chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 89726258 89726259 G A 27 GENIC homozygous 994894977 13 89727289 89727290 C T 23 GENIC homozygous 994894978 13 89728199 89728200 A G 31 GENIC possibly homozygous 994894979 13 89728283 89728284 G A 36 GENIC possibly homozygous 994894980 13 89728524 89728525 A G 28 GENIC homozygous 994894981 13 89729103 89729104 G A 26 GENIC homozygous 994894982 13 89730067 89730068 G A 26 GENIC possibly homozygous 994894983 13 89732436 89732437 G C 18 GENIC heterozygous 994894984 13 89735314 89735315 T C 21 GENIC possibly homozygous 994894985 13 89736067 89736068 G C 28 GENIC possibly homozygous 994894986 13 89738441 89738442 C G 21 GENIC homozygous 994894987 13 89740874 89740875 T C 27 GENIC homozygous 994894988 13 89740981 89740982 T G 27 GENIC homozygous 994894989 13 89741383 89741384 C G 25 GENIC homozygous 994894990 13 89742437 89742438 C T 25 GENIC homozygous 994894991 13 89743353 89743354 C T 21 GENIC homozygous 994894992