chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	29330972	29330973	C	T	53	GENIC	homozygous	110318197
18	29331783	29331784	G	C	30	GENIC	homozygous	110318201
18	29332231	29332232	G	C	41	GENIC	homozygous	110318203
18	29332511	29332512	G	C	16	GENIC	homozygous	110456477
18	29333118	29333119	C	G	51	GENIC	homozygous	110318205
18	29333345	29333346	G	A	38	GENIC	homozygous	110318207
18	29333521	29333522	G	C	46	GENIC	homozygous	110318209
18	29334061	29334062	A	G	35	GENIC	homozygous	110318211
18	29335475	29335476	G	A	52	GENIC	homozygous	110318213
18	29336243	29336244	C	T	35	GENIC	homozygous	110456478
18	29336854	29336855	T	G	45	GENIC	homozygous	110318217
18	29336941	29336942	C	T	49	GENIC	homozygous	110456479
18	29338079	29338080	G	T	45	GENIC	homozygous	110318219
18	29339204	29339205	T	C	35	GENIC	homozygous	110318221
18	29339423	29339424	C	G	38	GENIC	possibly homozygous	110456480
18	29339608	29339609	T	A	30	GENIC	homozygous	110318223
18	29340182	29340183	G	A	53	GENIC	homozygous	110318225
18	29339848	29339849	G	A	43	GENIC	homozygous	110723551
18	29339423	29339423		G	33	GENIC	possibly homozygous	129527267
18	29334065	29334072	AACTTCC		36	GENIC	homozygous	129527264
18	29335745	29335745		G	45	GENIC	homozygous	129527265
18	29338294	29338295	C		42	GENIC	homozygous	129527266