geneid | 5836 |
---|---|
ensemblid | ENSG00000100504.17 |
hgncid | 9725 |
symbol | PYGL |
name | glycogen phosphorylase L |
refseq_nuc | NM_002863.5 |
refseq_prot | NP_002854.3 |
ensembl_nuc | ENST00000216392.8 |
ensembl_prot | ENSP00000216392.7 |
mane_status | MANE Select |
chr | chr14 |
start | 50905217 |
end | 50944483 |
strand | - |
ver | v1.2 |
region | chr14:50905217-50944483 |
region5000 | chr14:50900217-50949483 |
regionname0 | PYGL_chr14_50905217_50944483 |
regionname5000 | PYGL_chr14_50900217_50949483 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 847 | 335 | 59 | 60 | 164 | 15 | 35 | 123 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0002 | 0/0 | 847 | 33 | 14 | 4 | 10 | 1 | 4 | 10 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0003 | 0/0 | 847 | 10 | 1 | 0 | 8 | 0 | 1 | 7 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0004 | 0/0 | 847 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0005 | 0/0 | 847 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0006 | 0/0 | 847 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0007 | 0/0 | 847 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0008 | 0/0 | 847 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2544 | 153 | 33 | 27 | 60 | 11 | 20 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0002 | 0/0 | 2544 | 90 | 6 | 16 | 57 | 3 | 8 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0003 | 0/0 | 2544 | 25 | 1 | 8 | 13 | 0 | 3 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0004 | 0/0 | 2544 | 22 | 13 | 3 | 1 | 1 | 4 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0005 | 0/0 | 2544 | 20 | 1 | 4 | 13 | 0 | 2 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0006 | 0/0 | 2544 | 19 | 5 | 0 | 13 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0007 | 0/0 | 2544 | 12 | 9 | 2 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0008 | 0/0 | 2544 | 9 | 0 | 1 | 8 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0009 | 0/0 | 2544 | 9 | 4 | 0 | 4 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0010 | 0/0 | 2544 | 9 | 0 | 0 | 8 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0011 | 0/0 | 2544 | 4 | 4 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0012 | 0/0 | 2544 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0013 | 0/0 | 2544 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0014 | 0/0 | 2544 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0015 | 0/0 | 2544 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0016 | 0/0 | 2544 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0017 | 0/0 | 2544 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0018 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0019 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0020 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0021 | 0/0 | 2544 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0022 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
c0023 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 256 | 170 | 34 | 28 | 70 | 12 | 24 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
t0002 | 0/0 | 255 | 114 | 45 | 16 | 45 | 1 | 7 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
t0003 | 0/0 | 255 | 104 | 6 | 20 | 67 | 3 | 8 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
t0004 | 0/0 | 256 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
t0005 | 0/0 | 255 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 0 | 0 | 13 | 0 | 2 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0002 | 0/0 | 12 | 0 | 0 | 8 | 2 | 2 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0005 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0007 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0009 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0017 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2544 | 153 | 33 | 27 | 60 | 11 | 20 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0002 | 0/0 | 2544 | 90 | 6 | 16 | 57 | 3 | 8 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0003 | 0/0 | 2544 | 25 | 1 | 8 | 13 | 0 | 3 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0005 | 0/0 | 2544 | 20 | 1 | 4 | 13 | 0 | 2 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0006 | 0/0 | 2544 | 19 | 5 | 0 | 13 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0007 | 0/0 | 2544 | 12 | 9 | 2 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0009 | 0/0 | 2544 | 9 | 4 | 0 | 4 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0012 | 0/0 | 2544 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0015 | 0/0 | 2544 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0017 | 0/0 | 2544 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0021 | 0/0 | 2544 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0002c0004 | 0/0 | 2544 | 22 | 13 | 3 | 1 | 1 | 4 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0002c0008 | 0/0 | 2544 | 9 | 0 | 1 | 8 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0002c0016 | 0/0 | 2544 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0002c0018 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0003c0010 | 0/0 | 2544 | 9 | 0 | 0 | 8 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0003c0019 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0004c0011 | 0/0 | 2544 | 4 | 4 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0004c0022 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0005c0013 | 0/0 | 2544 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0006c0014 | 0/0 | 2544 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0007c0023 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0008c0020 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2799 | 130 | 14 | 24 | 60 | 11 | 19 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0001t0002 | 0/0 | 2798 | 19 | 18 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0001t0003 | 0/0 | 2798 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0001t0004 | 0/0 | 2799 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0001t0005 | 0/0 | 2798 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0002t0001 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0002t0003 | 0/0 | 2798 | 89 | 6 | 16 | 56 | 3 | 8 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0003t0002 | 0/0 | 2798 | 25 | 1 | 8 | 13 | 0 | 3 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0005t0002 | 0/0 | 2798 | 20 | 1 | 4 | 13 | 0 | 2 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0006t0001 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0006t0002 | 0/0 | 2798 | 18 | 4 | 0 | 13 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0007t0001 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0007t0002 | 0/0 | 2798 | 11 | 8 | 2 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0009t0001 | 0/0 | 2799 | 3 | 1 | 0 | 1 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0009t0002 | 0/0 | 2798 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0009t0003 | 0/0 | 2798 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0012t0002 | 0/0 | 2798 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0015t0003 | 0/0 | 2798 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0017t0002 | 0/0 | 2798 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0001c0021t0002 | 0/0 | 2798 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0002c0004t0001 | 0/0 | 2799 | 22 | 13 | 3 | 1 | 1 | 4 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0002c0008t0001 | 0/0 | 2799 | 8 | 0 | 1 | 7 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0002c0008t0003 | 0/0 | 2798 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0002c0016t0003 | 0/0 | 2798 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0002c0018t0001 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0003c0010t0002 | 0/0 | 2798 | 3 | 0 | 0 | 2 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0003c0010t0003 | 0/0 | 2798 | 6 | 0 | 0 | 6 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0003c0019t0002 | 0/0 | 2798 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0004c0011t0002 | 0/0 | 2798 | 4 | 4 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0004c0022t0002 | 0/0 | 2798 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0005c0013t0002 | 0/0 | 2798 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0006c0014t0001 | 0/0 | 2799 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0007c0023t0002 | 0/0 | 2798 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
a0008c0020t0001 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | copy fasta | chr14 | 50900217 | 50949483 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 12 | 0 | 0 | 8 | 2 | 2 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0001 | 0/0 | 15 | 0 | 0 | 13 | 0 | 2 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0005 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0017 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0003t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0005t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0006t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0007t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0007t0002g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0007t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0007t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0007t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0007t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0007t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0007t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0007t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0007t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0007t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0009t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0009t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0009t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0009t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0009t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0009t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0009t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0009t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0012t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0012t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0012t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0015t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0017t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0001c0021t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0008t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0008t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0008t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0008t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0008t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0008t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0008t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0016t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0002c0018t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0003c0010t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0003c0010t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0003c0010t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0003c0010t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0003c0010t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0003c0010t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0003c0019t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0004c0011t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0004c0011t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0004c0011t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0004c0022t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0005c0013t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0006c0014t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0006c0014t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0007c0023t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
a0008c0020t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0004 | t0001 | g0099 | EUR | GBR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00280 | hp2 | a0001 | c0007 | t0002 | g0285 | EUR | FIN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00408 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00408 | hp2 | a0001 | c0003 | t0002 | g0080 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00423 | hp1 | a0001 | c0006 | t0002 | g0048 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00423 | hp2 | a0001 | c0002 | t0003 | g0224 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00438 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00544 | hp1 | a0001 | c0003 | t0002 | g0023 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00597 | hp1 | a0001 | c0009 | t0001 | g0069 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00597 | hp2 | a0001 | c0002 | t0003 | g0242 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00609 | hp1 | a0001 | c0002 | t0003 | g0190 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00609 | hp2 | a0001 | c0005 | t0002 | g0197 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00621 | hp1 | a0001 | c0006 | t0002 | g0048 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00642 | hp1 | a0001 | c0002 | t0003 | g0041 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00735 | hp1 | a0001 | c0003 | t0002 | g0083 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00741 | hp1 | a0002 | c0004 | t0001 | g0028 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0043 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0016 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01106 | hp2 | a0001 | c0007 | t0002 | g0277 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0216 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01168 | hp1 | a0001 | c0003 | t0002 | g0085 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01169 | hp1 | a0001 | c0003 | t0002 | g0086 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01175 | hp2 | a0002 | c0004 | t0001 | g0105 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01192 | hp1 | a0001 | c0003 | t0002 | g0027 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01243 | hp2 | a0001 | c0002 | t0003 | g0041 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01255 | hp1 | a0002 | c0004 | t0001 | g0103 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01257 | hp1 | a0001 | c0015 | t0003 | g0042 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01258 | hp2 | a0001 | c0015 | t0003 | g0042 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01346 | hp1 | a0001 | c0002 | t0003 | g0043 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01358 | hp1 | a0002 | c0008 | t0001 | g0064 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01361 | hp1 | a0001 | c0003 | t0002 | g0061 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01361 | hp2 | a0001 | c0002 | t0003 | g0219 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01496 | hp2 | a0001 | c0021 | t0002 | g0280 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01515 | hp1 | a0001 | c0002 | t0003 | g0217 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01516 | hp2 | a0001 | c0002 | t0003 | g0260 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0291 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01891 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01928 | hp2 | a0001 | c0003 | t0002 | g0081 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01952 | hp1 | a0001 | c0002 | t0003 | g0016 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01952 | hp2 | a0001 | c0002 | t0003 | g0233 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01978 | hp1 | a0001 | c0002 | t0003 | g0244 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01978 | hp2 | a0001 | c0002 | t0003 | g0113 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01981 | hp1 | a0001 | c0007 | t0002 | g0276 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01981 | hp2 | a0001 | c0005 | t0002 | g0198 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01993 | hp1 | a0001 | c0005 | t0002 | g0015 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG01993 | hp2 | a0001 | c0002 | t0003 | g0132 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02004 | hp1 | a0001 | c0005 | t0002 | g0015 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02004 | hp2 | a0001 | c0002 | t0003 | g0051 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02055 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02056 | hp1 | a0003 | c0010 | t0002 | g0019 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02071 | hp1 | a0001 | c0002 | t0003 | g0225 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02071 | hp2 | a0001 | c0002 | t0003 | g0265 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02080 | hp1 | a0001 | c0002 | t0003 | g0266 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0227 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02129 | hp1 | a0001 | c0006 | t0002 | g0201 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02129 | hp2 | a0001 | c0003 | t0002 | g0066 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02135 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02135 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02145 | hp2 | a0001 | c0002 | t0003 | g0245 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02148 | hp1 | a0001 | c0002 | t0003 | g0268 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02148 | hp2 | a0001 | c0003 | t0002 | g0026 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02155 | hp2 | a0001 | c0002 | t0003 | g0236 | EAS | CDX | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02257 | hp1 | a0005 | c0013 | t0002 | g0008 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02257 | hp2 | a0001 | c0009 | t0002 | g0063 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02258 | hp1 | a0008 | c0020 | t0001 | g0281 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02258 | hp2 | a0001 | c0002 | t0003 | g0248 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02273 | hp1 | a0001 | c0003 | t0002 | g0026 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02273 | hp2 | a0001 | c0002 | t0003 | g0241 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02280 | hp2 | a0001 | c0009 | t0002 | g0057 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02300 | hp1 | a0001 | c0002 | t0003 | g0051 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02300 | hp2 | a0001 | c0005 | t0002 | g0203 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02451 | hp2 | a0001 | c0006 | t0002 | g0252 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02523 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02572 | hp1 | a0001 | c0002 | t0003 | g0005 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0290 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02615 | hp1 | a0001 | c0007 | t0002 | g0287 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02622 | hp2 | a0002 | c0004 | t0001 | g0101 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02683 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02698 | hp2 | a0001 | c0003 | t0002 | g0006 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02717 | hp1 | a0001 | c0003 | t0002 | g0054 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02735 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02735 | hp2 | a0003 | c0010 | t0002 | g0059 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0211 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02809 | hp1 | a0002 | c0004 | t0001 | g0161 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02809 | hp2 | a0002 | c0004 | t0001 | g0092 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02818 | hp2 | a0002 | c0004 | t0001 | g0091 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02886 | hp2 | a0001 | c0006 | t0002 | g0167 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02895 | hp1 | a0002 | c0004 | t0001 | g0093 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02895 | hp2 | a0001 | c0007 | t0002 | g0286 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02896 | hp1 | a0001 | c0007 | t0002 | g0288 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02896 | hp2 | a0004 | c0011 | t0002 | g0034 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02922 | hp1 | a0001 | c0007 | t0002 | g0282 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02922 | hp2 | a0005 | c0013 | t0002 | g0008 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02970 | hp2 | a0001 | c0006 | t0001 | g0166 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02976 | hp2 | a0002 | c0004 | t0001 | g0162 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03098 | hp2 | a0001 | c0009 | t0002 | g0056 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03130 | hp2 | a0002 | c0004 | t0001 | g0094 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03195 | hp1 | a0006 | c0014 | t0001 | g0153 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03195 | hp2 | a0001 | c0007 | t0002 | g0052 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03209 | hp1 | a0001 | c0006 | t0002 | g0273 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03209 | hp2 | a0002 | c0018 | t0001 | g0158 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03225 | hp1 | a0001 | c0007 | t0002 | g0278 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03225 | hp2 | a0004 | c0011 | t0002 | g0168 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03239 | hp2 | a0001 | c0003 | t0002 | g0068 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03453 | hp1 | a0004 | c0011 | t0002 | g0034 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03453 | hp2 | a0002 | c0004 | t0001 | g0164 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03486 | hp2 | a0001 | c0006 | t0002 | g0274 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03516 | hp2 | a0002 | c0004 | t0001 | g0163 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03540 | hp1 | a0002 | c0004 | t0001 | g0104 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03540 | hp2 | a0006 | c0014 | t0001 | g0152 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03579 | hp1 | a0001 | c0009 | t0001 | g0053 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03579 | hp2 | a0002 | c0004 | t0001 | g0106 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03669 | hp1 | a0001 | c0005 | t0002 | g0202 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03688 | hp1 | a0002 | c0004 | t0001 | g0097 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03704 | hp1 | a0002 | c0004 | t0001 | g0028 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0230 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03831 | hp2 | a0001 | c0006 | t0002 | g0157 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03834 | hp1 | a0002 | c0004 | t0001 | g0096 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03927 | hp1 | a0001 | c0002 | t0003 | g0238 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03927 | hp2 | a0001 | c0005 | t0002 | g0205 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0065 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG04115 | hp2 | a0001 | c0002 | t0003 | g0218 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG04184 | hp1 | a0001 | c0009 | t0001 | g0084 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG04204 | hp2 | a0001 | c0002 | t0003 | g0232 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | YRI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18612 | hp1 | a0001 | c0002 | t0003 | g0088 | EAS | CHB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18747 | hp1 | a0001 | c0002 | t0003 | g0017 | EAS | CHB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0017 | EAS | CHB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18940 | hp1 | a0001 | c0003 | t0002 | g0062 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18940 | hp2 | a0001 | c0009 | t0003 | g0087 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18942 | hp1 | a0001 | c0005 | t0002 | g0195 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18943 | hp2 | a0002 | c0016 | t0003 | g0070 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18944 | hp1 | a0001 | c0017 | t0002 | g0078 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18944 | hp2 | a0001 | c0012 | t0002 | g0073 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18946 | hp1 | a0001 | c0002 | t0003 | g0253 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18947 | hp2 | a0001 | c0003 | t0002 | g0079 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18950 | hp1 | a0001 | c0002 | t0003 | g0047 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18950 | hp2 | a0001 | c0006 | t0002 | g0156 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18952 | hp2 | a0001 | c0006 | t0002 | g0011 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18953 | hp1 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18953 | hp2 | a0001 | c0002 | t0003 | g0267 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18956 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18959 | hp1 | a0001 | c0006 | t0002 | g0171 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18959 | hp2 | a0002 | c0008 | t0003 | g0071 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18960 | hp1 | a0001 | c0005 | t0002 | g0004 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18961 | hp1 | a0001 | c0002 | t0003 | g0036 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18961 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18962 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0239 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18963 | hp1 | a0001 | c0005 | t0002 | g0004 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18963 | hp2 | a0001 | c0006 | t0002 | g0033 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18964 | hp1 | a0003 | c0010 | t0003 | g0021 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18965 | hp1 | a0002 | c0008 | t0001 | g0024 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18965 | hp2 | a0001 | c0002 | t0003 | g0269 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18966 | hp2 | a0001 | c0002 | t0003 | g0039 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18968 | hp1 | a0001 | c0002 | t0003 | g0240 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18969 | hp2 | a0001 | c0006 | t0002 | g0011 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18972 | hp1 | a0001 | c0006 | t0002 | g0135 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18972 | hp2 | a0001 | c0003 | t0002 | g0082 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18973 | hp2 | a0001 | c0002 | t0003 | g0044 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18974 | hp1 | a0002 | c0008 | t0001 | g0024 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18974 | hp2 | a0001 | c0006 | t0002 | g0011 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18975 | hp1 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18975 | hp2 | a0002 | c0008 | t0001 | g0076 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18977 | hp1 | a0001 | c0002 | t0003 | g0249 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18979 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18979 | hp2 | a0001 | c0005 | t0002 | g0004 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18980 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18982 | hp2 | a0001 | c0005 | t0002 | g0200 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18983 | hp2 | a0001 | c0006 | t0002 | g0180 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18984 | hp2 | a0001 | c0002 | t0003 | g0044 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18988 | hp1 | a0001 | c0002 | t0003 | g0036 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18988 | hp2 | a0001 | c0006 | t0002 | g0033 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18989 | hp2 | a0001 | c0005 | t0002 | g0004 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18990 | hp1 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18990 | hp2 | a0001 | c0005 | t0002 | g0040 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18991 | hp1 | a0003 | c0010 | t0003 | g0060 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18991 | hp2 | a0001 | c0006 | t0002 | g0141 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18992 | hp2 | a0001 | c0002 | t0003 | g0262 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18995 | hp1 | a0002 | c0004 | t0001 | g0264 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18995 | hp2 | a0001 | c0002 | t0003 | g0263 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18998 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18998 | hp2 | a0003 | c0010 | t0003 | g0020 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18999 | hp1 | a0003 | c0010 | t0003 | g0020 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18999 | hp2 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19000 | hp1 | a0002 | c0008 | t0001 | g0025 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19000 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19001 | hp1 | a0003 | c0010 | t0002 | g0019 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19001 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19003 | hp1 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19004 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19006 | hp2 | a0001 | c0002 | t0003 | g0246 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19007 | hp1 | a0003 | c0010 | t0003 | g0021 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19007 | hp2 | a0001 | c0012 | t0002 | g0055 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19010 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19010 | hp2 | a0001 | c0003 | t0002 | g0027 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19012 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19030 | hp2 | a0002 | c0004 | t0001 | g0102 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19043 | hp2 | a0004 | c0022 | t0002 | g0279 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19054 | hp1 | a0001 | c0002 | t0003 | g0237 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19054 | hp2 | a0001 | c0003 | t0002 | g0022 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19056 | hp1 | a0001 | c0009 | t0003 | g0067 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19057 | hp2 | a0001 | c0005 | t0002 | g0004 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19058 | hp2 | a0003 | c0010 | t0003 | g0058 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19062 | hp1 | a0002 | c0008 | t0001 | g0025 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19062 | hp2 | a0001 | c0002 | t0003 | g0231 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19063 | hp1 | a0002 | c0008 | t0001 | g0074 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19065 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19066 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19074 | hp1 | a0001 | c0005 | t0002 | g0199 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19074 | hp2 | a0001 | c0012 | t0002 | g0072 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19076 | hp1 | a0001 | c0005 | t0002 | g0196 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19076 | hp2 | a0001 | c0002 | t0003 | g0039 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19079 | hp1 | a0001 | c0005 | t0002 | g0204 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19079 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19082 | hp1 | a0001 | c0002 | t0003 | g0047 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19082 | hp2 | a0002 | c0008 | t0001 | g0075 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19083 | hp2 | a0001 | c0002 | t0003 | g0247 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19086 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19087 | hp1 | a0001 | c0003 | t0002 | g0022 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19087 | hp2 | a0001 | c0005 | t0002 | g0040 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19088 | hp1 | a0001 | c0009 | t0003 | g0077 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19090 | hp1 | a0001 | c0002 | t0003 | g0220 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19240 | hp1 | a0001 | c0007 | t0001 | g0284 | AFR | YRI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA20129 | hp1 | a0001 | c0002 | t0003 | g0234 | AFR | ASW | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA20129 | hp2 | a0007 | c0023 | t0002 | g0289 | AFR | ASW | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA20805 | hp2 | a0001 | c0002 | t0003 | g0235 | EUR | TSI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA20905 | hp1 | a0001 | c0002 | t0003 | g0215 | SAS | GIH | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA20905 | hp2 | a0002 | c0004 | t0001 | g0098 | SAS | GIH | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02109 | hp2 | a0002 | c0004 | t0001 | g0095 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02559 | hp1 | a0001 | c0007 | t0002 | g0052 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG02559 | hp2 | a0005 | c0013 | t0002 | g0008 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03471 | hp1 | a0003 | c0019 | t0002 | g0271 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG06807 | hp1 | a0004 | c0011 | t0002 | g0169 | AFR | USA | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | USA | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA18955 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA20300 | hp1 | a0001 | c0007 | t0002 | g0283 | AFR | USA | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA20300 | hp2 | a0001 | c0005 | t0002 | g0015 | AFR | USA | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0090 | REF | REF | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0154 | REF | REF | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50905402
|
T | C | 2 | a0004a0005 | 8 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(5): Show |
missense_variant | MODERATE | c.2534A>G | p.Asn845Ser | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 20/20 | 2614/2799 | 2534/2544 | 845/847 | chr14 | 50905402 | ||
chr14:50905520
|
T | A | 1 | a0003 | 10 | HG02056.hp1 HG02735.hp2 HG03471.hp1 others(7): Show |
missense_variant | MODERATE | c.2416A>T | p.Ile806Leu | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 20/20 | 2496/2799 | 2416/2544 | 806/847 | chr14 | 50905520 | ||
chr14:50911988
|
A | G | 1 | a0008 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1817T>C | p.Ile606Thr | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 15/20 | 1897/2799 | 1817/2544 | 606/847 | chr14 | 50911988 | ||
chr14:50916999
|
C | T | 1 | a0006 | 2 | HG03195.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.962G>A | p.Arg321His | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 8/20 | 1042/2799 | 962/2544 | 321/847 | chr14 | 50916999 | ||
chr14:50917033
|
G | A | 1 | a0005 | 3 | HG02257.hp1 HG02559.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.928C>T | p.Arg310Cys | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 8/20 | 1008/2799 | 928/2544 | 310/847 | chr14 | 50917033 | ||
chr14:50921064
|
C | T | 1 | a0002 | 33 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(30): Show |
missense_variant | MODERATE | c.664G>A | p.Val222Ile | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/20 | 744/2799 | 664/2544 | 222/847 | chr14 | 50921064 | ||
chr14:50944228
|
G | A | 1 | a0007 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.176C>T | p.Thr59Met | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/20 | 256/2799 | 176/2544 | 59/847 | chr14 | 50944228 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50909960
|
A | G | 2 | a0001c0005a0001c0012 | 23 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(20): Show |
synonymous_variant | LOW | c.2112T>C | p.Ala704Ala | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/20 | 2192/2799 | 2112/2544 | 704/847 | chr14 | 50909960 | ||
chr14:50910056
|
G | A | 10 | a0001c0003a0001c0006a0001c0007others(7): Show | 97 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
synonymous_variant | LOW | c.2016C>T | p.Thr672Thr | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/20 | 2096/2799 | 2016/2544 | 672/847 | chr14 | 50910056 | ||
chr14:50913032
|
C | T | 1 | a0001c0017 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.1617G>A | p.Lys539Lys | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/20 | 1697/2799 | 1617/2544 | 539/847 | chr14 | 50913032 | ||
chr14:50916714
|
G | A | 3 | a0001c0002a0001c0015a0004c0022 | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
synonymous_variant | LOW | c.1020C>T | p.Asp340Asp | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/20 | 1100/2799 | 1020/2544 | 340/847 | chr14 | 50916714 | ||
chr14:50924026
|
C | A | 1 | a0001c0015 | 2 | HG01257.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.603G>T | p.Val201Val | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/20 | 683/2799 | 603/2544 | 201/847 | chr14 | 50924026 | ||
chr14:50944251
|
G | A | 5 | a0001c0007a0001c0021a0004c0022others(2): Show | 16 | HG00280.hp2 HG01106.hp2 HG01496.hp2 others(13): Show |
synonymous_variant | LOW | c.153C>T | p.Asp51Asp | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/20 | 233/2799 | 153/2544 | 51/847 | chr14 | 50944251 | ||
chr14:50944311
|
A | G | 7 | a0001c0003a0001c0009a0001c0012others(4): Show | 57 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(54): Show |
synonymous_variant | LOW | c.93T>C | p.Ser31Ser | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/20 | 173/2799 | 93/2544 | 31/847 | chr14 | 50944311 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50905380
|
CA | C | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(20): Show | 219 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*11delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 20/20 | 11 | chr14 | 50905380 | |||||
chr14:50905385
|
C | G | 7 | a0001c0001t0003a0001c0002t0003a0001c0009t0003others(4): Show | 104 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*7G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 20/20 | 7 | chr14 | 50905385 | |||||
chr14:50944432
|
T | G | 1 | a0001c0001t0004 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-29A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/20 | 29 | chr14 | 50944432 | |||||
chr14:50944474
|
G | A | 1 | a0001c0001t0005 | 1 | HG01891.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-71C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/20 | chr14 | 50944474 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50905597
|
C | T | 24 | a0001c0001t0002g0119a0001c0005t0002g0004a0001c0005t0002g0015others(21): Show | 34 | HG00609.hp2 HG01884.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.2380-41G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905597 | ||||||
chr14:50905615
|
A | G | 113 | a0001c0001t0002g0100a0001c0001t0002g0114a0001c0001t0002g0115others(110): Show | 159 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.2380-59T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905615 | ||||||
chr14:50905631
|
C | T | 1 | a0003c0010t0002g0059 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2380-75G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905631 | ||||||
chr14:50905639
|
C | A | 3 | a0001c0001t0002g0133a0001c0009t0002g0056a0001c0009t0002g0063 | 3 | HG02145.hp1 HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2380-83G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905639 | ||||||
chr14:50905687
|
A | G | 1 | a0001c0007t0002g0285 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2380-131T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905687 | ||||||
chr14:50905690
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2380-134A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905690 | ||||||
chr14:50905719
|
G | C | 1 | a0001c0009t0001g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2380-163C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905719 | ||||||
chr14:50905725
|
A | G | 2 | a0001c0006t0002g0167a0007c0023t0002g0289 | 2 | HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2380-169T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905725 | ||||||
chr14:50905820
|
A | G | 1 | a0002c0008t0003g0071 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2380-264T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905820 | ||||||
chr14:50905872
|
T | C | 103 | a0001c0001t0002g0100a0001c0001t0002g0114a0001c0001t0002g0115others(100): Show | 148 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.2380-316A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905872 | ||||||
chr14:50905888
|
G | A | 97 | a0001c0001t0002g0100a0001c0001t0002g0114a0001c0001t0002g0115others(94): Show | 139 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.2380-332C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905888 | ||||||
chr14:50905950
|
T | C | 1 | a0001c0003t0002g0061 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2380-394A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905950 | ||||||
chr14:50906203
|
T | C | 5 | a0004c0011t0002g0034a0004c0011t0002g0168a0004c0011t0002g0169others(2): Show | 8 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2380-647A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906203 | ||||||
chr14:50906256
|
G | A | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2380-700C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906256 | ||||||
chr14:50906323
|
A | G | 5 | a0004c0011t0002g0034a0004c0011t0002g0168a0004c0011t0002g0169others(2): Show | 8 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2380-767T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906323 | ||||||
chr14:50906456
|
C | T | 3 | a0001c0002t0003g0041a0001c0002t0003g0216a0001c0002t0003g0218 | 4 | HG00642.hp1 HG01109.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.2380-900G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906456 | ||||||
chr14:50906464
|
T | C | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2380-908A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906464 | ||||||
chr14:50906487
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2380-931A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906487 | ||||||
chr14:50906529
|
A | T | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2380-973T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906529 | ||||||
chr14:50906542
|
A | C | 2 | a0002c0004t0001g0161a0002c0018t0001g0158 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2380-986T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906542 | ||||||
chr14:50906583
|
G | A | 2 | a0001c0003t0002g0022a0001c0003t0002g0062 | 3 | NA18940.hp1 NA19054.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2380-1027C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906583 | ||||||
chr14:50906726
|
G | A | 1 | a0001c0003t0002g0080 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2380-1170C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906726 | ||||||
chr14:50906943
|
A | T | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+1328T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906943 | ||||||
chr14:50907004
|
A | C | 1 | a0001c0002t0003g0243 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2379+1267T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907004 | ||||||
chr14:50907005
|
C | A | 1 | a0001c0002t0003g0243 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2379+1266G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907005 | ||||||
chr14:50907203
|
C | T | 9 | a0001c0001t0002g0119a0001c0001t0005g0291a0003c0010t0002g0019others(6): Show | 12 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.2379+1068G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907203 | ||||||
chr14:50907205
|
C | T | 1 | a0002c0004t0001g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2379+1066G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907205 | ||||||
chr14:50907206
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2379+1065G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907206 | ||||||
chr14:50907225
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2379+1046G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907225 | ||||||
chr14:50907280
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2379+991G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907280 | ||||||
chr14:50907281
|
G | A | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+990C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907281 | ||||||
chr14:50907463
|
T | C | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+808A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907463 | ||||||
chr14:50907519
|
C | G | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+752G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907519 | ||||||
chr14:50907637
|
C | T | 1 | a0001c0007t0002g0288 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2379+634G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907637 | ||||||
chr14:50907707
|
A | T | 163 | a0001c0001t0002g0010a0001c0001t0002g0100a0001c0001t0002g0114others(160): Show | 222 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.2379+564T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907707 | ||||||
chr14:50907759
|
CA | C | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+511delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907759 | ||||||
chr14:50907776
|
T | G | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+495A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907776 | ||||||
chr14:50907779
|
C | T | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+492G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907779 | ||||||
chr14:50907872
|
T | C | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+399A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907872 | ||||||
chr14:50907983
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2379+288G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907983 | ||||||
chr14:50907993
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0251 | 2 | NA18966.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2379+278C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907993 | ||||||
chr14:50908020
|
C | CA | 81 | a0001c0001t0002g0010a0001c0001t0002g0100a0001c0001t0002g0114others(78): Show | 114 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.2379+250dupT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908020 | ||||||
chr14:50908020
|
C | CAA | 8 | a0001c0001t0002g0117a0001c0001t0002g0209a0001c0001t0005g0291others(5): Show | 9 | HG01261.hp2 HG01891.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2379+249_2379+250d others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908020 | ||||||
chr14:50908020
|
C | CAAA | 6 | a0003c0010t0002g0019a0003c0010t0002g0059a0003c0010t0003g0020others(3): Show | 9 | HG02056.hp1 HG02735.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2379+248_2379+250d others(5): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908020 | ||||||
chr14:50908020
|
CA | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(119): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.2379+250delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908020 | ||||||
chr14:50908020
|
CAA | C | 18 | a0001c0001t0001g0111a0001c0001t0001g0188a0001c0003t0002g0054others(15): Show | 20 | HG00280.hp2 HG01106.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.2379+249_2379+250d others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908020 | ||||||
chr14:50908100
|
G | A | 8 | a0001c0001t0002g0119a0003c0010t0002g0019a0003c0010t0002g0059others(5): Show | 11 | HG01884.hp2 HG02056.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.2379+171C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908100 | ||||||
chr14:50908101
|
G | GT | 6 | a0001c0001t0001g0122a0001c0001t0001g0187a0001c0002t0003g0211others(3): Show | 6 | HG01175.hp1 HG01175.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2379+169dupA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908101 | ||||||
chr14:50908139
|
GT | G | 10 | a0001c0001t0002g0119a0001c0001t0002g0155a0001c0001t0005g0291others(7): Show | 13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+131delA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908139 | ||||||
chr14:50908139
|
GTTT | G | 6 | a0001c0003t0002g0061a0004c0011t0002g0034a0004c0011t0002g0168others(3): Show | 9 | HG01361.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2379+129_2379+131d others(5): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908139 | ||||||
chr14:50908409
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0144a0001c0001t0001g0150 | 4 | HG01257.hp2 HG01261.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2313-72A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 18/19 | chr14 | 50908409 | ||||||
chr14:50908532
|
G | T | 107 | a0001c0001t0002g0100a0001c0001t0002g0114a0001c0001t0002g0115others(104): Show | 150 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.2313-195C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 18/19 | chr14 | 50908532 | ||||||
chr14:50908764
|
G | C | 1 | a0001c0001t0005g0291 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2312+57C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 18/19 | chr14 | 50908764 | ||||||
chr14:50908809
|
A | G | 1 | a0001c0001t0005g0291 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2312+12T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 18/19 | chr14 | 50908809 | ||||||
chr14:50908981
|
T | TA | 146 | a0001c0001t0002g0010a0001c0001t0002g0100a0001c0001t0002g0114others(143): Show | 198 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.2178-27dupT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50908981 | ||||||
chr14:50908990
|
G | C | 1 | a0008c0020t0001g0281 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2178-35C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50908990 | ||||||
chr14:50909079
|
T | G | 163 | a0001c0001t0002g0010a0001c0001t0002g0100a0001c0001t0002g0114others(160): Show | 222 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.2178-124A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909079 | ||||||
chr14:50909108
|
T | C | 140 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(137): Show | 192 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.2178-153A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909108 | ||||||
chr14:50909361
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2178-406C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909361 | ||||||
chr14:50909379
|
T | C | 23 | a0001c0001t0002g0100a0001c0001t0002g0114a0001c0001t0002g0115others(20): Show | 30 | HG00609.hp2 HG01496.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.2178-424A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909379 | ||||||
chr14:50909517
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2177+378C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909517 | ||||||
chr14:50909519
|
A | G | 72 | a0001c0001t0002g0100a0001c0001t0002g0114a0001c0001t0002g0115others(69): Show | 104 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2177+376T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909519 | ||||||
chr14:50909541
|
G | A | 1 | a0001c0002t0003g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2177+354C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909541 | ||||||
chr14:50909553
|
G | C | 24 | a0001c0001t0002g0119a0001c0005t0002g0004a0001c0005t0002g0015others(21): Show | 34 | HG00609.hp2 HG01884.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.2177+342C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909553 | ||||||
chr14:50909570
|
AC | A | 18 | a0001c0001t0002g0119a0001c0001t0002g0212a0001c0005t0002g0004others(15): Show | 25 | HG00609.hp2 HG01884.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.2177+324delG | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909570 | ||||||
chr14:50909624
|
C | T | 16 | a0001c0005t0002g0004a0001c0005t0002g0015a0001c0005t0002g0040others(13): Show | 23 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(20): Show |
intron_variant | MODIFIER | c.2177+271G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909624 | ||||||
chr14:50909795
|
T | C | 16 | a0001c0005t0002g0004a0001c0005t0002g0015a0001c0005t0002g0040others(13): Show | 23 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(20): Show |
intron_variant | MODIFIER | c.2177+100A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909795 | ||||||
chr14:50909850
|
G | C | 1 | a0001c0002t0003g0239 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2177+45C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909850 | ||||||
chr14:50909861
|
A | G | 12 | a0001c0005t0002g0004a0001c0005t0002g0040a0001c0005t0002g0195others(9): Show | 17 | HG00609.hp2 HG03669.hp1 HG03927.hp2 others(14): Show |
intron_variant | MODIFIER | c.2177+34T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909861 | ||||||
chr14:50910162
|
T | C | 81 | a0001c0001t0002g0212a0001c0003t0002g0006a0001c0003t0002g0022others(78): Show | 99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1970-60A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910162 | ||||||
chr14:50910209
|
T | C | 3 | a0001c0001t0002g0133a0001c0009t0002g0056a0001c0009t0002g0063 | 3 | HG02145.hp1 HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1970-107A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910209 | ||||||
chr14:50910314
|
C | T | 15 | a0001c0003t0002g0054a0001c0006t0002g0252a0001c0006t0002g0273others(12): Show | 16 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.1970-212G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910314 | ||||||
chr14:50910320
|
A | G | 1 | a0003c0019t0002g0271 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1970-218T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910320 | ||||||
chr14:50910349
|
G | A | 1 | a0002c0004t0001g0097 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1970-247C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910349 | ||||||
chr14:50910412
|
A | T | 1 | a0001c0002t0003g0243 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1970-310T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910412 | ||||||
chr14:50910413
|
T | A | 1 | a0001c0002t0003g0243 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1970-311A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910413 | ||||||
chr14:50910452
|
T | C | 28 | a0002c0004t0001g0028a0002c0004t0001g0091a0002c0004t0001g0092others(25): Show | 31 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.1970-350A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910452 | ||||||
chr14:50910514
|
G | T | 80 | a0001c0001t0002g0212a0001c0003t0002g0006a0001c0003t0002g0022others(77): Show | 98 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1970-412C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910514 | ||||||
chr14:50910660
|
C | T | 219 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0089others(216): Show | 285 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1970-558G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910660 | ||||||
chr14:50910789
|
T | C | 80 | a0001c0003t0002g0006a0001c0003t0002g0022a0001c0003t0002g0023others(77): Show | 98 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1970-687A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910789 | ||||||
chr14:50910804
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1970-702T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910804 | ||||||
chr14:50910833
|
C | A | 1 | a0001c0005t0002g0205 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1970-731G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910833 | ||||||
chr14:50910846
|
C | T | 1 | a0002c0008t0001g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1970-744G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910846 | ||||||
chr14:50910895
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0160 | 2 | NA19012.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1970-793G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910895 | ||||||
chr14:50910990
|
T | G | 8 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(5): Show | 10 | HG01261.hp2 HG01884.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1969+740A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910990 | ||||||
chr14:50911048
|
C | A | 1 | a0001c0001t0002g0119 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1969+682G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911048 | ||||||
chr14:50911078
|
C | T | 1 | a0001c0002t0003g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1969+652G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911078 | ||||||
chr14:50911152
|
C | T | 5 | a0004c0011t0002g0034a0004c0011t0002g0168a0004c0011t0002g0169others(2): Show | 8 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1969+578G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911152 | ||||||
chr14:50911159
|
C | T | 81 | a0001c0001t0002g0212a0001c0003t0002g0006a0001c0003t0002g0022others(78): Show | 99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1969+571G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911159 | ||||||
chr14:50911264
|
C | G | 1 | a0001c0003t0002g0079 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1969+466G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911264 | ||||||
chr14:50911326
|
G | C | 1 | a0001c0017t0002g0078 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1969+404C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911326 | ||||||
chr14:50911347
|
G | T | 1 | a0001c0002t0003g0235 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1969+383C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911347 | ||||||
chr14:50911371
|
T | C | 24 | a0001c0001t0001g0007a0001c0001t0001g0089a0001c0001t0001g0123others(21): Show | 27 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1969+359A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911371 | ||||||
chr14:50911438
|
C | A | 1 | a0004c0011t0002g0168 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1969+292G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911438 | ||||||
chr14:50911592
|
G | A | 9 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(6): Show | 11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1969+138C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911592 | ||||||
chr14:50911872
|
CT | C | 191 | a0001c0001t0002g0010a0001c0001t0002g0100a0001c0001t0002g0114others(188): Show | 253 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(250): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1828-2delA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 15/19 | chr14 | 50911872 | ||||||
chr14:50911892
|
C | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0144a0001c0001t0001g0150others(1): Show | 5 | HG01257.hp2 HG01261.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828-21G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 15/19 | chr14 | 50911892 | ||||||
chr14:50912128
|
G | A | 1 | a0001c0006t0002g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1768+28C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 14/19 | chr14 | 50912128 | ||||||
chr14:50912309
|
A | G | 9 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(6): Show | 11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1621-6T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912309 | ||||||
chr14:50912331
|
C | T | 1 | a0001c0003t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1621-28G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912331 | ||||||
chr14:50912382
|
G | A | 80 | a0001c0001t0002g0212a0001c0003t0002g0006a0001c0003t0002g0022others(77): Show | 98 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1621-79C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912382 | ||||||
chr14:50912435
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0144others(1): Show | 9 | HG00639.hp1 HG01081.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621-132G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912435 | ||||||
chr14:50912461
|
C | T | 2 | a0001c0003t0002g0023a0001c0003t0002g0068 | 3 | HG00544.hp1 HG03239.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1621-158G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912461 | ||||||
chr14:50912568
|
C | G | 1 | a0001c0002t0003g0241 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1621-265G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912568 | ||||||
chr14:50912631
|
C | T | 1 | a0001c0002t0003g0263 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1621-328G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912631 | ||||||
chr14:50912632
|
G | A | 10 | a0001c0001t0002g0133a0001c0009t0002g0056a0001c0009t0002g0057others(7): Show | 13 | HG02056.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1621-329C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912632 | ||||||
chr14:50912793
|
A | C | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1620+236T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912793 | ||||||
chr14:50912815
|
G | A | 3 | a0001c0005t0002g0015a0001c0005t0002g0198a0001c0005t0002g0203 | 5 | HG01981.hp2 HG01993.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1620+214C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912815 | ||||||
chr14:50912827
|
G | T | 5 | a0001c0001t0002g0100a0001c0001t0002g0114a0001c0001t0002g0115others(2): Show | 5 | HG01496.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1620+202C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912827 | ||||||
chr14:50912859
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1620+170G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912859 | ||||||
chr14:50912872
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1620+157A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912872 | ||||||
chr14:50912902
|
C | T | 1 | a0001c0001t0001g0037 | 2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.1620+127G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912902 | ||||||
chr14:50913390
|
G | T | 2 | a0001c0007t0002g0276a0001c0007t0002g0277 | 2 | HG01106.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1519-260C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913390 | ||||||
chr14:50913403
|
G | T | 1 | a0001c0001t0001g0037 | 2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.1519-273C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913403 | ||||||
chr14:50913418
|
C | A | 2 | a0002c0004t0001g0095a0002c0004t0001g0099 | 2 | HG00140.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1519-288G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913418 | ||||||
chr14:50913434
|
C | T | 9 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(6): Show | 11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1519-304G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913434 | ||||||
chr14:50913495
|
C | T | 19 | a0001c0005t0002g0004a0001c0005t0002g0015a0001c0005t0002g0040others(16): Show | 26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.1519-365G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913495 | ||||||
chr14:50913505
|
G | T | 1 | a0001c0002t0003g0172 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1519-375C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913505 | ||||||
chr14:50913517
|
G | A | 1 | a0001c0002t0003g0240 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1519-387C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913517 | ||||||
chr14:50913587
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0038others(8): Show | 15 | HG00558.hp1 HG00673.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1519-457T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913587 | ||||||
chr14:50913596
|
G | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0038others(6): Show | 13 | HG00558.hp1 HG02015.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1519-466C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913596 | ||||||
chr14:50913609
|
T | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0038others(8): Show | 15 | HG00558.hp1 HG00673.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1519-479A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913609 | ||||||
chr14:50913626
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1519-496C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913626 | ||||||
chr14:50913681
|
T | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0089a0001c0001t0001g0123others(14): Show | 20 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1519-551A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913681 | ||||||
chr14:50913765
|
C | A | 1 | a0004c0011t0002g0169 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1519-635G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913765 | ||||||
chr14:50913788
|
C | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0050a0001c0001t0001g0228others(4): Show | 10 | HG00741.hp2 HG01071.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1519-658G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913788 | ||||||
chr14:50913838
|
G | A | 1 | a0001c0006t0002g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1519-708C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913838 | ||||||
chr14:50913876
|
C | T | 5 | a0001c0001t0001g0151a0001c0001t0002g0100a0001c0001t0002g0115others(2): Show | 5 | HG01496.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1519-746G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913876 | ||||||
chr14:50913962
|
C | G | 5 | a0001c0006t0002g0011a0001c0006t0002g0033a0001c0006t0002g0135others(2): Show | 8 | NA18950.hp2 NA18952.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.1518+739G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913962 | ||||||
chr14:50914007
|
CACTGGTA others(1): Show |
C | 19 | a0001c0005t0002g0004a0001c0005t0002g0015a0001c0005t0002g0040others(16): Show | 26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.1518+686_1518+693d others(10): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914007 | ||||||
chr14:50914041
|
C | T | 2 | a0001c0003t0002g0026a0001c0003t0002g0081 | 3 | HG01928.hp2 HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1518+660G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914041 | ||||||
chr14:50914402
|
CAGG | C | 9 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(6): Show | 11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1518+296_1518+298d others(5): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914402 | ||||||
chr14:50914496
|
C | CAAT | 68 | a0001c0001t0001g0123a0001c0001t0001g0257a0001c0001t0002g0272others(65): Show | 103 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1518+202_1518+204d others(5): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914496 | ||||||
chr14:50914496
|
C | CAATAAT | 34 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(31): Show | 39 | HG00741.hp1 HG01175.hp2 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.1518+199_1518+204d others(8): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914496 | ||||||
chr14:50914496
|
C | CAATAATA others(2): Show |
47 | a0001c0002t0003g0237a0001c0003t0002g0006a0001c0003t0002g0022others(44): Show | 59 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1518+196_1518+204d others(11): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914496 | ||||||
chr14:50914496
|
C | CAATAATA others(5): Show |
3 | a0002c0004t0001g0097a0002c0004t0001g0102a0002c0004t0001g0103 | 3 | HG01255.hp1 HG03688.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1518+193_1518+204d others(14): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914496 | ||||||
chr14:50914496
|
C | CAATAATA others(17): Show |
2 | a0001c0001t0002g0212a0001c0003t0002g0061 | 2 | HG01361.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1518+181_1518+204d others(26): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914496 | ||||||
chr14:50914568
|
T | C | 190 | a0001c0001t0001g0165a0001c0001t0002g0010a0001c0001t0002g0100others(187): Show | 252 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.1518+133A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914568 | ||||||
chr14:50914662
|
C | T | 1 | a0001c0001t0005g0291 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1518+39G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914662 | ||||||
chr14:50915015
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1404-200T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 11/19 | chr14 | 50915015 | ||||||
chr14:50915167
|
CCTTTT | C | 2 | a0001c0001t0002g0114a0001c0002t0003g0047 | 3 | HG03471.hp2 NA18950.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1403+164_1403+168d others(7): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 11/19 | chr14 | 50915167 | ||||||
chr14:50915178
|
C | CT | 83 | a0001c0001t0001g0165a0001c0003t0002g0006a0001c0003t0002g0022others(80): Show | 101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1403+157dupA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 11/19 | chr14 | 50915178 | ||||||
chr14:50915181
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1403+155A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 11/19 | chr14 | 50915181 | ||||||
chr14:50915232
|
T | A | 60 | a0001c0002t0001g0221a0001c0002t0003g0001a0001c0002t0003g0005others(57): Show | 92 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1403+104A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 11/19 | chr14 | 50915232 | ||||||
chr14:50915550
|
A | G | 1 | a0001c0003t0002g0061 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1240-51T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 10/19 | chr14 | 50915550 | ||||||
chr14:50915619
|
G | A | 1 | a0001c0002t0003g0215 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1240-120C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 10/19 | chr14 | 50915619 | ||||||
chr14:50915640
|
T | C | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(287): Show | 389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.1240-141A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 10/19 | chr14 | 50915640 | ||||||
chr14:50915687
|
T | C | 191 | a0001c0001t0001g0149a0001c0001t0001g0165a0001c0001t0002g0010others(188): Show | 253 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.1239+138A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 10/19 | chr14 | 50915687 | ||||||
chr14:50915977
|
G | T | 1 | a0002c0004t0001g0096 | 1 | HG03834.hp1 | splice_region_variant&intron_variant | LOW | c.1093-6C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50915977 | ||||||
chr14:50916026
|
C | T | 92 | a0001c0001t0001g0149a0001c0001t0001g0165a0001c0001t0002g0010others(89): Show | 112 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1093-55G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916026 | ||||||
chr14:50916027
|
G | A | 1 | a0001c0006t0002g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1093-56C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916027 | ||||||
chr14:50916035
|
C | A | 19 | a0001c0005t0002g0004a0001c0005t0002g0015a0001c0005t0002g0040others(16): Show | 26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.1093-64G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916035 | ||||||
chr14:50916051
|
C | T | 1 | a0001c0006t0001g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1093-80G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916051 | ||||||
chr14:50916165
|
T | A | 2 | a0001c0001t0001g0151a0001c0001t0004g0290 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1093-194A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916165 | ||||||
chr14:50916188
|
A | T | 1 | a0001c0001t0002g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1093-217T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916188 | ||||||
chr14:50916216
|
A | C | 10 | a0001c0001t0002g0133a0001c0009t0002g0056a0001c0009t0002g0057others(7): Show | 13 | HG02056.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1093-245T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916216 | ||||||
chr14:50916223
|
T | C | 95 | a0001c0001t0001g0149a0001c0001t0001g0165a0001c0001t0002g0010others(92): Show | 115 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1093-252A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916223 | ||||||
chr14:50916328
|
A | G | 2 | a0001c0002t0001g0221a0001c0002t0003g0220 | 2 | NA18982.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1092+314T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916328 | ||||||
chr14:50916345
|
C | T | 19 | a0001c0005t0002g0004a0001c0005t0002g0015a0001c0005t0002g0040others(16): Show | 26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.1092+297G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916345 | ||||||
chr14:50916566
|
AAAG | A | 10 | a0001c0001t0002g0133a0001c0009t0002g0056a0001c0009t0002g0057others(7): Show | 13 | HG02056.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1092+73_1092+75del others(3): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916566 | ||||||
chr14:50916921
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.999+41G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 8/19 | chr14 | 50916921 | ||||||
chr14:50917326
|
G | C | 1 | a0002c0004t0001g0161 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.856-221C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917326 | ||||||
chr14:50917491
|
G | A | 81 | a0001c0001t0002g0212a0001c0003t0002g0006a0001c0003t0002g0022others(78): Show | 99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.856-386C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917491 | ||||||
chr14:50917529
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.856-424C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917529 | ||||||
chr14:50917566
|
A | G | 92 | a0001c0001t0002g0133a0001c0001t0002g0212a0001c0003t0002g0006others(89): Show | 113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.856-461T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917566 | ||||||
chr14:50917662
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.856-557C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917662 | ||||||
chr14:50917670
|
AACC | A | 10 | a0001c0002t0003g0043a0001c0002t0003g0051a0001c0002t0003g0230others(7): Show | 12 | HG01081.hp2 HG01346.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.856-568_856-566del others(3): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917670 | ||||||
chr14:50917751
|
G | A | 9 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(6): Show | 11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.856-646C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917751 | ||||||
chr14:50917930
|
T | C | 82 | a0001c0001t0001g0165a0001c0001t0002g0212a0001c0003t0002g0006others(79): Show | 100 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.856-825A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917930 | ||||||
chr14:50918085
|
C | G | 1 | a0004c0022t0002g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.856-980G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918085 | ||||||
chr14:50918215
|
AC | A | 61 | a0001c0002t0001g0221a0001c0002t0003g0001a0001c0002t0003g0005others(58): Show | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.856-1111delG | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918215 | ||||||
chr14:50918217
|
T | A | 61 | a0001c0002t0001g0221a0001c0002t0003g0001a0001c0002t0003g0005others(58): Show | 93 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.856-1112A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918217 | ||||||
chr14:50918286
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.856-1181C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918286 | ||||||
chr14:50918360
|
A | G | 1 | a0001c0002t0003g0246 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.856-1255T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918360 | ||||||
chr14:50918438
|
C | T | 81 | a0001c0001t0002g0212a0001c0003t0002g0006a0001c0003t0002g0022others(78): Show | 99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.856-1333G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918438 | ||||||
chr14:50918455
|
C | T | 6 | a0001c0001t0002g0100a0001c0001t0002g0114a0001c0001t0002g0115others(3): Show | 6 | HG01496.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.856-1350G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918455 | ||||||
chr14:50918517
|
C | A | 2 | a0001c0003t0002g0085a0001c0003t0002g0086 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.856-1412G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918517 | ||||||
chr14:50918587
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.856-1482T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918587 | ||||||
chr14:50918655
|
C | T | 1 | a0003c0010t0002g0059 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.856-1550G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918655 | ||||||
chr14:50919032
|
A | AAAAC | 33 | a0001c0002t0003g0041a0001c0002t0003g0215a0001c0002t0003g0216others(30): Show | 46 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.855+1505_855+1508d others(6): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919032 | ||||||
chr14:50919044
|
C | T | 5 | a0001c0001t0002g0100a0001c0001t0002g0114a0001c0001t0002g0115others(2): Show | 5 | HG01496.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+1497G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919044 | ||||||
chr14:50919093
|
A | G | 83 | a0001c0001t0002g0212a0001c0003t0002g0006a0001c0003t0002g0022others(80): Show | 101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.855+1448T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919093 | ||||||
chr14:50919331
|
G | C | 1 | a0001c0001t0002g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.855+1210C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919331 | ||||||
chr14:50919570
|
T | G | 1 | a0001c0005t0002g0197 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.855+971A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919570 | ||||||
chr14:50919576
|
A | T | 1 | a0001c0009t0003g0087 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.855+965T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919576 | ||||||
chr14:50919666
|
GGT | G | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(199): Show | 288 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.855+873_855+874del others(2): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919666 | ||||||
chr14:50919666
|
GGTGT | G | 62 | a0001c0001t0002g0100a0001c0001t0002g0114a0001c0001t0002g0115others(59): Show | 69 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.855+871_855+874del others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919666 | ||||||
chr14:50919904
|
G | C | 1 | a0001c0001t0002g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.855+637C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919904 | ||||||
chr14:50919947
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.855+594C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919947 | ||||||
chr14:50919948
|
T | C | 94 | a0001c0001t0001g0165a0001c0001t0002g0010a0001c0001t0002g0117others(91): Show | 114 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.855+593A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919948 | ||||||
chr14:50919990
|
G | GT | 7 | a0001c0001t0001g0031a0001c0001t0001g0184a0001c0001t0001g0256others(4): Show | 8 | HG02055.hp1 HG02071.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.855+550dupA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919990 | ||||||
chr14:50919990
|
GT | G | 9 | a0002c0004t0001g0028a0002c0004t0001g0105a0002c0008t0001g0024others(6): Show | 12 | HG00741.hp1 HG01175.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.855+550delA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919990 | ||||||
chr14:50920122
|
G | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0213 | 2 | HG00735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.855+419C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50920122 | ||||||
chr14:50920170
|
G | A | 1 | a0002c0018t0001g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.855+371C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50920170 | ||||||
chr14:50920223
|
A | T | 1 | a0001c0001t0001g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.855+318T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50920223 | ||||||
chr14:50920242
|
C | T | 1 | a0001c0002t0003g0235 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.855+299G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50920242 | ||||||
chr14:50920462
|
T | G | 1 | a0001c0005t0002g0204 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.855+79A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50920462 | ||||||
chr14:50920663
|
C | A | 1 | a0001c0006t0001g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.773-40G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920663 | ||||||
chr14:50920712
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.773-89T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920712 | ||||||
chr14:50920761
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG03017.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.773-138C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920761 | ||||||
chr14:50920836
|
G | C | 94 | a0001c0001t0002g0133a0001c0001t0002g0212a0001c0003t0002g0006others(91): Show | 115 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.772+120C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920836 | ||||||
chr14:50920838
|
G | T | 19 | a0001c0005t0002g0004a0001c0005t0002g0015a0001c0005t0002g0040others(16): Show | 26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.772+118C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920838 | ||||||
chr14:50920872
|
T | G | 30 | a0002c0004t0001g0028a0002c0004t0001g0091a0002c0004t0001g0092others(27): Show | 33 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.772+84A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920872 | ||||||
chr14:50920879
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.772+77T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920879 | ||||||
chr14:50920896
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.772+60T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920896 | ||||||
chr14:50920940
|
C | A | 27 | a0001c0003t0002g0006a0001c0003t0002g0022a0001c0003t0002g0023others(24): Show | 38 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.772+16G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920940 | ||||||
chr14:50921141
|
G | C | 1 | a0001c0001t0001g0182 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.661-74C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921141 | ||||||
chr14:50921165
|
G | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.661-98C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921165 | ||||||
chr14:50921257
|
G | C | 107 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(104): Show | 155 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.661-190C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921257 | ||||||
chr14:50921342
|
C | G | 1 | a0003c0010t0003g0058 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.661-275G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921342 | ||||||
chr14:50921363
|
G | T | 1 | a0001c0002t0003g0242 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.661-296C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921363 | ||||||
chr14:50921392
|
G | A | 9 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(6): Show | 11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.661-325C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921392 | ||||||
chr14:50921398
|
C | CT | 20 | a0001c0002t0003g0242a0001c0005t0002g0004a0001c0005t0002g0015others(17): Show | 27 | HG00597.hp2 HG00609.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.661-332dupA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921398 | ||||||
chr14:50921400
|
T | A | 11 | a0001c0001t0002g0133a0001c0003t0002g0061a0001c0009t0002g0056others(8): Show | 14 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.661-333A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921400 | ||||||
chr14:50921415
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.661-348T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921415 | ||||||
chr14:50921416
|
C | T | 1 | a0001c0002t0003g0235 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.661-349G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921416 | ||||||
chr14:50921522
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.661-455C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921522 | ||||||
chr14:50921523
|
G | T | 1 | a0001c0001t0002g0119 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.661-456C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921523 | ||||||
chr14:50921567
|
A | C | 1 | a0001c0002t0003g0190 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.661-500T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921567 | ||||||
chr14:50921786
|
C | A | 1 | a0001c0001t0002g0119 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.661-719G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921786 | ||||||
chr14:50921844
|
T | A | 53 | a0001c0001t0002g0212a0001c0006t0001g0166a0001c0006t0002g0167others(50): Show | 60 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.661-777A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921844 | ||||||
chr14:50922083
|
A | G | 20 | a0001c0003t0002g0006a0001c0003t0002g0022a0001c0003t0002g0023others(17): Show | 28 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.661-1016T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922083 | ||||||
chr14:50922114
|
C | T | 88 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(85): Show | 130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.661-1047G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922114 | ||||||
chr14:50922251
|
A | G | 128 | a0001c0001t0002g0133a0001c0001t0002g0212a0001c0002t0001g0221others(125): Show | 177 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.661-1184T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922251 | ||||||
chr14:50922368
|
G | A | 46 | a0001c0001t0002g0010a0001c0001t0002g0117a0001c0001t0002g0118others(43): Show | 56 | HG00280.hp2 HG00609.hp2 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.661-1301C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922368 | ||||||
chr14:50922371
|
A | G | 19 | a0001c0005t0002g0004a0001c0005t0002g0015a0001c0005t0002g0040others(16): Show | 26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.661-1304T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922371 | ||||||
chr14:50922374
|
A | T | 1 | a0001c0001t0001g0143 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.661-1307T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922374 | ||||||
chr14:50922447
|
A | G | 3 | a0001c0002t0003g0230a0001c0002t0003g0234a0001c0002t0003g0245 | 3 | HG02145.hp2 HG03710.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.661-1380T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922447 | ||||||
chr14:50922589
|
C | T | 29 | a0002c0004t0001g0028a0002c0004t0001g0091a0002c0004t0001g0092others(26): Show | 32 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.660+1380G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922589 | ||||||
chr14:50922687
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.660+1282C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922687 | ||||||
chr14:50922718
|
G | T | 11 | a0001c0001t0002g0133a0001c0003t0002g0061a0001c0009t0002g0056others(8): Show | 14 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.660+1251C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922718 | ||||||
chr14:50922820
|
G | A | 1 | a0001c0001t0002g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.660+1149C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922820 | ||||||
chr14:50922821
|
C | G | 1 | a0001c0003t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.660+1148G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922821 | ||||||
chr14:50922875
|
A | G | 1 | a0001c0003t0002g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.660+1094T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922875 | ||||||
chr14:50923040
|
T | C | 1 | a0001c0005t0002g0205 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.660+929A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923040 | ||||||
chr14:50923190
|
T | C | 219 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0089others(216): Show | 285 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.660+779A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923190 | ||||||
chr14:50923200
|
G | A | 111 | a0001c0001t0002g0133a0001c0001t0002g0212a0001c0002t0001g0221others(108): Show | 158 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.660+769C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923200 | ||||||
chr14:50923210
|
T | G | 1 | a0001c0002t0003g0242 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.660+759A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923210 | ||||||
chr14:50923227
|
A | G | 4 | a0004c0011t0002g0034a0004c0011t0002g0168a0004c0011t0002g0169others(1): Show | 7 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+742T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923227 | ||||||
chr14:50923296
|
TA | T | 11 | a0001c0001t0002g0133a0001c0003t0002g0061a0001c0009t0002g0056others(8): Show | 14 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.660+672delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923296 | ||||||
chr14:50923364
|
T | G | 26 | a0001c0001t0001g0007a0001c0001t0001g0089a0001c0001t0001g0123others(23): Show | 32 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.660+605A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923364 | ||||||
chr14:50923390
|
C | T | 6 | a0001c0001t0002g0119a0001c0001t0002g0212a0004c0011t0002g0034others(3): Show | 9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+579G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923390 | ||||||
chr14:50923414
|
T | A | 112 | a0001c0001t0002g0119a0001c0001t0002g0133a0001c0001t0002g0212others(109): Show | 159 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.660+555A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923414 | ||||||
chr14:50923455
|
T | C | 95 | a0001c0002t0001g0221a0001c0002t0003g0001a0001c0002t0003g0005others(92): Show | 136 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.660+514A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923455 | ||||||
chr14:50923539
|
C | T | 1 | a0001c0003t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.660+430G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923539 | ||||||
chr14:50923577
|
T | C | 5 | a0001c0001t0002g0212a0004c0011t0002g0034a0004c0011t0002g0168others(2): Show | 8 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+392A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923577 | ||||||
chr14:50923608
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.660+361A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923608 | ||||||
chr14:50923683
|
C | T | 1 | a0002c0004t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.660+286G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923683 | ||||||
chr14:50923687
|
C | CA | 30 | a0001c0001t0001g0120a0001c0001t0001g0131a0001c0001t0001g0142others(27): Show | 37 | HG00609.hp2 HG00621.hp2 HG01981.hp2 others(34): Show |
intron_variant | MODIFIER | c.660+281dupT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923687 | ||||||
chr14:50923687
|
C | CAA | 36 | a0001c0001t0005g0291a0001c0003t0002g0006a0001c0003t0002g0022others(33): Show | 47 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.660+280_660+281dup others(2): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923687 | ||||||
chr14:50923687
|
C | CAAA | 56 | a0001c0001t0002g0212a0001c0002t0001g0221a0001c0002t0003g0001others(53): Show | 86 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.660+279_660+281dup others(3): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923687 | ||||||
chr14:50923687
|
C | CAAAA | 7 | a0001c0001t0002g0119a0001c0002t0003g0044a0001c0002t0003g0045others(4): Show | 9 | HG01884.hp2 HG02071.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+278_660+281dup others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923687 | ||||||
chr14:50923687
|
CA | C | 7 | a0001c0001t0001g0037a0001c0001t0001g0134a0001c0001t0001g0174others(4): Show | 9 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+281delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923687 | ||||||
chr14:50923767
|
T | G | 1 | a0002c0008t0001g0074 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.660+202A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923767 | ||||||
chr14:50923768
|
C | G | 1 | a0002c0008t0001g0074 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.660+201G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923768 | ||||||
chr14:50923777
|
T | G | 7 | a0001c0003t0002g0061a0003c0010t0002g0019a0003c0010t0002g0059others(4): Show | 10 | HG01361.hp1 HG02056.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.660+192A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923777 | ||||||
chr14:50924122
|
C | T | 15 | a0001c0006t0002g0252a0001c0006t0002g0273a0001c0006t0002g0274others(12): Show | 16 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.529-22G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924122 | ||||||
chr14:50924288
|
T | C | 24 | a0001c0003t0002g0006a0001c0003t0002g0022a0001c0003t0002g0023others(21): Show | 35 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.529-188A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924288 | ||||||
chr14:50924390
|
C | T | 3 | a0001c0002t0003g0051a0001c0002t0003g0233a0001c0002t0003g0244 | 4 | HG01952.hp2 HG01978.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-290G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924390 | ||||||
chr14:50924391
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0160 | 2 | NA19012.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.529-291C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924391 | ||||||
chr14:50924538
|
A | G | 182 | a0001c0001t0001g0165a0001c0001t0002g0010a0001c0001t0002g0100others(179): Show | 241 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.529-438T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924538 | ||||||
chr14:50924753
|
C | T | 60 | a0001c0002t0001g0221a0001c0002t0003g0001a0001c0002t0003g0005others(57): Show | 92 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.529-653G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924753 | ||||||
chr14:50924824
|
C | T | 20 | a0001c0003t0002g0006a0001c0003t0002g0022a0001c0003t0002g0023others(17): Show | 28 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.529-724G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924824 | ||||||
chr14:50924861
|
A | T | 1 | a0002c0004t0001g0161 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.529-761T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924861 | ||||||
chr14:50925091
|
G | A | 1 | a0001c0001t0002g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.529-991C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50925091 | ||||||
chr14:50925536
|
T | G | 1 | a0001c0002t0003g0046 | 2 | NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.529-1436A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50925536 | ||||||
chr14:50925642
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0184 | 3 | NA18977.hp2 NA18992.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.529-1542C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50925642 | ||||||
chr14:50925881
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.529-1781C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50925881 | ||||||
chr14:50926016
|
C | T | 2 | a0001c0001t0002g0119a0001c0001t0002g0212 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.529-1916G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926016 | ||||||
chr14:50926021
|
AG | A | 4 | a0002c0004t0001g0093a0002c0004t0001g0101a0002c0004t0001g0104others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1922delC | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926021 | ||||||
chr14:50926115
|
T | C | 76 | a0001c0002t0001g0221a0001c0002t0003g0001a0001c0002t0003g0005others(73): Show | 109 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.529-2015A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926115 | ||||||
chr14:50926131
|
A | G | 114 | a0001c0001t0002g0119a0001c0001t0002g0133a0001c0001t0002g0212others(111): Show | 161 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.529-2031T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926131 | ||||||
chr14:50926315
|
T | C | 181 | a0001c0001t0002g0010a0001c0001t0002g0100a0001c0001t0002g0114others(178): Show | 240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.529-2215A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926315 | ||||||
chr14:50926455
|
G | A | 11 | a0001c0001t0002g0133a0001c0003t0002g0061a0001c0009t0002g0056others(8): Show | 14 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.529-2355C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926455 | ||||||
chr14:50926465
|
C | T | 1 | a0001c0002t0003g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.529-2365G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926465 | ||||||
chr14:50926595
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.529-2495C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926595 | ||||||
chr14:50926598
|
C | T | 11 | a0001c0001t0002g0133a0001c0003t0002g0061a0001c0009t0002g0056others(8): Show | 14 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.529-2498G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926598 | ||||||
chr14:50926599
|
A | G | 115 | a0001c0001t0001g0151a0001c0001t0002g0119a0001c0001t0002g0133others(112): Show | 162 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.529-2499T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926599 | ||||||
chr14:50926609
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.529-2509G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926609 | ||||||
chr14:50926687
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.529-2587G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926687 | ||||||
chr14:50926725
|
C | CA | 33 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0030others(30): Show | 43 | HG00438.hp2 HG00597.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.529-2626dupT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | ||||||
chr14:50926725
|
C | CAA | 10 | a0001c0001t0001g0014a0001c0001t0001g0186a0001c0001t0001g0187others(7): Show | 12 | HG00558.hp2 HG02523.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.529-2627_529-2626d others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | ||||||
chr14:50926725
|
CA | C | 63 | a0001c0001t0001g0007a0001c0001t0001g0089a0001c0001t0001g0124others(60): Show | 76 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.529-2626delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | ||||||
chr14:50926725
|
CAA | C | 92 | a0001c0001t0001g0134a0001c0001t0002g0010a0001c0001t0002g0100others(89): Show | 131 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.529-2627_529-2626d others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | ||||||
chr14:50926725
|
CAAAAAAA others(5): Show |
C | 13 | a0001c0001t0001g0109a0001c0001t0001g0213a0001c0001t0002g0133others(10): Show | 16 | HG00735.hp2 HG01361.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.529-2637_529-2626d others(14): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | ||||||
chr14:50926725
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0002g0115 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.529-2642_529-2626d others(19): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | ||||||
chr14:50926800
|
A | G | 1 | a0001c0002t0003g0231 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.529-2700T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926800 | ||||||
chr14:50926969
|
C | A | 1 | a0001c0007t0001g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.529-2869G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926969 | ||||||
chr14:50927012
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.529-2912G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927012 | ||||||
chr14:50927211
|
T | C | 103 | a0001c0001t0001g0151a0001c0001t0001g0188a0001c0001t0001g0189others(100): Show | 146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.529-3111A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927211 | ||||||
chr14:50927351
|
A | G | 63 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.529-3251T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927351 | ||||||
chr14:50927491
|
C | T | 4 | a0001c0007t0001g0284a0001c0007t0002g0052a0001c0007t0002g0282others(1): Show | 5 | HG02559.hp1 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.529-3391G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927491 | ||||||
chr14:50927537
|
T | C | 1 | a0004c0022t0002g0279 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.529-3437A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927537 | ||||||
chr14:50927549
|
T | A | 28 | a0001c0003t0002g0006a0001c0003t0002g0023a0001c0003t0002g0026others(25): Show | 36 | HG00408.hp2 HG00544.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.529-3449A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927549 | ||||||
chr14:50927685
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.529-3585G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927685 | ||||||
chr14:50927718
|
A | G | 13 | a0001c0003t0002g0022a0001c0003t0002g0061a0001c0003t0002g0062others(10): Show | 17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.529-3618T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927718 | ||||||
chr14:50927762
|
C | T | 125 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(122): Show | 174 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.529-3662G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927762 | ||||||
chr14:50927888
|
A | G | 28 | a0001c0003t0002g0006a0001c0003t0002g0023a0001c0003t0002g0026others(25): Show | 36 | HG00408.hp2 HG00544.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.528+3785T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927888 | ||||||
chr14:50927894
|
A | G | 4 | a0004c0011t0002g0034a0004c0011t0002g0168a0004c0011t0002g0169others(1): Show | 7 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.528+3779T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927894 | ||||||
chr14:50927919
|
C | T | 1 | a0004c0011t0002g0168 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.528+3754G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927919 | ||||||
chr14:50927978
|
G | A | 1 | a0001c0006t0001g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.528+3695C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927978 | ||||||
chr14:50928050
|
C | T | 1 | a0001c0006t0001g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.528+3623G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928050 | ||||||
chr14:50928123
|
G | A | 1 | a0003c0019t0002g0271 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.528+3550C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928123 | ||||||
chr14:50928171
|
G | C | 2 | a0001c0009t0002g0056a0001c0009t0002g0063 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.528+3502C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928171 | ||||||
chr14:50928200
|
T | C | 82 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(79): Show | 118 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.528+3473A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928200 | ||||||
chr14:50928273
|
T | A | 1 | a0001c0002t0001g0221 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.528+3400A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928273 | ||||||
chr14:50928273
|
T | C | 81 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(78): Show | 117 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.528+3400A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928273 | ||||||
chr14:50928365
|
C | T | 78 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(75): Show | 111 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.528+3308G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928365 | ||||||
chr14:50928387
|
G | A | 1 | a0001c0001t0002g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.528+3286C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928387 | ||||||
chr14:50928487
|
T | C | 78 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(75): Show | 111 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.528+3186A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928487 | ||||||
chr14:50928643
|
T | TATTTTCC | 77 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(74): Show | 110 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.528+3029_528+3030i others(9): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928643 | ||||||
chr14:50928666
|
T | G | 77 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(74): Show | 110 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.528+3007A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928666 | ||||||
chr14:50928694
|
A | C | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.528+2979T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928694 | ||||||
chr14:50928776
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0259 | 3 | NA18942.hp2 NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.528+2897C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928776 | ||||||
chr14:50928794
|
GT | G | 108 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(105): Show | 149 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.528+2878delA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928794 | ||||||
chr14:50928889
|
G | C | 13 | a0001c0003t0002g0022a0001c0003t0002g0061a0001c0003t0002g0062others(10): Show | 17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.528+2784C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928889 | ||||||
chr14:50928892
|
A | G | 77 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(74): Show | 110 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.528+2781T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928892 | ||||||
chr14:50929052
|
T | C | 29 | a0001c0003t0002g0006a0001c0003t0002g0023a0001c0003t0002g0026others(26): Show | 37 | HG00408.hp2 HG00544.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.528+2621A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929052 | ||||||
chr14:50929137
|
A | G | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+2536T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929137 | ||||||
chr14:50929138
|
T | C | 108 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(105): Show | 149 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.528+2535A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929138 | ||||||
chr14:50929209
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.528+2464G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929209 | ||||||
chr14:50929240
|
T | G | 108 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(105): Show | 149 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.528+2433A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929240 | ||||||
chr14:50929298
|
C | A | 63 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 95 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.528+2375G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929298 | ||||||
chr14:50929333
|
G | A | 2 | a0001c0021t0002g0280a0008c0020t0001g0281 | 2 | HG01496.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.528+2340C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929333 | ||||||
chr14:50929338
|
C | T | 9 | a0001c0003t0002g0022a0001c0003t0002g0061a0001c0003t0002g0062others(6): Show | 13 | HG01361.hp1 HG02056.hp1 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.528+2335G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929338 | ||||||
chr14:50929393
|
T | G | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+2280A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929393 | ||||||
chr14:50929663
|
G | A | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+2010C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929663 | ||||||
chr14:50929666
|
T | C | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+2007A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929666 | ||||||
chr14:50929700
|
T | C | 13 | a0001c0003t0002g0022a0001c0003t0002g0061a0001c0003t0002g0062others(10): Show | 17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.528+1973A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929700 | ||||||
chr14:50929790
|
T | C | 15 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(12): Show | 16 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.528+1883A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929790 | ||||||
chr14:50929837
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0174others(4): Show | 10 | HG00558.hp1 HG02015.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.528+1836G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929837 | ||||||
chr14:50929843
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.528+1830T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929843 | ||||||
chr14:50929903
|
T | A | 29 | a0001c0003t0002g0006a0001c0003t0002g0023a0001c0003t0002g0026others(26): Show | 37 | HG00408.hp2 HG00544.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.528+1770A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929903 | ||||||
chr14:50929909
|
A | G | 63 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(60): Show | 95 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.528+1764T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929909 | ||||||
chr14:50930002
|
C | G | 2 | a0001c0001t0002g0114a0001c0001t0005g0291 | 2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.528+1671G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930002 | ||||||
chr14:50930020
|
C | G | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+1653G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930020 | ||||||
chr14:50930076
|
C | T | 1 | a0001c0001t0005g0291 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.528+1597G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930076 | ||||||
chr14:50930337
|
T | C | 12 | a0001c0001t0002g0010a0001c0001t0002g0115a0001c0001t0002g0116others(9): Show | 14 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.528+1336A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930337 | ||||||
chr14:50930347
|
G | A | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+1326C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930347 | ||||||
chr14:50930353
|
A | G | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+1320T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930353 | ||||||
chr14:50930361
|
C | T | 3 | a0001c0002t0003g0016a0001c0002t0003g0225a0001c0002t0003g0268 | 5 | HG01099.hp2 HG01952.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+1312G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930361 | ||||||
chr14:50930425
|
G | C | 2 | a0001c0002t0003g0253a0001c0002t0003g0269 | 2 | NA18946.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.528+1248C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930425 | ||||||
chr14:50930567
|
A | T | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.528+1106T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930567 | ||||||
chr14:50930676
|
A | C | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+997T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930676 | ||||||
chr14:50930681
|
T | C | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+992A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930681 | ||||||
chr14:50930927
|
A | AT | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+745dupA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930927 | ||||||
chr14:50930977
|
A | C | 13 | a0001c0003t0002g0022a0001c0003t0002g0061a0001c0003t0002g0062others(10): Show | 17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.528+696T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930977 | ||||||
chr14:50931062
|
T | C | 1 | a0001c0001t0001g0031 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.528+611A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931062 | ||||||
chr14:50931096
|
A | C | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.528+577T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931096 | ||||||
chr14:50931134
|
A | G | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+539T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931134 | ||||||
chr14:50931154
|
ACT | A | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+517_528+518del others(2): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931154 | ||||||
chr14:50931212
|
G | T | 1 | a0001c0009t0003g0067 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.528+461C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931212 | ||||||
chr14:50931274
|
AC | A | 62 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(59): Show | 94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.528+398delG | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931274 | ||||||
chr14:50931299
|
A | T | 1 | a0002c0004t0001g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.528+374T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931299 | ||||||
chr14:50931374
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.528+299T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931374 | ||||||
chr14:50931469
|
G | A | 11 | a0001c0001t0002g0010a0001c0001t0002g0115a0001c0001t0002g0116others(8): Show | 13 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.528+204C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931469 | ||||||
chr14:50931618
|
G | A | 1 | a0001c0002t0003g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.528+55C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931618 | ||||||
chr14:50931862
|
C | T | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.425-86G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50931862 | ||||||
chr14:50932025
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.425-249G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932025 | ||||||
chr14:50932045
|
T | A | 2 | a0002c0004t0001g0028a0002c0004t0001g0105 | 3 | HG00741.hp1 HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.425-269A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932045 | ||||||
chr14:50932138
|
C | A | 1 | a0001c0009t0002g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.425-362G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932138 | ||||||
chr14:50932232
|
T | A | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.425-456A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932232 | ||||||
chr14:50932248
|
G | T | 61 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(58): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.425-472C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932248 | ||||||
chr14:50932429
|
T | A | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.425-653A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932429 | ||||||
chr14:50932505
|
G | A | 13 | a0001c0003t0002g0022a0001c0003t0002g0061a0001c0003t0002g0062others(10): Show | 17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.425-729C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932505 | ||||||
chr14:50932541
|
C | T | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.425-765G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932541 | ||||||
chr14:50932761
|
C | T | 4 | a0001c0009t0002g0056a0001c0009t0002g0057a0001c0009t0002g0063others(1): Show | 4 | HG01358.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-985G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932761 | ||||||
chr14:50933363
|
A | G | 175 | a0001c0001t0001g0210a0001c0001t0001g0226a0001c0001t0001g0250others(172): Show | 232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.425-1587T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933363 | ||||||
chr14:50933441
|
G | C | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.425-1665C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933441 | ||||||
chr14:50933442
|
G | A | 175 | a0001c0001t0001g0210a0001c0001t0001g0226a0001c0001t0001g0250others(172): Show | 232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.424+1665C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933442 | ||||||
chr14:50933683
|
T | C | 1 | a0001c0005t0002g0199 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.424+1424A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933683 | ||||||
chr14:50933697
|
G | A | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.424+1410C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933697 | ||||||
chr14:50933748
|
GTACACAC others(9): Show |
G | 1 | a0001c0001t0001g0130 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.424+1343_424+1358d others(18): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933748 | ||||||
chr14:50933773
|
C | A | 4 | a0004c0011t0002g0034a0004c0011t0002g0168a0004c0011t0002g0169others(1): Show | 7 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+1334G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933773 | ||||||
chr14:50933824
|
T | A | 93 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(90): Show | 132 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.424+1283A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933824 | ||||||
chr14:50933863
|
A | G | 1 | a0002c0008t0001g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.424+1244T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933863 | ||||||
chr14:50933913
|
C | T | 62 | a0001c0001t0001g0226a0001c0001t0001g0250a0001c0001t0001g0251others(59): Show | 93 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.424+1194G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933913 | ||||||
chr14:50933964
|
G | A | 1 | a0001c0002t0003g0260 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.424+1143C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933964 | ||||||
chr14:50934095
|
A | G | 1 | a0001c0002t0003g0230 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.424+1012T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934095 | ||||||
chr14:50934119
|
G | T | 13 | a0001c0003t0002g0022a0001c0003t0002g0061a0001c0003t0002g0062others(10): Show | 17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+988C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934119 | ||||||
chr14:50934659
|
GTA | G | 30 | a0001c0003t0002g0006a0001c0003t0002g0023a0001c0003t0002g0026others(27): Show | 38 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.424+446_424+447del others(2): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934659 | ||||||
chr14:50934661
|
A | G | 1 | a0002c0004t0001g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.424+446T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934661 | ||||||
chr14:50934673
|
G | A | 28 | a0001c0001t0001g0210a0001c0001t0002g0100a0001c0006t0001g0166others(25): Show | 32 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+434C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934673 | ||||||
chr14:50934694
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0129 | 3 | HG00639.hp2 HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.424+413G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934694 | ||||||
chr14:50934779
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+328C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934779 | ||||||
chr14:50934800
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.424+307C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934800 | ||||||
chr14:50934808
|
G | C | 23 | a0001c0001t0001g0165a0001c0001t0001g0210a0001c0001t0002g0100others(20): Show | 24 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.424+299C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934808 | ||||||
chr14:50934941
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.424+166T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934941 | ||||||
chr14:50934950
|
A | G | 1 | a0001c0005t0002g0202 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.424+157T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934950 | ||||||
chr14:50935010
|
T | C | 1 | a0007c0023t0002g0289 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.424+97A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50935010 | ||||||
chr14:50935101
|
A | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG02109.hp1 HG02886.hp1 |
splice_region_variant&intron_variant | LOW | c.424+6T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50935101 | ||||||
chr14:50935293
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.346-108T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935293 | ||||||
chr14:50935299
|
T | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0270 | 2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.346-114A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935299 | ||||||
chr14:50935337
|
G | A | 118 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(115): Show | 165 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.346-152C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935337 | ||||||
chr14:50935708
|
G | A | 188 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(185): Show | 249 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.346-523C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935708 | ||||||
chr14:50935908
|
C | A | 2 | a0001c0001t0001g0122a0001c0002t0003g0113 | 2 | HG01175.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.346-723G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935908 | ||||||
chr14:50935924
|
A | G | 25 | a0001c0001t0002g0010a0001c0001t0002g0114a0001c0001t0002g0115others(22): Show | 31 | HG01261.hp2 HG01358.hp1 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.346-739T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935924 | ||||||
chr14:50935978
|
C | T | 12 | a0001c0001t0002g0010a0001c0001t0002g0114a0001c0001t0002g0115others(9): Show | 14 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.346-793G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935978 | ||||||
chr14:50935992
|
G | A | 1 | a0001c0009t0002g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346-807C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935992 | ||||||
chr14:50935993
|
C | A | 1 | a0001c0009t0002g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346-808G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935993 | ||||||
chr14:50936043
|
C | T | 190 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(187): Show | 251 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.346-858G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936043 | ||||||
chr14:50936172
|
T | C | 1 | a0001c0002t0003g0262 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.346-987A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936172 | ||||||
chr14:50936309
|
C | A | 190 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(187): Show | 251 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.346-1124G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936309 | ||||||
chr14:50936365
|
T | A | 2 | a0006c0014t0001g0152a0006c0014t0001g0153 | 2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.346-1180A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936365 | ||||||
chr14:50936384
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.346-1199C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936384 | ||||||
chr14:50936507
|
G | A | 1 | a0001c0009t0001g0084 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.345+1229C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936507 | ||||||
chr14:50936645
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.345+1091G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936645 | ||||||
chr14:50936746
|
G | A | 1 | a0001c0007t0002g0288 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.345+990C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936746 | ||||||
chr14:50936785
|
C | T | 74 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(71): Show | 109 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.345+951G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936785 | ||||||
chr14:50936790
|
CA | C | 91 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(88): Show | 129 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.345+945delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936790 | ||||||
chr14:50936791
|
A | T | 1 | a0001c0001t0001g0228 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.345+945T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936791 | ||||||
chr14:50936813
|
T | C | 12 | a0001c0001t0002g0010a0001c0001t0002g0114a0001c0001t0002g0115others(9): Show | 14 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.345+923A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936813 | ||||||
chr14:50936954
|
A | G | 13 | a0001c0005t0002g0004a0001c0005t0002g0015a0001c0005t0002g0040others(10): Show | 20 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.345+782T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936954 | ||||||
chr14:50937007
|
C | T | 1 | a0001c0001t0001g0031 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.345+729G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937007 | ||||||
chr14:50937008
|
G | A | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.345+728C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937008 | ||||||
chr14:50937023
|
C | T | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.345+713G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937023 | ||||||
chr14:50937148
|
A | T | 2 | a0001c0012t0002g0055a0001c0012t0002g0073 | 2 | NA18944.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.345+588T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937148 | ||||||
chr14:50937243
|
C | G | 24 | a0001c0001t0001g0210a0001c0001t0002g0100a0001c0006t0001g0166others(21): Show | 25 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.345+493G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937243 | ||||||
chr14:50937281
|
A | G | 1 | a0003c0019t0002g0271 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.345+455T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937281 | ||||||
chr14:50937415
|
TAGC | T | 70 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(67): Show | 105 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.345+318_345+320del others(3): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937415 | ||||||
chr14:50937469
|
T | C | 1 | a0001c0001t0005g0291 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.345+267A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937469 | ||||||
chr14:50937544
|
C | G | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.345+192G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937544 | ||||||
chr14:50937549
|
T | C | 13 | a0001c0003t0002g0022a0001c0003t0002g0061a0001c0003t0002g0062others(10): Show | 17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.345+187A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937549 | ||||||
chr14:50937871
|
C | T | 14 | a0001c0003t0002g0022a0001c0003t0002g0054a0001c0003t0002g0061others(11): Show | 18 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.244-34G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50937871 | ||||||
chr14:50937940
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.244-103C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50937940 | ||||||
chr14:50938068
|
T | G | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.244-231A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938068 | ||||||
chr14:50938195
|
A | G | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.244-358T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938195 | ||||||
chr14:50938225
|
T | G | 1 | a0001c0001t0002g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244-388A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938225 | ||||||
chr14:50938406
|
TA | T | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(287): Show | 389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.244-570delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938406 | ||||||
chr14:50938431
|
C | T | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.244-594G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938431 | ||||||
chr14:50938494
|
G | A | 2 | a0001c0001t0002g0155a0001c0002t0003g0266 | 2 | HG02080.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.244-657C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938494 | ||||||
chr14:50938505
|
C | T | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.244-668G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938505 | ||||||
chr14:50938508
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.244-671C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938508 | ||||||
chr14:50938642
|
G | A | 2 | a0001c0006t0001g0166a0001c0006t0002g0167 | 2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.244-805C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938642 | ||||||
chr14:50938656
|
A | T | 1 | a0002c0004t0001g0093 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.244-819T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938656 | ||||||
chr14:50938702
|
C | T | 30 | a0001c0003t0002g0006a0001c0003t0002g0023a0001c0003t0002g0026others(27): Show | 38 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.244-865G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938702 | ||||||
chr14:50938723
|
A | C | 1 | a0002c0008t0001g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.244-886T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938723 | ||||||
chr14:50938746
|
A | G | 1 | a0001c0002t0003g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.244-909T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938746 | ||||||
chr14:50939031
|
A | T | 6 | a0001c0001t0001g0120a0001c0001t0001g0226a0001c0001t0002g0272others(3): Show | 6 | HG01891.hp1 HG02071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-1194T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939031 | ||||||
chr14:50939035
|
T | A | 21 | a0001c0001t0001g0192a0001c0002t0003g0267a0001c0003t0002g0022others(18): Show | 25 | HG01168.hp1 HG01169.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.244-1198A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939035 | ||||||
chr14:50939039
|
T | A | 14 | a0001c0003t0002g0022a0001c0003t0002g0054a0001c0003t0002g0061others(11): Show | 18 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.244-1202A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939039 | ||||||
chr14:50939061
|
G | A | 1 | a0001c0009t0003g0087 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.244-1224C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939061 | ||||||
chr14:50939188
|
C | G | 1 | a0001c0006t0002g0201 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.244-1351G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939188 | ||||||
chr14:50939291
|
C | T | 13 | a0001c0003t0002g0022a0001c0003t0002g0061a0001c0003t0002g0062others(10): Show | 17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.244-1454G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939291 | ||||||
chr14:50939398
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.244-1561G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939398 | ||||||
chr14:50939486
|
G | A | 1 | a0001c0002t0003g0268 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.244-1649C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939486 | ||||||
chr14:50939594
|
G | C | 1 | a0001c0001t0001g0193 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.244-1757C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939594 | ||||||
chr14:50939702
|
A | G | 1 | a0001c0002t0003g0224 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.244-1865T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939702 | ||||||
chr14:50939816
|
T | C | 178 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(175): Show | 235 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.244-1979A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939816 | ||||||
chr14:50939980
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244-2143G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939980 | ||||||
chr14:50940003
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.244-2166T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940003 | ||||||
chr14:50940050
|
T | C | 1 | a0002c0008t0001g0064 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.244-2213A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940050 | ||||||
chr14:50940097
|
G | A | 4 | a0004c0011t0002g0034a0004c0011t0002g0168a0004c0011t0002g0169others(1): Show | 7 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.244-2260C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940097 | ||||||
chr14:50940111
|
T | C | 1 | a0002c0004t0001g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.244-2274A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940111 | ||||||
chr14:50940150
|
C | T | 2 | a0002c0008t0003g0071a0002c0016t0003g0070 | 2 | NA18943.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.244-2313G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940150 | ||||||
chr14:50940257
|
T | TA | 29 | a0001c0001t0002g0010a0001c0001t0002g0114a0001c0001t0002g0115others(26): Show | 32 | HG00280.hp2 HG01106.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.244-2421dupT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940257 | ||||||
chr14:50940333
|
G | C | 1 | a0001c0002t0003g0269 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.244-2496C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940333 | ||||||
chr14:50940530
|
C | T | 3 | a0001c0003t0002g0023a0001c0003t0002g0068a0001c0009t0001g0069 | 4 | HG00544.hp1 HG00597.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-2693G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940530 | ||||||
chr14:50940862
|
C | T | 174 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(171): Show | 231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.244-3025G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940862 | ||||||
chr14:50940882
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.244-3045G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940882 | ||||||
chr14:50941132
|
G | T | 70 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(67): Show | 105 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.243+3029C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941132 | ||||||
chr14:50941176
|
C | T | 187 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(184): Show | 248 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.243+2985G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941176 | ||||||
chr14:50941210
|
G | A | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.243+2951C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941210 | ||||||
chr14:50941270
|
A | C | 1 | a0001c0001t0003g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.243+2891T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941270 | ||||||
chr14:50941336
|
AAAGT | A | 70 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(67): Show | 105 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.243+2821_243+2824d others(6): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941336 | ||||||
chr14:50941433
|
G | C | 1 | a0001c0001t0001g0270 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.243+2728C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941433 | ||||||
chr14:50941434
|
C | G | 17 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(14): Show | 18 | HG00280.hp2 HG01106.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.243+2727G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941434 | ||||||
chr14:50941485
|
A | G | 3 | a0001c0003t0002g0054a0001c0006t0001g0166a0001c0006t0002g0167 | 3 | HG02717.hp1 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.243+2676T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941485 | ||||||
chr14:50941507
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.243+2654C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941507 | ||||||
chr14:50941527
|
C | T | 1 | a0001c0007t0002g0278 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.243+2634G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941527 | ||||||
chr14:50941600
|
G | T | 7 | a0001c0002t0003g0041a0001c0002t0003g0215a0001c0002t0003g0216others(4): Show | 9 | HG00642.hp1 HG01109.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.243+2561C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941600 | ||||||
chr14:50941646
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.243+2515G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941646 | ||||||
chr14:50941803
|
G | A | 14 | a0001c0003t0002g0022a0001c0003t0002g0061a0001c0003t0002g0062others(11): Show | 18 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.243+2358C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941803 | ||||||
chr14:50941987
|
A | G | 2 | a0001c0003t0002g0023a0001c0003t0002g0068 | 3 | HG00544.hp1 HG03239.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.243+2174T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941987 | ||||||
chr14:50942031
|
T | C | 1 | a0001c0006t0002g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.243+2130A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942031 | ||||||
chr14:50942040
|
A | G | 76 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(73): Show | 111 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.243+2121T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942040 | ||||||
chr14:50942104
|
CCTACTTG others(11): Show |
C | 1 | a0001c0001t0001g0194 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.243+2039_243+2056d others(20): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942104 | ||||||
chr14:50942116
|
A | T | 24 | a0001c0001t0001g0165a0001c0001t0001g0210a0001c0001t0002g0100others(21): Show | 25 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.243+2045T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942116 | ||||||
chr14:50942142
|
T | C | 1 | a0001c0001t0002g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.243+2019A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942142 | ||||||
chr14:50942148
|
C | G | 1 | a0001c0009t0003g0067 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.243+2013G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942148 | ||||||
chr14:50942181
|
CACGTGTG others(624): Show |
C | 74 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(71): Show | 109 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.243+1349_243+1979d others(2): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942181 | ||||||
chr14:50942183
|
C | T | 2 | a0002c0004t0001g0091a0002c0004t0001g0092 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.243+1978G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942183 | ||||||
chr14:50942226
|
G | A | 2 | a0001c0001t0001g0159a0002c0018t0001g0158 | 2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.243+1935C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942226 | ||||||
chr14:50942269
|
C | T | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.243+1892G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942269 | ||||||
chr14:50942308
|
C | T | 12 | a0001c0001t0002g0010a0001c0001t0002g0114a0001c0001t0002g0115others(9): Show | 14 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.243+1853G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942308 | ||||||
chr14:50942515
|
T | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0160 | 2 | NA19012.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.243+1646A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942515 | ||||||
chr14:50942590
|
G | C | 29 | a0001c0003t0002g0006a0001c0003t0002g0023a0001c0003t0002g0026others(26): Show | 37 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.243+1571C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942590 | ||||||
chr14:50942822
|
C | CAAACA | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(44): Show | 76 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.243+1334_243+1338d others(7): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942822 | ||||||
chr14:50942822
|
C | CAAACAAA others(3): Show |
11 | a0001c0001t0002g0212a0001c0005t0002g0004a0001c0005t0002g0015others(8): Show | 18 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.243+1329_243+1338d others(12): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942822 | ||||||
chr14:50942822
|
C | CAAACAAA others(8): Show |
3 | a0001c0005t0002g0202a0001c0005t0002g0203a0001c0005t0002g0204 | 3 | HG02300.hp2 HG03669.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.243+1324_243+1338d others(17): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942822 | ||||||
chr14:50942822
|
C | CAAACAAA others(13): Show |
1 | a0001c0005t0002g0205 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.243+1319_243+1338d others(22): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942822 | ||||||
chr14:50942822
|
CAAACA | C | 148 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0029others(145): Show | 200 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.243+1334_243+1338d others(7): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942822 | ||||||
chr14:50942822
|
CAAACAAA others(3): Show |
C | 1 | a0001c0001t0001g0090 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.243+1329_243+1338d others(12): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942822 | ||||||
chr14:50942830
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.243+1331T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942830 | ||||||
chr14:50942962
|
G | A | 4 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0208others(1): Show | 4 | HG01261.hp2 HG02647.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+1199C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942962 | ||||||
chr14:50942987
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.243+1174A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942987 | ||||||
chr14:50943171
|
C | A | 14 | a0001c0006t0002g0273a0001c0006t0002g0274a0001c0007t0001g0284others(11): Show | 15 | HG00280.hp2 HG01496.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.243+990G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943171 | ||||||
chr14:50943199
|
C | G | 1 | a0001c0001t0002g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.243+962G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943199 | ||||||
chr14:50943207
|
C | T | 1 | a0001c0002t0003g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.243+954G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943207 | ||||||
chr14:50943309
|
C | T | 1 | a0001c0003t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.243+852G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943309 | ||||||
chr14:50943460
|
T | G | 139 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0050others(136): Show | 187 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.243+701A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943460 | ||||||
chr14:50943587
|
G | A | 28 | a0001c0003t0002g0006a0001c0003t0002g0023a0001c0003t0002g0026others(25): Show | 36 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.243+574C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943587 | ||||||
chr14:50943645
|
G | C | 1 | a0001c0001t0001g0089 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.243+516C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943645 | ||||||
chr14:50943646
|
C | G | 1 | a0001c0001t0001g0089 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.243+515G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943646 | ||||||
chr14:50943669
|
A | C | 1 | a0005c0013t0002g0008 | 3 | HG02257.hp1 HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.243+492T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943669 | ||||||
chr14:50943800
|
G | A | 45 | a0001c0003t0002g0006a0001c0003t0002g0022a0001c0003t0002g0023others(42): Show | 57 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.243+361C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943800 | ||||||
chr14:50943805
|
C | T | 1 | a0001c0002t0003g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.243+356G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943805 | ||||||
chr14:50943878
|
T | C | 18 | a0001c0001t0002g0272a0001c0006t0002g0273a0001c0006t0002g0274others(15): Show | 19 | HG00280.hp2 HG01106.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.243+283A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943878 | ||||||
chr14:50944041
|
C | A | 1 | a0001c0001t0002g0275 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.243+120G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50944041 |