chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5054470	5054471	A	G	30	GENIC	homozygous	109296742
20	5054562	5054563	G	C	38	GENIC	homozygous	109296744
20	5055733	5055734	T	C	33	GENIC	homozygous	109076231
20	5056402	5056403	G	A	27	GENIC	homozygous	124626747
20	5056517	5056518	A	G	41	GENIC	homozygous	109296746
20	5056545	5056546	G	C	38	GENIC	homozygous	109076233
20	5056547	5056548	T	C	39	GENIC	homozygous	109076235
20	5056638	5056639	T	C	18	GENIC	homozygous	109076237
20	5056643	5056644	T	C	18	GENIC	homozygous	109076239
20	5056387	5056387		TC	19	GENIC	homozygous	129653040
20	5056398	5056398		CTTTG	21	GENIC	homozygous	129653041
20	5056402	5056402		TCACAACTTCAC	22	GENIC	homozygous	129653042
20	5056493	5056495	AG		41	GENIC	homozygous	129653043