chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	44439003	44439004	G	A	39	GENIC	possibly homozygous	118449737
13	44439054	44439055	G	A	40	GENIC	homozygous	114755325
13	44439349	44439350	A	G	81	GENIC	heterozygous	118591530
13	44439377	44439378	A	G	79	GENIC	heterozygous	118449739
13	44439412	44439413	T	A	91	GENIC	heterozygous	118449740
13	44439442	44439443	A	T	76	GENIC	heterozygous	118449741
13	44439448	44439449	G	A	76	GENIC	heterozygous	118449742
13	44439451	44439452	T	G	71	GENIC	heterozygous	118449743
13	44439456	44439457	G	C	78	GENIC	heterozygous	118449744
13	44439469	44439470	G	T	99	GENIC	heterozygous	118449745
13	44439472	44439473	G	A	106	GENIC	heterozygous	118449746
13	44439523	44439524	T	A	103	GENIC	heterozygous	118591531
13	44439529	44439530	C	A	100	GENIC	heterozygous	118496828
13	44440258	44440259	A	G	49	GENIC	heterozygous	118580186
13	44441319	44441320	T	G	3	GENIC	homozygous	118449748
13	44441560	44441561	G	T	21	GENIC	possibly homozygous	118449749
13	44441582	44441583	G	A	20	GENIC	heterozygous	118449750
13	44441593	44441594	A	C	18	GENIC	homozygous	114546700
13	44445310	44445311	C	T	36	GENIC	heterozygous	118449751
13	44445314	44445315	C	T	33	GENIC	heterozygous	118496833
13	44445318	44445319	C	T	32	GENIC	heterozygous	118591532
13	44453349	44453350	A	G	13	GENIC	homozygous	114755327
13	44454097	44454098	A	G	39	GENIC	homozygous	114334685
13	44454163	44454164	A	C	13	GENIC	homozygous	114755329