chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	43048335	43048336	A	G	18	GENIC	homozygous	142366391
13	43050074	43050075	C	T	47	GENIC	homozygous	142366392
13	43050343	43050344	C	T	53	GENIC	homozygous	142366393
13	43052819	43052820	C	T	38	GENIC	homozygous	142366394
13	43054392	43054393	A	G	29	GENIC	homozygous	142366395
13	43054585	43054586	A	G	15	GENIC	homozygous	142366396
13	43055089	43055090	A		31	GENIC	homozygous	142343372
13	43055193	43055194	G	A	42	GENIC	homozygous	142366397
13	43055985	43055986	A	G	40	GENIC	homozygous	142366398
13	43056107	43056108	A	G	44	GENIC	homozygous	142366399
13	43056154	43056155	T	C	51	GENIC	homozygous	142366400
13	43056280	43056281	C	G	41	GENIC	homozygous	142366401
13	43056288	43056289	G	A	40	GENIC	homozygous	142366402
13	43056312	43056313	A	C	38	GENIC	homozygous	142366403
13	43056331	43056332	A	C	40	GENIC	homozygous	142366404
13	43056414	43056415	T	A	34	GENIC	homozygous	142366405
13	43056898	43056899	T	C	40	GENIC	homozygous	142366406
13	43056648	43056649	C	T	45	GENIC	homozygous	144929824
13	43057069	43057070	C	T	39	GENIC	homozygous	142366407
13	43054527	43054528	G	A	27	GENIC	homozygous	144929823