chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	80783493	80783494	T	C	13	GENIC	homozygous	109875592
2	80783937	80783938	C	T	23	GENIC	homozygous	110714117
2	80784212	80784213	C	A	12	GENIC	homozygous	110714118
2	80785190	80785191	T	C	10	GENIC	homozygous	110714119
2	80785401	80785402	A	C	16	GENIC	homozygous	109875600
2	80785523	80785524	A	G	20	GENIC	homozygous	110714120
2	80786231	80786232	T	C	20	GENIC	homozygous	110714121
2	80786802	80786803	T	C	25	GENIC	possibly homozygous	109875608
2	80786936	80786937	C	A	23	GENIC	homozygous	110714123
2	80787347	80787348	A	C	16	GENIC	homozygous	120465983
2	80787784	80787785	T	C	19	GENIC	homozygous	109875610
2	80787989	80787990	G	C	30	GENIC	homozygous	109875612
2	80788288	80788289	T	C	14	GENIC	homozygous	109875614
2	80788311	80788312	T	C	12	GENIC	homozygous	109875616
2	80788420	80788421	A	T	22	GENIC	homozygous	109875618
2	80788627	80788628	G	A	18	GENIC	homozygous	110714124
2	80789060	80789061	T	C	15	GENIC	homozygous	110714125
2	80789095	80789096	T	C	17	GENIC	homozygous	110714126
2	80789424	80789425	C	T	25	GENIC	homozygous	110714127
2	80789458	80789459	C	G	22	GENIC	homozygous	110714128
2	80789650	80789651	C	A	15	GENIC	homozygous	110714129
2	80790124	80790125	G	A	19	GENIC	homozygous	110714130
2	80791923	80791924	C	T	17	GENIC	homozygous	110714131
2	80792239	80792240	T	G	7	GENIC	homozygous	109875624
2	80792383	80792384	C	T	16	GENIC	homozygous	110714132
2	80788386	80788387	T	C	11	GENIC	heterozygous	125574037
2	80788387	80788388	G	T	10	GENIC	heterozygous	125574038
2	80788390	80788391	T	G	13	GENIC	homozygous	125574039