chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 39621955 39621956 G A 21 GENIC homozygous 114191238 5 39625630 39625631 A 20 GENIC homozygous 128172130 5 39625636 39625636 T 21 GENIC homozygous 128172131 5 39625649 39625649 G 22 GENIC homozygous 128172132 5 39625694 39625695 T 17 GENIC homozygous 128172133 5 39625699 39625699 A 17 GENIC homozygous 128172134 5 39625710 39625710 C 19 GENIC homozygous 128172135 5 39628444 39628445 C 13 GENIC homozygous 128172136 5 39629715 39629715 T 6 GENIC homozygous 128172137 5 39637737 39637737 A 28 GENIC homozygous 128172150 5 39649018 39649019 G A 28 GENIC homozygous 113758379 5 39649080 39649081 G A 26 GENIC homozygous 113758381 5 39649121 39649122 C A 24 GENIC homozygous 114191239 5 39649325 39649326 A G 32 GENIC homozygous 113758383 5 39650429 39650431 AA 23 GENIC homozygous 128172153 5 39650454 39650455 A G 24 GENIC homozygous 113758385 5 39650635 39650636 A G 13 GENIC homozygous 113758387 5 39650668 39650669 G C 9 GENIC homozygous 113758389 5 39650734 39650735 G T 20 GENIC possibly homozygous 114191240 5 39638924 39638931 CAGGGAC 37 GENIC homozygous 130952492 5 39649379 39649379 TATA 20 GENIC homozygous 130952493