chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 99125454 99125455 T TCTC 5 GENIC homozygous 51566914 10 99125467 99125469 TG -- 4 GENIC homozygous 51754709 10 99125565 99125566 T C 14 GENIC possibly homozygous 51566918 10 99126141 99126142 T A 13 GENIC heterozygous 51754711 10 99126932 99126933 C A 15 GENIC possibly homozygous 51754717 10 99127037 99127038 T TC 7 GENIC homozygous 51754718 10 99127638 99127639 G A 12 GENIC homozygous 51754720 10 99127889 99127890 G C 23 GENIC homozygous 51754722 10 99127988 99127989 C T 14 GENIC homozygous 51754724 10 99128161 99128162 T C 13 GENIC heterozygous 51566927 10 99128365 99128366 A T 17 GENIC possibly homozygous 51754726 10 99128592 99128593 C T 23 GENIC homozygous 51754728 10 99128779 99128780 G GGA 12 GENIC homozygous 51754730 10 99128825 99128826 C T 19 GENIC homozygous 51754732 10 99128909 99128910 C T 18 GENIC possibly homozygous 51754734 10 99129336 99129337 C CTT 8 GENIC possibly homozygous 51754736 10 99129343 99129344 C CCT 6 GENIC homozygous 51754738 10 99129389 99129394 TTTGT ----- 1 GENIC homozygous 51754740 10 99130361 99130362 T TTTTC 2 GENIC homozygous 51754742 10 99130393 99130394 A G 19 GENIC homozygous 51754744 10 99130442 99130443 T C 11 GENIC homozygous 51754746 10 99130576 99130577 A AT 2 GENIC heterozygous 51754748 10 99131955 99131956 A G 14 GENIC heterozygous 51566933 10 99132053 99132054 G A 15 GENIC possibly homozygous 51566935 10 99132143 99132144 G A 13 GENIC homozygous 51566937 10 99132194 99132195 T C 23 GENIC homozygous 51566939 10 99133722 99133723 C T 12 GENIC possibly homozygous 51754752 10 99134046 99134047 A G 18 GENIC possibly homozygous 51566955