chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	38433174	38433175	A	G	8	GENIC	possibly homozygous	46117258
19	38433282	38433283	G	-	7	GENIC	homozygous	46117259
19	38433294	38433295	A	G	8	GENIC	homozygous	46117260
19	38433385	38433386	T	A	1	GENIC	homozygous	46117261
19	38435137	38435138	T	TA	4	GENIC	homozygous	46117262
19	38435656	38435657	C	T	12	GENIC	homozygous	46117263
19	38436135	38436136	A	AAC	4	GENIC	heterozygous	46380191
19	38436271	38436272	G	A	15	GENIC	possibly homozygous	46117264
19	38438554	38438555	G	C	10	GENIC	possibly homozygous	46117265
19	38438555	38438556	T	C	9	GENIC	possibly homozygous	46117266
19	38439655	38439656	C	T	16	GENIC	homozygous	46117269
19	38443782	38443783	A	T	12	GENIC	homozygous	46117275
19	38444423	38444429	TGCTGC	------	4	GENIC	homozygous	46117276
19	38447995	38447996	A	G	5	GENIC	heterozygous	46117277
19	38451401	38451402	T	C	10	GENIC	heterozygous	46117282
19	38456965	38456966	T	TTA	3	GENIC	heterozygous	46117287
19	38459508	38459509	T	C	20	GENIC	homozygous	46117288
19	38459848	38459857	GTTTCCCCG	---------	5	GENIC	heterozygous	46117289
19	38460344	38460345	A	-	1	GENIC	homozygous	46117291
19	38460851	38460852	A	T	14	GENIC	homozygous	46117292
19	38461810	38461811	A	G	2	GENIC	homozygous	46380193