	90819679	G	A	24	GENIC	homozygous	126104390
13	90821270	90821271	C	T	10	GENIC	homozygous	126104392
13	90824672	90824673	C	T	9	GENIC	homozygous	126104394
13	90825255	90825256	A	T	13	GENIC	homozygous	126104396
13	90825271	90825272	T	C	13	GENIC	homozygous	126104398
13	90825564	90825565	G	A	6	GENIC	homozygous	126104400
13	90825885	90825886	C	T	9	GENIC	homozygous	126104402
13	90826023	90826024	A	G	15	GENIC	homozygous	126104404
13	90826657	90826658	T	C	17	GENIC	homozygous	126104406
13	90829064	90829065	T	C	10	GENIC	homozygous	126104408
13	90831431	90831432	C	G	22	GENIC	homozygous	126070687