chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	30015890	30015891	C	T	55	GENIC	homozygous	110319239
18	30080808	30080809	A	G	51	GENIC	heterozygous	130711989
18	30080804	30080805	T	A	46	GENIC	heterozygous	130711988
18	30081054	30081055	G	A	21	GENIC	heterozygous	124457194
18	30081156	30081157	G	A	61	GENIC	heterozygous	129570026
18	30081218	30081219	T	A	81	GENIC	heterozygous	129570030
18	30081221	30081222	G	T	83	GENIC	heterozygous	129570031
18	30081329	30081330	C	T	41	GENIC	heterozygous	124519179
18	30081024	30081025	G	C	27	GENIC	heterozygous	130798225
18	30081531	30081532	A	T	48	GENIC	heterozygous	130475683
18	30081539	30081540	T	C	50	GENIC	heterozygous	130475684
18	30081576	30081577	A	T	49	GENIC	heterozygous	130475685
18	30098978	30098979	T	A	28	GENIC	heterozygous	124457211
18	30098980	30098981	G	C	28	GENIC	heterozygous	124457212
18	30099022	30099023	C	T	29	GENIC	heterozygous	119571970
18	30140211	30140212	T	C	36	GENIC	homozygous	110319712
18	30167075	30167076	T	G	32	GENIC	heterozygous	131211701
18	30167102	30167103	C	T	37	GENIC	heterozygous	131211702
18	30167896	30167897	T	G	13	GENIC	heterozygous	131760734
18	30167926	30167927	G	A	12	GENIC	heterozygous	131211703
18	30168833	30168845	TGCTCTTTTTAT		48	GENIC	homozygous	134462340