chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 72266663 72266664 G A 9 GENIC homozygous 45963539 X 72286956 72286957 T A 9 GENIC homozygous 45963550 X 72295878 72295879 T C 8 GENIC homozygous 45963556 X 72297696 72297697 G GA 7 GENIC homozygous 45963558 X 72313152 72313153 A G 8 GENIC homozygous 45963564 X 72315382 72315383 C T 12 GENIC homozygous 45963566 X 72320197 72320198 A T 7 GENIC homozygous 45963568 X 72320219 72320220 T G 7 GENIC homozygous 45983397 X 72274578 72274579 A G 14 GENIC homozygous 45983388 X 72302629 72302630 G A 8 GENIC homozygous 45983390 X 72315420 72315421 G GA 9 GENIC homozygous 45983392 X 72320207 72320208 A - 7 GENIC homozygous 45983395 X 72320221 72320222 C G 7 GENIC homozygous 45983399 X 72320807 72320808 A G 14 GENIC homozygous 45963570 X 72320853 72320854 A AT 13 GENIC homozygous 45963572 X 72321946 72321947 A T 15 GENIC homozygous 45983401 X 72323323 72323324 A G 14 GENIC homozygous 45983403 X 72330606 72330607 T C 9 GENIC homozygous 45983405