chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	199665328	199665329	A	G	14	GENIC	homozygous	108501364
1	199665459	199665460	T	G	12	GENIC	homozygous	108501366
1	199665825	199665826	A	G	17	GENIC	homozygous	108501368
1	199666088	199666089	T	C	31	GENIC	homozygous	108501370
1	199666108	199666109	G	C	29	GENIC	homozygous	108501372
1	199666142	199666143	T	C	21	GENIC	homozygous	120475414
1	199666291	199666292	G	A	17	GENIC	homozygous	108501374
1	199666306	199666307	T	C	19	GENIC	homozygous	108501376
1	199666982	199666983	A	G	22	GENIC	homozygous	108501378
1	199667996	199667997	C	T	24	GENIC	homozygous	108501384
1	199668073	199668074	G	A	18	GENIC	homozygous	108501386
1	199668416	199668417	C	T	27	GENIC	homozygous	108501388
1	199668765	199668766	C	T	30	GENIC	homozygous	108501390
1	199668932	199668933	A	G	28	GENIC	homozygous	108501392
1	199669089	199669090	T	C	16	GENIC	homozygous	108501394
1	199669161	199669162	C	A	7	GENIC	homozygous	108501396
1	199669413	199669414	T	C	10	GENIC	homozygous	108501398
1	199670235	199670236	T	C	11	GENIC	homozygous	108501400
1	199670416	199670417	C	T	7	GENIC	homozygous	108501402
1	199670665	199670666	A	T	25	GENIC	homozygous	108501404
1	199670930	199670931	C	G	27	GENIC	homozygous	108501406