chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	100990278	100990279	C	T	40	GENIC	homozygous	114437747
13	100991019	100991020	A	G	28	GENIC	homozygous	114437749
13	100991268	100991269	C	A	4	GENIC	homozygous	114437751
13	100992297	100992298	G	A	76	GENIC	heterozygous	118529484
13	100992375	100992376	G	T	110	GENIC	heterozygous	118570173
13	100992376	100992377	C	T	112	GENIC	heterozygous	118600728
13	100992401	100992402	A	G	85	GENIC	heterozygous	118467476
13	100992402	100992403	T	C	92	GENIC	heterozygous	118467477
13	100993926	100993927	C	A	67	GENIC	heterozygous	118467478
13	100994233	100994234	G	A	57	GENIC	heterozygous	118506013
13	100994546	100994547	A	G	27	GENIC	heterozygous	118467479
13	100994575	100994576	A	C	12	GENIC	homozygous	118467480
13	100994651	100994652	A	T	4	GENIC	homozygous	118529486
13	100994653	100994654	A	C	4	GENIC	homozygous	118529487
13	100994693	100994694	A	T	6	GENIC	homozygous	118467481
13	100995451	100995452	C	T	129	GENIC	heterozygous	118467482
13	100995497	100995498	G	A	128	GENIC	heterozygous	118467483
13	100995531	100995532	G	C	90	GENIC	heterozygous	118467484
13	100995759	100995760	C	T	93	GENIC	heterozygous	118467485
13	100995763	100995764	A	G	84	GENIC	heterozygous	118467486
13	100995847	100995848	G	A	77	GENIC	heterozygous	118506018
13	101024473	101024474	G	A	47	GENIC	homozygous	114437759
13	101031462	101031463	A	C	25	GENIC	homozygous	118467487
13	101031631	101031632	G	C	41	GENIC	homozygous	114437761
13	101031634	101031635	A	T	41	GENIC	homozygous	114437763
13	101031924	101031925	G	A	25	GENIC	homozygous	114437765