chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 15134157 15134158 T TAA 1 GENIC homozygous 50070990 12 15134298 15134299 T TC 7 GENIC homozygous 50070992 12 15134791 15134792 A G 18 GENIC homozygous 50070994 12 15135448 15135449 G T 13 GENIC homozygous 50070996 12 15135506 15135507 T - 1 GENIC homozygous 50070998 12 15135661 15135662 G A 14 GENIC homozygous 50071000 12 15135904 15135905 T A 20 GENIC possibly homozygous 50071002 12 15139456 15139458 TT -- 2 GENIC homozygous 50071006 12 15139849 15139850 G A 9 GENIC possibly homozygous 50071010 12 15140786 15140787 T TC 12 GENIC heterozygous 50071012 12 15141359 15141360 G C 21 GENIC homozygous 50071014 12 15142799 15142800 T C 9 GENIC homozygous 50071016 12 15145622 15145623 T C 22 GENIC homozygous 50071018 12 15146149 15146150 T TGCTCA 2 GENIC heterozygous 50071020 12 15146825 15146826 C T 27 GENIC homozygous 50071022 12 15146993 15146994 A T 1 GENIC homozygous 50071024 12 15147430 15147431 G A 23 GENIC possibly homozygous 50071026 12 15148244 15148245 C CATGTATGTATGTATGT 1 GENIC homozygous 50533477 12 15148443 15148444 G GT 14 GENIC heterozygous 50071030 12 15148497 15148498 C T 20 GENIC homozygous 50071032 12 15148714 15148715 T G 23 GENIC homozygous 50071034 12 15148856 15148857 C G 18 GENIC homozygous 50071036 12 15149407 15149408 A ACTGGAACTCAAAGTTTACC 3 GENIC homozygous 50071038 12 15150331 15150332 C T 14 GENIC homozygous 50071040 12 15150789 15150790 C T 22 GENIC possibly homozygous 50071042 12 15152360 15152361 C T 25 GENIC homozygous 50071044 12 15152465 15152466 G A 19 GENIC homozygous 50071046