chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5055134	5055135	G	T	33	GENIC	homozygous	109076229
20	5055733	5055734	T	C	46	GENIC	homozygous	109076231
20	5056387	5056387		TC	17	GENIC	homozygous	129653040
20	5056398	5056398		CTTTG	22	GENIC	homozygous	129653041
20	5056402	5056403	G	A	27	GENIC	homozygous	124626747
20	5056402	5056402		TCACAACTTCAC	22	GENIC	homozygous	129653042
20	5056493	5056495	AG		46	GENIC	homozygous	129653043
20	5056517	5056518	A	G	51	GENIC	homozygous	109296746
20	5056545	5056546	G	C	50	GENIC	homozygous	109076233
20	5056547	5056548	T	C	49	GENIC	homozygous	109076235
20	5056638	5056639	T	C	28	GENIC	homozygous	109076237
20	5056643	5056644	T	C	27	GENIC	homozygous	109076239