chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	102258697	102258698	C	T	30	GENIC	homozygous	114919497
6	102259393	102259394	T	C	29	GENIC	possibly homozygous	114919499
6	102260309	102260310	A	G	30	GENIC	possibly homozygous	114919500
6	102260465	102260466	C	T	16	GENIC	possibly homozygous	114919502
6	102262955	102262956	C	T	34	GENIC	possibly homozygous	114919503
6	102263090	102263091	C	T	36	GENIC	possibly homozygous	114919505
6	102265100	102265101	G	A	24	GENIC	homozygous	114919506
6	102265329	102265330	A	G	15	GENIC	homozygous	114919508
6	102265506	102265507	T	C	21	GENIC	homozygous	114919509
6	102267062	102267063	C	G	20	GENIC	possibly homozygous	114919514
6	102268007	102268008	C	T	27	GENIC	homozygous	114919516
6	102268798	102268799	T	C	23	GENIC	possibly homozygous	114919517
6	102269519	102269520	C	T	30	GENIC	homozygous	114919519
6	102269833	102269834	A	G	19	GENIC	homozygous	114919521
6	102271608	102271609	T	C	28	GENIC	homozygous	114919522
6	102271762	102271763	G	A	43	GENIC	homozygous	114919524
6	102272301	102272302	A	T	20	GENIC	homozygous	114919525
6	102272416	102272417	A	G	20	GENIC	homozygous	114919526