chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	43510124	43510125	T	G	30	GENIC	homozygous	109707604
19	43510235	43510236	T	C	25	GENIC	homozygous	109707606
19	43510555	43510556	T	C	39	GENIC	homozygous	109783790
19	43512113	43512114	C	T	23	GENIC	homozygous	109707608
19	43513048	43513049	C	T	28	GENIC	homozygous	109707610
19	43513780	43513781	T	G	38	GENIC	homozygous	109707614
19	43514599	43514600	T	C	27	GENIC	homozygous	109707616
19	43515329	43515330	G	C	19	GENIC	homozygous	109928586
19	43516737	43516738	C	T	21	GENIC	homozygous	109928588
19	43517275	43517276	G	A	23	GENIC	homozygous	109707622
19	43517622	43517623	A	G	34	GENIC	homozygous	109707624
19	43523158	43523159	G	C	24	GENIC	homozygous	109783816
19	43524206	43524207	G	A	25	GENIC	homozygous	109707650
19	43524292	43524293	C	T	24	GENIC	homozygous	109928590
19	43524531	43524532	A	G	13	GENIC	homozygous	109707652
19	43525387	43525388	A	C	22	GENIC	homozygous	109928592
19	43525563	43525564	G	A	20	GENIC	homozygous	109928594
19	43525943	43525944	C	T	40	GENIC	homozygous	109707654
19	43529651	43529652	T	C	23	GENIC	homozygous	109707666
19	43530550	43530551	T	C	35	GENIC	homozygous	109707672
19	43530744	43530745	A	G	19	GENIC	homozygous	109928596
19	43534555	43534556	C	T	23	GENIC	homozygous	109928598
19	43534792	43534793	G	T	13	GENIC	homozygous	109707676