chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	30567152	30567153	T	G	42	GENIC	homozygous	115808743
11	30567180	30567181	T	G	39	GENIC	homozygous	115808745
11	30580466	30580467	C	G	18	GENIC	homozygous	115808755
11	30580470	30580471	C	A	18	GENIC	homozygous	116035200
11	30580481	30580482	C	A	13	GENIC	homozygous	116222183
11	30588710	30588711	T	C	79	GENIC	heterozygous	118228233
11	30610783	30610784	C	A	25	GENIC	homozygous	115808787
11	30656103	30656104	G	A	28	GENIC	homozygous	116351356
11	30656619	30656620	A	G	41	GENIC	homozygous	115959813
11	30656830	30656831	T	C	20	GENIC	homozygous	115808909
11	30656893	30656894	G	A	27	GENIC	homozygous	115808913
11	30656926	30656927	A	G	27	GENIC	homozygous	115808915
11	30656965	30656966	G	C	26	GENIC	homozygous	115959815
11	30657084	30657085	G	A	30	GENIC	homozygous	115808917
11	30657314	30657315	C	G	9	GENIC	homozygous	118141243
11	30657392	30657393	C	G	11	GENIC	homozygous	118141244
11	30657565	30657566	T	C	8	GENIC	homozygous	118141246
11	30657974	30657975	G	A	39	GENIC	homozygous	118141247
11	30658089	30658090	A	C	53	GENIC	homozygous	115808919
11	30658155	30658156	A	G	41	GENIC	homozygous	115808923
11	30659389	30659390	T	G	35	GENIC	heterozygous	118228234
11	30662530	30662531	T	C	34	GENIC	homozygous	115808965
11	30658108	30658109	G	A	48	GENIC	homozygous	116379223
11	30660025	30660026	C	G	31	GENIC	homozygous	116379224