geneid | 1666 |
---|---|
ensemblid | ENSG00000104325.7 |
hgncid | 2753 |
symbol | DECR1 |
name | 2,4-dienoyl-CoA reductase 1 |
refseq_nuc | NM_001359.2 |
refseq_prot | NP_001350.1 |
ensembl_nuc | ENST00000220764.7 |
ensembl_prot | ENSP00000220764.2 |
mane_status | MANE Select |
chr | chr8 |
start | 90001477 |
end | 90053633 |
strand | + |
ver | v1.2 |
region | chr8:90001477-90053633 |
region5000 | chr8:89996477-90058633 |
regionname0 | DECR1_chr8_90001477_90053633 |
regionname5000 | DECR1_chr8_89996477_90058633 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 335 | 375 | 86 | 64 | 169 | 14 | 40 | 127 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0002 | 0/0 | 335 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0003 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1008 | 375 | 86 | 64 | 169 | 14 | 40 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
c0002 | 0/0 | 1008 | 2 | 0 | 0 | 0 | 0 | 2 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
c0003 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1753 | 163 | 36 | 29 | 77 | 3 | 18 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0002 | 1/1 | 1753 | 116 | 13 | 21 | 53 | 6 | 21 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0003 | 0/0 | 1752 | 43 | 0 | 6 | 33 | 1 | 3 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0004 | 0/0 | 1754 | 29 | 25 | 2 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0005 | 0/0 | 1752 | 6 | 3 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0006 | 0/0 | 1753 | 5 | 4 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0007 | 0/0 | 1754 | 3 | 1 | 1 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0008 | 0/0 | 1753 | 3 | 0 | 1 | 0 | 2 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0009 | 0/0 | 1754 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0010 | 0/0 | 1753 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0011 | 0/0 | 1753 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0012 | 0/0 | 1753 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0013 | 0/0 | 1753 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0014 | 0/0 | 1753 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0015 | 0/0 | 1753 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0016 | 0/0 | 1753 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
t0017 | 0/0 | 1752 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 22 | 2 | 4 | 14 | 1 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0002 | 0/0 | 10 | 1 | 0 | 9 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0003 | 0/0 | 10 | 1 | 2 | 6 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0004 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0005 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0006 | 0/0 | 8 | 0 | 2 | 2 | 0 | 4 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0007 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0008 | 0/0 | 8 | 0 | 2 | 3 | 1 | 2 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0010 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0011 | 0/0 | 6 | 0 | 0 | 0 | 0 | 6 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0012 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0013 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0014 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0015 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1008 | 375 | 86 | 64 | 169 | 14 | 40 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0002c0002 | 0/0 | 1008 | 2 | 0 | 0 | 0 | 0 | 2 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0003c0003 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2760 | 163 | 36 | 29 | 77 | 3 | 18 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0002 | 1/1 | 2760 | 113 | 13 | 21 | 52 | 6 | 19 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0003 | 0/0 | 2759 | 43 | 0 | 6 | 33 | 1 | 3 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0004 | 0/0 | 2761 | 29 | 25 | 2 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0005 | 0/0 | 2759 | 6 | 3 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0006 | 0/0 | 2760 | 5 | 4 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0007 | 0/0 | 2761 | 3 | 1 | 1 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0008 | 0/0 | 2760 | 3 | 0 | 1 | 0 | 2 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0009 | 0/0 | 2761 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0010 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0011 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0012 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0013 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0014 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0015 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0016 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0001c0001t0017 | 0/0 | 2759 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0002c0002t0002 | 0/0 | 2760 | 2 | 0 | 0 | 0 | 0 | 2 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
a0003c0003t0002 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | copy fasta | chr8 | 89996477 | 90058633 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 10 | 1 | 0 | 9 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0004 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0007 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0001 | 0/0 | 21 | 1 | 4 | 14 | 1 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0003 | 0/0 | 9 | 1 | 2 | 5 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0011 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0005 | 0/0 | 9 | 0 | 3 | 6 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0008 | 0/0 | 8 | 0 | 2 | 3 | 1 | 2 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0006g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0007g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0007g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0008g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0009g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0010g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0011g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0012g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0013g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0015g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0016g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0001c0001t0017g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
a0003c0003t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | GBR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00099 | hp2 | a0001 | c0001 | t0008 | g0073 | EUR | GBR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | GBR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00140 | hp2 | a0001 | c0001 | t0010 | g0109 | EUR | GBR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | FIN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | FIN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0166 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG00741 | hp2 | a0001 | c0001 | t0016 | g0006 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0197 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0152 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01346 | hp1 | a0001 | c0001 | t0017 | g0015 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01891 | hp2 | a0001 | c0001 | t0015 | g0206 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01934 | hp1 | a0001 | c0001 | t0008 | g0006 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01934 | hp2 | a0001 | c0001 | t0012 | g0146 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CDX | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CDX | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0113 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03041 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0230 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03130 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0226 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0112 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0211 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | BEB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | STU | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | CHB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CHB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18990 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18993 | hp2 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0222 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19057 | hp2 | a0001 | c0001 | t0014 | g0105 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19062 | hp2 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ASW | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA20752 | hp1 | a0001 | c0001 | t0008 | g0080 | EUR | TSI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA20752 | hp2 | a0001 | c0001 | t0013 | g0141 | EUR | TSI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0162 | EUR | TSI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0011 | SAS | GIH | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | GIH | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | ACB | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | USA | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | USA | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0118 | AFR | LWK | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0147 | REF | REF | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0136 | REF | REF | DECR1_chr8_89996477_90058633 | DECR1 | chr8 | 89996477 | 90058633 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:90042781
|
C | T | 1 | a0002 | 2 | HG04184.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.719C>T | p.Pro240Leu | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/10 | 735/2760 | 719/1008 | 240/335 | chr8 | 90042781 | ||
chr8:90044993
|
G | A | 1 | a0003 | 1 | NA18990.hp2 | missense_variant&splice_region_variant | MODERATE | c.883G>A | p.Ala295Thr | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/10 | 899/2760 | 883/1008 | 295/335 | chr8 | 90044993 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:90051898
|
G | A | 1 | a0001c0001t0010 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 1 | chr8 | 90051898 | |||||
chr8:90051917
|
T | C | 1 | a0001c0001t0011 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*20T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 20 | chr8 | 90051917 | |||||
chr8:90052092
|
T | TA | 3 | a0001c0001t0004a0001c0001t0007a0001c0001t0009 | 34 | HG01070.hp1 HG01175.hp2 HG01243.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*208dupA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 209 | INFO_REALIGN_3_PRIME | chr8 | 90052092 | ||||
chr8:90052092
|
TA | T | 3 | a0001c0001t0003a0001c0001t0005a0001c0001t0017 | 50 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*208delA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 208 | INFO_REALIGN_3_PRIME | chr8 | 90052092 | ||||
chr8:90052227
|
C | G | 12 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(9): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*330C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 330 | chr8 | 90052227 | |||||
chr8:90052273
|
C | T | 1 | a0001c0001t0009 | 2 | HG03041.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*376C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 376 | chr8 | 90052273 | |||||
chr8:90052407
|
A | G | 2 | a0001c0001t0010a0001c0001t0016 | 2 | HG00140.hp2 HG00741.hp2 |
3_prime_UTR_variant | MODIFIER | c.*510A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 510 | chr8 | 90052407 | |||||
chr8:90052409
|
G | A | 1 | a0001c0001t0006 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*512G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 512 | chr8 | 90052409 | |||||
chr8:90052517
|
G | A | 1 | a0001c0001t0008 | 3 | HG00099.hp2 HG01934.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*620G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 620 | chr8 | 90052517 | |||||
chr8:90052844
|
C | T | 2 | a0001c0001t0003a0001c0001t0011 | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*947C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 947 | chr8 | 90052844 | |||||
chr8:90052919
|
C | G | 1 | a0001c0001t0015 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1022C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 1022 | chr8 | 90052919 | |||||
chr8:90052935
|
C | T | 1 | a0001c0001t0013 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1038C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 1038 | chr8 | 90052935 | |||||
chr8:90053035
|
G | A | 1 | a0001c0001t0012 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1138G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 1138 | chr8 | 90053035 | |||||
chr8:90053347
|
C | T | 1 | a0001c0001t0014 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1450C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 10/10 | 1450 | chr8 | 90053347 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:90001772
|
C | T | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.69+211C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90001772 | ||||||
chr8:90001926
|
G | T | 20 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(17): Show | 24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.69+365G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90001926 | ||||||
chr8:90001932
|
C | T | 1 | a0001c0001t0003g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.69+371C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90001932 | ||||||
chr8:90002028
|
G | C | 1 | a0001c0001t0002g0047 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.69+467G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002028 | ||||||
chr8:90002045
|
A | T | 1 | a0001c0001t0002g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.69+484A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002045 | ||||||
chr8:90002074
|
G | A | 1 | a0001c0001t0004g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.69+513G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002074 | ||||||
chr8:90002100
|
G | A | 1 | a0001c0001t0004g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+539G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002100 | ||||||
chr8:90002497
|
G | C | 4 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(1): Show | 7 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+936G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002497 | ||||||
chr8:90002499
|
AGCAATAA others(4): Show |
A | 4 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(1): Show | 7 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+939_69+949delGC others(9): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002499 | ||||||
chr8:90002511
|
C | A | 4 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(1): Show | 7 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+950C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002511 | ||||||
chr8:90002814
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.69+1253A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002814 | ||||||
chr8:90002823
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.69+1262A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002823 | ||||||
chr8:90002901
|
G | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0213others(4): Show | 9 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+1340G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90002901 | ||||||
chr8:90003274
|
T | G | 20 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(17): Show | 24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.69+1713T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003274 | ||||||
chr8:90003289
|
A | T | 3 | a0001c0001t0006g0021a0001c0001t0006g0211a0001c0001t0006g0212 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+1728A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003289 | ||||||
chr8:90003313
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.69+1752A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003313 | ||||||
chr8:90003315
|
A | C | 9 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(6): Show | 9 | HG01261.hp2 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+1754A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003315 | ||||||
chr8:90003383
|
ATATT | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG01261.hp2 HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.69+1827_69+1830del others(4): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90003383 | |||||
chr8:90003442
|
TA | T | 10 | a0001c0001t0001g0195a0001c0001t0001g0201a0001c0001t0004g0039others(7): Show | 11 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+1887delA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90003442 | |||||
chr8:90003541
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+1980A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003541 | ||||||
chr8:90003615
|
A | G | 1 | a0001c0001t0003g0192 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.69+2054A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003615 | ||||||
chr8:90003673
|
C | T | 1 | a0001c0001t0002g0020 | 3 | NA18946.hp2 NA19010.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.69+2112C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003673 | ||||||
chr8:90003707
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.69+2146T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003707 | ||||||
chr8:90003735
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+2174A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003735 | ||||||
chr8:90003765
|
C | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG01261.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.69+2204C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003765 | ||||||
chr8:90003851
|
A | G | 3 | a0001c0001t0002g0019a0001c0001t0002g0190a0001c0001t0002g0191 | 5 | HG00609.hp1 HG02083.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+2290A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003851 | ||||||
chr8:90003853
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.69+2292C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003853 | ||||||
chr8:90003896
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0213 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.69+2335G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003896 | ||||||
chr8:90003981
|
T | G | 1 | a0001c0001t0002g0048 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.69+2420T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90003981 | ||||||
chr8:90004352
|
GA | G | 8 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(5): Show | 8 | HG00673.hp2 HG01261.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+2805delA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90004352 | |||||
chr8:90004386
|
T | C | 1 | a0001c0001t0002g0051 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.69+2825T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90004386 | ||||||
chr8:90004528
|
A | G | 28 | a0001c0001t0001g0185a0001c0001t0002g0186a0001c0001t0003g0005others(25): Show | 46 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.69+2967A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90004528 | ||||||
chr8:90004602
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.69+3041C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90004602 | ||||||
chr8:90004652
|
T | A | 1 | a0001c0001t0005g0166 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.69+3091T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90004652 | ||||||
chr8:90005002
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+3441G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005002 | ||||||
chr8:90005003
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+3442A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005003 | ||||||
chr8:90005036
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+3475A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005036 | ||||||
chr8:90005037
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+3476G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005037 | ||||||
chr8:90005086
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.69+3525A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005086 | ||||||
chr8:90005238
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+3677G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005238 | ||||||
chr8:90005373
|
T | C | 9 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(6): Show | 9 | HG01261.hp2 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+3812T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005373 | ||||||
chr8:90005382
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.69+3821G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005382 | ||||||
chr8:90005445
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.69+3884C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005445 | ||||||
chr8:90005517
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.69+3956T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005517 | ||||||
chr8:90005551
|
A | G | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0213others(4): Show | 9 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+3990A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005551 | ||||||
chr8:90005612
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0053 | 3 | HG02723.hp1 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.69+4051G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005612 | ||||||
chr8:90005763
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.69+4202C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005763 | ||||||
chr8:90005883
|
G | GGGGTGTT others(29): Show |
1 | a0001c0001t0001g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.69+4376_69+4411dup others(36): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90005883 | |||||
chr8:90005903
|
C | T | 1 | a0001c0001t0002g0162 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.69+4342C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005903 | ||||||
chr8:90005986
|
A | G | 4 | a0001c0001t0002g0015a0001c0001t0002g0160a0001c0001t0002g0161others(1): Show | 6 | HG00099.hp1 HG01346.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+4425A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90005986 | ||||||
chr8:90006052
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.69+4491C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006052 | ||||||
chr8:90006081
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.69+4520C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006081 | ||||||
chr8:90006082
|
C | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+4521C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006082 | ||||||
chr8:90006260
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+4699C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006260 | ||||||
chr8:90006261
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.69+4700T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006261 | ||||||
chr8:90006279
|
T | A | 49 | a0001c0001t0001g0185a0001c0001t0001g0195a0001c0001t0001g0203others(46): Show | 70 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.69+4718T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006279 | ||||||
chr8:90006612
|
A | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.69+5051A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006612 | ||||||
chr8:90006614
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.69+5053G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006614 | ||||||
chr8:90006756
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0004g0194 | 2 | HG01109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.69+5195T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006756 | ||||||
chr8:90006757
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | NA18940.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.69+5196A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006757 | ||||||
chr8:90006772
|
C | T | 1 | a0001c0001t0004g0200 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.69+5211C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006772 | ||||||
chr8:90006778
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0114a0001c0001t0001g0115 | 5 | NA18966.hp2 NA18986.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+5217A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006778 | ||||||
chr8:90006819
|
C | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.69+5258C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006819 | ||||||
chr8:90006823
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(90): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.69+5262G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006823 | ||||||
chr8:90006830
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.69+5269A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006830 | ||||||
chr8:90006832
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(117): Show | 183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.69+5271C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90006832 | ||||||
chr8:90007254
|
C | G | 1 | a0001c0001t0002g0159 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.69+5693C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007254 | ||||||
chr8:90007401
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.69+5840A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007401 | ||||||
chr8:90007550
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0055a0001c0001t0001g0056others(1): Show | 7 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+5989G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007550 | ||||||
chr8:90007575
|
G | C | 1 | a0001c0001t0001g0058 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.69+6014G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007575 | ||||||
chr8:90007728
|
A | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(90): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.69+6167A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007728 | ||||||
chr8:90007910
|
G | A | 1 | a0001c0001t0002g0051 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.69+6349G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90007910 | ||||||
chr8:90008185
|
T | G | 20 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(17): Show | 24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.69+6624T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008185 | ||||||
chr8:90008397
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.69+6836A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008397 | ||||||
chr8:90008510
|
A | G | 3 | a0001c0001t0006g0021a0001c0001t0006g0211a0001c0001t0006g0212 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+6949A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008510 | ||||||
chr8:90008606
|
A | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(111): Show | 175 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.69+7045A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008606 | ||||||
chr8:90008631
|
A | G | 1 | a0001c0001t0003g0184 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.69+7070A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008631 | ||||||
chr8:90008757
|
G | T | 1 | a0001c0001t0010g0109 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.69+7196G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008757 | ||||||
chr8:90008956
|
T | A | 1 | a0001c0001t0001g0203 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.69+7395T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90008956 | ||||||
chr8:90009054
|
T | C | 23 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(20): Show | 27 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.69+7493T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009054 | ||||||
chr8:90009069
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.69+7508G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009069 | ||||||
chr8:90009089
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.69+7528T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009089 | ||||||
chr8:90009175
|
C | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(107): Show | 169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.69+7614C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009175 | ||||||
chr8:90009452
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 6 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-7672A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009452 | ||||||
chr8:90009502
|
G | GT | 81 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(78): Show | 121 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.70-7610dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90009502 | |||||
chr8:90009514
|
T | TA | 5 | a0001c0001t0001g0195a0001c0001t0004g0039a0001c0001t0004g0194others(2): Show | 6 | HG01109.hp1 HG01243.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-7609dupA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90009514 | |||||
chr8:90009799
|
A | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-7325A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009799 | ||||||
chr8:90009941
|
G | A | 1 | a0001c0001t0004g0042 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.70-7183G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90009941 | ||||||
chr8:90010125
|
C | T | 5 | a0001c0001t0003g0038a0001c0001t0003g0180a0001c0001t0003g0181others(2): Show | 6 | HG00544.hp1 NA18612.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-6999C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010125 | ||||||
chr8:90010234
|
G | A | 3 | a0001c0001t0006g0021a0001c0001t0006g0211a0001c0001t0006g0212 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-6890G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010234 | ||||||
chr8:90010540
|
G | T | 1 | a0001c0001t0001g0104 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.70-6584G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010540 | ||||||
chr8:90010548
|
G | A | 2 | a0001c0001t0004g0223a0001c0001t0004g0224 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.70-6576G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010548 | ||||||
chr8:90010639
|
G | A | 55 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(52): Show | 89 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.70-6485G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010639 | ||||||
chr8:90010758
|
T | C | 1 | a0001c0001t0003g0167 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.70-6366T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010758 | ||||||
chr8:90010816
|
T | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(24): Show | 43 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.70-6308T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010816 | ||||||
chr8:90010890
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.70-6234T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010890 | ||||||
chr8:90010893
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.70-6231T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010893 | ||||||
chr8:90010925
|
G | C | 1 | a0001c0001t0001g0061 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.70-6199G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90010925 | ||||||
chr8:90011304
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.70-5820A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011304 | ||||||
chr8:90011314
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.70-5810A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011314 | ||||||
chr8:90011329
|
T | C | 28 | a0001c0001t0001g0185a0001c0001t0003g0005a0001c0001t0003g0008others(25): Show | 46 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.70-5795T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011329 | ||||||
chr8:90011399
|
A | G | 22 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(19): Show | 26 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-5725A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011399 | ||||||
chr8:90011582
|
C | T | 3 | a0001c0001t0004g0233a0001c0001t0004g0234a0001c0001t0004g0235 | 3 | HG01884.hp2 HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.70-5542C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011582 | ||||||
chr8:90011617
|
T | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-5507T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011617 | ||||||
chr8:90011622
|
A | G | 1 | a0001c0001t0002g0122 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.70-5502A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011622 | ||||||
chr8:90011784
|
A | G | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.70-5340A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011784 | ||||||
chr8:90011850
|
T | A | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.70-5274T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90011850 | ||||||
chr8:90012069
|
G | C | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.70-5055G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012069 | ||||||
chr8:90012156
|
CT | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0062others(4): Show | 8 | HG02723.hp1 HG02922.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-4954delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90012156 | |||||
chr8:90012161
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0214a0001c0001t0001g0215 | 4 | HG02486.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-4963T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012161 | ||||||
chr8:90012164
|
T | A | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.70-4960T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012164 | ||||||
chr8:90012193
|
C | T | 2 | a0001c0001t0003g0178a0001c0001t0003g0179 | 2 | NA18977.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.70-4931C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012193 | ||||||
chr8:90012262
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.70-4862C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012262 | ||||||
chr8:90012277
|
C | T | 1 | a0001c0001t0002g0024 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.70-4847C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012277 | ||||||
chr8:90012314
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.70-4810G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012314 | ||||||
chr8:90012343
|
G | C | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.70-4781G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012343 | ||||||
chr8:90012388
|
G | T | 8 | a0001c0001t0001g0195a0001c0001t0004g0039a0001c0001t0004g0194others(5): Show | 9 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-4736G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012388 | ||||||
chr8:90012432
|
T | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.70-4692T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012432 | ||||||
chr8:90012585
|
A | G | 1 | a0001c0001t0003g0183 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.70-4539A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012585 | ||||||
chr8:90012654
|
C | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0119a0001c0001t0001g0120 | 4 | HG02896.hp2 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-4470C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012654 | ||||||
chr8:90012879
|
T | C | 27 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(24): Show | 45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.70-4245T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012879 | ||||||
chr8:90012949
|
G | T | 20 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(17): Show | 24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.70-4175G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90012949 | ||||||
chr8:90013018
|
C | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-4106C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013018 | ||||||
chr8:90013299
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.70-3825T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013299 | ||||||
chr8:90013343
|
T | A | 1 | a0001c0001t0015g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.70-3781T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013343 | ||||||
chr8:90013399
|
G | GT | 72 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0028others(69): Show | 102 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.70-3702dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | |||||
chr8:90013399
|
G | GTT | 20 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0016others(17): Show | 32 | HG00642.hp2 HG00673.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.70-3703_70-3702dup others(2): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | |||||
chr8:90013399
|
G | GTTTT | 16 | a0001c0001t0003g0008a0001c0001t0003g0036a0001c0001t0003g0037others(13): Show | 26 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.70-3705_70-3702dup others(4): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | |||||
chr8:90013399
|
G | GTTTTT | 8 | a0001c0001t0003g0005a0001c0001t0003g0173a0001c0001t0003g0174others(5): Show | 16 | HG00438.hp1 HG01952.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.70-3706_70-3702dup others(5): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | |||||
chr8:90013399
|
G | T | 1 | a0001c0001t0002g0157 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.70-3725G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013399 | ||||||
chr8:90013399
|
GT | G | 11 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0067others(8): Show | 13 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-3702delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | |||||
chr8:90013399
|
GTTTTTTT others(2): Show |
G | 5 | a0001c0001t0001g0025a0001c0001t0001g0062a0001c0001t0001g0208others(2): Show | 6 | HG01891.hp2 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-3710_70-3702del others(9): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr8 | 90013399 | |||||
chr8:90013423
|
G | T | 2 | a0001c0001t0002g0154a0001c0001t0002g0155 | 2 | NA18940.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.70-3701G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013423 | ||||||
chr8:90013970
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70-3154A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013970 | ||||||
chr8:90013996
|
G | T | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.70-3128G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90013996 | ||||||
chr8:90014137
|
C | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70-2987C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90014137 | ||||||
chr8:90014236
|
A | G | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.70-2888A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90014236 | ||||||
chr8:90014299
|
C | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(8): Show | 25 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.70-2825C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90014299 | ||||||
chr8:90014673
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.70-2451G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90014673 | ||||||
chr8:90014702
|
A | T | 1 | a0001c0001t0002g0147 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.70-2422A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90014702 | ||||||
chr8:90014921
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.70-2203G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90014921 | ||||||
chr8:90015173
|
A | T | 1 | a0001c0001t0001g0016 | 3 | HG02027.hp1 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.70-1951A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015173 | ||||||
chr8:90015197
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.70-1927C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015197 | ||||||
chr8:90015521
|
T | C | 1 | a0001c0001t0003g0169 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.70-1603T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015521 | ||||||
chr8:90015641
|
C | A | 9 | a0001c0001t0001g0195a0001c0001t0004g0039a0001c0001t0004g0194others(6): Show | 10 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-1483C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015641 | ||||||
chr8:90015661
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG01261.hp2 HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.70-1463G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015661 | ||||||
chr8:90015697
|
A | G | 1 | a0001c0001t0004g0228 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.70-1427A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015697 | ||||||
chr8:90015902
|
G | A | 20 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(17): Show | 24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.70-1222G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015902 | ||||||
chr8:90015934
|
T | G | 1 | a0001c0001t0001g0064 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.70-1190T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90015934 | ||||||
chr8:90016046
|
C | G | 35 | a0001c0001t0001g0195a0001c0001t0001g0227a0001c0001t0001g0231others(32): Show | 42 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.70-1078C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016046 | ||||||
chr8:90016068
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.70-1056G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016068 | ||||||
chr8:90016131
|
G | A | 90 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(87): Show | 131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.70-993G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016131 | ||||||
chr8:90016166
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(74): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.70-958A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016166 | ||||||
chr8:90016393
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.70-731T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016393 | ||||||
chr8:90016403
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.70-721G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016403 | ||||||
chr8:90016473
|
A | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.70-651A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016473 | ||||||
chr8:90016498
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.70-626G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016498 | ||||||
chr8:90016797
|
T | C | 1 | a0001c0001t0002g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.70-327T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 1/9 | chr8 | 90016797 | ||||||
chr8:90017578
|
T | C | 27 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(24): Show | 45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.272+252T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90017578 | ||||||
chr8:90018054
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.272+728T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018054 | ||||||
chr8:90018177
|
C | G | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.273-732C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018177 | ||||||
chr8:90018308
|
G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.273-601G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018308 | ||||||
chr8:90018508
|
AT | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(79): Show | 125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.273-397delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 90018508 | |||||
chr8:90018526
|
A | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(79): Show | 125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.273-383A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018526 | ||||||
chr8:90018533
|
GT | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(25): Show | 44 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.273-368delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr8 | 90018533 | |||||
chr8:90018682
|
A | G | 22 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(19): Show | 26 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.273-227A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018682 | ||||||
chr8:90018782
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.273-127T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018782 | ||||||
chr8:90018846
|
G | A | 48 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(45): Show | 72 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.273-63G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 2/9 | chr8 | 90018846 | ||||||
chr8:90019205
|
G | A | 35 | a0001c0001t0001g0195a0001c0001t0001g0227a0001c0001t0001g0231others(32): Show | 42 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.417+33G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019205 | ||||||
chr8:90019350
|
G | A | 6 | a0001c0001t0004g0223a0001c0001t0004g0224a0001c0001t0004g0226others(3): Show | 7 | HG02257.hp2 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.417+178G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019350 | ||||||
chr8:90019352
|
A | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0057 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.417+180A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019352 | ||||||
chr8:90019386
|
G | A | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.417+214G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019386 | ||||||
chr8:90019490
|
A | G | 2 | a0001c0001t0004g0234a0001c0001t0004g0235 | 2 | HG01884.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.417+318A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019490 | ||||||
chr8:90019671
|
G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.417+499G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019671 | ||||||
chr8:90019705
|
A | G | 90 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(87): Show | 131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.417+533A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019705 | ||||||
chr8:90019734
|
A | G | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0049others(5): Show | 10 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.417+562A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019734 | ||||||
chr8:90019825
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.417+653A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019825 | ||||||
chr8:90019930
|
G | A | 1 | a0001c0001t0005g0207 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.417+758G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019930 | ||||||
chr8:90019960
|
T | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.417+788T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90019960 | ||||||
chr8:90020103
|
G | C | 3 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0153 | 3 | HG01070.hp2 HG01071.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.418-806G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020103 | ||||||
chr8:90020107
|
G | A | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.418-802G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020107 | ||||||
chr8:90020206
|
G | T | 1 | a0001c0001t0012g0146 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.418-703G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020206 | ||||||
chr8:90020308
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.418-601T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020308 | ||||||
chr8:90020348
|
T | C | 90 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(87): Show | 131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.418-561T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020348 | ||||||
chr8:90020492
|
G | A | 4 | a0001c0001t0003g0036a0001c0001t0003g0168a0001c0001t0003g0173others(1): Show | 5 | HG02132.hp1 NA19004.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.418-417G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020492 | ||||||
chr8:90020504
|
T | G | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.418-405T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020504 | ||||||
chr8:90020605
|
C | G | 90 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(87): Show | 131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.418-304C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020605 | ||||||
chr8:90020852
|
A | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.418-57A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 4/9 | chr8 | 90020852 | ||||||
chr8:90021235
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+179T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021235 | ||||||
chr8:90021361
|
A | G | 31 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(28): Show | 49 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.565+305A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021361 | ||||||
chr8:90021511
|
A | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(8): Show | 25 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.565+455A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021511 | ||||||
chr8:90021518
|
A | G | 31 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(28): Show | 49 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.565+462A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021518 | ||||||
chr8:90021760
|
T | A | 1 | a0001c0001t0003g0184 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.565+704T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021760 | ||||||
chr8:90021854
|
C | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.565+798C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90021854 | ||||||
chr8:90022129
|
T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(55): Show | 94 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.565+1073T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022129 | ||||||
chr8:90022207
|
T | C | 3 | a0001c0001t0006g0021a0001c0001t0006g0211a0001c0001t0006g0212 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+1151T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022207 | ||||||
chr8:90022274
|
T | C | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+1218T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022274 | ||||||
chr8:90022433
|
T | C | 9 | a0001c0001t0001g0195a0001c0001t0004g0039a0001c0001t0004g0194others(6): Show | 10 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+1377T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022433 | ||||||
chr8:90022589
|
C | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.565+1533C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022589 | ||||||
chr8:90022590
|
G | A | 1 | a0001c0001t0009g0043 | 2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.565+1534G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022590 | ||||||
chr8:90022647
|
G | A | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+1591G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022647 | ||||||
chr8:90022895
|
G | T | 1 | a0001c0001t0003g0169 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.565+1839G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90022895 | ||||||
chr8:90023061
|
A | T | 1 | a0001c0001t0001g0227 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.565+2005A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90023061 | ||||||
chr8:90023318
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.565+2262A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90023318 | ||||||
chr8:90023343
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+2287T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90023343 | ||||||
chr8:90023387
|
G | GT | 28 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(25): Show | 44 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+2340dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 90023387 | |||||
chr8:90023676
|
A | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.565+2620A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90023676 | ||||||
chr8:90023685
|
G | A | 90 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(87): Show | 131 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.565+2629G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90023685 | ||||||
chr8:90024190
|
G | A | 2 | a0001c0001t0006g0021a0001c0001t0006g0211 | 4 | HG01081.hp2 HG02486.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.565+3134G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024190 | ||||||
chr8:90024250
|
G | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0148 | 2 | NA18747.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.565+3194G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024250 | ||||||
chr8:90024403
|
C | T | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.565+3347C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024403 | ||||||
chr8:90024467
|
A | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0125 | 3 | HG02055.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.565+3411A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024467 | ||||||
chr8:90024647
|
A | C | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+3591A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024647 | ||||||
chr8:90024738
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.565+3682T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024738 | ||||||
chr8:90024813
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.565+3757G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024813 | ||||||
chr8:90024857
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.565+3801G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024857 | ||||||
chr8:90024916
|
A | G | 48 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(45): Show | 72 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.565+3860A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90024916 | ||||||
chr8:90025008
|
G | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0082 | 3 | HG00735.hp2 HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.565+3952G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025008 | ||||||
chr8:90025191
|
T | A | 2 | a0001c0001t0003g0175a0001c0001t0005g0071 | 2 | NA19062.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.565+4135T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025191 | ||||||
chr8:90025216
|
G | A | 1 | a0001c0001t0004g0229 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.565+4160G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025216 | ||||||
chr8:90025387
|
T | C | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.565+4331T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025387 | ||||||
chr8:90025396
|
A | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+4340A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025396 | ||||||
chr8:90025573
|
T | A | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+4517T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025573 | ||||||
chr8:90025651
|
A | G | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0049others(5): Show | 10 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.565+4595A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025651 | ||||||
chr8:90025682
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.565+4626C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025682 | ||||||
chr8:90025753
|
A | C | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+4697A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025753 | ||||||
chr8:90025891
|
G | A | 4 | a0001c0001t0005g0072a0001c0001t0006g0021a0001c0001t0006g0211others(1): Show | 6 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+4835G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025891 | ||||||
chr8:90025919
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.565+4863T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025919 | ||||||
chr8:90025936
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.565+4880G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025936 | ||||||
chr8:90025950
|
G | A | 38 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0062others(35): Show | 46 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.565+4894G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90025950 | ||||||
chr8:90026021
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.565+4965C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026021 | ||||||
chr8:90026106
|
G | T | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.565+5050G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026106 | ||||||
chr8:90026135
|
C | T | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+5079C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026135 | ||||||
chr8:90026369
|
G | A | 1 | a0001c0001t0008g0073 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.565+5313G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026369 | ||||||
chr8:90026427
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.565+5371C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026427 | ||||||
chr8:90026455
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0074a0001c0001t0001g0089others(2): Show | 11 | HG00438.hp2 HG00673.hp1 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.565+5399G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026455 | ||||||
chr8:90026612
|
C | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+5556C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026612 | ||||||
chr8:90026639
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.565+5583A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026639 | ||||||
chr8:90026939
|
T | G | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.565+5883T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90026939 | ||||||
chr8:90027105
|
G | C | 1 | a0001c0001t0015g0206 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.565+6049G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027105 | ||||||
chr8:90027149
|
G | A | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.565+6093G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027149 | ||||||
chr8:90027302
|
G | T | 2 | a0001c0001t0002g0154a0001c0001t0002g0155 | 2 | NA18940.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.565+6246G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027302 | ||||||
chr8:90027367
|
G | A | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.565+6311G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027367 | ||||||
chr8:90027575
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0002g0190 | 2 | HG02145.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.565+6519A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027575 | ||||||
chr8:90027576
|
T | G | 2 | a0001c0001t0001g0236a0001c0001t0002g0190 | 2 | HG02145.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.565+6520T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027576 | ||||||
chr8:90027577
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0002g0190 | 2 | HG02145.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.565+6521C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027577 | ||||||
chr8:90027587
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.565+6531C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027587 | ||||||
chr8:90027630
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.565+6574T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027630 | ||||||
chr8:90027694
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.565+6638A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027694 | ||||||
chr8:90027702
|
C | T | 3 | a0001c0001t0006g0021a0001c0001t0006g0211a0001c0001t0006g0212 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.565+6646C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027702 | ||||||
chr8:90027717
|
C | T | 20 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(17): Show | 24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.565+6661C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027717 | ||||||
chr8:90027773
|
T | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0050a0001c0001t0001g0075others(3): Show | 7 | HG02698.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.565+6717T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027773 | ||||||
chr8:90027774
|
T | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(105): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.565+6718T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027774 | ||||||
chr8:90027775
|
A | T | 27 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(24): Show | 45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.565+6719A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027775 | ||||||
chr8:90027846
|
A | G | 3 | a0001c0001t0002g0142a0001c0001t0002g0156a0001c0001t0013g0141 | 3 | HG01433.hp1 HG03491.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.565+6790A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027846 | ||||||
chr8:90027854
|
G | T | 2 | a0001c0001t0002g0034a0001c0001t0002g0159 | 3 | HG00741.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.565+6798G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027854 | ||||||
chr8:90027941
|
A | G | 1 | a0001c0001t0004g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.565+6885A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90027941 | ||||||
chr8:90028096
|
T | G | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.565+7040T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028096 | ||||||
chr8:90028166
|
C | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(17): Show | 34 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.565+7110C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028166 | ||||||
chr8:90028349
|
T | G | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.565+7293T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028349 | ||||||
chr8:90028385
|
A | T | 1 | a0001c0001t0007g0152 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.565+7329A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028385 | ||||||
chr8:90028478
|
G | A | 27 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(24): Show | 45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.565+7422G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028478 | ||||||
chr8:90028638
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.565+7582G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028638 | ||||||
chr8:90028693
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.565+7637C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028693 | ||||||
chr8:90028725
|
CT | C | 20 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(17): Show | 24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.565+7676delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 90028725 | |||||
chr8:90028730
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.565+7674T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028730 | ||||||
chr8:90028880
|
G | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0062others(2): Show | 6 | HG01167.hp1 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.565+7824G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028880 | ||||||
chr8:90028920
|
G | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(8): Show | 25 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.565+7864G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028920 | ||||||
chr8:90028957
|
C | T | 6 | a0001c0001t0004g0039a0001c0001t0004g0196a0001c0001t0004g0197others(3): Show | 7 | HG01070.hp1 HG01243.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.566-7884C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90028957 | ||||||
chr8:90029066
|
T | A | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-7775T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029066 | ||||||
chr8:90029079
|
AAG | A | 15 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(12): Show | 29 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.566-7760_566-7759d others(4): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 90029079 | |||||
chr8:90029126
|
A | G | 3 | a0001c0001t0006g0021a0001c0001t0006g0211a0001c0001t0006g0212 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-7715A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029126 | ||||||
chr8:90029511
|
C | G | 10 | a0001c0001t0001g0195a0001c0001t0004g0039a0001c0001t0004g0054others(7): Show | 11 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.566-7330C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029511 | ||||||
chr8:90029591
|
G | A | 1 | a0001c0001t0004g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.566-7250G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029591 | ||||||
chr8:90029642
|
A | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.566-7199A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029642 | ||||||
chr8:90029645
|
A | T | 1 | a0001c0001t0002g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.566-7196A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029645 | ||||||
chr8:90029708
|
G | A | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.566-7133G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029708 | ||||||
chr8:90029739
|
T | A | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.566-7102T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029739 | ||||||
chr8:90029821
|
C | T | 1 | a0001c0001t0005g0072 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.566-7020C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029821 | ||||||
chr8:90029823
|
A | C | 1 | a0001c0001t0001g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.566-7018A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029823 | ||||||
chr8:90029823
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.566-7018A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029823 | ||||||
chr8:90029998
|
A | G | 2 | a0001c0001t0002g0033a0001c0001t0002g0151 | 3 | NA18939.hp2 NA18952.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.566-6843A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90029998 | ||||||
chr8:90030004
|
G | A | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.566-6837G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030004 | ||||||
chr8:90030158
|
A | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-6683A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030158 | ||||||
chr8:90030215
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.566-6626G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030215 | ||||||
chr8:90030319
|
A | T | 1 | a0001c0001t0002g0155 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.566-6522A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030319 | ||||||
chr8:90030441
|
C | T | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-6400C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030441 | ||||||
chr8:90030475
|
T | G | 27 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(24): Show | 45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.566-6366T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030475 | ||||||
chr8:90030599
|
A | G | 3 | a0001c0001t0006g0021a0001c0001t0006g0211a0001c0001t0006g0212 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-6242A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030599 | ||||||
chr8:90030623
|
T | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0092 | 2 | NA18985.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.566-6218T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030623 | ||||||
chr8:90030913
|
T | A | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.566-5928T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90030913 | ||||||
chr8:90031088
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.566-5753T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031088 | ||||||
chr8:90031327
|
C | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0093 | 2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.566-5514C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031327 | ||||||
chr8:90031414
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.566-5427A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031414 | ||||||
chr8:90031473
|
G | C | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.566-5368G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031473 | ||||||
chr8:90031547
|
G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.566-5294G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031547 | ||||||
chr8:90031822
|
A | G | 1 | a0001c0001t0002g0163 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.566-5019A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031822 | ||||||
chr8:90031824
|
A | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.566-5017A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031824 | ||||||
chr8:90031877
|
G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.566-4964G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031877 | ||||||
chr8:90031904
|
A | T | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.566-4937A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90031904 | ||||||
chr8:90032030
|
T | A | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.566-4811T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032030 | ||||||
chr8:90032053
|
G | A | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-4788G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032053 | ||||||
chr8:90032162
|
A | T | 3 | a0001c0001t0006g0021a0001c0001t0006g0211a0001c0001t0006g0212 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.566-4679A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032162 | ||||||
chr8:90032180
|
C | T | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-4661C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032180 | ||||||
chr8:90032266
|
A | G | 2 | a0001c0001t0002g0032a0001c0001t0002g0140 | 3 | NA18943.hp2 NA18964.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.566-4575A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032266 | ||||||
chr8:90032444
|
C | T | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-4397C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032444 | ||||||
chr8:90032600
|
C | T | 1 | a0001c0001t0008g0080 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.566-4241C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032600 | ||||||
chr8:90032605
|
A | G | 1 | a0001c0001t0006g0212 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.566-4236A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032605 | ||||||
chr8:90032643
|
A | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.566-4198A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032643 | ||||||
chr8:90032849
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.566-3992C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032849 | ||||||
chr8:90032864
|
T | A | 1 | a0001c0001t0001g0213 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.566-3977T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032864 | ||||||
chr8:90032910
|
A | G | 9 | a0001c0001t0001g0195a0001c0001t0004g0039a0001c0001t0004g0194others(6): Show | 10 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.566-3931A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90032910 | ||||||
chr8:90033038
|
C | T | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.566-3803C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90033038 | ||||||
chr8:90033060
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.566-3781A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90033060 | ||||||
chr8:90033513
|
A | C | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.566-3328A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90033513 | ||||||
chr8:90033665
|
A | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.566-3176A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90033665 | ||||||
chr8:90033667
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.566-3174T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90033667 | ||||||
chr8:90034251
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.566-2590G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90034251 | ||||||
chr8:90034257
|
C | A | 4 | a0001c0001t0004g0197a0001c0001t0004g0198a0001c0001t0004g0199others(1): Show | 4 | HG01070.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.566-2584C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90034257 | ||||||
chr8:90034533
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.566-2308C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90034533 | ||||||
chr8:90035107
|
A | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(8): Show | 25 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.566-1734A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035107 | ||||||
chr8:90035113
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.566-1728A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035113 | ||||||
chr8:90035281
|
C | T | 9 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0049others(6): Show | 11 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.566-1560C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035281 | ||||||
chr8:90035511
|
G | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(175): Show | 266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.566-1330G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035511 | ||||||
chr8:90035659
|
G | A | 20 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(17): Show | 24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.566-1182G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035659 | ||||||
chr8:90035797
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-1044T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035797 | ||||||
chr8:90035886
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.566-955A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90035886 | ||||||
chr8:90035931
|
A | AT | 27 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(24): Show | 45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.566-901dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr8 | 90035931 | |||||
chr8:90036049
|
A | G | 36 | a0001c0001t0001g0195a0001c0001t0001g0217a0001c0001t0001g0227others(33): Show | 43 | HG01070.hp1 HG01081.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.566-792A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90036049 | ||||||
chr8:90036090
|
A | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.566-751A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90036090 | ||||||
chr8:90036138
|
A | G | 2 | a0001c0001t0002g0139a0001c0001t0002g0150 | 2 | HG02027.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.566-703A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90036138 | ||||||
chr8:90036585
|
G | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0126 | 3 | NA18948.hp2 NA18998.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.566-256G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90036585 | ||||||
chr8:90036744
|
C | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.566-97C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 5/9 | chr8 | 90036744 | ||||||
chr8:90037151
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01167.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.665+211G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037151 | ||||||
chr8:90037266
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665+326T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037266 | ||||||
chr8:90037325
|
C | G | 2 | a0001c0001t0003g0038a0001c0001t0003g0183 | 3 | NA18939.hp1 NA18949.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.665+385C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037325 | ||||||
chr8:90037448
|
C | CT | 27 | a0001c0001t0001g0097a0001c0001t0003g0005a0001c0001t0003g0008others(24): Show | 45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.665+524dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 90037448 | |||||
chr8:90037511
|
A | G | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.665+571A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037511 | ||||||
chr8:90037603
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0079a0001c0001t0001g0081others(2): Show | 6 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(3): Show |
intron_variant | MODIFIER | c.665+663C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037603 | ||||||
chr8:90037735
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.665+795C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037735 | ||||||
chr8:90037823
|
A | C | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.665+883A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90037823 | ||||||
chr8:90038049
|
T | A | 4 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(1): Show | 7 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.665+1109T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038049 | ||||||
chr8:90038052
|
T | C | 1 | a0001c0001t0005g0112 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.665+1112T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038052 | ||||||
chr8:90038068
|
A | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(8): Show | 25 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.665+1128A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038068 | ||||||
chr8:90038128
|
A | G | 1 | a0001c0001t0004g0232 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.665+1188A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038128 | ||||||
chr8:90038262
|
A | T | 3 | a0001c0001t0006g0021a0001c0001t0006g0211a0001c0001t0006g0212 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.665+1322A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038262 | ||||||
chr8:90038454
|
C | CT | 32 | a0001c0001t0001g0013a0001c0001t0001g0055a0001c0001t0001g0056others(29): Show | 40 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.665+1535dupT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 90038454 | |||||
chr8:90038454
|
CT | C | 53 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0049others(50): Show | 74 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.665+1535delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 90038454 | |||||
chr8:90038463
|
T | C | 1 | a0001c0001t0004g0196 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.665+1523T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038463 | ||||||
chr8:90038536
|
G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.665+1596G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90038536 | ||||||
chr8:90039104
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.665+2164T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039104 | ||||||
chr8:90039162
|
A | G | 1 | a0001c0001t0003g0181 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.665+2222A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039162 | ||||||
chr8:90039199
|
C | A | 1 | a0001c0001t0002g0133 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.665+2259C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039199 | ||||||
chr8:90039234
|
A | G | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.665+2294A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039234 | ||||||
chr8:90039268
|
CTGAGACT others(8): Show |
C | 28 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(25): Show | 44 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.665+2330_665+2344d others(17): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 90039268 | |||||
chr8:90039397
|
T | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(79): Show | 125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.665+2457T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039397 | ||||||
chr8:90039400
|
TC | T | 3 | a0001c0001t0001g0208a0001c0001t0005g0207a0001c0001t0015g0206 | 3 | HG01891.hp2 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.665+2462delC | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr8 | 90039400 | |||||
chr8:90039624
|
C | A | 9 | a0001c0001t0004g0042a0001c0001t0004g0044a0001c0001t0004g0222others(6): Show | 11 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.665+2684C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90039624 | ||||||
chr8:90040016
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.666-2712G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040016 | ||||||
chr8:90040039
|
G | GC | 3 | a0001c0001t0001g0208a0001c0001t0005g0207a0001c0001t0015g0206 | 3 | HG01891.hp2 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.666-2689_666-2688i others(3): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040039 | ||||||
chr8:90040040
|
T | A | 3 | a0001c0001t0001g0208a0001c0001t0005g0207a0001c0001t0015g0206 | 3 | HG01891.hp2 HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.666-2688T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040040 | ||||||
chr8:90040447
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0002g0186 | 2 | HG00735.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.666-2281C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040447 | ||||||
chr8:90040463
|
T | C | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666-2265T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040463 | ||||||
chr8:90040484
|
T | A | 1 | a0001c0001t0002g0134 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.666-2244T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040484 | ||||||
chr8:90040598
|
A | T | 2 | a0001c0001t0002g0154a0001c0001t0002g0155 | 2 | NA18940.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.666-2130A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040598 | ||||||
chr8:90040604
|
C | T | 8 | a0001c0001t0001g0195a0001c0001t0004g0039a0001c0001t0004g0194others(5): Show | 9 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.666-2124C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040604 | ||||||
chr8:90040678
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.666-2050G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040678 | ||||||
chr8:90040712
|
G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666-2016G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040712 | ||||||
chr8:90040782
|
A | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(171): Show | 261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.666-1946A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040782 | ||||||
chr8:90040800
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.666-1928A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040800 | ||||||
chr8:90040888
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.666-1840G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040888 | ||||||
chr8:90040896
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.666-1832T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90040896 | ||||||
chr8:90041025
|
T | C | 10 | a0001c0001t0001g0195a0001c0001t0004g0039a0001c0001t0004g0054others(7): Show | 11 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.666-1703T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041025 | ||||||
chr8:90041261
|
A | G | 4 | a0001c0001t0003g0037a0001c0001t0003g0171a0001c0001t0003g0172others(1): Show | 5 | HG01943.hp1 NA18943.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.666-1467A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041261 | ||||||
chr8:90041369
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.666-1359C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041369 | ||||||
chr8:90041569
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.666-1159A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041569 | ||||||
chr8:90041610
|
G | A | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.666-1118G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041610 | ||||||
chr8:90041644
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.666-1084A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041644 | ||||||
chr8:90041747
|
A | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.666-981A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041747 | ||||||
chr8:90041811
|
G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666-917G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041811 | ||||||
chr8:90041882
|
A | C | 1 | a0001c0001t0004g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.666-846A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90041882 | ||||||
chr8:90042319
|
G | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666-409G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 6/9 | chr8 | 90042319 | ||||||
chr8:90042953
|
G | A | 1 | a0001c0001t0002g0124 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.738+153G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90042953 | ||||||
chr8:90042973
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.738+173C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90042973 | ||||||
chr8:90043117
|
A | G | 27 | a0001c0001t0001g0090a0001c0001t0003g0005a0001c0001t0003g0008others(24): Show | 45 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.738+317A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043117 | ||||||
chr8:90043159
|
A | T | 32 | a0001c0001t0001g0195a0001c0001t0001g0227a0001c0001t0001g0231others(29): Show | 37 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.738+359A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043159 | ||||||
chr8:90043183
|
A | T | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.738+383A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043183 | ||||||
chr8:90043221
|
A | T | 1 | a0001c0001t0003g0170 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.738+421A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043221 | ||||||
chr8:90043225
|
G | A | 3 | a0001c0001t0002g0142a0001c0001t0002g0156a0001c0001t0013g0141 | 3 | HG01433.hp1 HG03491.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.738+425G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043225 | ||||||
chr8:90043241
|
G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(76): Show | 121 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.738+441G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043241 | ||||||
chr8:90043265
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.738+465A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043265 | ||||||
chr8:90043477
|
A | C | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.738+677A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043477 | ||||||
chr8:90043622
|
G | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.738+822G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043622 | ||||||
chr8:90043636
|
T | TA | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(175): Show | 266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.738+841dupA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr8 | 90043636 | |||||
chr8:90043687
|
G | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(80): Show | 126 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.738+887G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043687 | ||||||
chr8:90043757
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0074a0001c0001t0001g0089others(2): Show | 11 | HG00438.hp2 HG00673.hp1 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.738+957A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043757 | ||||||
chr8:90043956
|
A | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.739-893A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90043956 | ||||||
chr8:90044205
|
C | T | 27 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(24): Show | 45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.739-644C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90044205 | ||||||
chr8:90044393
|
C | T | 27 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(24): Show | 43 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.739-456C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90044393 | ||||||
chr8:90044418
|
C | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(240): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.739-431C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90044418 | ||||||
chr8:90044495
|
T | C | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.739-354T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90044495 | ||||||
chr8:90044582
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0053 | 3 | HG02723.hp1 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.739-267T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90044582 | ||||||
chr8:90044611
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.739-238G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 7/9 | chr8 | 90044611 | ||||||
chr8:90045001
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02630.hp2 | splice_region_variant&intron_variant | LOW | c.885+6C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045001 | ||||||
chr8:90045002
|
GT | G | 4 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(1): Show | 7 | HG01884.hp1 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.885+9delT | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 90045002 | |||||
chr8:90045160
|
T | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.885+165T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045160 | ||||||
chr8:90045385
|
C | T | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.885+390C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045385 | ||||||
chr8:90045392
|
G | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0091others(1): Show | 4 | HG01123.hp2 HG03654.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.885+397G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045392 | ||||||
chr8:90045679
|
G | A | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.885+684G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045679 | ||||||
chr8:90045899
|
A | G | 54 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(51): Show | 88 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.885+904A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90045899 | ||||||
chr8:90046122
|
C | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0049others(5): Show | 10 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.885+1127C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046122 | ||||||
chr8:90046163
|
C | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(80): Show | 126 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.885+1168C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046163 | ||||||
chr8:90046179
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(7): Show | 24 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.885+1184G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046179 | ||||||
chr8:90046255
|
G | A | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.885+1260G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046255 | ||||||
chr8:90046279
|
G | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0213a0001c0001t0001g0216 | 4 | HG02055.hp1 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.885+1284G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046279 | ||||||
chr8:90046298
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.885+1303G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046298 | ||||||
chr8:90046773
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(24): Show | 43 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.885+1778G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046773 | ||||||
chr8:90046855
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.885+1860T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046855 | ||||||
chr8:90046898
|
T | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.885+1903T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046898 | ||||||
chr8:90046902
|
T | G | 22 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(19): Show | 26 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.885+1907T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046902 | ||||||
chr8:90046988
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.885+1993A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90046988 | ||||||
chr8:90047019
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.885+2024A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047019 | ||||||
chr8:90047148
|
C | T | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.885+2153C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047148 | ||||||
chr8:90047169
|
T | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0049others(5): Show | 10 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.885+2174T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047169 | ||||||
chr8:90047316
|
C | T | 22 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(19): Show | 26 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.885+2321C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047316 | ||||||
chr8:90047359
|
CA | C | 9 | a0001c0001t0001g0195a0001c0001t0004g0039a0001c0001t0004g0194others(6): Show | 10 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.885+2373delA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 90047359 | |||||
chr8:90047596
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0004g0194 | 2 | HG01109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.885+2601C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047596 | ||||||
chr8:90047625
|
C | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.885+2630C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047625 | ||||||
chr8:90047737
|
T | C | 63 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(60): Show | 86 | HG00642.hp2 HG00673.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.885+2742T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90047737 | ||||||
chr8:90048117
|
T | G | 1 | a0001c0001t0002g0031 | 2 | HG00323.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.885+3122T>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048117 | ||||||
chr8:90048208
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0095 | 3 | HG01496.hp1 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.885+3213G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048208 | ||||||
chr8:90048267
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.885+3272A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048267 | ||||||
chr8:90048286
|
T | C | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.885+3291T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048286 | ||||||
chr8:90048359
|
C | T | 1 | a0001c0001t0002g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.886-3318C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048359 | ||||||
chr8:90048385
|
C | T | 10 | a0001c0001t0001g0195a0001c0001t0004g0039a0001c0001t0004g0054others(7): Show | 11 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.886-3292C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048385 | ||||||
chr8:90048527
|
A | T | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.886-3150A>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048527 | ||||||
chr8:90048697
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.886-2980T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048697 | ||||||
chr8:90048754
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.886-2923C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048754 | ||||||
chr8:90048842
|
C | G | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.886-2835C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048842 | ||||||
chr8:90048843
|
G | C | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.886-2834G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048843 | ||||||
chr8:90048889
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886-2788C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048889 | ||||||
chr8:90048974
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0062others(3): Show | 7 | HG01167.hp1 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-2703C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90048974 | ||||||
chr8:90049031
|
G | T | 1 | a0001c0001t0002g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.886-2646G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049031 | ||||||
chr8:90049253
|
T | C | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.886-2424T>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049253 | ||||||
chr8:90049377
|
C | T | 6 | a0001c0001t0004g0223a0001c0001t0004g0224a0001c0001t0004g0226others(3): Show | 7 | HG02257.hp2 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-2300C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049377 | ||||||
chr8:90049446
|
A | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.886-2231A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049446 | ||||||
chr8:90049567
|
A | G | 2 | a0001c0001t0005g0112a0001c0001t0005g0113 | 2 | HG02630.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.886-2110A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049567 | ||||||
chr8:90049661
|
A | G | 1 | a0001c0001t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.886-2016A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049661 | ||||||
chr8:90049710
|
A | G | 99 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(96): Show | 143 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.886-1967A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049710 | ||||||
chr8:90049742
|
A | G | 1 | a0001c0001t0001g0046 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.886-1935A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049742 | ||||||
chr8:90049813
|
C | CT | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0049others(5): Show | 10 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.886-1864_886-1863i others(3): Show |
DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049813 | ||||||
chr8:90049814
|
G | A | 1 | a0001c0001t0004g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.886-1863G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049814 | ||||||
chr8:90049837
|
C | T | 6 | a0001c0001t0004g0039a0001c0001t0004g0196a0001c0001t0004g0197others(3): Show | 7 | HG01070.hp1 HG01243.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.886-1840C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049837 | ||||||
chr8:90049890
|
G | A | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.886-1787G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049890 | ||||||
chr8:90049914
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.886-1763C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049914 | ||||||
chr8:90049918
|
A | C | 28 | a0001c0001t0002g0011a0001c0001t0002g0014a0001c0001t0002g0015others(25): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.886-1759A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049918 | ||||||
chr8:90049928
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.886-1749A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049928 | ||||||
chr8:90049982
|
A | G | 20 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(17): Show | 24 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.886-1695A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90049982 | ||||||
chr8:90050008
|
C | G | 1 | a0001c0001t0011g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.886-1669C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050008 | ||||||
chr8:90050143
|
A | G | 1 | a0001c0001t0002g0023 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.886-1534A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050143 | ||||||
chr8:90050162
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.886-1515C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050162 | ||||||
chr8:90050274
|
C | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0119a0001c0001t0001g0120 | 4 | HG02896.hp2 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.886-1403C>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050274 | ||||||
chr8:90050289
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.886-1388G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050289 | ||||||
chr8:90050315
|
T | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0079a0001c0001t0001g0081others(2): Show | 6 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(3): Show |
intron_variant | MODIFIER | c.886-1362T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050315 | ||||||
chr8:90050499
|
G | T | 3 | a0001c0001t0006g0021a0001c0001t0006g0211a0001c0001t0006g0212 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.886-1178G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050499 | ||||||
chr8:90050566
|
G | A | 27 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(24): Show | 45 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.886-1111G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050566 | ||||||
chr8:90050592
|
A | C | 46 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0236others(43): Show | 68 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.886-1085A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050592 | ||||||
chr8:90050683
|
G | A | 5 | a0001c0001t0003g0038a0001c0001t0003g0180a0001c0001t0003g0181others(2): Show | 6 | HG00544.hp1 NA18612.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.886-994G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90050683 | ||||||
chr8:90051020
|
G | A | 8 | a0001c0001t0001g0195a0001c0001t0004g0039a0001c0001t0004g0194others(5): Show | 9 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.886-657G>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051020 | ||||||
chr8:90051022
|
C | G | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(80): Show | 126 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.886-655C>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051022 | ||||||
chr8:90051174
|
T | TA | 37 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(34): Show | 69 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.886-490dupA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 90051174 | |||||
chr8:90051174
|
TA | T | 11 | a0001c0001t0001g0187a0001c0001t0001g0195a0001c0001t0002g0123others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.886-490delA | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr8 | 90051174 | |||||
chr8:90051376
|
T | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0016others(27): Show | 48 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.886-301T>A | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051376 | ||||||
chr8:90051389
|
C | T | 26 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0036others(23): Show | 44 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.886-288C>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051389 | ||||||
chr8:90051471
|
A | G | 1 | a0001c0001t0003g0171 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.886-206A>G | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051471 | ||||||
chr8:90051500
|
A | C | 3 | a0001c0001t0006g0021a0001c0001t0006g0211a0001c0001t0006g0212 | 5 | HG01081.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.886-177A>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051500 | ||||||
chr8:90051559
|
G | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(75): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.886-118G>T | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 8/9 | chr8 | 90051559 | ||||||
chr8:90051808
|
G | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(169): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.949-30G>C | DECR1 | ENSG00000104325.7 | transcript | ENST00000220764.7 | protein_coding | 9/9 | chr8 | 90051808 |