chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 37609275 37609276 G C 2 GENIC homozygous 112807899 15 37609301 37609302 A 1 GENIC homozygous 129246358 15 37636462 37636464 CG 12 GENIC homozygous 129246361 15 37636475 37636475 G 11 GENIC homozygous 129246362 15 37636480 37636480 GGGGA 11 GENIC homozygous 129246363 15 37636486 37636487 A 10 GENIC possibly homozygous 129246364 15 37636498 37636499 A 10 GENIC homozygous 129246365 15 37636500 37636501 G A 10 GENIC homozygous 124064695 15 37636517 37636518 A 10 GENIC homozygous 129246366 15 37636521 37636521 G 10 GENIC homozygous 129246367 15 37639578 37639578 TGGG 6 GENIC homozygous 129246368 15 37639580 37639580 TTT 6 GENIC homozygous 129246369 15 37639581 37639581 GCTCAGTGGT 6 GENIC homozygous 129246370 15 37639584 37639585 A C 7 GENIC homozygous 124064702 15 37639584 37639584 GCG 6 GENIC homozygous 129246371 15 37639589 37639589 CTAGCAAGCA 7 GENIC homozygous 129246372 15 37644184 37644186 TG 17 GENIC heterozygous 129246373 15 37644214 37644216 AG 13 GENIC heterozygous 129246374 15 37661648 37661650 AC 28 GENIC heterozygous 130149005