geneid | 7095 |
---|---|
ensemblid | ENSG00000008952.17 |
hgncid | 11846 |
symbol | SEC62 |
name | SEC62 homolog, preprotein translocation factor |
refseq_nuc | NM_003262.4 |
refseq_prot | NP_003253.1 |
ensembl_nuc | ENST00000337002.9 |
ensembl_prot | ENSP00000337688.4 |
mane_status | MANE Select |
chr | chr3 |
start | 169966807 |
end | 169998373 |
strand | + |
ver | v1.2 |
region | chr3:169966807-169998373 |
region5000 | chr3:169961807-170003373 |
regionname0 | SEC62_chr3_169966807_169998373 |
regionname5000 | SEC62_chr3_169961807_170003373 |
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 | 399 | 328 | 92 | 46 | 142 | 6 | 40 | 110 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0002 | 0/0 | 399 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0003 | 0/0 | 399 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
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 | 1200 | 309 | 74 | 45 | 142 | 6 | 40 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
c0002 | 0/0 | 1200 | 12 | 11 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
c0003 | 0/0 | 1200 | 7 | 7 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
c0004 | 0/0 | 1200 | 6 | 0 | 0 | 6 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
c0005 | 0/0 | 1200 | 2 | 0 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
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 | 1/1 | 5327 | 158 | 35 | 31 | 68 | 4 | 18 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0002 | 0/0 | 5327 | 55 | 9 | 6 | 27 | 2 | 11 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0003 | 0/0 | 5328 | 34 | 0 | 0 | 32 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0004 | 0/0 | 5329 | 11 | 10 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0005 | 0/0 | 5326 | 11 | 8 | 3 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0006 | 0/0 | 5327 | 11 | 0 | 5 | 6 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0007 | 0/0 | 5327 | 4 | 0 | 0 | 0 | 0 | 4 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0008 | 0/0 | 5327 | 3 | 0 | 0 | 3 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0009 | 0/0 | 5327 | 3 | 0 | 0 | 3 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0010 | 0/0 | 5327 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0011 | 0/0 | 5327 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0012 | 0/0 | 5326 | 3 | 0 | 0 | 0 | 0 | 3 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0013 | 0/0 | 5326 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0014 | 0/0 | 5327 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0015 | 0/0 | 5327 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0016 | 0/0 | 5326 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0017 | 0/0 | 5327 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0018 | 0/0 | 5327 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0019 | 0/0 | 5328 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0020 | 0/0 | 5327 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0021 | 0/0 | 5326 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0022 | 0/0 | 5327 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0023 | 0/0 | 5327 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0024 | 0/0 | 5327 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0025 | 0/0 | 5327 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0026 | 0/0 | 5327 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0027 | 0/0 | 5327 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0028 | 0/0 | 5327 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0029 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0030 | 0/0 | 5329 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0031 | 0/0 | 5326 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0032 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0033 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0034 | 0/0 | 5328 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0035 | 0/0 | 5328 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0036 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0037 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0038 | 0/0 | 5327 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0039 | 0/0 | 5326 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0040 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0041 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
t0042 | 0/0 | 5327 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
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 | 43 | 2 | 6 | 29 | 1 | 5 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0002 | 0/0 | 20 | 1 | 0 | 17 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0003 | 0/0 | 17 | 4 | 3 | 6 | 1 | 3 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0004 | 0/0 | 14 | 0 | 0 | 13 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0005 | 0/0 | 10 | 1 | 1 | 0 | 2 | 6 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0006 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0008 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0009 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0010 | 0/0 | 5 | 1 | 2 | 0 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0012 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0015 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0017 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0024 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0025 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0026 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0039 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
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 | 1200 | 309 | 74 | 45 | 142 | 6 | 40 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0002 | 0/0 | 1200 | 12 | 11 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0003 | 0/0 | 1200 | 7 | 7 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0002c0004 | 0/0 | 1200 | 6 | 0 | 0 | 6 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0003c0005 | 0/0 | 1200 | 2 | 0 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 6526 | 156 | 35 | 29 | 68 | 4 | 18 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0002 | 0/0 | 6526 | 55 | 9 | 6 | 27 | 2 | 11 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0003 | 0/0 | 6527 | 28 | 0 | 0 | 26 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0004 | 0/0 | 6528 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0005 | 0/0 | 6525 | 11 | 8 | 3 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0006 | 0/0 | 6526 | 11 | 0 | 5 | 6 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0007 | 0/0 | 6526 | 4 | 0 | 0 | 0 | 0 | 4 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0008 | 0/0 | 6526 | 3 | 0 | 0 | 3 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0009 | 0/0 | 6526 | 3 | 0 | 0 | 3 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0010 | 0/0 | 6526 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0011 | 0/0 | 6526 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0012 | 0/0 | 6525 | 3 | 0 | 0 | 0 | 0 | 3 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0014 | 0/0 | 6526 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0015 | 0/0 | 6526 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0017 | 0/0 | 6526 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0018 | 0/0 | 6526 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0019 | 0/0 | 6527 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0020 | 0/0 | 6526 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0022 | 0/0 | 6526 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0023 | 0/0 | 6526 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0024 | 0/0 | 6526 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0025 | 0/0 | 6526 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0026 | 0/0 | 6526 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0027 | 0/0 | 6526 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0028 | 0/0 | 6526 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0032 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0033 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0034 | 0/0 | 6527 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0035 | 0/0 | 6527 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0036 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0037 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0038 | 0/0 | 6526 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0039 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0040 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0041 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0001t0042 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0002t0004 | 0/0 | 6528 | 10 | 9 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0002t0029 | 0/0 | 6526 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0002t0030 | 0/0 | 6528 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0003t0013 | 0/0 | 6525 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0003t0016 | 0/0 | 6525 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0003t0021 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0001c0003t0031 | 0/0 | 6525 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0002c0004t0003 | 0/0 | 6527 | 6 | 0 | 0 | 6 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
a0003c0005t0001 | 0/0 | 6526 | 2 | 0 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | copy fasta | chr3 | 169961807 | 170003373 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 35 | 2 | 4 | 23 | 1 | 5 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0003 | 0/0 | 16 | 4 | 2 | 6 | 1 | 3 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0009 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0017 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0024 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0025 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0039 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0004 | 0/0 | 14 | 0 | 0 | 13 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0005 | 0/0 | 8 | 1 | 1 | 0 | 2 | 4 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0010 | 0/0 | 5 | 1 | 2 | 0 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0002 | 0/0 | 13 | 0 | 0 | 11 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0005g0026 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0005g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0006g0008 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0006g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0007g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0008g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0009g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0011g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0012g0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0014g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0015g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0017g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0018g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0019g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0020g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0022g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0023g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0024g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0025g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0026g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0027g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0028g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0032g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0033g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0034g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0035g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0036g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0037g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0038g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0039g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0040g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0041g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0001t0042g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0002t0004g0006 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0002t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0002t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0002t0029g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0002t0030g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0003t0013g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0003t0016g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0003t0021g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0001c0003t0031g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0002c0004t0003g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0002c0004t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
a0003c0005t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | GBR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | CHS | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01081 | hp2 | a0001 | c0001 | t0025 | g0122 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01106 | hp1 | a0003 | c0005 | t0001 | g0001 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01167 | hp1 | a0003 | c0005 | t0001 | g0001 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01243 | hp1 | a0001 | c0001 | t0027 | g0003 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01243 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01255 | hp2 | a0001 | c0001 | t0005 | g0134 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01261 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01884 | hp2 | a0001 | c0001 | t0037 | g0032 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01952 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01981 | hp2 | a0001 | c0001 | t0006 | g0008 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02015 | hp1 | a0001 | c0001 | t0026 | g0090 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02055 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02145 | hp2 | a0001 | c0001 | t0010 | g0066 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02148 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | CDX | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CDX | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CDX | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02257 | hp2 | a0001 | c0002 | t0004 | g0080 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02451 | hp1 | a0001 | c0003 | t0016 | g0031 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02602 | hp2 | a0001 | c0001 | t0012 | g0015 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02622 | hp1 | a0001 | c0003 | t0016 | g0031 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02622 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02809 | hp2 | a0001 | c0001 | t0017 | g0027 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02895 | hp2 | a0001 | c0002 | t0004 | g0030 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02896 | hp2 | a0001 | c0001 | t0036 | g0063 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0030 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02922 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02922 | hp2 | a0001 | c0001 | t0041 | g0015 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02965 | hp2 | a0001 | c0001 | t0014 | g0038 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02970 | hp1 | a0001 | c0001 | t0010 | g0087 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02976 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03017 | hp2 | a0001 | c0001 | t0007 | g0084 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0136 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03041 | hp2 | a0001 | c0001 | t0018 | g0034 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03098 | hp2 | a0001 | c0002 | t0030 | g0079 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03130 | hp2 | a0001 | c0002 | t0029 | g0006 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03139 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03195 | hp1 | a0001 | c0001 | t0011 | g0076 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03209 | hp1 | a0001 | c0003 | t0013 | g0022 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03453 | hp1 | a0001 | c0003 | t0031 | g0078 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03453 | hp2 | a0001 | c0003 | t0013 | g0022 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03486 | hp2 | a0001 | c0001 | t0010 | g0072 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03491 | hp2 | a0001 | c0001 | t0024 | g0092 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03516 | hp1 | a0001 | c0001 | t0040 | g0074 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ESN | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03540 | hp1 | a0001 | c0001 | t0039 | g0069 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03579 | hp2 | a0001 | c0003 | t0013 | g0022 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0082 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03710 | hp1 | a0001 | c0001 | t0023 | g0059 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03710 | hp2 | a0001 | c0001 | t0007 | g0005 | SAS | PJL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03831 | hp1 | a0001 | c0001 | t0012 | g0015 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03927 | hp1 | a0001 | c0001 | t0012 | g0015 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03942 | hp1 | a0001 | c0001 | t0007 | g0005 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | STU | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | CHB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18945 | hp1 | a0001 | c0001 | t0034 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18947 | hp1 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18954 | hp1 | a0001 | c0001 | t0019 | g0150 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18959 | hp2 | a0001 | c0001 | t0022 | g0065 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18960 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18963 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18963 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18968 | hp1 | a0001 | c0001 | t0038 | g0131 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18975 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18979 | hp1 | a0002 | c0004 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18984 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18993 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18998 | hp1 | a0002 | c0004 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19001 | hp1 | a0002 | c0004 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19005 | hp1 | a0002 | c0004 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19030 | hp1 | a0001 | c0001 | t0033 | g0068 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19030 | hp2 | a0001 | c0001 | t0018 | g0034 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0137 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19043 | hp2 | a0001 | c0001 | t0011 | g0077 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19057 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19064 | hp2 | a0002 | c0004 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19076 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19077 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19077 | hp2 | a0001 | c0001 | t0020 | g0121 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19081 | hp1 | a0001 | c0001 | t0028 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19082 | hp1 | a0002 | c0004 | t0003 | g0152 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19084 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19240 | hp1 | a0001 | c0001 | t0032 | g0138 | AFR | YRI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | ASW | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA20129 | hp2 | a0001 | c0001 | t0014 | g0038 | AFR | ASW | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | GIH | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02109 | hp1 | a0001 | c0001 | t0017 | g0027 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG02559 | hp2 | a0001 | c0001 | t0035 | g0002 | AFR | ACB | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG03471 | hp2 | a0001 | c0001 | t0011 | g0088 | AFR | MSL | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | USA | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA20300 | hp2 | a0001 | c0003 | t0021 | g0086 | AFR | USA | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA21309 | hp1 | a0001 | c0001 | t0042 | g0107 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0039 | REF | REF | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0093 | REF | REF | SEC62_chr3_169961807_170003373 | SEC62 | chr3 | 169961807 | 170003373 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:169992826
|
G | C | 1 | a0003 | 2 | HG01106.hp1 HG01167.hp1 |
missense_variant | MODERATE | c.963G>C | p.Glu321Asp | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 979/6526 | 963/1200 | 321/399 | chr3 | 169992826 | ||
chr3:169993051
|
T | G | 1 | a0002 | 6 | NA18979.hp1 NA18998.hp1 NA19001.hp1 others(3): Show |
missense_variant | MODERATE | c.1188T>G | p.His396Gln | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1204/6526 | 1188/1200 | 396/399 | chr3 | 169993051 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:169975646
|
C | G | 1 | a0001c0002 | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
synonymous_variant | LOW | c.75C>G | p.Ala25Ala | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/8 | 91/6526 | 75/1200 | 25/399 | chr3 | 169975646 | ||
chr3:169982737
|
C | G | 1 | a0001c0003 | 7 | HG02451.hp1 HG02622.hp1 HG03209.hp1 others(4): Show |
synonymous_variant | LOW | c.282C>G | p.Ala94Ala | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 4/8 | 298/6526 | 282/1200 | 94/399 | chr3 | 169982737 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:169966811
|
G | A | 1 | a0001c0001t0019 | 1 | NA18954.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/8 | 12 | chr3 | 169966811 | |||||
chr3:169993242
|
G | T | 1 | a0001c0001t0007 | 4 | HG03017.hp2 HG03704.hp2 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*179G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 179 | chr3 | 169993242 | |||||
chr3:169993310
|
T | C | 1 | a0001c0001t0020 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*247T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 247 | chr3 | 169993310 | |||||
chr3:169993709
|
G | A | 1 | a0001c0003t0021 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*646G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 646 | chr3 | 169993709 | |||||
chr3:169993773
|
G | A | 1 | a0001c0001t0008 | 3 | NA18963.hp2 NA19077.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*710G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 710 | chr3 | 169993773 | |||||
chr3:169993920
|
C | A | 1 | a0001c0001t0022 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*857C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 857 | chr3 | 169993920 | |||||
chr3:169994033
|
C | T | 1 | a0001c0001t0042 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*970C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 970 | chr3 | 169994033 | |||||
chr3:169994223
|
G | T | 1 | a0001c0001t0041 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1160G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1160 | chr3 | 169994223 | |||||
chr3:169994441
|
A | G | 1 | a0001c0001t0018 | 2 | HG03041.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1378A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1378 | chr3 | 169994441 | |||||
chr3:169994521
|
C | T | 1 | a0001c0001t0040 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1458C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1458 | chr3 | 169994521 | |||||
chr3:169994623
|
A | G | 1 | a0001c0001t0039 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1560A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1560 | chr3 | 169994623 | |||||
chr3:169994642
|
C | T | 1 | a0001c0003t0013 | 3 | HG03209.hp1 HG03453.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1579C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1579 | chr3 | 169994642 | |||||
chr3:169994770
|
A | G | 12 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(9): Show | 86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1707A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 1707 | chr3 | 169994770 | |||||
chr3:169995247
|
T | C | 1 | a0001c0001t0011 | 3 | HG03195.hp1 HG03471.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2184T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2184 | chr3 | 169995247 | |||||
chr3:169995506
|
A | G | 1 | a0001c0001t0036 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2443A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2443 | chr3 | 169995506 | |||||
chr3:169995624
|
A | AT | 5 | a0001c0001t0003a0001c0001t0019a0001c0001t0034others(2): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2571dupT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2572 | INFO_REALIGN_3_PRIME | chr3 | 169995624 | ||||
chr3:169995634
|
T | A | 1 | a0001c0001t0037 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2571T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2571 | chr3 | 169995634 | |||||
chr3:169995694
|
AC | A | 1 | a0001c0001t0012 | 3 | HG02602.hp2 HG03831.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2632delC | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2632 | chr3 | 169995694 | |||||
chr3:169995695
|
C | T | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(26): Show | 157 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2632C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2632 | chr3 | 169995695 | |||||
chr3:169995696
|
G | T | 1 | a0001c0001t0012 | 3 | HG02602.hp2 HG03831.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2633G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2633 | chr3 | 169995696 | |||||
chr3:169995887
|
T | C | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2824T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2824 | chr3 | 169995887 | |||||
chr3:169995888
|
G | T | 6 | a0001c0001t0003a0001c0001t0019a0001c0001t0032others(3): Show | 38 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2825G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2825 | chr3 | 169995888 | |||||
chr3:169995889
|
C | T | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2826C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2826 | chr3 | 169995889 | |||||
chr3:169995890
|
C | G | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2827C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2827 | chr3 | 169995890 | |||||
chr3:169995896
|
G | T | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2833G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2833 | chr3 | 169995896 | |||||
chr3:169995898
|
A | T | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2835A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2835 | chr3 | 169995898 | |||||
chr3:169995899
|
G | T | 1 | a0001c0001t0034 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2836 | chr3 | 169995899 | |||||
chr3:169995944
|
A | G | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(26): Show | 157 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2881A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2881 | chr3 | 169995944 | |||||
chr3:169995976
|
A | G | 3 | a0001c0003t0013a0001c0003t0021a0001c0003t0031 | 5 | HG03209.hp1 HG03453.hp1 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2913A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2913 | chr3 | 169995976 | |||||
chr3:169996006
|
CA | C | 6 | a0001c0001t0005a0001c0001t0039a0001c0003t0013others(3): Show | 19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2950delA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 2950 | INFO_REALIGN_3_PRIME | chr3 | 169996006 | ||||
chr3:169996208
|
A | G | 4 | a0001c0001t0004a0001c0002t0004a0001c0002t0029others(1): Show | 13 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3145A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3145 | chr3 | 169996208 | |||||
chr3:169996305
|
C | G | 1 | a0001c0001t0028 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3242C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3242 | chr3 | 169996305 | |||||
chr3:169996353
|
C | T | 3 | a0001c0001t0006a0001c0001t0008a0001c0001t0012 | 17 | HG01261.hp1 HG01934.hp1 HG01952.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3290C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3290 | chr3 | 169996353 | |||||
chr3:169996354
|
A | G | 30 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(27): Show | 160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*3291A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3291 | chr3 | 169996354 | |||||
chr3:169996363
|
C | T | 1 | a0001c0001t0017 | 2 | HG02109.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3300C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3300 | chr3 | 169996363 | |||||
chr3:169996515
|
C | T | 1 | a0001c0003t0016 | 2 | HG02451.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3452C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3452 | chr3 | 169996515 | |||||
chr3:169996562
|
C | T | 1 | a0001c0001t0038 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3499C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3499 | chr3 | 169996562 | |||||
chr3:169996605
|
G | C | 1 | a0001c0001t0032 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3542G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3542 | chr3 | 169996605 | |||||
chr3:169996777
|
G | A | 1 | a0001c0001t0023 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3714G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3714 | chr3 | 169996777 | |||||
chr3:169996781
|
G | A | 2 | a0001c0001t0005a0001c0001t0039 | 12 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3718G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3718 | chr3 | 169996781 | |||||
chr3:169996939
|
G | A | 1 | a0001c0001t0035 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3876G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3876 | chr3 | 169996939 | |||||
chr3:169996942
|
C | T | 1 | a0001c0001t0020 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3879C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3879 | chr3 | 169996942 | |||||
chr3:169997013
|
T | C | 12 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(9): Show | 86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3950T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 3950 | chr3 | 169997013 | |||||
chr3:169997176
|
G | A | 1 | a0001c0001t0009 | 3 | NA18947.hp1 NA18984.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4113G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4113 | chr3 | 169997176 | |||||
chr3:169997281
|
G | A | 1 | a0001c0001t0024 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4218G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4218 | chr3 | 169997281 | |||||
chr3:169997313
|
A | G | 1 | a0001c0002t0030 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4250A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4250 | chr3 | 169997313 | |||||
chr3:169997459
|
G | GTT | 3 | a0001c0001t0004a0001c0002t0004a0001c0002t0030 | 12 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4403_*4404dupTT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4405 | INFO_REALIGN_3_PRIME | chr3 | 169997459 | ||||
chr3:169997460
|
T | G | 7 | a0001c0001t0005a0001c0001t0025a0001c0001t0039others(4): Show | 20 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4397T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4397 | chr3 | 169997460 | |||||
chr3:169997542
|
T | A | 1 | a0001c0001t0005 | 11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4479T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4479 | chr3 | 169997542 | |||||
chr3:169997747
|
C | T | 1 | a0001c0001t0015 | 2 | NA19057.hp1 NA19076.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4684C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4684 | chr3 | 169997747 | |||||
chr3:169997849
|
T | C | 1 | a0001c0001t0005 | 11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4786T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4786 | chr3 | 169997849 | |||||
chr3:169997897
|
C | T | 1 | a0001c0001t0027 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4834C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4834 | chr3 | 169997897 | |||||
chr3:169997939
|
A | G | 1 | a0001c0001t0033 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4876A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4876 | chr3 | 169997939 | |||||
chr3:169997945
|
A | G | 1 | a0001c0001t0010 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4882A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4882 | chr3 | 169997945 | |||||
chr3:169998011
|
T | C | 1 | a0001c0003t0016 | 2 | HG02451.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4948T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 4948 | chr3 | 169998011 | |||||
chr3:169998248
|
A | G | 1 | a0001c0001t0014 | 2 | HG02965.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5185A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 5185 | chr3 | 169998248 | |||||
chr3:169998356
|
T | A | 1 | a0001c0001t0026 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5293T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 8/8 | 5293 | chr3 | 169998356 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:169966899
|
G | C | 37 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0017others(34): Show | 87 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.36+41G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169966899 | ||||||
chr3:169966954
|
AGGTGGGG others(3): Show |
A | 19 | a0001c0001t0001g0140a0001c0001t0003g0002a0001c0001t0003g0016others(16): Show | 38 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.36+110_36+119delGG others(8): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169966954 | |||||
chr3:169967027
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.36+169G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967027 | ||||||
chr3:169967027
|
G | C | 1 | a0001c0001t0001g0029 | 2 | HG00639.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.36+169G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967027 | ||||||
chr3:169967090
|
A | T | 1 | a0001c0001t0010g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.36+232A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967090 | ||||||
chr3:169967286
|
G | A | 1 | a0001c0001t0017g0027 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.36+428G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967286 | ||||||
chr3:169967319
|
A | G | 1 | a0001c0001t0022g0065 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.36+461A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967319 | ||||||
chr3:169967412
|
T | C | 1 | a0001c0002t0004g0030 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.36+554T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967412 | ||||||
chr3:169967493
|
C | T | 1 | a0001c0001t0032g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.36+635C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967493 | ||||||
chr3:169967494
|
G | T | 7 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(4): Show | 11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.36+636G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967494 | ||||||
chr3:169967525
|
T | C | 1 | a0001c0001t0005g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.36+667T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967525 | ||||||
chr3:169967586
|
G | C | 92 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0019others(89): Show | 182 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.36+728G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967586 | ||||||
chr3:169967620
|
T | A | 2 | a0001c0001t0001g0023a0001c0001t0018g0034 | 5 | HG02257.hp1 HG02572.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.36+762T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967620 | ||||||
chr3:169967691
|
C | T | 1 | a0001c0001t0011g0088 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.36+833C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967691 | ||||||
chr3:169967859
|
T | C | 1 | a0001c0001t0033g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.36+1001T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967859 | ||||||
chr3:169967881
|
C | CT | 53 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0020others(50): Show | 105 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.36+1034dupT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169967881 | |||||
chr3:169967989
|
A | G | 2 | a0001c0001t0010g0087a0001c0003t0021g0086 | 2 | HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.36+1131A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967989 | ||||||
chr3:169967998
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.36+1140A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169967998 | ||||||
chr3:169968349
|
G | A | 1 | a0001c0003t0016g0031 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.36+1491G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169968349 | ||||||
chr3:169968535
|
CA | C | 55 | a0001c0001t0001g0057a0001c0001t0001g0133a0001c0001t0002g0004others(52): Show | 116 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.36+1690delA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169968535 | |||||
chr3:169968567
|
T | G | 1 | a0001c0001t0005g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.36+1709T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169968567 | ||||||
chr3:169968605
|
T | C | 1 | a0001c0001t0003g0145 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.36+1747T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169968605 | ||||||
chr3:169968652
|
A | G | 4 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087others(1): Show | 5 | HG02109.hp1 HG02145.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.36+1794A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169968652 | ||||||
chr3:169969049
|
A | G | 1 | a0001c0001t0032g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.36+2191A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969049 | ||||||
chr3:169969217
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.36+2359G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969217 | ||||||
chr3:169969439
|
A | G | 7 | a0001c0001t0002g0032a0001c0001t0002g0071a0001c0001t0002g0075others(4): Show | 7 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+2581A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969439 | ||||||
chr3:169969489
|
A | G | 2 | a0001c0001t0006g0008a0001c0001t0008g0018 | 9 | HG01261.hp1 HG01934.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.36+2631A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969489 | ||||||
chr3:169969515
|
GC | G | 5 | a0001c0002t0004g0006a0001c0002t0004g0030a0001c0002t0004g0080others(2): Show | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.36+2659delC | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169969515 | |||||
chr3:169969566
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0089a0001c0001t0026g0090 | 4 | HG02015.hp1 HG02135.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+2708G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969566 | ||||||
chr3:169969591
|
C | T | 20 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(17): Show | 39 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.36+2733C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969591 | ||||||
chr3:169969592
|
G | A | 7 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(4): Show | 11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.36+2734G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969592 | ||||||
chr3:169969649
|
TC | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(15): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.36+2792delC | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969649 | ||||||
chr3:169969795
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.36+2937C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969795 | ||||||
chr3:169969819
|
A | G | 25 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(22): Show | 51 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.36+2961A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969819 | ||||||
chr3:169969845
|
T | C | 2 | a0001c0001t0003g0146a0001c0001t0003g0147 | 2 | NA18940.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.36+2987T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169969845 | ||||||
chr3:169970119
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.36+3261T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970119 | ||||||
chr3:169970202
|
C | T | 1 | a0001c0001t0032g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.36+3344C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970202 | ||||||
chr3:169970230
|
T | C | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(77): Show | 159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.36+3372T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970230 | ||||||
chr3:169970291
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.36+3433A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970291 | ||||||
chr3:169970542
|
A | G | 1 | a0001c0001t0033g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.36+3684A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970542 | ||||||
chr3:169970579
|
C | T | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(77): Show | 159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.36+3721C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970579 | ||||||
chr3:169970740
|
C | T | 1 | a0001c0001t0039g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.36+3882C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970740 | ||||||
chr3:169970799
|
T | G | 3 | a0001c0001t0002g0073a0001c0001t0017g0027a0001c0001t0040g0074 | 4 | HG02109.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+3941T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169970799 | ||||||
chr3:169971011
|
G | A | 18 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(15): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.36+4153G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971011 | ||||||
chr3:169971068
|
C | CT | 11 | a0001c0001t0001g0127a0001c0001t0002g0056a0001c0001t0002g0132others(8): Show | 15 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.36+4227dupT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169971068 | |||||
chr3:169971068
|
CT | C | 9 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 16 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.36+4227delT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169971068 | |||||
chr3:169971130
|
A | T | 1 | a0001c0001t0001g0126 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.36+4272A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971130 | ||||||
chr3:169971376
|
A | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 4 | NA18948.hp2 NA18984.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.37-4232A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971376 | ||||||
chr3:169971399
|
A | G | 37 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(34): Show | 82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.37-4209A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971399 | ||||||
chr3:169971419
|
A | C | 12 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(9): Show | 19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.37-4189A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971419 | ||||||
chr3:169971564
|
G | A | 65 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(62): Show | 137 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.37-4044G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971564 | ||||||
chr3:169971592
|
C | T | 3 | a0001c0001t0002g0073a0001c0001t0017g0027a0001c0001t0040g0074 | 4 | HG02109.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-4016C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971592 | ||||||
chr3:169971899
|
T | C | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(77): Show | 159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.37-3709T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971899 | ||||||
chr3:169971989
|
G | C | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(77): Show | 159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.37-3619G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169971989 | ||||||
chr3:169972005
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0124a0001c0001t0001g0125 | 4 | HG00735.hp1 HG01258.hp1 NA21309.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-3603A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972005 | ||||||
chr3:169972166
|
G | A | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(77): Show | 159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.37-3442G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972166 | ||||||
chr3:169972197
|
T | C | 1 | a0001c0001t0024g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.37-3411T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972197 | ||||||
chr3:169972301
|
G | A | 3 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.37-3307G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972301 | ||||||
chr3:169972356
|
A | T | 5 | a0001c0002t0004g0006a0001c0002t0004g0030a0001c0002t0004g0080others(2): Show | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-3252A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972356 | ||||||
chr3:169972385
|
A | G | 3 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.37-3223A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972385 | ||||||
chr3:169972404
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.37-3204C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972404 | ||||||
chr3:169972580
|
C | CT | 60 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(57): Show | 133 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.37-3008dupT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169972580 | |||||
chr3:169972580
|
C | CTT | 28 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0023others(25): Show | 54 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.37-3009_37-3008dup others(2): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169972580 | |||||
chr3:169972580
|
CT | C | 7 | a0001c0001t0002g0075a0001c0001t0003g0141a0001c0001t0007g0082others(4): Show | 10 | HG02451.hp1 HG02622.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.37-3008delT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169972580 | |||||
chr3:169972602
|
T | G | 20 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(17): Show | 39 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.37-3006T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972602 | ||||||
chr3:169972672
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.37-2936C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972672 | ||||||
chr3:169972749
|
ATT | A | 8 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(5): Show | 12 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-2854_37-2853del others(2): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169972749 | |||||
chr3:169972797
|
G | A | 1 | a0001c0001t0032g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.37-2811G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972797 | ||||||
chr3:169972871
|
G | A | 1 | a0001c0001t0033g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.37-2737G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972871 | ||||||
chr3:169972923
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.37-2685C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972923 | ||||||
chr3:169972971
|
C | A | 1 | a0001c0001t0005g0135 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.37-2637C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169972971 | ||||||
chr3:169973057
|
A | T | 1 | a0001c0001t0025g0122 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.37-2551A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973057 | ||||||
chr3:169973270
|
A | T | 1 | a0001c0001t0002g0021 | 3 | HG02258.hp2 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.37-2338A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973270 | ||||||
chr3:169973307
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.37-2301A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973307 | ||||||
chr3:169973577
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.37-2031C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973577 | ||||||
chr3:169973645
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.37-1963A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973645 | ||||||
chr3:169973662
|
C | CA | 6 | a0001c0001t0001g0089a0001c0001t0001g0096a0001c0001t0001g0112others(3): Show | 7 | HG00544.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.37-1930dupA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169973662 | |||||
chr3:169973662
|
C | CAA | 22 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(19): Show | 48 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.37-1931_37-1930dup others(2): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169973662 | |||||
chr3:169973662
|
CA | C | 12 | a0001c0001t0002g0055a0001c0001t0002g0071a0001c0001t0005g0026others(9): Show | 16 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.37-1930delA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169973662 | |||||
chr3:169973887
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.37-1721C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169973887 | ||||||
chr3:169974095
|
A | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(15): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.37-1513A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974095 | ||||||
chr3:169974097
|
A | T | 12 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(9): Show | 19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.37-1511A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974097 | ||||||
chr3:169974282
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0114a0001c0001t0004g0070 | 8 | HG00639.hp1 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-1326T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974282 | ||||||
chr3:169974317
|
A | T | 1 | a0001c0001t0001g0064 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.37-1291A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974317 | ||||||
chr3:169974347
|
A | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(15): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.37-1261A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974347 | ||||||
chr3:169974649
|
A | T | 77 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(74): Show | 156 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.37-959A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169974649 | ||||||
chr3:169974835
|
CCTT | C | 5 | a0001c0002t0004g0006a0001c0002t0004g0030a0001c0002t0004g0080others(2): Show | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-770_37-768delTC others(1): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169974835 | |||||
chr3:169975003
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.37-605G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975003 | ||||||
chr3:169975056
|
G | A | 3 | a0001c0001t0011g0076a0001c0001t0011g0077a0001c0001t0011g0088 | 3 | HG03195.hp1 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.37-552G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975056 | ||||||
chr3:169975084
|
C | T | 3 | a0001c0002t0004g0030a0001c0002t0004g0080a0001c0002t0030g0079 | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-524C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975084 | ||||||
chr3:169975103
|
A | G | 1 | a0001c0002t0030g0079 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.37-505A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975103 | ||||||
chr3:169975123
|
A | T | 1 | a0001c0001t0039g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.37-485A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975123 | ||||||
chr3:169975126
|
C | A | 1 | a0001c0001t0001g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.37-482C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975126 | ||||||
chr3:169975222
|
A | C | 3 | a0001c0002t0004g0030a0001c0002t0004g0080a0001c0002t0030g0079 | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-386A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975222 | ||||||
chr3:169975229
|
C | T | 1 | a0001c0001t0032g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.37-379C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975229 | ||||||
chr3:169975280
|
C | CA | 36 | a0001c0001t0001g0058a0001c0001t0001g0098a0001c0001t0001g0116others(33): Show | 81 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.37-310dupA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 169975280 | |||||
chr3:169975341
|
A | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0036g0063 | 3 | HG02615.hp2 HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.37-267A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975341 | ||||||
chr3:169975443
|
C | T | 19 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(16): Show | 38 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.37-165C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975443 | ||||||
chr3:169975511
|
A | G | 1 | a0001c0001t0032g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.37-97A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975511 | ||||||
chr3:169975555
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0033g0068 | 2 | NA19030.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.37-53G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 1/7 | chr3 | 169975555 | ||||||
chr3:169975885
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.145+169A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169975885 | ||||||
chr3:169975987
|
G | A | 6 | a0001c0001t0003g0016a0001c0001t0003g0141a0001c0001t0003g0142others(3): Show | 9 | NA18961.hp1 NA18969.hp1 NA18979.hp2 others(6): Show |
intron_variant | MODIFIER | c.145+271G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169975987 | ||||||
chr3:169976005
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0032g0138 | 2 | NA18977.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.145+289A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976005 | ||||||
chr3:169976027
|
A | G | 1 | a0001c0001t0003g0151 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.145+311A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976027 | ||||||
chr3:169976130
|
C | T | 5 | a0001c0002t0004g0006a0001c0002t0004g0030a0001c0002t0004g0080others(2): Show | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.145+414C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976130 | ||||||
chr3:169976194
|
C | T | 1 | a0001c0001t0042g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.145+478C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976194 | ||||||
chr3:169976206
|
A | G | 3 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.145+490A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976206 | ||||||
chr3:169976215
|
A | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG02965.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.145+499A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976215 | ||||||
chr3:169976263
|
G | T | 1 | a0001c0003t0031g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.145+547G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976263 | ||||||
chr3:169976264
|
C | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(15): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.145+548C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976264 | ||||||
chr3:169976338
|
A | T | 7 | a0001c0001t0002g0032a0001c0001t0002g0071a0001c0001t0002g0075others(4): Show | 7 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.146-608A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976338 | ||||||
chr3:169976374
|
G | GA | 37 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(34): Show | 82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.146-562dupA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 169976374 | |||||
chr3:169976609
|
C | G | 1 | a0001c0003t0016g0031 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.146-337C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 2/7 | chr3 | 169976609 | ||||||
chr3:169977222
|
T | TTATACTT others(319): Show |
4 | a0001c0001t0002g0032a0001c0001t0002g0071a0001c0001t0002g0075others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+180_251+181ins others(326): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 169977222 | |||||
chr3:169977415
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.251+364G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977415 | ||||||
chr3:169977437
|
C | T | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(77): Show | 159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.251+386C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977437 | ||||||
chr3:169977631
|
T | G | 3 | a0001c0001t0002g0073a0001c0001t0017g0027a0001c0001t0040g0074 | 4 | HG02109.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+580T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977631 | ||||||
chr3:169977774
|
T | C | 18 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(15): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.251+723T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977774 | ||||||
chr3:169977798
|
A | AT | 5 | a0001c0002t0004g0006a0001c0002t0004g0030a0001c0002t0004g0080others(2): Show | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+751dupT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 169977798 | |||||
chr3:169977799
|
T | A | 4 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0136others(1): Show | 7 | HG01167.hp2 HG01169.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.251+748T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977799 | ||||||
chr3:169977853
|
G | C | 1 | a0001c0001t0010g0087 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.251+802G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977853 | ||||||
chr3:169977980
|
T | C | 3 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.251+929T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169977980 | ||||||
chr3:169978075
|
C | T | 1 | a0001c0001t0025g0122 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.251+1024C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978075 | ||||||
chr3:169978095
|
A | C | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(77): Show | 159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.251+1044A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978095 | ||||||
chr3:169978104
|
C | T | 8 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(5): Show | 12 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+1053C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978104 | ||||||
chr3:169978134
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.251+1083C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978134 | ||||||
chr3:169978235
|
C | G | 1 | a0001c0003t0031g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.251+1184C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978235 | ||||||
chr3:169978236
|
G | A | 1 | a0001c0003t0016g0031 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.251+1185G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978236 | ||||||
chr3:169978417
|
G | T | 1 | a0001c0001t0005g0137 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.251+1366G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978417 | ||||||
chr3:169978430
|
G | A | 77 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(74): Show | 156 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.251+1379G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978430 | ||||||
chr3:169978555
|
A | G | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(77): Show | 159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.251+1504A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978555 | ||||||
chr3:169978587
|
G | A | 1 | a0001c0001t0005g0136 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.251+1536G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978587 | ||||||
chr3:169978616
|
C | G | 1 | a0001c0001t0039g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.251+1565C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978616 | ||||||
chr3:169978745
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.251+1694C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978745 | ||||||
chr3:169978785
|
A | T | 1 | a0001c0001t0017g0027 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.251+1734A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169978785 | ||||||
chr3:169979134
|
G | A | 3 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.251+2083G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979134 | ||||||
chr3:169979195
|
A | T | 1 | a0001c0001t0020g0121 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.251+2144A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979195 | ||||||
chr3:169979237
|
A | G | 37 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(34): Show | 82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.251+2186A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979237 | ||||||
chr3:169979296
|
C | T | 1 | a0001c0001t0040g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.251+2245C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979296 | ||||||
chr3:169979588
|
A | G | 66 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(63): Show | 138 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.251+2537A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979588 | ||||||
chr3:169979845
|
A | G | 12 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(9): Show | 19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+2794A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979845 | ||||||
chr3:169979888
|
A | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(15): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.252-2819A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979888 | ||||||
chr3:169979998
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.252-2709A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169979998 | ||||||
chr3:169980081
|
G | A | 3 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.252-2626G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980081 | ||||||
chr3:169980111
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.252-2596T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980111 | ||||||
chr3:169980274
|
A | G | 4 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0136others(1): Show | 7 | HG01167.hp2 HG01169.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-2433A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980274 | ||||||
chr3:169980320
|
G | A | 4 | a0001c0003t0013g0022a0001c0003t0016g0031a0001c0003t0021g0086others(1): Show | 7 | HG02451.hp1 HG02622.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-2387G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980320 | ||||||
chr3:169980355
|
CAG | C | 40 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(37): Show | 86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.252-2347_252-2346d others(4): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 169980355 | |||||
chr3:169980699
|
G | A | 40 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(37): Show | 86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.252-2008G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980699 | ||||||
chr3:169980795
|
G | A | 3 | a0001c0003t0013g0022a0001c0003t0021g0086a0001c0003t0031g0078 | 5 | HG03209.hp1 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-1912G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980795 | ||||||
chr3:169980952
|
T | C | 81 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(78): Show | 160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.252-1755T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980952 | ||||||
chr3:169980969
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.252-1738A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169980969 | ||||||
chr3:169981004
|
A | G | 1 | a0001c0001t0011g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.252-1703A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981004 | ||||||
chr3:169981144
|
G | A | 81 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(78): Show | 160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.252-1563G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981144 | ||||||
chr3:169981395
|
A | T | 1 | a0001c0001t0019g0150 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.252-1312A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981395 | ||||||
chr3:169981521
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.252-1186G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981521 | ||||||
chr3:169981534
|
G | A | 1 | a0001c0001t0033g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.252-1173G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981534 | ||||||
chr3:169981661
|
C | A | 4 | a0001c0003t0013g0022a0001c0003t0016g0031a0001c0003t0021g0086others(1): Show | 7 | HG02451.hp1 HG02622.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-1046C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981661 | ||||||
chr3:169981726
|
G | A | 1 | a0001c0003t0016g0031 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.252-981G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981726 | ||||||
chr3:169981727
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.252-980G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981727 | ||||||
chr3:169981967
|
G | A | 3 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.252-740G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169981967 | ||||||
chr3:169982042
|
A | C | 4 | a0001c0001t0002g0032a0001c0001t0002g0071a0001c0001t0002g0075others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-665A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982042 | ||||||
chr3:169982090
|
AT | A | 3 | a0001c0003t0013g0022a0001c0003t0021g0086a0001c0003t0031g0078 | 5 | HG03209.hp1 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-616delT | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982090 | ||||||
chr3:169982124
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0120 | 2 | HG01109.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.252-583A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982124 | ||||||
chr3:169982216
|
C | G | 81 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(78): Show | 160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.252-491C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982216 | ||||||
chr3:169982316
|
T | C | 1 | a0001c0001t0039g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.252-391T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982316 | ||||||
chr3:169982366
|
G | A | 1 | a0001c0001t0002g0013 | 4 | NA18957.hp2 NA18961.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-341G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982366 | ||||||
chr3:169982608
|
T | C | 8 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(5): Show | 12 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-99T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982608 | ||||||
chr3:169982669
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.252-38A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982669 | ||||||
chr3:169982673
|
G | T | 8 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(5): Show | 12 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-34G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982673 | ||||||
chr3:169982686
|
C | A | 7 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(4): Show | 11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-21C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 3/7 | chr3 | 169982686 | ||||||
chr3:169982991
|
G | A | 6 | a0001c0001t0004g0070a0001c0002t0004g0006a0001c0002t0004g0030others(3): Show | 13 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.456+80G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 4/7 | chr3 | 169982991 | ||||||
chr3:169983082
|
T | G | 1 | a0001c0001t0002g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.457-79T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 4/7 | chr3 | 169983082 | ||||||
chr3:169983375
|
A | G | 1 | a0001c0001t0003g0144 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.549+122A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169983375 | ||||||
chr3:169983667
|
A | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG02165.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.549+414A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169983667 | ||||||
chr3:169983690
|
G | C | 81 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(78): Show | 160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.549+437G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169983690 | ||||||
chr3:169983885
|
A | G | 37 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(34): Show | 82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.549+632A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169983885 | ||||||
chr3:169984044
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0019others(7): Show | 22 | HG00280.hp2 HG00438.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.549+791C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984044 | ||||||
chr3:169984477
|
C | T | 2 | a0001c0002t0004g0006a0001c0002t0029g0006 | 8 | HG01243.hp2 HG02055.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.549+1224C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984477 | ||||||
chr3:169984555
|
C | T | 1 | a0001c0001t0040g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.550-1250C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984555 | ||||||
chr3:169984627
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0064 | 7 | NA18944.hp1 NA18946.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.550-1178A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984627 | ||||||
chr3:169984877
|
T | C | 1 | a0001c0001t0001g0036 | 2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.550-928T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984877 | ||||||
chr3:169984924
|
A | G | 40 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(37): Show | 86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.550-881A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984924 | ||||||
chr3:169984971
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.550-834C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169984971 | ||||||
chr3:169985058
|
G | A | 12 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(9): Show | 19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.550-747G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985058 | ||||||
chr3:169985145
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.550-660C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985145 | ||||||
chr3:169985167
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.550-638A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985167 | ||||||
chr3:169985296
|
C | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0101a0001c0001t0001g0102 | 7 | HG00140.hp2 HG01123.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-509C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985296 | ||||||
chr3:169985351
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0103a0001c0001t0001g0119 | 5 | HG00741.hp2 HG02280.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-454C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985351 | ||||||
chr3:169985423
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.550-382G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985423 | ||||||
chr3:169985447
|
G | A | 1 | a0001c0001t0002g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.550-358G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985447 | ||||||
chr3:169985485
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | NA18959.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.550-320G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985485 | ||||||
chr3:169985556
|
T | A | 7 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(4): Show | 11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.550-249T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 5/7 | chr3 | 169985556 | ||||||
chr3:169985883
|
A | C | 15 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0013others(12): Show | 37 | HG00597.hp1 HG01257.hp2 HG01258.hp2 others(34): Show |
intron_variant | MODIFIER | c.610+18A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169985883 | ||||||
chr3:169985890
|
A | G | 3 | a0001c0001t0002g0073a0001c0001t0017g0027a0001c0001t0040g0074 | 4 | HG02109.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.610+25A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169985890 | ||||||
chr3:169985929
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.610+64A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169985929 | ||||||
chr3:169986085
|
G | A | 18 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(15): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.610+220G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986085 | ||||||
chr3:169986110
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.610+245A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986110 | ||||||
chr3:169986140
|
A | G | 1 | a0001c0001t0001g0020 | 3 | HG02572.hp1 HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.610+275A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986140 | ||||||
chr3:169986153
|
A | G | 1 | a0001c0001t0032g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.610+288A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986153 | ||||||
chr3:169986246
|
A | G | 1 | a0001c0001t0002g0028 | 2 | NA18946.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.610+381A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986246 | ||||||
chr3:169986268
|
G | A | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(77): Show | 159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.610+403G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986268 | ||||||
chr3:169986542
|
T | TA | 4 | a0001c0003t0013g0022a0001c0003t0016g0031a0001c0003t0021g0086others(1): Show | 7 | HG02451.hp1 HG02622.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.610+684dupA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 169986542 | |||||
chr3:169986543
|
A | T | 3 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.610+678A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986543 | ||||||
chr3:169986567
|
C | A | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.610+702C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986567 | ||||||
chr3:169986567
|
C | T | 1 | a0001c0001t0018g0034 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.610+702C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986567 | ||||||
chr3:169986615
|
T | C | 15 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0013others(12): Show | 37 | HG00597.hp1 HG01257.hp2 HG01258.hp2 others(34): Show |
intron_variant | MODIFIER | c.610+750T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986615 | ||||||
chr3:169986712
|
T | C | 1 | a0001c0001t0001g0040 | 2 | NA18948.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.610+847T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986712 | ||||||
chr3:169986764
|
G | A | 77 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(74): Show | 156 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.610+899G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986764 | ||||||
chr3:169986859
|
G | A | 2 | a0001c0001t0006g0014a0001c0001t0006g0054 | 5 | HG02056.hp2 HG02155.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.610+994G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986859 | ||||||
chr3:169986887
|
C | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0071a0001c0001t0002g0075others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.610+1022C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986887 | ||||||
chr3:169986924
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.610+1059G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169986924 | ||||||
chr3:169987065
|
G | GA | 2 | a0001c0001t0002g0010a0001c0001t0002g0056 | 6 | HG01257.hp2 HG01258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.611-1163dupA | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 169987065 | |||||
chr3:169987230
|
C | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(15): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.611-1010C>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987230 | ||||||
chr3:169987256
|
G | A | 20 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(17): Show | 39 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.611-984G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987256 | ||||||
chr3:169987283
|
G | A | 7 | a0001c0001t0005g0026a0001c0001t0005g0043a0001c0001t0005g0044others(4): Show | 11 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.611-957G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987283 | ||||||
chr3:169987305
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0060 | 4 | HG01099.hp2 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.611-935A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987305 | ||||||
chr3:169987581
|
G | A | 2 | a0001c0001t0005g0044a0001c0001t0005g0135 | 3 | HG02055.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.611-659G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987581 | ||||||
chr3:169987913
|
G | A | 80 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(77): Show | 159 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.611-327G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987913 | ||||||
chr3:169987951
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.611-289G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987951 | ||||||
chr3:169987987
|
T | C | 1 | a0001c0001t0001g0036 | 2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.611-253T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169987987 | ||||||
chr3:169988150
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.611-90G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 6/7 | chr3 | 169988150 | ||||||
chr3:169988395
|
G | A | 1 | a0001c0001t0032g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.730+36G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169988395 | ||||||
chr3:169988398
|
G | A | 3 | a0001c0002t0004g0030a0001c0002t0004g0080a0001c0002t0030g0079 | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+39G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169988398 | ||||||
chr3:169988770
|
A | G | 1 | a0001c0001t0025g0122 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.730+411A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169988770 | ||||||
chr3:169989002
|
A | G | 3 | a0001c0002t0004g0030a0001c0002t0004g0080a0001c0002t0030g0079 | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+643A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989002 | ||||||
chr3:169989034
|
A | C | 5 | a0001c0002t0004g0006a0001c0002t0004g0030a0001c0002t0004g0080others(2): Show | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.730+675A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989034 | ||||||
chr3:169989072
|
A | G | 4 | a0001c0001t0002g0032a0001c0001t0002g0071a0001c0001t0002g0075others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+713A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989072 | ||||||
chr3:169989109
|
TTAGAGGC others(9): Show |
T | 1 | a0001c0001t0001g0037 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.730+751_730+766del others(16): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989109 | ||||||
chr3:169989126
|
C | A | 1 | a0001c0001t0001g0037 | 2 | HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.730+767C>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989126 | ||||||
chr3:169989223
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.730+864A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989223 | ||||||
chr3:169989255
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0064 | 7 | NA18944.hp1 NA18946.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.730+896G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989255 | ||||||
chr3:169989288
|
C | CCCAGGCT others(403): Show |
95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(92): Show | 195 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.730+936_730+937ins others(410): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989288 | |||||
chr3:169989288
|
C | CCTAGGCT others(403): Show |
3 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.730+930_730+931ins others(410): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989288 | |||||
chr3:169989290
|
C | CAGGCTGA others(403): Show |
1 | a0001c0001t0008g0018 | 3 | NA18963.hp2 NA19077.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.730+936_730+937ins others(410): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989290 | |||||
chr3:169989290
|
C | CAGGCTGG others(403): Show |
25 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(22): Show | 51 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.730+936_730+937ins others(410): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989290 | |||||
chr3:169989290
|
C | CAGGCTGG others(403): Show |
39 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(36): Show | 83 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.730+936_730+937ins others(410): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989290 | |||||
chr3:169989362
|
G | A | 1 | a0001c0001t0032g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.730+1003G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989362 | ||||||
chr3:169989424
|
C | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(15): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.730+1065C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989424 | ||||||
chr3:169989425
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.730+1066T>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989425 | ||||||
chr3:169989641
|
T | A | 1 | a0001c0001t0005g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.730+1282T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989641 | ||||||
chr3:169989744
|
C | T | 1 | a0001c0003t0016g0031 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.730+1385C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989744 | ||||||
chr3:169989792
|
T | A | 1 | a0001c0001t0017g0027 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.730+1433T>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989792 | ||||||
chr3:169989845
|
T | G | 81 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(78): Show | 160 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.730+1486T>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989845 | ||||||
chr3:169989944
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.730+1585G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169989944 | ||||||
chr3:169989978
|
TATATATG others(8): Show |
T | 1 | a0001c0001t0003g0143 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.730+1633_730+1647d others(17): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169989978 | |||||
chr3:169990000
|
GATATATC others(8): Show |
G | 40 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(37): Show | 86 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.730+1652_730+1666d others(17): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169990000 | |||||
chr3:169990002
|
TATATC | T | 7 | a0001c0001t0001g0101a0001c0001t0010g0087a0001c0002t0004g0006others(4): Show | 14 | HG01123.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.730+1647_730+1651d others(7): Show |
SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 169990002 | |||||
chr3:169990051
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.730+1692A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990051 | ||||||
chr3:169990166
|
A | G | 1 | a0001c0001t0005g0026 | 3 | HG01167.hp2 HG01169.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.730+1807A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990166 | ||||||
chr3:169990313
|
A | G | 1 | a0001c0001t0042g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.730+1954A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990313 | ||||||
chr3:169990488
|
G | A | 1 | a0001c0003t0021g0086 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.731-2106G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990488 | ||||||
chr3:169990503
|
A | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0139others(15): Show | 37 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.731-2091A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990503 | ||||||
chr3:169990646
|
A | G | 3 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.731-1948A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990646 | ||||||
chr3:169990696
|
A | C | 1 | a0001c0001t0003g0142 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.731-1898A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990696 | ||||||
chr3:169990743
|
C | T | 1 | a0001c0001t0003g0149 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.731-1851C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990743 | ||||||
chr3:169990846
|
C | T | 3 | a0001c0003t0013g0022a0001c0003t0021g0086a0001c0003t0031g0078 | 5 | HG03209.hp1 HG03453.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1748C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169990846 | ||||||
chr3:169991094
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.731-1500C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991094 | ||||||
chr3:169991192
|
A | C | 4 | a0001c0001t0002g0032a0001c0001t0002g0071a0001c0001t0002g0075others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-1402A>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991192 | ||||||
chr3:169991316
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.731-1278G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991316 | ||||||
chr3:169991700
|
C | T | 1 | a0001c0001t0008g0018 | 3 | NA18963.hp2 NA19077.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.731-894C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991700 | ||||||
chr3:169991732
|
A | G | 3 | a0001c0001t0010g0066a0001c0001t0010g0072a0001c0001t0010g0087 | 3 | HG02145.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.731-862A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991732 | ||||||
chr3:169991754
|
G | C | 7 | a0001c0001t0002g0032a0001c0001t0002g0071a0001c0001t0002g0075others(4): Show | 7 | HG01884.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.731-840G>C | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169991754 | ||||||
chr3:169992002
|
C | T | 37 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(34): Show | 82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.731-592C>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169992002 | ||||||
chr3:169992137
|
A | G | 1 | a0001c0001t0026g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.731-457A>G | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169992137 | ||||||
chr3:169992311
|
G | A | 1 | a0001c0001t0033g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.731-283G>A | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169992311 | ||||||
chr3:169992324
|
A | T | 37 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(34): Show | 82 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.731-270A>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169992324 | ||||||
chr3:169992575
|
G | T | 65 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0010others(62): Show | 137 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.731-19G>T | SEC62 | ENSG00000008952.17 | transcript | ENST00000337002.9 | protein_coding | 7/7 | chr3 | 169992575 |