chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 65376727 65376728 G A 22 GENIC homozygous 796710318 X 65385795 65385796 C T 94 GENIC heterozygous 796710319 X 65386324 65386325 G A 42 GENIC heterozygous 796710320 X 65386390 65386391 G A 92 GENIC heterozygous 796710321 X 65386394 65386395 G T 99 GENIC heterozygous 796710322 X 65386419 65386420 T G 107 GENIC heterozygous 796710323 X 65387998 65387999 T G 18 GENIC possibly homozygous 796710324 X 65388009 65388010 T G 15 GENIC homozygous 796710325 X 65388034 65388035 C A 8 GENIC homozygous 796710326 X 65390812 65390813 A G 108 GENIC heterozygous 796710327 X 65390836 65390837 A T 146 GENIC heterozygous 796710328 X 65393956 65393957 G A 44 GENIC homozygous 796710329 X 65394268 65394269 T A 31 GENIC possibly homozygous 796710330 X 65394962 65394963 G A 63 GENIC heterozygous 796710331 X 65395038 65395039 A G 48 GENIC heterozygous 796710332 X 65395065 65395066 C T 50 GENIC heterozygous 796710333 X 65395490 65395491 C T 70 GENIC heterozygous 796710334 X 65395570 65395571 G T 81 GENIC heterozygous 796710335 X 65395612 65395613 G A 104 GENIC heterozygous 796710336 X 65395623 65395624 T G 102 GENIC heterozygous 796710337 X 65395626 65395627 A G 103 GENIC heterozygous 796710338