chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 7853351 7853352 G A 19 GENIC possibly homozygous 993366433 4 7853494 7853495 C T 27 GENIC homozygous 993366434 4 7853514 7853515 T C 26 GENIC homozygous 993366435 4 7853986 7853987 A G 10 GENIC homozygous 993366436 4 7854219 7854220 G A 8 GENIC homozygous 993366437 4 7854265 7854266 A G 18 GENIC homozygous 993366438 4 7854419 7854420 A G 22 GENIC possibly homozygous 993366439 4 7855517 7855518 T C 22 GENIC possibly homozygous 993366440 4 7856767 7856768 A G 27 GENIC homozygous 993366441 4 7857153 7857154 G A 18 GENIC possibly homozygous 993366442 4 7859550 7859551 C T 12 GENIC homozygous 993366443 4 7860068 7860069 C T 27 GENIC possibly homozygous 993366444 4 7862653 7862654 T C 27 GENIC possibly homozygous 993366445 4 7862768 7862769 C T 26 GENIC homozygous 993366446 4 7863146 7863147 T C 26 GENIC possibly homozygous 993366447 4 7864059 7864060 T C 27 GENIC homozygous 993366448 4 7864456 7864457 A G 18 GENIC homozygous 993366449 4 7864658 7864659 T A 23 GENIC possibly homozygous 993366450 4 7865851 7865852 C A 13 GENIC heterozygous 993366451 4 7865852 7865853 C T 13 GENIC heterozygous 993366452 4 7866356 7866357 G A 26 GENIC homozygous 993366453 4 7866663 7866664 C T 27 GENIC possibly homozygous 993366454 4 7866801 7866802 A C 6 GENIC homozygous 993366455 4 7869226 7869227 T A 28 GENIC homozygous 993366456 4 7869227 7869228 A T 29 GENIC homozygous 993366457 4 7874445 7874446 G C 31 GENIC homozygous 993366458 4 7875505 7875506 C T 26 GENIC homozygous 993366459 4 7875806 7875807 C T 36 GENIC possibly homozygous 993366460 4 7875811 7875812 G A 34 GENIC possibly homozygous 993366461 4 7878676 7878677 C T 38 GENIC homozygous 993366462 4 7880026 7880027 G C 22 GENIC homozygous 993366463 4 7880071 7880072 T A 15 GENIC homozygous 993366464 4 7880101 7880102 T A 10 GENIC homozygous 993366465 4 7880104 7880105 G C 11 GENIC homozygous 993366466