chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	30284233	30284234	T	G	23	GENIC	homozygous	56792301
5	30284704	30284705	A	ACTGGG	28	GENIC	homozygous	55270009
5	30286711	30286712	G	A	28	GENIC	homozygous	55270012
5	30286913	30286914	A	C	23	GENIC	homozygous	55270015
5	30286984	30286985	T	C	27	GENIC	homozygous	55270018
5	30287351	30287353	AA	--	24	GENIC	homozygous	55270021
5	30287434	30287435	C	A	26	GENIC	homozygous	55270024
5	30288510	30288511	T	TC	16	GENIC	homozygous	55270027
5	30288868	30288870	TT	--	22	GENIC	homozygous	55270030
5	30289074	30289075	A	C	27	GENIC	homozygous	55270033
5	30289260	30289261	C	CT	16	GENIC	homozygous	55270036
5	30289311	30289312	C	G	21	GENIC	homozygous	55270039
5	30289708	30289709	C	T	13	GENIC	homozygous	55270042
5	30289846	30289847	C	T	17	GENIC	homozygous	55270045
5	30289927	30289928	T	C	14	GENIC	homozygous	55270048
5	30290047	30290048	G	GGACAGCAGCAGC	9	GENIC	homozygous	55270051
5	30290282	30290283	A	T	11	GENIC	homozygous	55270054
5	30290483	30290484	C	CTG	8	GENIC	homozygous	55270057
5	30290576	30290577	C	A	8	GENIC	homozygous	55270060
5	30290593	30290594	T	C	8	GENIC	homozygous	55270063
5	30290624	30290625	G	A	7	GENIC	homozygous	55270066
5	30290664	30290665	G	A	10	GENIC	homozygous	55270068