chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 40697264 40697265 G GAA 13 GENIC heterozygous 50204346 12 40697265 40697266 A - 13 GENIC heterozygous 50543733 12 40697505 40697509 ACAC ---- 4 GENIC homozygous 50543734 12 40697972 40697973 G A 25 GENIC homozygous 50422914 12 40698750 40698751 T C 19 GENIC homozygous 50204351 12 40699327 40699328 C G 16 GENIC homozygous 50422915 12 40699950 40699956 GAGGGG ------ 2 INTERGENIC homozygous 50422916 12 40701978 40701979 C CA 12 INTERGENIC homozygous 50204363 12 40701982 40701983 T - 12 INTERGENIC homozygous 50204364 12 40701984 40701985 T C 12 INTERGENIC homozygous 50204365 12 40702025 40702026 C CA 3 INTERGENIC homozygous 50204366 12 40702453 40702454 T TA 13 INTERGENIC possibly homozygous 50204370 12 40702463 40702464 T TAA 15 INTERGENIC homozygous 50422917 12 40702468 40702469 G A 15 INTERGENIC homozygous 50543735 12 40703905 40703906 T A 19 INTERGENIC homozygous 50422918 12 40704330 40704331 T G 18 INTERGENIC homozygous 50422919 12 40704413 40704414 G A 14 INTERGENIC homozygous 50204375 12 40704576 40704577 C T 7 INTERGENIC homozygous 50422920 12 40704877 40704878 G - 6 INTERGENIC homozygous 50204376 12 40707206 40707207 T TC 18 INTERGENIC homozygous 50422921 12 40707463 40707464 G A 27 INTERGENIC homozygous 50422922 12 40707605 40707606 C T 17 INTERGENIC homozygous 50422923 12 40707622 40707623 G A 12 INTERGENIC homozygous 50422924 12 40707870 40707871 A ATAGC 8 INTERGENIC homozygous 50422926 12 40708142 40708143 C CA 9 INTERGENIC homozygous 50422927 12 40708783 40708784 G C 10 INTERGENIC homozygous 50422928 12 40708784 40708785 A C 10 INTERGENIC homozygous 50422929 12 40708832 40708833 T TTTTTTTG 12 INTERGENIC heterozygous 50543736 12 40708845 40708846 G T 13 INTERGENIC homozygous 50543737 12 40708941 40708942 T C 13 INTERGENIC homozygous 50422930 12 40709100 40709101 T C 6 INTERGENIC homozygous 50204379 12 40709254 40709255 C T 16 INTERGENIC homozygous 50422931 12 40708835 40708836 C T 15 INTERGENIC homozygous 50512453