chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	10555621	10555622	T	C	30	GENIC	possibly homozygous	111933389
16	10556040	10556041	T	C	27	GENIC	homozygous	111933391
16	10556427	10556428	G	C	40	GENIC	homozygous	111723840
16	10556580	10556581	T	A	35	GENIC	homozygous	112319751
16	10556630	10556631	C	T	35	GENIC	heterozygous	112274697
16	10556812	10556813	A	G	18	GENIC	homozygous	111933393
16	10557957	10557958	G	A	42	GENIC	homozygous	111723844
16	10558844	10558845	A	G	28	GENIC	homozygous	111933395
16	10559105	10559106	G	A	45	GENIC	homozygous	111933397
16	10559271	10559272	T	G	31	GENIC	homozygous	111933399
16	10559318	10559319	T	C	29	GENIC	homozygous	111933401
16	10559605	10559606	A	G	11	GENIC	homozygous	111933403
16	10559693	10559694	T	G	21	GENIC	homozygous	111933405
16	10560336	10560337	C	T	41	GENIC	homozygous	111933407
16	10560831	10560832	G	C	34	GENIC	homozygous	111933409
16	10561273	10561274	T	C	46	GENIC	homozygous	111933411
16	10562398	10562399	C	T	27	GENIC	homozygous	111933413
16	10562489	10562490	T	C	35	GENIC	homozygous	111933415
16	10562524	10562525	G	T	35	GENIC	homozygous	111933417
16	10562697	10562698	C	T	44	GENIC	homozygous	111933419
16	10563412	10563413	G	A	40	GENIC	homozygous	111933421
16	10563418	10563419	T	C	41	GENIC	homozygous	111933423
16	10563451	10563452	T	C	37	GENIC	homozygous	111933425
16	10563466	10563467	G	A	39	GENIC	homozygous	111933427
16	10563526	10563527	A	G	47	GENIC	homozygous	111723848
16	10563766	10563767	A	T	29	GENIC	homozygous	111933429
16	10563982	10563983	T	C	40	GENIC	homozygous	111933431
16	10564142	10564143	C	T	42	GENIC	homozygous	111933433
16	10564256	10564257	T	C	20	GENIC	homozygous	111933435
16	10564560	10564561	C	T	24	GENIC	homozygous	111933437
16	10564639	10564640	T	C	48	GENIC	homozygous	111723850
16	10562468	10562469	T	C	30	GENIC	homozygous	112050623