chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10575336	10575337	G	A	54	GENIC	homozygous	134899251
19	10575578	10575579	C	T	56	GENIC	homozygous	134899252
19	10575630	10575631	T	C	48	GENIC	homozygous	134899253
19	10575633	10575634	C	T	49	GENIC	homozygous	134899254
19	10575650	10575651	T	C	49	GENIC	homozygous	134899255
19	10575698	10575699	G	T	45	GENIC	homozygous	134899256
19	10575714	10575715	T	C	44	GENIC	homozygous	134899257
19	10576058	10576059	C	T	42	GENIC	homozygous	134899258
19	10576271	10576272	C	A	50	GENIC	possibly homozygous	134899259
19	10576331	10576332	G	A	48	GENIC	possibly homozygous	134899260
19	10576424	10576425	T	C	43	GENIC	homozygous	110076256
19	10576534	10576535	T	C	42	GENIC	homozygous	134899261
19	10577358	10577359	T	G	49	GENIC	homozygous	110130850
19	10577399	10577400	G	C	40	GENIC	homozygous	134899262
19	10577456	10577457	C	G	40	GENIC	homozygous	134899263
19	10578337	10578337		C	49	GENIC	homozygous	134895590
19	10576529	10576531	AA		44	GENIC	homozygous	134895588
19	10576533	10576533		CCC	44	GENIC	homozygous	134895589
19	10577291	10577292	T	C	50	GENIC	homozygous	109634266
19	10577388	10577389	A	G	43	GENIC	homozygous	109993853
19	10578422	10578423	C	T	46	GENIC	homozygous	134899264
19	10578495	10578496	G	C	52	GENIC	homozygous	109634272
19	10578553	10578554	T	A	48	GENIC	homozygous	109634274
19	10579051	10579052	T	C	47	GENIC	homozygous	134899265
19	10579285	10579286	T	C	56	GENIC	homozygous	109634278
19	10579352	10579353	G	A	36	GENIC	homozygous	134899266
19	10580734	10580734		GC	12	GENIC	heterozygous	134895591
19	10581140	10581144	ACAG		37	GENIC	homozygous	134895592
19	10579097	10579098	A		29	GENIC	homozygous	129583623
19	10580738	10580739	T	G	13	GENIC	heterozygous	109956576