chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 129652598 129652599 T C 24 GENIC homozygous 582007465 3 129652599 129652600 G A 24 GENIC homozygous 582007466 3 129653298 129653299 G A 14 GENIC homozygous 582007467 3 129653987 129653988 C T 31 GENIC homozygous 582007468 3 129654504 129654505 T TGTATGTTTCTC 44 GENIC homozygous 719283938 3 129654838 129654839 G A 47 GENIC homozygous 582007469 3 129656308 129656325 CAGGTCCCCCGGAAAGG ----------------- 41 GENIC homozygous 719283939 3 129656985 129656986 G A 35 GENIC homozygous 584084080 3 129657111 129657112 C T 47 GENIC homozygous 584084081 3 129657568 129657569 G GA 18 GENIC heterozygous 719283940 3 129658097 129658098 A AT 21 GENIC homozygous 719283942 3 129658262 129658263 C CTT 18 GENIC heterozygous 719283944 3 129659438 129659439 C T 35 GENIC homozygous 582007470 3 129659588 129659589 G C 25 GENIC homozygous 584084082 3 129660226 129660227 T - 26 GENIC homozygous 719283945 3 129661042 129661043 C T 45 GENIC homozygous 584084083 3 129663140 129663141 G A 22 GENIC homozygous 584084084 3 129664167 129664168 G GA 35 GENIC possibly homozygous 719283946 3 129665319 129665320 A AT 13 GENIC heterozygous 719283947 3 129665363 129665364 T TGTGCTTGCTAGGCAA 3 GENIC homozygous 719283948 3 129665366 129665367 G GCTCT 4 GENIC homozygous 719283949 3 129665367 129665368 A AC 4 GENIC homozygous 719283950 3 129665369 129665370 A ACTGAGC 4 GENIC homozygous 719283951 3 129665374 129665375 T TCCC 4 GENIC homozygous 719283952 3 129665568 129665569 C G 33 GENIC homozygous 582007471 3 129666506 129666507 A T 21 GENIC homozygous 584084085 3 129667397 129667407 TTTTTTTTTT ---------- 7 GENIC heterozygous 719283953 3 129668229 129668230 C T 27 GENIC homozygous 582007472 3 129668628 129668629 A - 32 GENIC homozygous 719283954 3 129668632 129668633 A C 32 GENIC homozygous 584084086 3 129669216 129669217 G A 41 GENIC homozygous 582007473 3 129669784 129669785 C T 37 GENIC homozygous 582007474