chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 247502531 247502532 C T 31 GENIC homozygous 109017655 1 247503300 247503301 A C 41 GENIC homozygous 108775547 1 247503323 247503324 C T 36 GENIC homozygous 108775548 1 247503327 247503328 C T 35 GENIC homozygous 108775549 1 247505170 247505171 A C 53 GENIC homozygous 108602890 1 247505282 247505283 C T 54 GENIC homozygous 108602891 1 247505976 247505977 T A 37 GENIC homozygous 108602892 1 247508430 247508431 G T 46 GENIC homozygous 108602898 1 247508947 247508965 CAGTGGATTCCCGACACT 39 GENIC homozygous 127501463 1 247509726 247509727 A C 28 GENIC homozygous 109017657 1 247510104 247510105 C G 36 GENIC homozygous 108602899 1 247510190 247510191 C T 34 GENIC homozygous 109017658 1 247511468 247511469 A G 37 GENIC homozygous 108602902 1 247511571 247511572 A G 38 GENIC homozygous 108602903 1 247512289 247512290 T C 45 GENIC homozygous 108602904 1 247512314 247512314 T 41 GENIC homozygous 127501467 1 247513265 247513265 TTCCCTCCGTCCCTTGACCTGTTCTA 24 GENIC homozygous 131265587 1 247513612 247513613 C A 53 GENIC homozygous 109017659 1 247514372 247514373 G A 56 GENIC homozygous 109017660 1 247514378 247514379 G A 55 GENIC homozygous 108602907