chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	39621570	39621571	C	T	9	GENIC	homozygous	113758357
5	39623964	39623965	A	G	26	GENIC	homozygous	119152479
5	39627853	39627854	G	A	35	GENIC	homozygous	119152481
5	39628281	39628282	T	C	11	GENIC	homozygous	119152483
5	39630661	39630662	G	A	27	GENIC	homozygous	119152485
5	39633259	39633260	C	T	21	GENIC	homozygous	119152487
5	39633439	39633440	C	A	26	GENIC	homozygous	119152489
5	39633633	39633634	G	A	38	GENIC	homozygous	119152492
5	39634732	39634733	A	G	23	GENIC	homozygous	119152494
5	39635380	39635381	T	A	43	GENIC	homozygous	119152496
5	39635449	39635450	C	A	37	GENIC	homozygous	119152498
5	39636167	39636168	A	G	25	GENIC	homozygous	119152500
5	39636721	39636722	C	G	41	GENIC	homozygous	119152502
5	39639351	39639352	A	T	7	GENIC	homozygous	119152504
5	39639858	39639859	C	G	18	GENIC	homozygous	119152506
5	39646581	39646582	C	T	26	GENIC	homozygous	119152508
5	39646641	39646642	T	C	15	GENIC	homozygous	119152510
5	39646944	39646945	G	A	30	GENIC	homozygous	119152512
5	39649080	39649081	G	A	22	GENIC	homozygous	113758381
5	39650127	39650128	A	T	8	GENIC	homozygous	119152514
5	39650454	39650455	A	G	20	GENIC	homozygous	113758385
5	39650635	39650636	A	G	38	GENIC	homozygous	113758387
5	39650668	39650669	G	C	50	GENIC	homozygous	113758389