chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 38095835 38095836 A C 47 GENIC possibly homozygous 795373312 12 38096899 38096900 T G 41 GENIC heterozygous 795373313 12 38096954 38096955 G C 44 GENIC possibly homozygous 795373314 12 38100973 38100974 G C 35 GENIC homozygous 795373315 12 38101113 38101114 G A 29 GENIC homozygous 795373316 12 38101123 38101124 G T 25 GENIC homozygous 795373317 12 38103175 38103176 A C 34 GENIC homozygous 795373318 12 38103344 38103345 A C 37 GENIC homozygous 795373319 12 38104417 38104418 A T 46 GENIC homozygous 795373320 12 38104891 38104892 G C 45 GENIC homozygous 795373321 12 38106139 38106140 C T 48 GENIC homozygous 795373322 12 38106408 38106409 G A 39 GENIC homozygous 795373323 12 38106726 38106727 A G 45 GENIC possibly homozygous 795373324 12 38110578 38110579 A G 34 GENIC homozygous 795373325 12 38110996 38110997 G A 40 GENIC homozygous 795373326 12 38113923 38113924 G C 37 GENIC homozygous 795373327 12 38113945 38113946 T C 25 GENIC homozygous 795373328 12 38113977 38113978 G A 12 GENIC homozygous 795373329 12 38114516 38114517 A T 43 GENIC homozygous 795373330 12 38116443 38116444 C T 56 GENIC homozygous 795373331