chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 3995632 3995633 G A 12 INTERGENIC homozygous 45374463 20 3995774 3995775 A G 23 INTERGENIC homozygous 45374464 20 3996374 3996375 G A 11 GENIC homozygous 45374465 20 3996471 3996472 T G 12 GENIC homozygous 45374466 20 3996647 3996648 C T 9 GENIC homozygous 45374467 20 3996651 3996652 G A 11 GENIC homozygous 45374468 20 4001368 4001369 A G 16 GENIC homozygous 45374476 20 4001887 4001888 A - 13 GENIC homozygous 45374477 20 4002532 4002533 A G 16 GENIC homozygous 45374478 20 4002638 4002639 T A 13 GENIC homozygous 45374479 20 4004135 4004136 T C 15 GENIC homozygous 45374485 20 4004589 4004590 G A 25 GENIC homozygous 45374487 20 4004755 4004756 T G 15 GENIC homozygous 45374488 20 4004756 4004757 C A 15 GENIC homozygous 45374489 20 4004763 4004764 C T 15 GENIC homozygous 45374490 20 4005284 4005285 G A 18 GENIC homozygous 45374491 20 4006217 4006218 A G 9 GENIC homozygous 45374494 20 4006440 4006441 A G 14 GENIC homozygous 45374495 20 4007628 4007629 A C 14 GENIC homozygous 45374498 20 4008294 4008295 C T 10 GENIC homozygous 45374499 20 4009398 4009399 G - 15 GENIC homozygous 45374500 20 4003546 4003547 C G 19 GENIC heterozygous 46035619