chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 47644395 47644396 G A 54 GENIC homozygous 114548321 13 47644605 47644606 T C 47 GENIC homozygous 114548323 13 47645152 47645153 T C 44 GENIC homozygous 114548324 13 47645586 47645586 TC 44 GENIC homozygous 132171400 13 47645990 47645991 A G 60 GENIC homozygous 114548326 13 47646370 47646372 AG 47 GENIC homozygous 131501499 13 47646492 47646492 CCAGCATTTTATATTT 43 GENIC homozygous 131501500 13 47648071 47648072 G A 54 GENIC homozygous 114548328 13 47648323 47648324 C T 68 GENIC homozygous 114548330 13 47649984 47649984 G 42 GENIC homozygous 129050853 13 47649951 47649952 A 40 GENIC homozygous 129050850 13 47649958 47649959 A 40 GENIC homozygous 129050851 13 47649977 47649977 A 41 GENIC homozygous 129050852 13 47649988 47649988 T 41 GENIC homozygous 129050854 13 47650005 47650005 T 38 GENIC homozygous 129050855 13 47650042 47650043 A 47 GENIC homozygous 129050856 13 47650107 47650108 A C 30 GENIC homozygous 114548331 13 47650115 47650115 G 28 GENIC homozygous 129050857 13 47651397 47651398 C T 61 GENIC homozygous 118566818 13 47651464 47651465 T C 67 GENIC homozygous 118566819 13 47650579 47650580 A G 36 GENIC homozygous 114615075