chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	60258148	60258149	A	G	71	GENIC	homozygous	113474460
14	60259642	60259643	T	C	69	GENIC	homozygous	113474462
14	60259674	60259675	C	T	66	GENIC	homozygous	113474464
14	60260327	60260328	T	C	42	GENIC	homozygous	113474466
14	60261658	60261659	G	A	54	GENIC	homozygous	113474468
14	60261801	60261802	G	A	56	GENIC	homozygous	113474470
14	60266992	60266993	C	T	52	GENIC	homozygous	113474472
14	60268920	60268921	A	G	59	GENIC	homozygous	113474474
14	60270155	60270156	A	C	36	GENIC	heterozygous	118759515
14	60270282	60270283	A	C	71	GENIC	heterozygous	118699582
14	60270171	60270172	C	A	50	GENIC	heterozygous	118699579
14	60270198	60270199	C	A	71	GENIC	heterozygous	118699580
14	60270202	60270203	A	C	77	GENIC	heterozygous	118699581
14	60270298	60270299	G	C	34	GENIC	homozygous	118699583
14	60270576	60270577	G	A	66	GENIC	homozygous	113474476
14	60271353	60271354	T	C	45	GENIC	homozygous	113474478
14	60272491	60272492	G	A	48	GENIC	homozygous	113474480
14	60274034	60274035	T	C	51	GENIC	possibly homozygous	113474482
14	60270313	60270314	A	G	34	GENIC	possibly homozygous	113677757