chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 53595888 53595889 T C 32 GENIC homozygous 116887332 10 53596200 53596201 T C 33 GENIC homozygous 116887334 10 53597930 53597931 T C 11 GENIC homozygous 116887336 10 53600029 53600030 T C 23 GENIC homozygous 116887338 10 53600073 53600074 A G 23 GENIC homozygous 116887340 10 53600376 53600377 G C 30 GENIC homozygous 116887342 10 53601096 53601097 C T 13 GENIC homozygous 116887344 10 53601524 53601525 T C 18 GENIC homozygous 116887346 10 53602896 53602897 T C 20 GENIC homozygous 116887348 10 53603902 53603903 A G 18 GENIC homozygous 116887350 10 53604160 53604161 A G 24 GENIC homozygous 116887352 10 53604349 53604350 A G 34 GENIC homozygous 116887354 10 53604896 53604897 G A 28 GENIC homozygous 116887356 10 53605006 53605007 C A 23 GENIC homozygous 116887358 10 53605117 53605118 T C 15 GENIC homozygous 116887360 10 53605274 53605275 T C 21 GENIC homozygous 116887362 10 53605952 53605953 A G 31 GENIC homozygous 116887364 10 53606461 53606462 A G 22 GENIC homozygous 116887366 10 53606719 53606720 C T 26 GENIC homozygous 116887368 10 53607446 53607447 A G 27 GENIC homozygous 116887370 10 53608437 53608438 A G 26 GENIC homozygous 116887372 10 53608104 53608105 C G 26 GENIC homozygous 116933687