chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 15133929 15133930 T TCCCC 8 GENIC heterozygous 727703094 12 15133931 15133932 A C 8 GENIC heterozygous 605297117 12 15134157 15134158 T TAAA 12 GENIC homozygous 727703097 12 15134298 15134299 T TC 16 GENIC possibly homozygous 727703099 12 15134514 15134515 T - 9 GENIC possibly homozygous 727703100 12 15134791 15134792 A G 19 GENIC homozygous 604262714 12 15135506 15135507 T - 19 GENIC homozygous 727703101 12 15135661 15135662 G A 14 GENIC homozygous 604262715 12 15136399 15136400 G A 29 GENIC homozygous 605297118 12 15137573 15137574 G GCT 6 GENIC homozygous 727703102 12 15137596 15137597 A AAC 3 GENIC heterozygous 727703103 12 15138115 15138119 TGTA ---- 1 GENIC homozygous 727703106 12 15138318 15138319 C CCTGTCTGT 10 GENIC homozygous 727703107 12 15138416 15138417 C CGTGTGTGT 1 GENIC homozygous 727703111 12 15139455 15139456 G GT 3 GENIC heterozygous 727703114 12 15139849 15139850 G A 24 GENIC homozygous 604262716 12 15140786 15140787 T TC 18 GENIC homozygous 727703115 12 15141359 15141360 G C 25 GENIC homozygous 604262717 12 15141633 15141634 A C 20 GENIC homozygous 605297119 12 15145622 15145623 T C 18 GENIC homozygous 604262718 12 15146825 15146826 C T 12 GENIC homozygous 604262719 12 15146993 15146994 A T 28 GENIC homozygous 604262720 12 15147430 15147431 G A 33 GENIC homozygous 604262721 12 15148244 15148245 C CATGT 11 GENIC homozygous 727703116 12 15148443 15148444 G GT 14 GENIC homozygous 727703118 12 15148497 15148498 C T 19 GENIC homozygous 604262722 12 15149407 15149408 A ACTGGAACTCAAAGTTTACC 29 GENIC homozygous 727703119 12 15150331 15150332 C T 16 GENIC homozygous 604262723 12 15152360 15152361 C T 28 GENIC homozygous 604262724 12 15152465 15152466 G A 16 GENIC homozygous 604262725