chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	67754224	67754228	TGTC		37	GENIC	homozygous	133190877
8	67754451	67754452	A	C	50	GENIC	homozygous	117947317
8	67754990	67754991	G	A	50	GENIC	homozygous	117947318
8	67755268	67755272	CTTG		47	GENIC	homozygous	133190878
8	67755877	67755878	A	G	49	GENIC	homozygous	117947319
8	67757469	67757470	T	C	48	GENIC	homozygous	117947320
8	67757604	67757605	T	C	47	GENIC	homozygous	117947321
8	67759305	67759306	T	C	53	GENIC	homozygous	117947322
8	67759620	67759621	A	T	52	GENIC	homozygous	117947323
8	67759647	67759648	T	C	43	GENIC	homozygous	117947324
8	67761696	67761697	C	G	46	GENIC	homozygous	117947325
8	67762576	67762577	A	T	31	GENIC	homozygous	118027178
8	67764450	67764451	T	C	56	GENIC	homozygous	117947326
8	67762889	67762889		A	30	GENIC	homozygous	128600137
8	67761121	67761122	G	C	39	GENIC	homozygous	133414437
8	67762715	67762716	G	A	31	GENIC	homozygous	118099788
8	67762786	67762787	G	T	21	GENIC	homozygous	116520103