chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 49017334 49017335 T G 21 GENIC homozygous 109721723 19 49017515 49017516 G C 11 GENIC homozygous 109721725 19 49019954 49019955 G A 43 GENIC homozygous 109721729 19 49020256 49020257 A T 22 GENIC homozygous 109721730 19 49020278 49020279 A G 27 GENIC homozygous 109721732 19 49022637 49022638 C T 34 GENIC homozygous 110025217 19 49023271 49023272 T C 27 GENIC homozygous 110025219 19 49023511 49023512 T C 28 GENIC homozygous 109721738 19 49023572 49023573 A T 34 GENIC homozygous 110025221 19 49023679 49023680 G A 32 GENIC homozygous 109721740 19 49024273 49024274 G A 33 GENIC homozygous 109721742 19 49024399 49024400 A T 27 GENIC homozygous 110025223 19 49024704 49024705 G A 22 GENIC homozygous 109721746 19 49024828 49024829 G A 14 GENIC homozygous 109721748 19 49025311 49025312 G A 35 GENIC homozygous 109721752 19 49025351 49025352 G T 46 GENIC homozygous 109721754 19 49026037 49026038 A C 17 GENIC homozygous 109721756 19 49026081 49026082 A G 17 GENIC homozygous 109721758 19 49026093 49026094 A G 17 GENIC homozygous 109721760 19 49026936 49026937 C G 24 GENIC homozygous 109721764 19 49027237 49027238 T C 28 GENIC homozygous 109721768 19 49027527 49027528 G A 29 GENIC homozygous 109721770