chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	80783272	80783273	G	C	23	GENIC	homozygous	109875590
2	80783493	80783494	T	C	18	GENIC	homozygous	109875592
2	80783911	80783912	G	A	12	GENIC	homozygous	109875594
2	80784098	80784099	C	T	18	GENIC	homozygous	109875596
2	80785268	80785269	C	T	17	GENIC	homozygous	109875598
2	80785401	80785402	A	C	22	GENIC	homozygous	109875600
2	80785503	80785504	T	G	22	GENIC	homozygous	109875602
2	80786034	80786035	C	T	17	GENIC	heterozygous	109875604
2	80786797	80786798	C	T	15	GENIC	homozygous	109875606
2	80786802	80786803	T	C	17	GENIC	homozygous	109875608
2	80787784	80787785	T	C	22	GENIC	homozygous	109875610
2	80787989	80787990	G	C	21	GENIC	homozygous	109875612
2	80788288	80788289	T	C	7	GENIC	homozygous	109875614
2	80788311	80788312	T	C	13	GENIC	homozygous	109875616
2	80788386	80788387	T	C	11	GENIC	homozygous	125574037
2	80788387	80788388	G	T	11	GENIC	homozygous	125574038
2	80788390	80788391	T	G	11	GENIC	homozygous	125574039
2	80788420	80788421	A	T	24	GENIC	homozygous	109875618
2	80790270	80790271	T	A	15	GENIC	homozygous	109875620
2	80791660	80791661	C	T	20	GENIC	homozygous	109875622
2	80792239	80792240	T	G	17	GENIC	homozygous	109875624