chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 4054814 4054819 TTTTC ----- 3 GENIC homozygous 45927814 20 4054987 4054988 G A 16 GENIC possibly homozygous 46027336 20 4055046 4055047 T A 10 GENIC heterozygous 46027337 20 4056308 4056309 T C 12 GENIC homozygous 45374707 20 4056546 4056547 C T 24 GENIC possibly homozygous 46027338 20 4056659 4056660 C T 24 GENIC homozygous 46027339 20 4057087 4057088 G A 22 GENIC homozygous 46027340 20 4058346 4058347 G A 28 GENIC homozygous 45374710 20 4058587 4058588 G C 13 GENIC homozygous 46027342 20 4058748 4058749 T G 13 GENIC homozygous 46027343 20 4059062 4059063 C T 19 GENIC possibly homozygous 46027344 20 4059249 4059250 G A 13 GENIC heterozygous 45374713 20 4059373 4059374 G GT 14 GENIC possibly homozygous 46027345 20 4059374 4059375 G GTGTGTGTGTGTGTGT 14 GENIC possibly homozygous 46027346 20 4059429 4059430 A G 19 GENIC homozygous 45374715 20 4059686 4059687 T TATCC 9 GENIC homozygous 46027347 20 4060055 4060056 C T 19 GENIC homozygous 45374717 20 4060099 4060100 A - 10 GENIC homozygous 45374718 20 4060140 4060141 G C 9 GENIC homozygous 45374719 20 4060741 4060742 A G 18 GENIC heterozygous 46027349 20 4060874 4060875 T C 3 GENIC homozygous 46013627