chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 29 GENIC homozygous 997794365 9 94238781 94238782 T C 31 GENIC homozygous 997794366 9 94238917 94238918 G A 22 GENIC homozygous 997794367 9 94238963 94238964 A G 22 GENIC homozygous 997794368 9 94239001 94239002 C T 23 GENIC homozygous 997794369 9 94239188 94239189 T C 26 GENIC homozygous 997794370 9 94239326 94239327 G A 27 GENIC homozygous 997794371 9 94242072 94242073 G C 24 GENIC possibly homozygous 997794372 9 94242332 94242333 A G 21 GENIC homozygous 997794373 9 94242364 94242365 A C 20 GENIC homozygous 997794374 9 94244297 94244298 G C 17 GENIC homozygous 997794375 9 94245634 94245635 G A 11 GENIC homozygous 997794376 9 94246622 94246623 G A 18 GENIC homozygous 997794377 9 94247630 94247631 A C 22 GENIC homozygous 997794378 9 94247969 94247970 A G 13 GENIC homozygous 997794379 9 94248493 94248494 C T 18 GENIC homozygous 997794380 9 94249423 94249424 T C 31 GENIC homozygous 997794381 9 94250831 94250832 C T 13 GENIC homozygous 997794382 9 94252124 94252125 A G 12 GENIC homozygous 997794383