chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	42711201	42711202	C	-	19	GENIC	homozygous	49307377
14	42711204	42711205	C	CA	20	GENIC	homozygous	49307378
14	42711383	42711384	A	G	31	GENIC	homozygous	48685119
14	42711501	42711502	T	C	38	GENIC	homozygous	48685120
14	42712304	42712305	A	G	33	GENIC	homozygous	49178650
14	42712735	42712736	C	A	35	GENIC	homozygous	48685122
14	42712839	42712840	T	C	40	GENIC	homozygous	48685123
14	42713594	42713595	T	C	39	GENIC	homozygous	49178651
14	42713714	42713715	A	G	25	GENIC	homozygous	48685125
14	42713870	42713871	T	TA	18	GENIC	homozygous	49178652
14	42714470	42714471	A	G	25	GENIC	homozygous	48685127
14	42716112	42716115	GGG	---	31	GENIC	homozygous	49178653
14	42716157	42716158	C	T	30	GENIC	homozygous	49178654
14	42716180	42716181	T	C	38	GENIC	homozygous	48685131
14	42716826	42716827	A	-	12	GENIC	homozygous	49178655
14	42716882	42716883	C	A	24	GENIC	homozygous	49178656
14	42716947	42716948	G	A	34	GENIC	homozygous	49178657
14	42717412	42717413	T	C	33	GENIC	homozygous	48685133
14	42718587	42718588	T	A	39	GENIC	homozygous	49178658