geneid | 132671 |
---|---|
ensemblid | ENSG00000163071.11 |
hgncid | 29579 |
symbol | SPATA18 |
name | spermatogenesis associated 18 |
refseq_nuc | NM_145263.4 |
refseq_prot | NP_660306.1 |
ensembl_nuc | ENST00000295213.9 |
ensembl_prot | ENSP00000295213.4 |
mane_status | MANE Select |
chr | chr4 |
start | 52051304 |
end | 52097299 |
strand | + |
ver | v1.2 |
region | chr4:52051304-52097299 |
region5000 | chr4:52046304-52102299 |
regionname0 | SPATA18_chr4_52051304_52097299 |
regionname5000 | SPATA18_chr4_52046304_52102299 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 538 | 196 | 61 | 22 | 84 | 7 | 20 | 65 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0002 | 0/0 | 538 | 98 | 8 | 22 | 50 | 9 | 9 | 39 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0003 | 0/0 | 538 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0004 | 0/0 | 538 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0005 | 0/0 | 538 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0006 | 0/0 | 538 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0007 | 0/0 | 538 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0008 | 0/0 | 497 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0009 | 0/0 | 538 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0010 | 0/0 | 538 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1617 | 190 | 60 | 22 | 79 | 7 | 20 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
c0002 | 0/0 | 1617 | 98 | 8 | 22 | 50 | 9 | 9 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
c0003 | 0/0 | 1617 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
c0004 | 0/0 | 1617 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
c0005 | 0/0 | 1617 | 3 | 2 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
c0006 | 0/0 | 1617 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
c0007 | 0/0 | 1617 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
c0008 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
c0009 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
c0010 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
c0011 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
c0012 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2813 | 102 | 9 | 21 | 54 | 9 | 9 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0002 | 0/1 | 2814 | 77 | 5 | 12 | 53 | 0 | 6 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0003 | 0/0 | 2813 | 61 | 7 | 7 | 32 | 6 | 9 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0004 | 1/0 | 2814 | 45 | 40 | 3 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0005 | 0/0 | 2815 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0006 | 0/0 | 2815 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0007 | 0/0 | 2813 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0008 | 0/0 | 2813 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0009 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0010 | 0/0 | 2814 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0011 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0012 | 0/0 | 2813 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0013 | 0/0 | 2814 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0014 | 0/0 | 2813 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0015 | 0/0 | 2814 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0016 | 0/0 | 2814 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0017 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0018 | 0/0 | 2814 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0019 | 0/0 | 2814 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0020 | 0/0 | 2815 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
t0021 | 0/0 | 2815 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 0 | 7 | 4 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0003 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0005 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0006 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0025 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1617 | 190 | 60 | 22 | 79 | 7 | 20 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0003 | 0/0 | 1617 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0011 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0002c0002 | 0/0 | 1617 | 98 | 8 | 22 | 50 | 9 | 9 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0003c0005 | 0/0 | 1617 | 3 | 2 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0004c0004 | 0/0 | 1617 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0005c0007 | 0/0 | 1617 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0006c0006 | 0/0 | 1617 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0007c0009 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0008c0010 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0009c0012 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0010c0008 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4429 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0002 | 0/1 | 4430 | 73 | 5 | 11 | 50 | 0 | 6 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0003 | 0/0 | 4429 | 54 | 5 | 7 | 27 | 6 | 9 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0004 | 1/0 | 4430 | 42 | 38 | 3 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0005 | 0/0 | 4431 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0006 | 0/0 | 4431 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0007 | 0/0 | 4429 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0009 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0010 | 0/0 | 4430 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0011 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0012 | 0/0 | 4429 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0013 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0015 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0016 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0018 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0019 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0020 | 0/0 | 4431 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0001t0021 | 0/0 | 4431 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0003t0003 | 0/0 | 4429 | 5 | 0 | 0 | 5 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0001c0011t0004 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0002c0002t0001 | 0/0 | 4429 | 95 | 8 | 21 | 49 | 9 | 8 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0002c0002t0002 | 0/0 | 4430 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0002c0002t0004 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0002c0002t0008 | 0/0 | 4429 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0003c0005t0001 | 0/0 | 4429 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0003c0005t0004 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0003c0005t0017 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0004c0004t0001 | 0/0 | 4429 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0005c0007t0002 | 0/0 | 4430 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0006c0006t0003 | 0/0 | 4429 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0007c0009t0001 | 0/0 | 4429 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0008c0010t0001 | 0/0 | 4429 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0009c0012t0002 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
a0010c0008t0014 | 0/0 | 4429 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | copy fasta | chr4 | 52046304 | 52102299 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0025 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0006 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0005g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0006g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0010g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0011g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0012g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0015g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0018g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0019g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0020g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0001t0021g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0003t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0001c0011t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0001 | 0/0 | 12 | 0 | 7 | 4 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0002c0002t0008g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0003c0005t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0003c0005t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0003c0005t0017g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0004c0004t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0004c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0005c0007t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0006c0006t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0006c0006t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0007c0009t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0008c0010t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0009c0012t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
a0010c0008t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0168 | EUR | GBR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0216 | EUR | GBR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0169 | EUR | FIN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0153 | EUR | FIN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0130 | EUR | FIN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0159 | EUR | FIN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0179 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01168 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0209 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0097 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0148 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0125 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0035 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0035 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01884 | hp2 | a0001 | c0001 | t0021 | g0217 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0155 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0143 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0171 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0213 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02027 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02132 | hp1 | a0005 | c0007 | t0002 | g0003 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02132 | hp2 | a0007 | c0009 | t0001 | g0033 | EAS | KHV | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0205 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02258 | hp1 | a0010 | c0008 | t0014 | g0037 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | PEL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0165 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0134 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02895 | hp2 | a0001 | c0001 | t0015 | g0121 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03225 | hp1 | a0001 | c0001 | t0016 | g0005 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0094 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03516 | hp2 | a0001 | c0001 | t0019 | g0218 | AFR | ESN | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03540 | hp2 | a0003 | c0005 | t0001 | g0118 | AFR | GWD | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0157 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03669 | hp1 | a0003 | c0005 | t0017 | g0119 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | STU | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | STU | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0083 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03710 | hp2 | a0001 | c0001 | t0009 | g0077 | SAS | PJL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0176 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0044 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03927 | hp1 | a0002 | c0002 | t0004 | g0207 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03942 | hp1 | a0001 | c0001 | t0007 | g0088 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | BEB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG04228 | hp1 | a0001 | c0001 | t0018 | g0003 | SAS | STU | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | STU | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18522 | hp2 | a0006 | c0006 | t0003 | g0132 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | CHB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | CHB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18940 | hp2 | a0005 | c0007 | t0002 | g0003 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18943 | hp2 | a0004 | c0004 | t0001 | g0015 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18957 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18959 | hp1 | a0001 | c0003 | t0003 | g0110 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18959 | hp2 | a0001 | c0001 | t0012 | g0144 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18967 | hp2 | a0008 | c0010 | t0001 | g0210 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18969 | hp2 | a0002 | c0002 | t0008 | g0187 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18984 | hp2 | a0001 | c0003 | t0003 | g0091 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18995 | hp2 | a0004 | c0004 | t0001 | g0195 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19010 | hp2 | a0001 | c0003 | t0003 | g0051 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | LWK | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19030 | hp2 | a0001 | c0011 | t0004 | g0112 | AFR | LWK | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19043 | hp1 | a0003 | c0005 | t0004 | g0120 | AFR | LWK | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | LWK | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19083 | hp2 | a0009 | c0012 | t0002 | g0004 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19085 | hp1 | a0004 | c0004 | t0001 | g0015 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19085 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | YRI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA20129 | hp1 | a0001 | c0001 | t0020 | g0221 | AFR | ASW | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0208 | AFR | ASW | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0043 | EUR | TSI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0158 | EUR | TSI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0042 | EUR | TSI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA20805 | hp2 | a0001 | c0001 | t0011 | g0117 | EUR | TSI | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0122 | AFR | ACB | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | MSL | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | USA | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
HG06807 | hp2 | a0006 | c0006 | t0003 | g0133 | AFR | USA | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | USA | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0096 | AFR | USA | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0025 | REF | REF | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0113 | REF | REF | SPATA18_chr4_52046304_52102299 | SPATA18 | chr4 | 52046304 | 52102299 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:52069832
|
C | T | 1 | a0003 | 3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.434C>T | p.Thr145Ile | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/13 | 835/4430 | 434/1617 | 145/538 | chr4 | 52069832 | ||
chr4:52071925
|
C | A | 1 | a0010 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.527C>A | p.Ser176Tyr | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/13 | 928/4430 | 527/1617 | 176/538 | chr4 | 52071925 | ||
chr4:52071973
|
G | A | 1 | a0004 | 3 | NA18943.hp2 NA18995.hp2 NA19085.hp1 |
missense_variant | MODERATE | c.575G>A | p.Ser192Asn | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/13 | 976/4430 | 575/1617 | 192/538 | chr4 | 52071973 | ||
chr4:52072077
|
T | C | 4 | a0002a0004a0007others(1): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
missense_variant | MODERATE | c.679T>C | p.Ser227Pro | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/13 | 1080/4430 | 679/1617 | 227/538 | chr4 | 52072077 | ||
chr4:52076820
|
G | C | 1 | a0007 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.800G>C | p.Arg267Pro | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/13 | 1201/4430 | 800/1617 | 267/538 | chr4 | 52076820 | ||
chr4:52076858
|
G | A | 1 | a0006 | 2 | HG06807.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.838G>A | p.Ala280Thr | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/13 | 1239/4430 | 838/1617 | 280/538 | chr4 | 52076858 | ||
chr4:52079908
|
T | A | 1 | a0009 | 1 | NA19083.hp2 | missense_variant | MODERATE | c.1344T>A | p.Phe448Leu | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/13 | 1745/4430 | 1344/1617 | 448/538 | chr4 | 52079908 | ||
chr4:52082391
|
C | T | 1 | a0005 | 2 | HG02132.hp1 NA18940.hp2 |
missense_variant | MODERATE | c.1360C>T | p.Arg454Cys | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/13 | 1761/4430 | 1360/1617 | 454/538 | chr4 | 52082391 | ||
chr4:52084928
|
C | T | 1 | a0008 | 1 | NA18967.hp2 | stop_gained | HIGH | c.1492C>T | p.Arg498* | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/13 | 1893/4430 | 1492/1617 | 498/538 | chr4 | 52084928 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:52076983
|
G | A | 1 | a0001c0011 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.963G>A | p.Leu321Leu | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/13 | 1364/4430 | 963/1617 | 321/538 | chr4 | 52076983 | ||
chr4:52079857
|
G | A | 1 | a0001c0003 | 5 | NA18957.hp2 NA18959.hp1 NA18984.hp2 others(2): Show |
synonymous_variant | LOW | c.1293G>A | p.Gln431Gln | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/13 | 1694/4430 | 1293/1617 | 431/538 | chr4 | 52079857 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:52051461
|
G | T | 3 | a0001c0001t0019a0001c0001t0020a0001c0001t0021 | 3 | HG01884.hp2 HG03516.hp2 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-244G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/13 | 244 | chr4 | 52051461 | |||||
chr4:52051472
|
C | T | 1 | a0001c0001t0018 | 1 | HG04228.hp1 | 5_prime_UTR_variant | MODIFIER | c.-233C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/13 | 233 | chr4 | 52051472 | |||||
chr4:52051626
|
C | T | 1 | a0003c0005t0017 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-79C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/13 | 79 | chr4 | 52051626 | |||||
chr4:52095199
|
C | T | 1 | a0001c0001t0016 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 312 | chr4 | 52095199 | |||||
chr4:52095203
|
C | T | 1 | a0001c0001t0015 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 316 | chr4 | 52095203 | |||||
chr4:52095444
|
A | T | 1 | a0010c0008t0014 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*557A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 557 | chr4 | 52095444 | |||||
chr4:52095558
|
C | T | 1 | a0001c0001t0013 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*671C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 671 | chr4 | 52095558 | |||||
chr4:52095609
|
G | T | 1 | a0010c0008t0014 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*722G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 722 | chr4 | 52095609 | |||||
chr4:52095751
|
C | T | 1 | a0010c0008t0014 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*864C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 864 | chr4 | 52095751 | |||||
chr4:52095772
|
A | G | 2 | a0001c0001t0005a0001c0001t0021 | 5 | HG01884.hp2 HG02630.hp2 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*885A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 885 | chr4 | 52095772 | |||||
chr4:52095964
|
C | A | 1 | a0001c0001t0007 | 2 | HG03704.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1077C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1077 | chr4 | 52095964 | |||||
chr4:52096234
|
T | G | 1 | a0002c0002t0008 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1347T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1347 | chr4 | 52096234 | |||||
chr4:52096299
|
T | C | 9 | a0001c0001t0002a0001c0001t0009a0001c0001t0013others(6): Show | 82 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1412T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1412 | chr4 | 52096299 | |||||
chr4:52096363
|
C | T | 8 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(5): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1476C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1476 | chr4 | 52096363 | |||||
chr4:52096761
|
C | CA | 4 | a0001c0001t0005a0001c0001t0006a0001c0001t0020others(1): Show | 9 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1887dupA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1888 | INFO_REALIGN_3_PRIME | chr4 | 52096761 | ||||
chr4:52096761
|
CA | C | 13 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(10): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1887delA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1887 | INFO_REALIGN_3_PRIME | chr4 | 52096761 | ||||
chr4:52096773
|
A | C | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(13): Show | 148 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1886A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 1886 | chr4 | 52096773 | |||||
chr4:52097010
|
C | T | 1 | a0001c0001t0011 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2123C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 2123 | chr4 | 52097010 | |||||
chr4:52097165
|
G | A | 8 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(5): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2278G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 2278 | chr4 | 52097165 | |||||
chr4:52097214
|
G | A | 1 | a0001c0001t0009 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2327G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 2327 | chr4 | 52097214 | |||||
chr4:52097290
|
A | G | 1 | a0001c0001t0012 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2403A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 13/13 | 2403 | chr4 | 52097290 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:52051821
|
CGCCCTCC others(77): Show |
C | 5 | a0001c0001t0004g0219a0001c0001t0004g0220a0001c0001t0019g0218others(2): Show | 5 | HG01884.hp2 HG02258.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+33_87+116delCCT others(81): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52051821 | |||||
chr4:52052096
|
G | A | 1 | a0010c0008t0014g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.87+305G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052096 | ||||||
chr4:52052127
|
A | C | 1 | a0010c0008t0014g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.87+336A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052127 | ||||||
chr4:52052302
|
T | C | 1 | a0001c0001t0003g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.87+511T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052302 | ||||||
chr4:52052382
|
T | C | 1 | a0001c0001t0002g0039 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.87+591T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052382 | ||||||
chr4:52052537
|
C | T | 73 | a0001c0001t0002g0032a0001c0001t0002g0166a0001c0001t0002g0183others(70): Show | 96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.87+746C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052537 | ||||||
chr4:52052572
|
G | A | 5 | a0002c0002t0001g0016a0002c0002t0001g0040a0002c0002t0001g0041others(2): Show | 6 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.87+781G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052572 | ||||||
chr4:52052726
|
G | C | 1 | a0002c0002t0001g0044 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.87+935G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52052726 | ||||||
chr4:52053073
|
A | G | 2 | a0001c0001t0003g0153a0001c0001t0003g0154 | 2 | HG00280.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.87+1282A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52053073 | ||||||
chr4:52053453
|
C | A | 1 | a0001c0001t0002g0045 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.87+1662C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52053453 | ||||||
chr4:52053482
|
A | T | 1 | a0002c0002t0001g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.87+1691A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52053482 | ||||||
chr4:52053709
|
C | T | 1 | a0002c0002t0001g0215 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.87+1918C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52053709 | ||||||
chr4:52053955
|
C | A | 1 | a0002c0002t0001g0046 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.87+2164C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52053955 | ||||||
chr4:52054100
|
G | T | 1 | a0001c0001t0020g0221 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.87+2309G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054100 | ||||||
chr4:52054172
|
T | C | 1 | a0001c0001t0021g0217 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.87+2381T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054172 | ||||||
chr4:52054320
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.87+2529A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054320 | ||||||
chr4:52054388
|
C | G | 2 | a0001c0001t0002g0045a0001c0001t0002g0151 | 2 | NA18967.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.87+2597C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054388 | ||||||
chr4:52054393
|
G | A | 4 | a0001c0001t0004g0017a0001c0001t0004g0047a0001c0001t0004g0048others(1): Show | 5 | HG02109.hp2 HG02622.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+2602G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054393 | ||||||
chr4:52054431
|
A | G | 1 | a0001c0001t0004g0150 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.87+2640A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054431 | ||||||
chr4:52054469
|
A | C | 1 | a0002c0002t0001g0216 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.87+2678A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52054469 | ||||||
chr4:52054897
|
A | AACATGGT others(35): Show |
1 | a0002c0002t0001g0046 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.87+3107_87+3148dup others(42): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52054897 | |||||
chr4:52055288
|
C | G | 127 | a0001c0001t0001g0129a0001c0001t0002g0032a0001c0001t0002g0142others(124): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.87+3497C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52055288 | ||||||
chr4:52055835
|
G | A | 1 | a0001c0001t0011g0117 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.87+4044G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52055835 | ||||||
chr4:52056169
|
C | G | 2 | a0001c0001t0004g0027a0001c0001t0004g0116 | 3 | HG02486.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.88-4250C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056169 | ||||||
chr4:52056269
|
T | G | 1 | a0001c0001t0002g0050 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.88-4150T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056269 | ||||||
chr4:52056455
|
A | G | 4 | a0001c0001t0004g0017a0001c0001t0004g0047a0001c0001t0004g0048others(1): Show | 5 | HG02109.hp2 HG02622.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-3964A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056455 | ||||||
chr4:52056498
|
GATCAGTA | G | 2 | a0002c0002t0001g0036a0002c0002t0001g0214 | 3 | NA18957.hp1 NA19005.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.88-3918_88-3912del others(7): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52056498 | |||||
chr4:52056543
|
T | C | 3 | a0003c0005t0001g0118a0003c0005t0004g0120a0003c0005t0017g0119 | 3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.88-3876T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056543 | ||||||
chr4:52056560
|
C | CT | 75 | a0001c0001t0002g0032a0001c0001t0002g0166a0001c0001t0002g0183others(72): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.88-3857dupT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52056560 | |||||
chr4:52056646
|
C | T | 1 | a0002c0002t0001g0213 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.88-3773C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056646 | ||||||
chr4:52056785
|
C | G | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.88-3634C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52056785 | ||||||
chr4:52057026
|
C | T | 3 | a0002c0002t0001g0211a0002c0002t0001g0212a0008c0010t0001g0210 | 3 | NA18967.hp2 NA18993.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.88-3393C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057026 | ||||||
chr4:52057039
|
C | T | 117 | a0001c0001t0001g0129a0001c0001t0002g0032a0001c0001t0002g0142others(114): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.88-3380C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057039 | ||||||
chr4:52057297
|
T | G | 75 | a0001c0001t0002g0032a0001c0001t0002g0166a0001c0001t0002g0183others(72): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.88-3122T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057297 | ||||||
chr4:52057517
|
C | G | 3 | a0003c0005t0001g0118a0003c0005t0004g0120a0003c0005t0017g0119 | 3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.88-2902C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057517 | ||||||
chr4:52057795
|
T | C | 1 | a0002c0002t0001g0155 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.88-2624T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057795 | ||||||
chr4:52057882
|
G | A | 2 | a0001c0001t0019g0218a0001c0001t0020g0221 | 2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.88-2537G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52057882 | ||||||
chr4:52058099
|
A | G | 1 | a0002c0002t0001g0035 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.88-2320A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058099 | ||||||
chr4:52058239
|
G | C | 1 | a0001c0003t0003g0051 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.88-2180G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058239 | ||||||
chr4:52058270
|
T | G | 127 | a0001c0001t0001g0129a0001c0001t0002g0032a0001c0001t0002g0142others(124): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.88-2149T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058270 | ||||||
chr4:52058272
|
T | C | 122 | a0001c0001t0001g0129a0001c0001t0002g0032a0001c0001t0002g0142others(119): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.88-2147T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058272 | ||||||
chr4:52058298
|
T | TTTTGGGA others(10): Show |
2 | a0002c0002t0001g0042a0002c0002t0001g0043 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.88-2120_88-2104dup others(17): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52058298 | |||||
chr4:52058331
|
G | GA | 4 | a0003c0005t0001g0118a0003c0005t0004g0120a0003c0005t0017g0119others(1): Show | 4 | HG02258.hp1 HG03540.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-2082dupA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 52058331 | |||||
chr4:52058462
|
G | A | 3 | a0003c0005t0001g0118a0003c0005t0004g0120a0003c0005t0017g0119 | 3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.88-1957G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058462 | ||||||
chr4:52058612
|
G | A | 77 | a0001c0001t0002g0032a0001c0001t0002g0166a0001c0001t0002g0183others(74): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.88-1807G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058612 | ||||||
chr4:52058774
|
A | T | 1 | a0001c0001t0004g0026 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.88-1645A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52058774 | ||||||
chr4:52059210
|
A | T | 1 | a0002c0002t0001g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.88-1209A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52059210 | ||||||
chr4:52059340
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.88-1079A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52059340 | ||||||
chr4:52059343
|
C | T | 1 | a0001c0001t0002g0115 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.88-1076C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52059343 | ||||||
chr4:52059789
|
T | C | 1 | a0001c0001t0003g0052 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.88-630T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52059789 | ||||||
chr4:52060020
|
A | C | 1 | a0001c0001t0019g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.88-399A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52060020 | ||||||
chr4:52060050
|
T | A | 122 | a0001c0001t0001g0129a0001c0001t0002g0032a0001c0001t0002g0142others(119): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.88-369T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52060050 | ||||||
chr4:52060099
|
A | T | 4 | a0001c0001t0003g0038a0001c0001t0003g0145a0001c0001t0003g0146others(1): Show | 4 | HG02559.hp1 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-320A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52060099 | ||||||
chr4:52060234
|
G | A | 2 | a0002c0002t0001g0156a0002c0002t0001g0157 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.88-185G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 1/12 | chr4 | 52060234 | ||||||
chr4:52060947
|
C | A | 82 | a0001c0001t0002g0032a0001c0001t0002g0166a0001c0001t0002g0183others(79): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.309+50C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52060947 | ||||||
chr4:52061048
|
A | T | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.309+151A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061048 | ||||||
chr4:52061063
|
A | G | 122 | a0001c0001t0001g0129a0001c0001t0002g0032a0001c0001t0002g0142others(119): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.309+166A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061063 | ||||||
chr4:52061231
|
C | A | 2 | a0001c0001t0004g0018a0001c0001t0004g0053 | 3 | HG02280.hp2 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.309+334C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061231 | ||||||
chr4:52061315
|
T | G | 1 | a0002c0002t0001g0158 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.309+418T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061315 | ||||||
chr4:52061487
|
A | AAAT | 10 | a0001c0001t0002g0032a0001c0001t0003g0028a0001c0001t0003g0123others(7): Show | 13 | HG00099.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.309+623_309+625dup others(3): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | |||||
chr4:52061487
|
A | AAATAAT | 57 | a0001c0001t0002g0166a0001c0001t0002g0183a0001c0001t0002g0184others(54): Show | 72 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.309+620_309+625dup others(6): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | |||||
chr4:52061487
|
A | AAATAATA others(2): Show |
21 | a0001c0001t0001g0129a0001c0001t0003g0029a0001c0001t0003g0030others(18): Show | 28 | HG01257.hp1 HG01258.hp1 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.309+617_309+625dup others(9): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | |||||
chr4:52061487
|
A | AAATAATA others(5): Show |
22 | a0001c0001t0003g0006a0001c0001t0003g0031a0001c0001t0003g0130others(19): Show | 26 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.309+614_309+625dup others(12): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | |||||
chr4:52061487
|
A | AAATAATA others(8): Show |
11 | a0001c0001t0002g0142a0001c0001t0003g0038a0001c0001t0003g0143others(8): Show | 11 | HG01978.hp1 HG01993.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.309+611_309+625dup others(15): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | |||||
chr4:52061487
|
AAAT | A | 95 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(92): Show | 141 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.309+623_309+625del others(3): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | |||||
chr4:52061487
|
AAATAAT | A | 4 | a0001c0001t0002g0045a0001c0001t0002g0151a0001c0001t0004g0219others(1): Show | 4 | HG02258.hp2 HG03098.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.309+620_309+625del others(6): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52061487 | |||||
chr4:52061645
|
A | G | 5 | a0002c0002t0001g0015a0002c0002t0001g0194a0002c0002t0001g0196others(2): Show | 6 | HG02027.hp1 NA18943.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-575A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061645 | ||||||
chr4:52061895
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.310-325A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | chr4 | 52061895 | ||||||
chr4:52062186
|
GT | G | 192 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(189): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.310-16delT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52062186 | |||||
chr4:52062186
|
GTT | G | 7 | a0001c0001t0003g0125a0001c0001t0003g0130a0001c0001t0004g0055others(4): Show | 7 | HG00323.hp1 HG01433.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-17_310-16delTT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 52062186 | |||||
chr4:52062431
|
G | A | 1 | a0001c0001t0003g0154 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.422+99G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062431 | ||||||
chr4:52062469
|
T | C | 1 | a0001c0001t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.422+137T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062469 | ||||||
chr4:52062479
|
T | A | 1 | a0001c0001t0004g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.422+147T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062479 | ||||||
chr4:52062568
|
A | G | 2 | a0001c0001t0004g0122a0001c0001t0015g0121 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.422+236A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062568 | ||||||
chr4:52062698
|
GGAAA | G | 3 | a0002c0002t0001g0158a0002c0002t0001g0162a0002c0002t0001g0192 | 3 | HG01433.hp1 HG02273.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.422+370_422+373del others(4): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 52062698 | |||||
chr4:52062724
|
C | G | 1 | a0002c0002t0001g0191 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.422+392C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062724 | ||||||
chr4:52062813
|
T | A | 82 | a0001c0001t0002g0032a0001c0001t0002g0166a0001c0001t0002g0183others(79): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.422+481T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062813 | ||||||
chr4:52062986
|
C | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0099 | 5 | HG00597.hp2 NA18970.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+654C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52062986 | ||||||
chr4:52063006
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.422+674G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063006 | ||||||
chr4:52063155
|
T | A | 2 | a0001c0001t0019g0218a0001c0001t0020g0221 | 2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.422+823T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063155 | ||||||
chr4:52063156
|
A | T | 4 | a0001c0001t0003g0030a0001c0001t0003g0154a0002c0002t0001g0189others(1): Show | 5 | HG02280.hp1 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+824A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063156 | ||||||
chr4:52063317
|
A | G | 1 | a0001c0001t0003g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.422+985A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063317 | ||||||
chr4:52063386
|
A | G | 1 | a0001c0001t0003g0141 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.422+1054A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063386 | ||||||
chr4:52063408
|
C | G | 35 | a0001c0001t0001g0129a0001c0001t0002g0142a0001c0001t0003g0006others(32): Show | 42 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.422+1076C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063408 | ||||||
chr4:52063598
|
C | T | 1 | a0001c0011t0004g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.422+1266C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063598 | ||||||
chr4:52063655
|
C | A | 1 | a0001c0001t0004g0150 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.422+1323C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063655 | ||||||
chr4:52063819
|
G | C | 1 | a0002c0002t0001g0046 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.422+1487G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52063819 | ||||||
chr4:52064183
|
C | CTA | 16 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0039others(13): Show | 18 | HG00673.hp2 HG02258.hp2 HG03098.hp1 others(15): Show |
intron_variant | MODIFIER | c.422+1871_422+1872d others(4): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 52064183 | |||||
chr4:52064183
|
C | CTATA | 88 | a0001c0001t0001g0129a0001c0001t0002g0032a0001c0001t0002g0142others(85): Show | 111 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.422+1869_422+1872d others(6): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 52064183 | |||||
chr4:52064183
|
C | CTATATA | 27 | a0001c0001t0002g0166a0001c0001t0004g0122a0001c0001t0015g0121others(24): Show | 35 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.422+1867_422+1872d others(8): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 52064183 | |||||
chr4:52064248
|
G | A | 3 | a0003c0005t0001g0118a0003c0005t0004g0120a0003c0005t0017g0119 | 3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.422+1916G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064248 | ||||||
chr4:52064354
|
T | C | 7 | a0001c0001t0003g0168a0002c0002t0001g0035a0002c0002t0001g0159others(4): Show | 8 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.422+2022T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064354 | ||||||
chr4:52064381
|
G | A | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.422+2049G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064381 | ||||||
chr4:52064383
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.422+2051G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064383 | ||||||
chr4:52064476
|
C | G | 3 | a0001c0001t0019g0218a0001c0001t0020g0221a0001c0001t0021g0217 | 3 | HG01884.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.422+2144C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064476 | ||||||
chr4:52064504
|
C | G | 1 | a0002c0002t0001g0046 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.422+2172C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064504 | ||||||
chr4:52064507
|
A | G | 75 | a0001c0001t0002g0032a0001c0001t0002g0166a0001c0001t0002g0183others(72): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.422+2175A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064507 | ||||||
chr4:52064581
|
T | C | 1 | a0001c0001t0003g0126 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.422+2249T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064581 | ||||||
chr4:52064679
|
G | T | 1 | a0001c0001t0004g0109 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.422+2347G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064679 | ||||||
chr4:52064696
|
G | T | 1 | a0002c0002t0001g0200 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.422+2364G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064696 | ||||||
chr4:52064822
|
T | A | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.422+2490T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064822 | ||||||
chr4:52064897
|
A | G | 1 | a0002c0002t0008g0187 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.422+2565A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064897 | ||||||
chr4:52064974
|
A | G | 7 | a0001c0001t0004g0026a0001c0001t0004g0094a0001c0001t0004g0095others(4): Show | 8 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.422+2642A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064974 | ||||||
chr4:52064996
|
A | T | 1 | a0001c0001t0002g0093 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.422+2664A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52064996 | ||||||
chr4:52065006
|
G | C | 1 | a0002c0002t0001g0170 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.422+2674G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065006 | ||||||
chr4:52065048
|
T | C | 1 | a0002c0002t0001g0198 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.422+2716T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065048 | ||||||
chr4:52065142
|
T | G | 1 | a0001c0003t0003g0051 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.422+2810T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065142 | ||||||
chr4:52065345
|
T | G | 1 | a0001c0001t0002g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.422+3013T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065345 | ||||||
chr4:52065408
|
C | T | 1 | a0001c0001t0012g0144 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.422+3076C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065408 | ||||||
chr4:52065857
|
A | G | 1 | a0001c0001t0003g0123 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.422+3525A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065857 | ||||||
chr4:52065893
|
T | C | 1 | a0002c0002t0002g0171 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.422+3561T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52065893 | ||||||
chr4:52066119
|
A | G | 4 | a0003c0005t0001g0118a0003c0005t0004g0120a0003c0005t0017g0119others(1): Show | 4 | HG02258.hp1 HG03540.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-3702A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066119 | ||||||
chr4:52066224
|
C | T | 1 | a0001c0001t0002g0093 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.423-3597C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066224 | ||||||
chr4:52066300
|
G | A | 1 | a0001c0001t0004g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.423-3521G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066300 | ||||||
chr4:52066524
|
G | A | 3 | a0003c0005t0001g0118a0003c0005t0004g0120a0003c0005t0017g0119 | 3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.423-3297G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066524 | ||||||
chr4:52066659
|
C | T | 122 | a0001c0001t0001g0129a0001c0001t0002g0032a0001c0001t0002g0142others(119): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.423-3162C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066659 | ||||||
chr4:52066813
|
C | T | 127 | a0001c0001t0001g0129a0001c0001t0002g0032a0001c0001t0002g0142others(124): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.423-3008C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066813 | ||||||
chr4:52066990
|
T | A | 1 | a0001c0001t0015g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.423-2831T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52066990 | ||||||
chr4:52067049
|
G | A | 1 | a0001c0001t0002g0010 | 3 | NA19009.hp2 NA19063.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.423-2772G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067049 | ||||||
chr4:52067130
|
G | T | 1 | a0001c0003t0003g0051 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.423-2691G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067130 | ||||||
chr4:52067151
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.423-2670C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067151 | ||||||
chr4:52067238
|
T | A | 2 | a0002c0002t0001g0172a0002c0002t0001g0190 | 2 | HG00738.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.423-2583T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067238 | ||||||
chr4:52067332
|
AT | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0099 | 5 | HG00597.hp2 NA18970.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.423-2483delT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 52067332 | |||||
chr4:52067354
|
T | G | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.423-2467T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067354 | ||||||
chr4:52067453
|
C | A | 1 | a0004c0004t0001g0195 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.423-2368C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067453 | ||||||
chr4:52067608
|
C | T | 1 | a0001c0011t0004g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.423-2213C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067608 | ||||||
chr4:52067644
|
C | T | 1 | a0002c0002t0001g0169 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.423-2177C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067644 | ||||||
chr4:52067701
|
T | C | 1 | a0001c0001t0002g0142 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.423-2120T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067701 | ||||||
chr4:52067742
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.423-2079T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067742 | ||||||
chr4:52067881
|
G | A | 1 | a0002c0002t0001g0201 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.423-1940G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067881 | ||||||
chr4:52067977
|
A | G | 1 | a0002c0002t0001g0186 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.423-1844A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52067977 | ||||||
chr4:52068396
|
A | G | 1 | a0010c0008t0014g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.423-1425A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52068396 | ||||||
chr4:52068802
|
T | G | 1 | a0001c0001t0002g0066 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.423-1019T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52068802 | ||||||
chr4:52069174
|
T | A | 1 | a0001c0001t0002g0099 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.423-647T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069174 | ||||||
chr4:52069279
|
A | T | 77 | a0001c0001t0002g0032a0001c0001t0002g0166a0001c0001t0002g0183others(74): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.423-542A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069279 | ||||||
chr4:52069289
|
C | T | 3 | a0003c0005t0001g0118a0003c0005t0004g0120a0003c0005t0017g0119 | 3 | HG03540.hp2 HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.423-532C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069289 | ||||||
chr4:52069349
|
G | A | 1 | a0010c0008t0014g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.423-472G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069349 | ||||||
chr4:52069481
|
G | C | 1 | a0002c0002t0001g0173 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.423-340G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069481 | ||||||
chr4:52069486
|
T | A | 1 | a0002c0002t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.423-335T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069486 | ||||||
chr4:52069515
|
A | G | 127 | a0001c0001t0001g0129a0001c0001t0002g0032a0001c0001t0002g0142others(124): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.423-306A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069515 | ||||||
chr4:52069645
|
A | G | 1 | a0001c0001t0004g0108 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.423-176A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069645 | ||||||
chr4:52069652
|
C | G | 1 | a0002c0002t0001g0157 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.423-169C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069652 | ||||||
chr4:52069679
|
T | C | 2 | a0001c0001t0004g0100a0001c0001t0004g0109 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.423-142T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 4/12 | chr4 | 52069679 | ||||||
chr4:52070040
|
TTA | T | 60 | a0001c0001t0001g0129a0001c0001t0002g0152a0001c0001t0003g0002others(57): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.518+140_518+141del others(2): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 52070040 | |||||
chr4:52070046
|
A | G | 8 | a0001c0001t0003g0002a0001c0001t0003g0090a0001c0001t0003g0092others(5): Show | 17 | HG00597.hp1 HG02074.hp1 NA18945.hp2 others(14): Show |
intron_variant | MODIFIER | c.518+130A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070046 | ||||||
chr4:52070158
|
G | A | 7 | a0001c0001t0004g0026a0001c0001t0004g0094a0001c0001t0004g0095others(4): Show | 8 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.518+242G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070158 | ||||||
chr4:52070243
|
T | A | 1 | a0001c0001t0003g0107 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.518+327T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070243 | ||||||
chr4:52070323
|
G | A | 1 | a0001c0001t0007g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.518+407G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070323 | ||||||
chr4:52070397
|
G | A | 1 | a0001c0001t0004g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.518+481G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070397 | ||||||
chr4:52070419
|
A | C | 122 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(119): Show | 165 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.518+503A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070419 | ||||||
chr4:52070472
|
T | A | 1 | a0001c0001t0002g0142 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.518+556T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070472 | ||||||
chr4:52070534
|
T | G | 2 | a0006c0006t0003g0132a0006c0006t0003g0133 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.518+618T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070534 | ||||||
chr4:52070535
|
G | A | 3 | a0001c0001t0005g0011a0001c0001t0005g0134a0001c0001t0021g0217 | 5 | HG01884.hp2 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.518+619G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070535 | ||||||
chr4:52070540
|
A | G | 50 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(47): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.518+624A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070540 | ||||||
chr4:52070545
|
G | T | 49 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(46): Show | 65 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.518+629G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070545 | ||||||
chr4:52070561
|
C | T | 1 | a0001c0001t0003g0145 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.518+645C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070561 | ||||||
chr4:52070562
|
A | T | 49 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(46): Show | 64 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.518+646A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070562 | ||||||
chr4:52070578
|
A | T | 1 | a0003c0005t0017g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.518+662A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070578 | ||||||
chr4:52070699
|
A | G | 7 | a0001c0001t0004g0026a0001c0001t0004g0094a0001c0001t0004g0095others(4): Show | 8 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.518+783A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070699 | ||||||
chr4:52070758
|
T | A | 107 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(104): Show | 148 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.518+842T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070758 | ||||||
chr4:52070880
|
TG | T | 25 | a0001c0001t0002g0022a0001c0001t0002g0056a0001c0001t0002g0070others(22): Show | 31 | HG00673.hp2 HG01243.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.518+975delG | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 52070880 | |||||
chr4:52070880
|
TGG | T | 110 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(107): Show | 151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.518+974_518+975del others(2): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 52070880 | |||||
chr4:52070933
|
C | A | 12 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0094others(9): Show | 14 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.519-984C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52070933 | ||||||
chr4:52071006
|
T | C | 3 | a0002c0002t0001g0015a0004c0004t0001g0015a0004c0004t0001g0195 | 4 | NA18943.hp2 NA18964.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.519-911T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071006 | ||||||
chr4:52071010
|
A | G | 1 | a0002c0002t0001g0186 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.519-907A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071010 | ||||||
chr4:52071054
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.519-863A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071054 | ||||||
chr4:52071061
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.519-856A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071061 | ||||||
chr4:52071213
|
T | G | 2 | a0001c0001t0004g0027a0001c0001t0004g0116 | 3 | HG02486.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.519-704T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071213 | ||||||
chr4:52071630
|
A | G | 1 | a0010c0008t0014g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.519-287A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071630 | ||||||
chr4:52071768
|
T | G | 1 | a0002c0002t0001g0204 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.519-149T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 5/12 | chr4 | 52071768 | ||||||
chr4:52072216
|
G | T | 2 | a0002c0002t0001g0172a0002c0002t0001g0190 | 2 | HG00738.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.758+60G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072216 | ||||||
chr4:52072217
|
G | A | 2 | a0001c0001t0004g0027a0001c0001t0004g0116 | 3 | HG02486.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.758+61G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072217 | ||||||
chr4:52072445
|
C | T | 3 | a0001c0001t0003g0082a0001c0001t0003g0089a0001c0001t0003g0106 | 3 | HG02738.hp1 HG03017.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.758+289C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072445 | ||||||
chr4:52072596
|
C | T | 1 | a0001c0001t0003g0138 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.758+440C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072596 | ||||||
chr4:52072617
|
G | C | 1 | a0002c0002t0001g0044 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.758+461G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072617 | ||||||
chr4:52072625
|
C | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0070a0001c0001t0002g0081 | 4 | NA18961.hp2 NA18974.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.758+469C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072625 | ||||||
chr4:52072802
|
C | A | 1 | a0001c0001t0002g0183 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.758+646C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072802 | ||||||
chr4:52072889
|
G | A | 1 | a0001c0001t0003g0052 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.758+733G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52072889 | ||||||
chr4:52073298
|
C | T | 1 | a0002c0002t0001g0181 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.758+1142C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073298 | ||||||
chr4:52073374
|
C | T | 1 | a0010c0008t0014g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.758+1218C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073374 | ||||||
chr4:52073556
|
G | A | 51 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(48): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.758+1400G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073556 | ||||||
chr4:52073583
|
G | A | 3 | a0001c0001t0003g0084a0001c0001t0003g0085a0001c0001t0003g0086 | 3 | HG00558.hp2 HG00673.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.758+1427G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073583 | ||||||
chr4:52073624
|
T | G | 3 | a0001c0001t0005g0011a0001c0001t0005g0134a0001c0001t0021g0217 | 5 | HG01884.hp2 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.758+1468T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073624 | ||||||
chr4:52073655
|
T | G | 3 | a0001c0001t0002g0152a0001c0001t0004g0219a0001c0001t0004g0220 | 3 | HG02258.hp2 HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.758+1499T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073655 | ||||||
chr4:52073816
|
G | C | 16 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0010others(13): Show | 27 | HG00597.hp2 HG00673.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.758+1660G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073816 | ||||||
chr4:52073816
|
G | T | 1 | a0001c0001t0002g0080 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.758+1660G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073816 | ||||||
chr4:52073986
|
C | T | 51 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(48): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.758+1830C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52073986 | ||||||
chr4:52074041
|
C | T | 12 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0094others(9): Show | 14 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.758+1885C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074041 | ||||||
chr4:52074339
|
T | C | 1 | a0001c0001t0004g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.758+2183T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074339 | ||||||
chr4:52074399
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.758+2243C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074399 | ||||||
chr4:52074459
|
C | T | 1 | a0001c0001t0003g0125 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.758+2303C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074459 | ||||||
chr4:52074460
|
G | A | 73 | a0001c0001t0002g0020a0001c0001t0002g0060a0001c0001t0002g0065others(70): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.758+2304G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074460 | ||||||
chr4:52074480
|
A | G | 3 | a0001c0001t0005g0011a0001c0001t0005g0134a0001c0001t0021g0217 | 5 | HG01884.hp2 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.759-2299A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074480 | ||||||
chr4:52074536
|
T | C | 5 | a0001c0001t0004g0017a0001c0001t0004g0047a0001c0001t0004g0048others(2): Show | 6 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.759-2243T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074536 | ||||||
chr4:52074558
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.759-2221A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074558 | ||||||
chr4:52074572
|
G | C | 1 | a0001c0001t0003g0168 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.759-2207G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074572 | ||||||
chr4:52074607
|
A | T | 46 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(43): Show | 62 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.759-2172A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074607 | ||||||
chr4:52074684
|
G | C | 7 | a0001c0001t0002g0004a0001c0001t0002g0022a0001c0001t0002g0070others(4): Show | 14 | NA18612.hp2 NA18961.hp2 NA18968.hp2 others(11): Show |
intron_variant | MODIFIER | c.759-2095G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52074684 | ||||||
chr4:52075020
|
G | A | 1 | a0001c0001t0003g0136 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.759-1759G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52075020 | ||||||
chr4:52075101
|
G | T | 1 | a0001c0001t0002g0025 | 2 | NA19012.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.759-1678G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52075101 | ||||||
chr4:52075639
|
C | T | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.759-1140C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52075639 | ||||||
chr4:52075897
|
A | G | 201 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.759-882A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52075897 | ||||||
chr4:52076021
|
A | G | 52 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(49): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.759-758A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076021 | ||||||
chr4:52076100
|
C | T | 55 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(52): Show | 80 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.759-679C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076100 | ||||||
chr4:52076117
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.759-662T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076117 | ||||||
chr4:52076208
|
C | T | 201 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.759-571C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076208 | ||||||
chr4:52076239
|
A | T | 131 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(128): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.759-540A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076239 | ||||||
chr4:52076392
|
T | C | 11 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0094others(8): Show | 13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.759-387T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076392 | ||||||
chr4:52076613
|
G | T | 79 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0009others(76): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.759-166G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 6/12 | chr4 | 52076613 | ||||||
chr4:52077132
|
T | A | 1 | a0001c0001t0003g0139 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1020+92T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077132 | ||||||
chr4:52077174
|
T | G | 1 | a0001c0001t0003g0126 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1020+134T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077174 | ||||||
chr4:52077244
|
TTCCCTCC others(1): Show |
T | 50 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(47): Show | 66 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1020+212_1020+219d others(10): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52077244 | |||||
chr4:52077244
|
TTCCCTCC others(5): Show |
T | 1 | a0001c0001t0003g0092 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1020+212_1020+223d others(14): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52077244 | |||||
chr4:52077341
|
T | TCTCTTTC others(5): Show |
3 | a0002c0002t0001g0167a0002c0002t0001g0209a0002c0002t0001g0213 | 3 | HG01081.hp1 HG01168.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1020+306_1020+317d others(14): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52077341 | |||||
chr4:52077348
|
C | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0070 | 3 | NA18961.hp2 NA18974.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1020+308C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077348 | ||||||
chr4:52077415
|
CCTCT | C | 80 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0009others(77): Show | 104 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1020+381_1020+384d others(6): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52077415 | |||||
chr4:52077422
|
CTCCT | C | 3 | a0001c0001t0002g0050a0001c0001t0004g0219a0001c0001t0004g0220 | 3 | HG02258.hp2 HG03098.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1020+398_1020+401d others(6): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52077422 | |||||
chr4:52077572
|
G | A | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1020+532G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077572 | ||||||
chr4:52077687
|
G | A | 1 | a0001c0001t0004g0024 | 2 | HG01167.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1020+647G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077687 | ||||||
chr4:52077794
|
C | T | 51 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(48): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1020+754C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52077794 | ||||||
chr4:52078108
|
T | TA | 85 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(82): Show | 119 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.1021-614dupA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52078108 | |||||
chr4:52078108
|
TA | T | 128 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(125): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1021-614delA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 52078108 | |||||
chr4:52078143
|
A | C | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1021-592A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078143 | ||||||
chr4:52078173
|
C | A | 2 | a0002c0002t0001g0046a0002c0002t0001g0199 | 2 | HG02074.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1021-562C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078173 | ||||||
chr4:52078277
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1021-458G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078277 | ||||||
chr4:52078478
|
T | A | 52 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(49): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1021-257T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078478 | ||||||
chr4:52078554
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1021-181T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078554 | ||||||
chr4:52078664
|
C | A | 2 | a0003c0005t0004g0120a0003c0005t0017g0119 | 2 | HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1021-71C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078664 | ||||||
chr4:52078721
|
A | G | 1 | a0001c0001t0002g0045 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1021-14A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 7/12 | chr4 | 52078721 | ||||||
chr4:52078975
|
C | T | 1 | a0002c0002t0001g0205 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1179+82C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52078975 | ||||||
chr4:52078998
|
G | A | 2 | a0001c0001t0003g0028a0001c0001t0003g0123 | 3 | NA18954.hp2 NA18962.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1179+105G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52078998 | ||||||
chr4:52079041
|
G | A | 79 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0009others(76): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1179+148G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079041 | ||||||
chr4:52079084
|
G | A | 2 | a0002c0002t0001g0174a0002c0002t0001g0181 | 2 | NA18951.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1179+191G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079084 | ||||||
chr4:52079603
|
G | A | 1 | a0010c0008t0014g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1180-141G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079603 | ||||||
chr4:52079633
|
C | T | 204 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(201): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1180-111C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079633 | ||||||
chr4:52079652
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1180-92T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079652 | ||||||
chr4:52079732
|
T | C | 1 | a0002c0002t0001g0175 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1180-12T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 8/12 | chr4 | 52079732 | ||||||
chr4:52079995
|
A | G | 201 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1355+76A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52079995 | ||||||
chr4:52080005
|
C | CAA | 7 | a0002c0002t0001g0033a0002c0002t0001g0149a0002c0002t0001g0163others(4): Show | 7 | HG00438.hp2 HG00609.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1355+86_1355+87ins others(2): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080005 | ||||||
chr4:52080007
|
C | T | 7 | a0002c0002t0001g0033a0002c0002t0001g0149a0002c0002t0001g0163others(4): Show | 7 | HG00438.hp2 HG00609.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1355+88C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080007 | ||||||
chr4:52080009
|
G | A | 7 | a0002c0002t0001g0033a0002c0002t0001g0149a0002c0002t0001g0163others(4): Show | 7 | HG00438.hp2 HG00609.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1355+90G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080009 | ||||||
chr4:52080109
|
C | G | 6 | a0002c0002t0001g0016a0002c0002t0001g0040a0002c0002t0001g0041others(3): Show | 7 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1355+190C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080109 | ||||||
chr4:52080243
|
A | G | 3 | a0001c0001t0003g0084a0001c0001t0003g0085a0001c0001t0003g0086 | 3 | HG00558.hp2 HG00673.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1355+324A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080243 | ||||||
chr4:52080398
|
C | G | 1 | a0002c0002t0001g0179 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1355+479C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080398 | ||||||
chr4:52080405
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1355+486T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080405 | ||||||
chr4:52080432
|
G | A | 9 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0094others(6): Show | 11 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1355+513G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080432 | ||||||
chr4:52080467
|
G | T | 1 | a0001c0001t0007g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1355+548G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080467 | ||||||
chr4:52080479
|
C | T | 56 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 81 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1355+560C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080479 | ||||||
chr4:52080523
|
G | T | 1 | a0001c0001t0002g0059 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1355+604G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080523 | ||||||
chr4:52080593
|
C | G | 1 | a0001c0001t0003g0086 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1355+674C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080593 | ||||||
chr4:52080679
|
C | T | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1355+760C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080679 | ||||||
chr4:52080772
|
G | T | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1355+853G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080772 | ||||||
chr4:52080990
|
T | C | 4 | a0001c0001t0002g0063a0001c0001t0002g0073a0001c0001t0002g0079others(1): Show | 4 | HG02071.hp1 NA18974.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1355+1071T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52080990 | ||||||
chr4:52081029
|
T | A | 1 | a0002c0002t0001g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1355+1110T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081029 | ||||||
chr4:52081325
|
T | G | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1356-1062T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081325 | ||||||
chr4:52081541
|
T | C | 200 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(197): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1356-846T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081541 | ||||||
chr4:52081542
|
G | A | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1356-845G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081542 | ||||||
chr4:52081649
|
A | G | 1 | a0001c0001t0003g0143 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1356-738A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081649 | ||||||
chr4:52081825
|
A | G | 1 | a0001c0001t0009g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1356-562A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081825 | ||||||
chr4:52081827
|
C | CT | 79 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0009others(76): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1356-550dupT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 52081827 | |||||
chr4:52081851
|
A | G | 1 | a0001c0001t0003g0031 | 2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1356-536A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081851 | ||||||
chr4:52081883
|
C | G | 1 | a0001c0001t0003g0124 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1356-504C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081883 | ||||||
chr4:52081945
|
G | GGTTTCTA others(141): Show |
79 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0009others(76): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1356-436_1356-435i others(150): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 52081945 | |||||
chr4:52081945
|
G | GGTTTCTG others(141): Show |
53 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(50): Show | 77 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1356-408_1356-407i others(150): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 52081945 | |||||
chr4:52081945
|
G | GGTTTCTG others(141): Show |
67 | a0001c0001t0001g0129a0001c0001t0002g0152a0001c0001t0003g0002others(64): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1356-295_1356-294i others(150): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 52081945 | |||||
chr4:52081980
|
T | G | 3 | a0001c0001t0002g0032a0001c0001t0002g0059a0001c0001t0002g0184 | 3 | HG02129.hp2 HG04184.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1356-407T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52081980 | ||||||
chr4:52082043
|
A | ATTTTGTC others(141): Show |
3 | a0001c0001t0002g0032a0001c0001t0002g0059a0001c0001t0002g0184 | 3 | HG02129.hp2 HG04184.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1356-295_1356-294i others(150): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 52082043 | |||||
chr4:52082043
|
A | G | 1 | a0001c0001t0002g0032 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1356-344A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52082043 | ||||||
chr4:52082072
|
T | G | 1 | a0002c0002t0001g0158 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1356-315T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52082072 | ||||||
chr4:52082180
|
C | T | 1 | a0001c0001t0004g0097 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1356-207C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 9/12 | chr4 | 52082180 | ||||||
chr4:52082668
|
C | G | 52 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(49): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1479+158C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082668 | ||||||
chr4:52082827
|
G | A | 1 | a0001c0001t0004g0103 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1479+317G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082827 | ||||||
chr4:52082846
|
A | T | 51 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(48): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1479+336A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082846 | ||||||
chr4:52082857
|
A | T | 1 | a0006c0006t0003g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1479+347A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082857 | ||||||
chr4:52082874
|
G | A | 2 | a0003c0005t0004g0120a0003c0005t0017g0119 | 2 | HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1479+364G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082874 | ||||||
chr4:52082896
|
G | A | 201 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1479+386G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52082896 | ||||||
chr4:52083083
|
G | C | 1 | a0003c0005t0004g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1479+573G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083083 | ||||||
chr4:52083093
|
TAAA | T | 212 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(209): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1479+589_1479+591d others(5): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 52083093 | |||||
chr4:52083137
|
G | A | 2 | a0003c0005t0004g0120a0003c0005t0017g0119 | 2 | HG03669.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1479+627G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083137 | ||||||
chr4:52083343
|
A | C | 11 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0094others(8): Show | 13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1479+833A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083343 | ||||||
chr4:52083489
|
C | A | 2 | a0001c0001t0004g0122a0001c0001t0015g0121 | 2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1479+979C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083489 | ||||||
chr4:52083515
|
C | T | 1 | a0002c0002t0001g0214 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1479+1005C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083515 | ||||||
chr4:52083572
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1479+1062T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083572 | ||||||
chr4:52083708
|
C | T | 52 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(49): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1479+1198C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083708 | ||||||
chr4:52083739
|
G | T | 1 | a0001c0001t0004g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1480-1177G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083739 | ||||||
chr4:52083741
|
C | CT | 7 | a0001c0001t0002g0058a0001c0001t0002g0093a0001c0001t0002g0105others(4): Show | 9 | HG01884.hp2 HG01981.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1480-1157dupT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 52083741 | |||||
chr4:52083741
|
CT | C | 83 | a0001c0001t0002g0023a0001c0001t0002g0057a0001c0001t0002g0061others(80): Show | 108 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1480-1157delT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 52083741 | |||||
chr4:52083825
|
C | G | 44 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(41): Show | 60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1480-1091C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083825 | ||||||
chr4:52083843
|
C | T | 52 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(49): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1480-1073C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52083843 | ||||||
chr4:52084009
|
G | A | 52 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(49): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1480-907G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084009 | ||||||
chr4:52084050
|
CA | C | 187 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(184): Show | 252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1480-851delA | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 52084050 | |||||
chr4:52084094
|
G | A | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1480-822G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084094 | ||||||
chr4:52084146
|
C | T | 55 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(52): Show | 80 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1480-770C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084146 | ||||||
chr4:52084153
|
A | G | 1 | a0001c0001t0020g0221 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1480-763A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084153 | ||||||
chr4:52084243
|
A | G | 1 | a0001c0001t0020g0221 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1480-673A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084243 | ||||||
chr4:52084494
|
A | C | 79 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0009others(76): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1480-422A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084494 | ||||||
chr4:52084706
|
G | A | 2 | a0001c0001t0007g0083a0001c0001t0007g0088 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1480-210G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084706 | ||||||
chr4:52084801
|
C | A | 1 | a0002c0002t0001g0067 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1480-115C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 10/12 | chr4 | 52084801 | ||||||
chr4:52085047
|
CT | C | 87 | a0001c0001t0002g0152a0001c0001t0004g0026a0001c0001t0004g0027others(84): Show | 113 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1563+62delT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 52085047 | |||||
chr4:52085047
|
CTT | C | 110 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(107): Show | 151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1563+61_1563+62del others(2): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 52085047 | |||||
chr4:52085236
|
A | G | 1 | a0001c0001t0004g0069 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1563+237A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085236 | ||||||
chr4:52085525
|
A | G | 1 | a0001c0001t0002g0114 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1563+526A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085525 | ||||||
chr4:52085546
|
A | T | 1 | a0010c0008t0014g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1563+547A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085546 | ||||||
chr4:52085690
|
T | A | 51 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(48): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1563+691T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085690 | ||||||
chr4:52085790
|
T | A | 4 | a0001c0001t0002g0019a0001c0001t0002g0056a0001c0001t0002g0057others(1): Show | 5 | HG00673.hp2 NA18951.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.1563+791T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085790 | ||||||
chr4:52085920
|
G | C | 133 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(130): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1563+921G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52085920 | ||||||
chr4:52086026
|
T | C | 1 | a0002c0002t0001g0054 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1563+1027T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086026 | ||||||
chr4:52086027
|
G | A | 11 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0094others(8): Show | 13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1563+1028G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086027 | ||||||
chr4:52086185
|
A | G | 79 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0009others(76): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1563+1186A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086185 | ||||||
chr4:52086312
|
A | G | 1 | a0001c0001t0003g0168 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1563+1313A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086312 | ||||||
chr4:52086319
|
T | A | 52 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(49): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1563+1320T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086319 | ||||||
chr4:52086369
|
C | T | 55 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(52): Show | 80 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1563+1370C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086369 | ||||||
chr4:52086375
|
C | T | 1 | a0001c0001t0019g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1563+1376C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086375 | ||||||
chr4:52086520
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1563+1521G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086520 | ||||||
chr4:52086747
|
G | A | 1 | a0010c0008t0014g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1563+1748G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52086747 | ||||||
chr4:52087072
|
A | G | 201 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1563+2073A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087072 | ||||||
chr4:52087076
|
C | T | 1 | a0001c0001t0004g0122 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1563+2077C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087076 | ||||||
chr4:52087259
|
C | T | 1 | a0001c0001t0002g0071 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1563+2260C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087259 | ||||||
chr4:52087326
|
C | T | 1 | a0003c0005t0004g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1563+2327C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087326 | ||||||
chr4:52087406
|
C | T | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1563+2407C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087406 | ||||||
chr4:52087451
|
T | A | 1 | a0001c0001t0012g0144 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1563+2452T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087451 | ||||||
chr4:52087588
|
G | A | 1 | a0001c0001t0004g0122 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1563+2589G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087588 | ||||||
chr4:52087682
|
A | G | 3 | a0001c0001t0003g0084a0001c0001t0003g0085a0001c0001t0003g0086 | 3 | HG00558.hp2 HG00673.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1563+2683A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087682 | ||||||
chr4:52087786
|
G | GT | 13 | a0001c0001t0003g0002a0001c0001t0003g0052a0001c0001t0003g0082others(10): Show | 22 | HG00597.hp1 HG02738.hp1 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.1563+2793dupT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 52087786 | |||||
chr4:52087834
|
G | A | 52 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(49): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1563+2835G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087834 | ||||||
chr4:52087900
|
G | A | 1 | a0002c0002t0001g0179 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1563+2901G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087900 | ||||||
chr4:52087932
|
T | G | 11 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0094others(8): Show | 13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1563+2933T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087932 | ||||||
chr4:52087962
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1563+2963C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087962 | ||||||
chr4:52087975
|
G | A | 1 | a0002c0002t0001g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1563+2976G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52087975 | ||||||
chr4:52088098
|
T | C | 1 | a0001c0001t0004g0101 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1563+3099T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088098 | ||||||
chr4:52088183
|
C | G | 131 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(128): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1563+3184C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088183 | ||||||
chr4:52088203
|
C | A | 11 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0094others(8): Show | 13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1563+3204C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088203 | ||||||
chr4:52088350
|
G | A | 6 | a0002c0002t0001g0016a0002c0002t0001g0040a0002c0002t0001g0041others(3): Show | 7 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1563+3351G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088350 | ||||||
chr4:52088488
|
C | G | 131 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(128): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1563+3489C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088488 | ||||||
chr4:52088493
|
G | T | 131 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(128): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1563+3494G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088493 | ||||||
chr4:52088663
|
G | A | 57 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(54): Show | 82 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1563+3664G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088663 | ||||||
chr4:52088678
|
G | T | 1 | a0001c0001t0004g0122 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1563+3679G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088678 | ||||||
chr4:52088682
|
G | A | 1 | a0002c0002t0001g0174 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1563+3683G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088682 | ||||||
chr4:52088689
|
T | G | 56 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 81 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1563+3690T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088689 | ||||||
chr4:52088768
|
T | A | 63 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(60): Show | 81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1563+3769T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52088768 | ||||||
chr4:52089132
|
CT | C | 3 | a0001c0001t0005g0011a0001c0001t0005g0134a0001c0001t0021g0217 | 5 | HG01884.hp2 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1563+4134delT | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089132 | ||||||
chr4:52089179
|
C | G | 1 | a0001c0001t0011g0117 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1563+4180C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089179 | ||||||
chr4:52089603
|
T | G | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1563+4604T>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089603 | ||||||
chr4:52089813
|
C | G | 201 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1564-4714C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089813 | ||||||
chr4:52089900
|
A | G | 80 | a0001c0001t0001g0129a0002c0002t0001g0001a0002c0002t0001g0007others(77): Show | 104 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1564-4627A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089900 | ||||||
chr4:52089968
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1564-4559T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52089968 | ||||||
chr4:52090058
|
C | G | 1 | a0004c0004t0001g0195 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1564-4469C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090058 | ||||||
chr4:52090274
|
G | A | 1 | a0001c0001t0003g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1564-4253G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090274 | ||||||
chr4:52090306
|
T | A | 201 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1564-4221T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090306 | ||||||
chr4:52090445
|
G | A | 1 | a0001c0001t0003g0136 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1564-4082G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090445 | ||||||
chr4:52090445
|
G | T | 138 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(135): Show | 187 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1564-4082G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090445 | ||||||
chr4:52090527
|
C | CTTCCTCT others(26): Show |
1 | a0002c0002t0001g0179 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1564-4000_1564-399 others(37): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090527 | ||||||
chr4:52090530
|
T | A | 1 | a0002c0002t0001g0179 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1564-3997T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090530 | ||||||
chr4:52090597
|
T | C | 57 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(54): Show | 82 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1564-3930T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090597 | ||||||
chr4:52090614
|
C | T | 1 | a0001c0001t0020g0221 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1564-3913C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090614 | ||||||
chr4:52090753
|
G | T | 1 | a0002c0002t0001g0178 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1564-3774G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090753 | ||||||
chr4:52090808
|
A | G | 1 | a0002c0002t0001g0209 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1564-3719A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090808 | ||||||
chr4:52090849
|
G | A | 79 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0009others(76): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1564-3678G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090849 | ||||||
chr4:52090850
|
A | T | 79 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0009others(76): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1564-3677A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52090850 | ||||||
chr4:52091159
|
A | T | 52 | a0001c0001t0001g0129a0001c0001t0003g0002a0001c0001t0003g0006others(49): Show | 68 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1564-3368A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091159 | ||||||
chr4:52091193
|
T | C | 1 | a0001c0001t0002g0076 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1564-3334T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091193 | ||||||
chr4:52091270
|
G | A | 7 | a0001c0001t0002g0020a0001c0001t0002g0023a0001c0001t0002g0025others(4): Show | 10 | HG01943.hp2 HG02004.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.1564-3257G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091270 | ||||||
chr4:52091292
|
G | A | 56 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 81 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1564-3235G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091292 | ||||||
chr4:52091548
|
G | A | 55 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(52): Show | 80 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1564-2979G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091548 | ||||||
chr4:52091580
|
TGCCTGGG others(26): Show |
T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2946_1564-291 others(37): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091580 | ||||||
chr4:52091614
|
C | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2913C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091614 | ||||||
chr4:52091616
|
A | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2911A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091616 | ||||||
chr4:52091617
|
A | ATTTTTTT others(25): Show |
1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2910_1564-290 others(36): Show |
SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091617 | ||||||
chr4:52091618
|
G | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2909G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091618 | ||||||
chr4:52091622
|
G | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2905G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091622 | ||||||
chr4:52091623
|
C | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2904C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091623 | ||||||
chr4:52091625
|
G | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2902G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091625 | ||||||
chr4:52091626
|
C | A | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2901C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091626 | ||||||
chr4:52091627
|
C | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2900C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091627 | ||||||
chr4:52091629
|
G | A | 6 | a0002c0002t0001g0016a0002c0002t0001g0040a0002c0002t0001g0041others(3): Show | 7 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1564-2898G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091629 | ||||||
chr4:52091629
|
G | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2898G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091629 | ||||||
chr4:52091632
|
C | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2895C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091632 | ||||||
chr4:52091636
|
C | A | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2891C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091636 | ||||||
chr4:52091637
|
C | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2890C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091637 | ||||||
chr4:52091639
|
C | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2888C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091639 | ||||||
chr4:52091641
|
G | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2886G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091641 | ||||||
chr4:52091642
|
G | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2885G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091642 | ||||||
chr4:52091644
|
A | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2883A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091644 | ||||||
chr4:52091645
|
G | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2882G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091645 | ||||||
chr4:52091646
|
C | T | 1 | a0001c0001t0004g0098 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-2881C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091646 | ||||||
chr4:52091712
|
C | A | 51 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0028others(48): Show | 67 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1564-2815C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091712 | ||||||
chr4:52091770
|
G | A | 7 | a0001c0001t0004g0026a0001c0001t0004g0094a0001c0001t0004g0095others(4): Show | 8 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1564-2757G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091770 | ||||||
chr4:52091772
|
A | G | 1 | a0001c0011t0004g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1564-2755A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091772 | ||||||
chr4:52091846
|
G | A | 56 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(53): Show | 81 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1564-2681G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091846 | ||||||
chr4:52091997
|
A | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0075 | 2 | HG03492.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1564-2530A>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52091997 | ||||||
chr4:52092144
|
C | T | 1 | a0002c0002t0001g0177 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1564-2383C>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092144 | ||||||
chr4:52092243
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1564-2284G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092243 | ||||||
chr4:52092291
|
A | G | 201 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1564-2236A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092291 | ||||||
chr4:52092307
|
C | A | 2 | a0001c0001t0004g0219a0001c0001t0004g0220 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1564-2220C>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092307 | ||||||
chr4:52092453
|
G | T | 2 | a0001c0001t0003g0089a0001c0001t0003g0106 | 2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1564-2074G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092453 | ||||||
chr4:52092459
|
G | A | 79 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0009others(76): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1564-2068G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092459 | ||||||
chr4:52092537
|
A | C | 1 | a0003c0005t0017g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1564-1990A>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52092537 | ||||||
chr4:52093154
|
A | G | 1 | a0002c0002t0001g0176 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1564-1373A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52093154 | ||||||
chr4:52093425
|
A | G | 1 | a0001c0001t0004g0116 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1564-1102A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52093425 | ||||||
chr4:52093551
|
G | A | 7 | a0001c0001t0004g0026a0001c0001t0004g0094a0001c0001t0004g0095others(4): Show | 8 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1564-976G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52093551 | ||||||
chr4:52093641
|
A | G | 1 | a0001c0001t0002g0070 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1564-886A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52093641 | ||||||
chr4:52093977
|
A | G | 55 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(52): Show | 80 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1564-550A>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52093977 | ||||||
chr4:52094222
|
G | A | 201 | a0001c0001t0001g0129a0001c0001t0002g0003a0001c0001t0002g0004others(198): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1564-305G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52094222 | ||||||
chr4:52094246
|
G | T | 2 | a0001c0001t0006g0013a0001c0001t0020g0221 | 4 | HG02145.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1564-281G>T | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52094246 | ||||||
chr4:52094407
|
T | C | 1 | a0001c0001t0004g0094 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1564-120T>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52094407 | ||||||
chr4:52094435
|
G | C | 11 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0094others(8): Show | 13 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1564-92G>C | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 11/12 | chr4 | 52094435 | ||||||
chr4:52094625
|
C | G | 1 | a0001c0001t0002g0060 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1609+53C>G | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 12/12 | chr4 | 52094625 | ||||||
chr4:52094742
|
T | A | 79 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0009others(76): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1610-138T>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 12/12 | chr4 | 52094742 | ||||||
chr4:52094802
|
G | A | 1 | a0001c0001t0003g0031 | 2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1610-78G>A | SPATA18 | ENSG00000163071.11 | transcript | ENST00000295213.9 | protein_coding | 12/12 | chr4 | 52094802 |