chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 141040769 141040770 C A 61 GENIC homozygous 116232947 7 141041132 141041133 C T 58 GENIC homozygous 115939685 7 141041404 141041405 A 34 GENIC possibly homozygous 128529393 7 141041587 141041588 A T 63 GENIC homozygous 115939686 7 141042385 141042385 A 43 GENIC possibly homozygous 132112853 7 141044353 141044354 T C 50 GENIC homozygous 116232948 7 141045765 141045765 A 55 GENIC homozygous 128529395 7 141046228 141046229 C T 67 GENIC homozygous 116232949 7 141052572 141052573 C 22 GENIC homozygous 128529396 7 141053521 141053522 C G 71 GENIC homozygous 115939690 7 141053995 141053996 G A 43 GENIC homozygous 116232952 7 141054282 141054283 A G 69 GENIC homozygous 115939691 7 141042950 141042951 C 14 GENIC heterozygous 135187304 7 141042954 141042954 G 15 GENIC heterozygous 135187305 7 141056875 141056876 A 71 GENIC homozygous 135187306 7 141045824 141045825 C T 70 GENIC homozygous 135189964 7 141060510 141060511 A G 70 GENIC homozygous 115939693 7 141061219 141061219 C 37 GENIC possibly homozygous 128529397 7 141063700 141063700 TGTT 66 GENIC homozygous 128529399 7 141064516 141064517 C T 29 GENIC homozygous 116232956 7 141064517 141064518 C T 30 GENIC homozygous 116232957 7 141066932 141066933 C T 68 GENIC homozygous 116232958 7 141067470 141067471 T C 60 GENIC homozygous 118288112 7 141067934 141067935 T A 59 GENIC possibly homozygous 116232959 7 141069363 141069363 TTTTTTAAATTGTCAACCGTTGTTACTGATTGGTCTCC 55 GENIC homozygous 128529401 7 141069637 141069637 G 67 GENIC homozygous 128529402 7 141067843 141067844 T 52 GENIC homozygous 132658986 7 141062434 141062442 GTTTGTTT 30 GENIC homozygous 132658984 7 141066028 141066028 TTTA 58 GENIC homozygous 132658985