chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 50913689 50913690 C T 27 INTERGENIC homozygous 50035342 13 50913817 50913818 A G 26 INTERGENIC homozygous 50035344 13 50913853 50913854 G T 27 INTERGENIC homozygous 50035346 13 50913866 50913867 C T 25 INTERGENIC homozygous 50035348 13 50913900 50913901 A G 28 INTERGENIC homozygous 50035350 13 50913939 50913940 G T 25 INTERGENIC homozygous 50035352 13 50914256 50914257 T C 27 INTERGENIC homozygous 50035354 13 50914458 50914459 G - 29 INTERGENIC homozygous 50035356 13 50914476 50914477 A - 26 INTERGENIC homozygous 50035358 13 50914507 50914508 T C 23 INTERGENIC homozygous 50035360 13 50914818 50914819 T C 39 INTERGENIC homozygous 50035362 13 50915003 50915004 A T 27 INTERGENIC homozygous 50035364 13 50915109 50915110 G A 41 INTERGENIC homozygous 50035366 13 50915167 50915168 C T 43 INTERGENIC homozygous 50035368 13 50915200 50915201 G A 37 INTERGENIC homozygous 50035370 13 50915288 50915289 G C 33 INTERGENIC homozygous 50035371 13 50915401 50915402 A T 41 INTERGENIC homozygous 50035373 13 50915642 50915643 C A 38 INTERGENIC homozygous 50035375 13 50916592 50916593 T C 26 INTERGENIC homozygous 50035377 13 50916666 50916667 T C 21 INTERGENIC homozygous 50035381 13 50916900 50916902 AA -- 19 INTERGENIC homozygous 50035383