chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 15134157 15134158 T TAA 17 GENIC heterozygous 752660475 12 15134158 15134159 A - 17 GENIC possibly homozygous 752660474 12 15134299 15134300 C - 26 GENIC homozygous 752660477 12 15134526 15134532 TTAACC ------ 13 GENIC heterozygous 752660479 12 15134791 15134792 A G 23 GENIC homozygous 642585127 12 15135661 15135662 G A 17 GENIC homozygous 642585128 12 15137596 15137597 A AACACACACACAC 1 GENIC homozygous 752660482 12 15138318 15138319 C CCTGTCTGT 16 GENIC homozygous 752660483 12 15138416 15138417 C CGTGTGTGT 3 GENIC homozygous 752660487 12 15139455 15139456 G GT 5 GENIC heterozygous 752660490 12 15139635 15139636 A G 20 GENIC homozygous 642585129 12 15140786 15140787 T TC 26 GENIC possibly homozygous 752660491 12 15141700 15141701 G A 25 GENIC possibly homozygous 642585130 12 15141767 15141768 C T 20 GENIC homozygous 642585131 12 15144902 15144903 G A 23 GENIC homozygous 642585132 12 15145622 15145623 T C 22 GENIC homozygous 642585133 12 15146825 15146826 C T 20 GENIC homozygous 642585134 12 15146993 15146994 A T 22 GENIC possibly homozygous 642585135 12 15147430 15147431 G A 36 GENIC homozygous 642585136 12 15148244 15148245 C CATGT 20 GENIC heterozygous 752660492 12 15148244 15148245 C CATGTATGTATGTATGT 20 GENIC possibly homozygous 752660493 12 15148415 15148416 T TGGTGTG 24 GENIC homozygous 752660494 12 15148443 15148444 G GT 29 GENIC homozygous 752660495 12 15148497 15148498 C T 24 GENIC homozygous 642585137 12 15148886 15148887 A G 30 GENIC homozygous 642585138 12 15149291 15149292 C T 30 GENIC homozygous 642585139 12 15149407 15149408 A ACTGGAACTCAAAGTTTACC 37 GENIC homozygous 752660496 12 15149910 15149911 G C 23 GENIC homozygous 642585140 12 15150331 15150332 C T 16 GENIC homozygous 642585141 12 15150501 15150502 T A 25 GENIC homozygous 642585142 12 15152360 15152361 C T 22 GENIC homozygous 642585143