Item | Value |
---|---|
geneid | 1996 |
ensemblid | ENSG00000162374.18 |
hgncid | 3315 |
symbol | ELAVL4 |
name | ELAV like RNA binding protein 4 |
refseq_nuc | NM_001144774.3 |
refseq_prot | NP_001138246.1 |
ensembl_nuc | ENST00000371824.7 |
ensembl_prot | ENSP00000360889.2 |
mane_status | MANE Select |
chr | chr1 |
start | 50108920 |
end | 50203772 |
strand | + |
ver | v1.2 |
region | chr1:50108920-50203772 |
region5000 | chr1:50103920-50208772 |
regionname0 | ELAVL4_chr1_50108920_50203772 |
regionname5000 | ELAVL4_chr1_50103920_50208772 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 366 | 276 | 90 | 46 | 102 | 12 | 24 | 80 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2865 | 187 | 57 | 37 | 63 | 10 | 18 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0002 | 0/0 | 2865 | 48 | 2 | 1 | 38 | 2 | 5 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0003 | 0/0 | 2864 | 16 | 13 | 3 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0004 | 0/0 | 2865 | 8 | 7 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0005 | 0/0 | 2865 | 4 | 4 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0006 | 0/0 | 2865 | 3 | 0 | 3 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0007 | 0/0 | 2865 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0008 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0009 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0010 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0011 | 0/0 | 2865 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0012 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0013 | 0/0 | 2864 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
t0014 | 0/0 | 2865 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1101 | 215 | 37 | 39 | 102 | 12 | 24 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0002 | 1/0 | 1101 | 61 | 53 | 7 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3965 | 159 | 33 | 34 | 63 | 10 | 18 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0001t0002 | 0/0 | 3965 | 48 | 2 | 1 | 38 | 2 | 5 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0001t0006 | 0/0 | 3965 | 3 | 0 | 3 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0001t0009 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0001t0010 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0001t0011 | 0/0 | 3965 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0001t0012 | 0/0 | 3965 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0001t0014 | 0/0 | 3965 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0002t0001 | 1/0 | 3965 | 28 | 24 | 3 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0002t0003 | 0/0 | 3964 | 16 | 13 | 3 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0002t0004 | 0/0 | 3965 | 8 | 7 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0002t0005 | 0/0 | 3965 | 4 | 4 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0002t0007 | 0/0 | 3965 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0002t0008 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
a0001c0002t0013 | 0/0 | 3964 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | copy fasta | chr1 | 50103920 | 50208772 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0006g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0006g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0010g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0011g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0012g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0001t0014g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0007g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
a0001c0002t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | GBR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0115 | EUR | FIN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | FIN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | FIN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01169 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01243 | hp2 | a0001 | c0002 | t0004 | g0055 | AMR | PUR | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01346 | hp2 | a0001 | c0002 | t0003 | g0027 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01891 | hp1 | a0001 | c0002 | t0004 | g0054 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0128 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02135 | hp2 | a0001 | c0001 | t0012 | g0148 | EAS | KHV | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02145 | hp2 | a0001 | c0002 | t0004 | g0270 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02257 | hp1 | a0001 | c0002 | t0003 | g0268 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02258 | hp1 | a0001 | c0002 | t0004 | g0004 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0101 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0110 | AMR | PEL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0234 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0003 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02622 | hp1 | a0001 | c0002 | t0003 | g0175 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02630 | hp1 | a0001 | c0002 | t0003 | g0173 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0273 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02723 | hp1 | a0001 | c0002 | t0004 | g0244 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0245 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0203 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02895 | hp2 | a0001 | c0002 | t0004 | g0098 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02922 | hp1 | a0001 | c0002 | t0005 | g0237 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02922 | hp2 | a0001 | c0002 | t0004 | g0068 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02965 | hp2 | a0001 | c0002 | t0003 | g0249 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02970 | hp2 | a0001 | c0002 | t0005 | g0240 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03098 | hp1 | a0001 | c0002 | t0007 | g0242 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03098 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03130 | hp1 | a0001 | c0002 | t0004 | g0236 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03139 | hp2 | a0001 | c0002 | t0003 | g0196 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0252 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03195 | hp2 | a0001 | c0002 | t0008 | g0130 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0109 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | ESN | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03540 | hp1 | a0001 | c0002 | t0007 | g0241 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03579 | hp1 | a0001 | c0002 | t0003 | g0166 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03669 | hp1 | a0001 | c0001 | t0011 | g0219 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | BEB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | BEB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18522 | hp1 | a0001 | c0002 | t0003 | g0003 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18522 | hp2 | a0001 | c0002 | t0005 | g0239 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19030 | hp1 | a0001 | c0002 | t0013 | g0090 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19043 | hp1 | a0001 | c0002 | t0007 | g0238 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | ASW | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ASW | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | GIH | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | GIH | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01123 | hp1 | a0001 | c0001 | t0014 | g0021 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG01123 | hp2 | a0001 | c0001 | t0006 | g0111 | AMR | CLM | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0225 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02486 | hp2 | a0001 | c0002 | t0005 | g0243 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0131 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG06807 | hp1 | a0001 | c0002 | t0003 | g0248 | AFR | USA | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | USA | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | USA | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0165 | AFR | USA | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0214 | REF | REF | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0064 | REF | REF | ELAVL4_chr1_50103920_50208772 | ELAVL4 | chr1 | 50103920 | 50208772 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:50195739
|
C | T | 1 | a0001c0001 | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
synonymous_variant | LOW | c.687C>T | p.Pro229Pro | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/7 | 957/3965 | 687/1101 | 229/366 | chr1 | 50195739 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:50108973
|
G | A | 3 | a0001c0001t0009a0001c0001t0010a0001c0002t0008 | 3 | HG02055.hp2 HG02559.hp1 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-217G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/7 | 217 | chr1 | 50108973 | |||||
chr1:50201234
|
C | T | 1 | a0001c0002t0003 | 16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*56C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 56 | chr1 | 50201234 | |||||
chr1:50201290
|
A | T | 1 | a0001c0001t0014 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 112 | chr1 | 50201290 | |||||
chr1:50201390
|
GA | G | 2 | a0001c0002t0003a0001c0002t0013 | 17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*224delA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 224 | INFO_REALIGN_3_PRIME | chr1 | 50201390 | ||||
chr1:50202183
|
C | T | 1 | a0001c0001t0012 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1005C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 1005 | chr1 | 50202183 | |||||
chr1:50202874
|
G | A | 1 | a0001c0002t0005 | 4 | HG02486.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1696G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 1696 | chr1 | 50202874 | |||||
chr1:50202958
|
G | A | 1 | a0001c0001t0006 | 3 | HG01123.hp2 HG02273.hp2 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1780G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 1780 | chr1 | 50202958 | |||||
chr1:50202973
|
C | T | 2 | a0001c0001t0010a0001c0002t0004 | 9 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1795C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 1795 | chr1 | 50202973 | |||||
chr1:50203286
|
T | C | 2 | a0001c0001t0002a0001c0001t0011 | 49 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2108T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 2108 | chr1 | 50203286 | |||||
chr1:50203481
|
T | C | 1 | a0001c0002t0008 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2303T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 2303 | chr1 | 50203481 | |||||
chr1:50203698
|
T | C | 2 | a0001c0001t0002a0001c0001t0011 | 49 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2520T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 2520 | chr1 | 50203698 | |||||
chr1:50203707
|
T | A | 1 | a0001c0002t0007 | 3 | HG03098.hp1 HG03540.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2529T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 2529 | chr1 | 50203707 | |||||
chr1:50203741
|
T | C | 1 | a0001c0001t0011 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2563T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 7/7 | 2563 | chr1 | 50203741 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:50109452
|
G | T | 1 | a0001c0002t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.9+254G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50109452 | ||||||
chr1:50109540
|
G | A | 1 | a0001c0002t0004g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.9+342G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50109540 | ||||||
chr1:50109604
|
C | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG00609.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.9+406C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50109604 | ||||||
chr1:50109736
|
A | T | 1 | a0001c0002t0004g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.9+538A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50109736 | ||||||
chr1:50110003
|
C | CTG | 33 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0250others(30): Show | 34 | HG00642.hp1 HG02083.hp1 HG02148.hp2 others(31): Show |
intron_variant | MODIFIER | c.9+828_9+829dupTG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50110003 | |||||
chr1:50110003
|
C | CTGTG | 3 | a0001c0001t0002g0269a0001c0002t0003g0268a0001c0002t0004g0270 | 3 | HG02145.hp2 HG02257.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.9+826_9+829dupTGTG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50110003 | |||||
chr1:50110459
|
G | A | 1 | a0001c0002t0003g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9+1261G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50110459 | ||||||
chr1:50110461
|
A | G | 1 | a0001c0002t0004g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9+1263A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50110461 | ||||||
chr1:50110710
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.9+1512C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50110710 | ||||||
chr1:50110843
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.9+1645G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50110843 | ||||||
chr1:50111038
|
T | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(38): Show | 42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.9+1840T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111038 | ||||||
chr1:50111362
|
A | G | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0002t0001g0233others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+2164A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111362 | ||||||
chr1:50111663
|
C | G | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | NA18959.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.9+2465C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111663 | ||||||
chr1:50111845
|
T | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+2647T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111845 | ||||||
chr1:50111886
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.9+2688C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111886 | ||||||
chr1:50111982
|
G | T | 64 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0182others(61): Show | 64 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.9+2784G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50111982 | ||||||
chr1:50112004
|
C | T | 31 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0171others(28): Show | 32 | HG00642.hp1 HG01891.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.9+2806C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112004 | ||||||
chr1:50112401
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.9+3203A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112401 | ||||||
chr1:50112665
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.9+3467A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112665 | ||||||
chr1:50112784
|
T | A | 1 | a0001c0002t0004g0244 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.9+3586T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112784 | ||||||
chr1:50112796
|
G | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0002t0001g0233others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+3598G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112796 | ||||||
chr1:50112905
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.9+3707G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50112905 | ||||||
chr1:50113116
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.9+3918G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113116 | ||||||
chr1:50113220
|
C | CT | 8 | a0001c0001t0001g0167a0001c0002t0005g0237a0001c0002t0005g0239others(5): Show | 8 | HG02486.hp2 HG02922.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.9+4033dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50113220 | |||||
chr1:50113220
|
CT | C | 32 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0171others(29): Show | 33 | HG00642.hp1 HG01167.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.9+4033delT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50113220 | |||||
chr1:50113375
|
A | T | 1 | a0001c0001t0001g0227 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.9+4177A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113375 | ||||||
chr1:50113542
|
A | G | 2 | a0001c0002t0001g0165a0001c0002t0003g0166 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.9+4344A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113542 | ||||||
chr1:50113565
|
A | C | 123 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0093others(120): Show | 124 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.9+4367A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113565 | ||||||
chr1:50113653
|
G | A | 1 | a0001c0002t0013g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9+4455G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113653 | ||||||
chr1:50113748
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.9+4550A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50113748 | ||||||
chr1:50114070
|
C | A | 11 | a0001c0001t0002g0092a0001c0002t0001g0091a0001c0002t0001g0273others(8): Show | 11 | HG02055.hp1 HG02486.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+4872C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114070 | ||||||
chr1:50114125
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | NA18948.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.9+4927T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114125 | ||||||
chr1:50114247
|
G | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0002t0001g0233others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+5049G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114247 | ||||||
chr1:50114394
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.9+5196A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114394 | ||||||
chr1:50114429
|
G | A | 1 | a0001c0002t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.9+5231G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114429 | ||||||
chr1:50114602
|
C | T | 2 | a0001c0001t0001g0267a0001c0002t0003g0225 | 2 | HG02486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.9+5404C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114602 | ||||||
chr1:50114603
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.9+5405G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50114603 | ||||||
chr1:50115056
|
G | C | 1 | a0001c0001t0001g0167 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.9+5858G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115056 | ||||||
chr1:50115060
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.9+5862C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115060 | ||||||
chr1:50115074
|
G | C | 1 | a0001c0001t0001g0167 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.9+5876G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115074 | ||||||
chr1:50115120
|
T | C | 11 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0171others(8): Show | 11 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+5922T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115120 | ||||||
chr1:50115151
|
C | T | 92 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0096others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.9+5953C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115151 | ||||||
chr1:50115155
|
C | A | 1 | a0001c0002t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.9+5957C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115155 | ||||||
chr1:50115406
|
G | A | 27 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0171others(24): Show | 28 | HG00642.hp1 HG02145.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.9+6208G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115406 | ||||||
chr1:50115446
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.9+6248A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115446 | ||||||
chr1:50115637
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.9+6439G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115637 | ||||||
chr1:50115787
|
G | T | 92 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0096others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.9+6589G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115787 | ||||||
chr1:50115962
|
A | G | 3 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0002t0001g0088 | 3 | HG02109.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.9+6764A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115962 | ||||||
chr1:50115971
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.9+6773G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50115971 | ||||||
chr1:50116395
|
GGT | G | 10 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0002t0003g0003others(7): Show | 11 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+7213_9+7214delTG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50116395 | |||||
chr1:50116397
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.9+7199T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116397 | ||||||
chr1:50116409
|
TGTGC | T | 90 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0096others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.9+7215_9+7218delCG others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50116409 | |||||
chr1:50116411
|
T | C | 5 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 5 | HG00642.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+7213T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116411 | ||||||
chr1:50116411
|
TGC | T | 64 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(61): Show | 64 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.9+7215_9+7216delCG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50116411 | |||||
chr1:50116413
|
C | CGTGT | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0002t0001g0233others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+7238_9+7241dupGT others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50116413 | |||||
chr1:50116413
|
C | T | 6 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0254others(3): Show | 6 | HG00642.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+7215C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116413 | ||||||
chr1:50116413
|
CGT | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0167a0001c0001t0001g0171others(8): Show | 11 | HG01891.hp1 HG01993.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+7240_9+7241delGT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50116413 | |||||
chr1:50116415
|
T | C | 1 | a0001c0002t0001g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.9+7217T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116415 | ||||||
chr1:50116417
|
T | C | 64 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(61): Show | 64 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.9+7219T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116417 | ||||||
chr1:50116419
|
T | C | 90 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0096others(87): Show | 90 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.9+7221T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116419 | ||||||
chr1:50116500
|
A | C | 155 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0096others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.9+7302A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50116500 | ||||||
chr1:50117066
|
G | A | 1 | a0001c0002t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.9+7868G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117066 | ||||||
chr1:50117407
|
C | T | 31 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0171others(28): Show | 32 | HG00642.hp1 HG01891.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.9+8209C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117407 | ||||||
chr1:50117469
|
G | A | 1 | a0001c0002t0004g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9+8271G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117469 | ||||||
chr1:50117518
|
C | T | 31 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0171others(28): Show | 32 | HG00642.hp1 HG01891.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.9+8320C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117518 | ||||||
chr1:50117565
|
C | T | 5 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0254others(2): Show | 5 | HG00642.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+8367C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117565 | ||||||
chr1:50117753
|
G | A | 1 | a0001c0002t0003g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.9+8555G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117753 | ||||||
chr1:50117813
|
C | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0002t0001g0233others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+8615C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117813 | ||||||
chr1:50117946
|
A | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0163others(2): Show | 5 | HG01069.hp1 HG01109.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.9+8748A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117946 | ||||||
chr1:50117950
|
G | T | 1 | a0001c0001t0002g0266 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.9+8752G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50117950 | ||||||
chr1:50118140
|
T | G | 1 | a0001c0002t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.9+8942T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118140 | ||||||
chr1:50118204
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.9+9006T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118204 | ||||||
chr1:50118207
|
A | AT | 10 | a0001c0001t0002g0092a0001c0002t0001g0091a0001c0002t0005g0237others(7): Show | 10 | HG02055.hp1 HG02486.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+9017dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118207 | |||||
chr1:50118263
|
A | G | 1 | a0001c0002t0013g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9+9065A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118263 | ||||||
chr1:50118494
|
GA | G | 13 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0159others(10): Show | 13 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.9+9305delA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118494 | |||||
chr1:50118503
|
AG | A | 169 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0096others(166): Show | 170 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.9+9306delG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118503 | ||||||
chr1:50118516
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.9+9318A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118516 | ||||||
chr1:50118723
|
C | T | 3 | a0001c0001t0001g0158a0001c0002t0001g0094a0001c0002t0004g0236 | 3 | HG02717.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.9+9525C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50118723 | ||||||
chr1:50118944
|
A | AAG | 82 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.9+9765_9+9766dupAG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118944 | |||||
chr1:50118961
|
A | AGAGAGG | 10 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0171others(7): Show | 10 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+9766_9+9767insAG others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118961 | |||||
chr1:50118961
|
A | AGAGAGGG others(3): Show |
1 | a0001c0001t0001g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.9+9766_9+9767insAG others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118961 | |||||
chr1:50118981
|
G | GGA | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0002t0001g0233others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+9798_9+9799dupGA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50118981 | |||||
chr1:50119010
|
A | G | 63 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(60): Show | 63 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.9+9812A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119010 | ||||||
chr1:50119034
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.9+9836G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119034 | ||||||
chr1:50119036
|
A | AAAAG | 27 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(24): Show | 27 | HG00140.hp2 HG00609.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.9+9894_9+9897dupGA others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
A | AAAAGAAA others(1): Show |
27 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0039others(24): Show | 29 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.9+9890_9+9897dupGA others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
A | AAAAGAAA others(5): Show |
12 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0176others(9): Show | 12 | HG02615.hp1 HG02965.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+9886_9+9897dupGA others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
A | AAAAGAAA others(9): Show |
1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.9+9882_9+9897dupGA others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
A | AAAAGAAA others(13): Show |
2 | a0001c0001t0002g0045a0001c0002t0003g0175 | 2 | HG02622.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.9+9878_9+9897dupGA others(18): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
A | AAAGAAAG others(8): Show |
1 | a0001c0001t0001g0085 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.9+9840_9+9841insGA others(13): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
A | AAGAAAGA others(3): Show |
1 | a0001c0001t0002g0265 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.9+9839_9+9840insGA others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.9+9838A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119036 | ||||||
chr1:50119036
|
AAAAG | A | 17 | a0001c0001t0001g0012a0001c0001t0001g0060a0001c0001t0001g0061others(14): Show | 17 | HG00140.hp1 HG02717.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.9+9894_9+9897delGA others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
AAAAGAAA others(1): Show |
A | 28 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(25): Show | 28 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.9+9890_9+9897delGA others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
AAAAGAAA others(5): Show |
A | 18 | a0001c0001t0001g0006a0001c0001t0001g0194a0001c0001t0001g0197others(15): Show | 18 | HG01243.hp2 HG01361.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.9+9886_9+9897delGA others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
AAAAGAAA others(9): Show |
A | 7 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG00323.hp2 HG01255.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+9882_9+9897delGA others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
AAAAGAAA others(13): Show |
A | 5 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0185others(2): Show | 5 | HG00438.hp1 HG00673.hp1 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.9+9878_9+9897delGA others(18): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
AAAAGAAA others(17): Show |
A | 1 | a0001c0002t0001g0181 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9+9874_9+9897delGA others(22): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119036
|
AAAAGAAA others(25): Show |
A | 1 | a0001c0001t0001g0180 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.9+9866_9+9897delGA others(30): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119036 | |||||
chr1:50119072
|
GAAAGAAA others(15): Show |
G | 3 | a0001c0001t0001g0099a0001c0001t0001g0193a0001c0002t0004g0098 | 3 | HG02895.hp2 NA19043.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.9+9882_9+9903delGA others(20): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119072 | |||||
chr1:50119076
|
GAAAGAAA others(11): Show |
G | 1 | a0001c0001t0001g0093 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.9+9886_9+9903delGA others(16): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119076 | |||||
chr1:50119080
|
GAAAGAAA others(7): Show |
G | 2 | a0001c0001t0002g0100a0001c0001t0006g0101 | 2 | HG02273.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.9+9890_9+9903delGA others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119080 | |||||
chr1:50119084
|
GAAAGAAA others(3): Show |
G | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(2): Show | 5 | HG02896.hp1 HG03579.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+9894_9+9903delGA others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119084 | |||||
chr1:50119088
|
GAAAGAA | G | 13 | a0001c0001t0001g0089a0001c0001t0001g0107a0001c0001t0001g0112others(10): Show | 13 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.9+9902_9+9907delAA others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119088 | |||||
chr1:50119092
|
GAA | G | 17 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0118others(14): Show | 17 | HG00099.hp2 HG00609.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.9+9898_9+9899delAA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119092 | |||||
chr1:50119094
|
A | AAG | 26 | a0001c0001t0001g0095a0001c0001t0001g0129a0001c0001t0001g0132others(23): Show | 26 | HG00423.hp2 HG01069.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.9+9897_9+9898insGA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119094 | |||||
chr1:50119094
|
A | AAGAAAG | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG00741.hp2 HG01243.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+9897_9+9898insGA others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119094 | |||||
chr1:50119094
|
A | AAGAAAGA others(3): Show |
5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01261.hp2 HG02647.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.9+9897_9+9898insGA others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50119094 | |||||
chr1:50119095
|
A | AGAAAGAA others(6): Show |
1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.9+9897_9+9898insGA others(11): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119095 | ||||||
chr1:50119343
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.9+10145T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119343 | ||||||
chr1:50119566
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.9+10368G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119566 | ||||||
chr1:50119611
|
A | C | 83 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+10413A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50119611 | ||||||
chr1:50120046
|
T | C | 17 | a0001c0001t0001g0104a0001c0001t0001g0118a0001c0001t0001g0129others(14): Show | 17 | HG01167.hp1 HG01243.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.9+10848T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50120046 | ||||||
chr1:50120060
|
A | AAT | 129 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.9+10880_9+10881dup others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50120060 | |||||
chr1:50120060
|
A | AATAT | 7 | a0001c0001t0001g0099a0001c0001t0001g0153a0001c0001t0001g0163others(4): Show | 7 | HG02280.hp1 HG02723.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.9+10878_9+10881dup others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50120060 | |||||
chr1:50120078
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0070 | 2 | NA18975.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.9+10880T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50120078 | ||||||
chr1:50120402
|
G | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0002t0001g0233others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+11204G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50120402 | ||||||
chr1:50120852
|
G | C | 2 | a0001c0001t0001g0186a0001c0001t0002g0187 | 2 | NA19060.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.9+11654G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50120852 | ||||||
chr1:50120956
|
G | A | 1 | a0001c0002t0003g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9+11758G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50120956 | ||||||
chr1:50121611
|
G | C | 6 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0002g0119others(3): Show | 6 | HG01123.hp2 HG01358.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+12413G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50121611 | ||||||
chr1:50121622
|
G | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(38): Show | 42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.9+12424G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50121622 | ||||||
chr1:50121853
|
C | T | 83 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+12655C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50121853 | ||||||
chr1:50121907
|
C | T | 1 | a0001c0002t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.9+12709C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50121907 | ||||||
chr1:50122013
|
C | T | 7 | a0001c0002t0005g0237a0001c0002t0005g0239a0001c0002t0005g0240others(4): Show | 7 | HG02486.hp2 HG02922.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+12815C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122013 | ||||||
chr1:50122114
|
A | G | 2 | a0001c0002t0001g0165a0001c0002t0003g0166 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.9+12916A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122114 | ||||||
chr1:50122117
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.9+12919G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122117 | ||||||
chr1:50122210
|
C | T | 83 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+13012C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122210 | ||||||
chr1:50122217
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.9+13019T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122217 | ||||||
chr1:50122421
|
A | G | 63 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(60): Show | 63 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.9+13223A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122421 | ||||||
chr1:50122754
|
G | C | 1 | a0001c0002t0001g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.9+13556G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122754 | ||||||
chr1:50122913
|
A | G | 3 | a0001c0001t0001g0186a0001c0001t0001g0228a0001c0001t0002g0187 | 3 | HG01361.hp1 NA19060.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.9+13715A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122913 | ||||||
chr1:50122971
|
T | C | 1 | a0001c0002t0001g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.9+13773T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122971 | ||||||
chr1:50122993
|
C | T | 189 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0089others(186): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.9+13795C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50122993 | ||||||
chr1:50123053
|
C | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014 | 3 | HG00280.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.9+13855C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50123053 | ||||||
chr1:50123171
|
G | T | 104 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0171others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.9+13973G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50123171 | ||||||
chr1:50123173
|
G | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0002t0001g0233others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+13975G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50123173 | ||||||
chr1:50123354
|
A | G | 15 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0250others(12): Show | 16 | HG00642.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.9+14156A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50123354 | ||||||
chr1:50123485
|
T | TA | 83 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+14292dupA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50123485 | |||||
chr1:50123766
|
T | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+14568T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50123766 | ||||||
chr1:50124034
|
G | A | 1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.9+14836G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124034 | ||||||
chr1:50124070
|
C | G | 50 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0183others(47): Show | 50 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.9+14872C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124070 | ||||||
chr1:50124119
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.9+14921C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124119 | ||||||
chr1:50124126
|
G | A | 83 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+14928G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124126 | ||||||
chr1:50124802
|
C | T | 1 | a0001c0002t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.9+15604C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124802 | ||||||
chr1:50124848
|
G | A | 83 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+15650G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124848 | ||||||
chr1:50124934
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.9+15736A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124934 | ||||||
chr1:50124966
|
G | A | 82 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.9+15768G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124966 | ||||||
chr1:50124977
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.9+15779G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50124977 | ||||||
chr1:50125049
|
T | C | 1 | a0001c0002t0001g0102 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.9+15851T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50125049 | ||||||
chr1:50125060
|
G | A | 82 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.9+15862G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50125060 | ||||||
chr1:50125130
|
C | G | 1 | a0001c0001t0001g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.9+15932C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50125130 | ||||||
chr1:50125733
|
G | T | 104 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0171others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.9+16535G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50125733 | ||||||
chr1:50125893
|
G | A | 63 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.9+16695G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50125893 | ||||||
chr1:50126032
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.9+16834C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126032 | ||||||
chr1:50126033
|
C | G | 83 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+16835C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126033 | ||||||
chr1:50126071
|
C | T | 104 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0171others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.9+16873C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126071 | ||||||
chr1:50126179
|
G | A | 77 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0095others(74): Show | 77 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.9+16981G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126179 | ||||||
chr1:50126419
|
G | A | 104 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0171others(101): Show | 105 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.9+17221G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126419 | ||||||
chr1:50126568
|
A | C | 1 | a0001c0002t0003g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.9+17370A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126568 | ||||||
chr1:50126776
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.9+17578C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126776 | ||||||
chr1:50126929
|
G | C | 146 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.9+17731G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126929 | ||||||
chr1:50126998
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+17800G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50126998 | ||||||
chr1:50127334
|
C | A | 10 | a0001c0001t0001g0129a0001c0001t0001g0177a0001c0002t0001g0051others(7): Show | 10 | HG01167.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.10-17623C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127334 | ||||||
chr1:50127460
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.10-17497G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127460 | ||||||
chr1:50127469
|
T | C | 5 | a0001c0001t0001g0116a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 5 | NA18954.hp1 NA18977.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.10-17488T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127469 | ||||||
chr1:50127569
|
C | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0069others(18): Show | 23 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.10-17388C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127569 | ||||||
chr1:50127725
|
T | C | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-17232T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127725 | ||||||
chr1:50127857
|
A | G | 1 | a0001c0001t0009g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.10-17100A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127857 | ||||||
chr1:50127939
|
C | T | 12 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0069others(9): Show | 13 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.10-17018C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127939 | ||||||
chr1:50127949
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.10-17008G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127949 | ||||||
chr1:50127988
|
G | T | 1 | a0001c0002t0003g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.10-16969G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50127988 | ||||||
chr1:50127994
|
ATTGGCT | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0157 | 2 | HG02129.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.10-16941_10-16936d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50127994 | |||||
chr1:50128137
|
C | T | 1 | a0001c0002t0008g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.10-16820C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128137 | ||||||
chr1:50128166
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.10-16791G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128166 | ||||||
chr1:50128520
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.10-16437G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128520 | ||||||
chr1:50128755
|
G | A | 1 | a0001c0002t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.10-16202G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128755 | ||||||
chr1:50128764
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.10-16193T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128764 | ||||||
chr1:50128810
|
T | C | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG00673.hp1 HG01109.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.10-16147T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128810 | ||||||
chr1:50128810
|
T | G | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0002t0001g0233 | 3 | HG01891.hp2 HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.10-16147T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128810 | ||||||
chr1:50128913
|
A | C | 11 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0160others(8): Show | 11 | HG01069.hp1 HG01109.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.10-16044A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128913 | ||||||
chr1:50128925
|
C | G | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-16032C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50128925 | ||||||
chr1:50129274
|
G | A | 103 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(100): Show | 105 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.10-15683G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50129274 | ||||||
chr1:50129514
|
T | C | 2 | a0001c0001t0001g0177a0001c0002t0001g0170 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.10-15443T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50129514 | ||||||
chr1:50129867
|
T | C | 2 | a0001c0001t0001g0118a0001c0002t0013g0090 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.10-15090T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50129867 | ||||||
chr1:50130006
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.10-14951T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130006 | ||||||
chr1:50130063
|
C | T | 1 | a0001c0002t0004g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.10-14894C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130063 | ||||||
chr1:50130115
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.10-14842A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130115 | ||||||
chr1:50130311
|
G | A | 155 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(152): Show | 157 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.10-14646G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130311 | ||||||
chr1:50130324
|
G | A | 157 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.10-14633G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130324 | ||||||
chr1:50130725
|
A | G | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-14232A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130725 | ||||||
chr1:50130785
|
A | G | 157 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.10-14172A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50130785 | ||||||
chr1:50131015
|
T | C | 51 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.10-13942T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131015 | ||||||
chr1:50131172
|
C | A | 52 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.10-13785C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131172 | ||||||
chr1:50131330
|
A | G | 2 | a0001c0001t0001g0118a0001c0002t0013g0090 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.10-13627A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131330 | ||||||
chr1:50131408
|
T | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0213 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.10-13549T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131408 | ||||||
chr1:50131781
|
T | C | 1 | a0001c0001t0002g0147 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.10-13176T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131781 | ||||||
chr1:50131886
|
TA | T | 30 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0031others(27): Show | 32 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.10-13055delA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50131886 | |||||
chr1:50131946
|
A | G | 1 | a0001c0002t0004g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.10-13011A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50131946 | ||||||
chr1:50132063
|
A | G | 6 | a0001c0001t0001g0048a0001c0001t0001g0246a0001c0002t0004g0004others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-12894A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50132063 | ||||||
chr1:50132082
|
A | T | 1 | a0001c0001t0002g0184 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.10-12875A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50132082 | ||||||
chr1:50132696
|
C | T | 103 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(100): Show | 105 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.10-12261C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50132696 | ||||||
chr1:50133078
|
G | T | 51 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.10-11879G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133078 | ||||||
chr1:50133215
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.10-11742T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133215 | ||||||
chr1:50133598
|
G | GA | 3 | a0001c0001t0001g0247a0001c0002t0003g0175a0001c0002t0003g0268 | 3 | HG02257.hp1 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.10-11355dupA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133598 | |||||
chr1:50133599
|
A | AAAAAG | 3 | a0001c0002t0003g0248a0001c0002t0003g0249a0001c0002t0004g0068 | 3 | HG02922.hp2 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.10-11355_10-11354i others(7): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
A | AAAAAGAA others(6): Show |
1 | a0001c0002t0003g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.10-11355_10-11354i others(15): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
A | AAAAG | 44 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0020others(41): Show | 45 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.10-11308_10-11305d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
A | AAAAGAAA others(1): Show |
56 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(53): Show | 56 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.10-11312_10-11305d others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
A | AAAAGAAA others(5): Show |
27 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0079others(24): Show | 27 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.10-11316_10-11305d others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
A | AAAAGAAA others(9): Show |
10 | a0001c0001t0001g0052a0001c0001t0001g0060a0001c0001t0001g0200others(7): Show | 10 | HG02056.hp1 HG02109.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.10-11320_10-11305d others(18): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
A | AAAGAAAG others(8): Show |
1 | a0001c0002t0003g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10-11356_10-11355i others(17): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
A | AAAGAAAG others(12): Show |
1 | a0001c0001t0001g0183 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.10-11356_10-11355i others(21): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
AAAAG | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(22): Show | 26 | HG00735.hp1 HG01069.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.10-11308_10-11305d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
AAAAGAAA others(1): Show |
A | 22 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0046others(19): Show | 22 | HG00609.hp2 HG01167.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.10-11312_10-11305d others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
AAAAGAAA others(5): Show |
A | 13 | a0001c0001t0001g0062a0001c0001t0001g0077a0001c0001t0001g0078others(10): Show | 13 | HG00642.hp1 HG02132.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.10-11316_10-11305d others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
AAAAGAAA others(9): Show |
A | 1 | a0001c0002t0013g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.10-11320_10-11305d others(18): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133599
|
AAAAGAAA others(13): Show |
A | 2 | a0001c0001t0001g0065a0001c0002t0001g0146 | 2 | HG01243.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.10-11324_10-11305d others(22): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133599 | |||||
chr1:50133635
|
GAAAGAAA others(3): Show |
G | 3 | a0001c0001t0001g0188a0001c0001t0001g0193a0001c0001t0001g0194 | 3 | HG02280.hp2 NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.10-11320_10-11311d others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133635 | |||||
chr1:50133649
|
AAG | A | 4 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0193others(1): Show | 4 | HG02280.hp2 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-11304_10-11303d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133649 | |||||
chr1:50133651
|
G | GAA | 3 | a0001c0001t0002g0037a0001c0001t0002g0187a0001c0002t0001g0273 | 3 | HG00438.hp2 HG02647.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.10-11305_10-11304i others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133651 | |||||
chr1:50133651
|
G | GAAAGAAA others(3): Show |
1 | a0001c0001t0001g0186 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.10-11305_10-11304i others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133651 | |||||
chr1:50133651
|
G | GAAAGAAG others(3): Show |
1 | a0001c0001t0002g0072 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.10-11305_10-11304i others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133651 | |||||
chr1:50133652
|
A | G | 1 | a0001c0001t0002g0045 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.10-11305A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133652 | ||||||
chr1:50133653
|
G | A | 2 | a0001c0001t0002g0222a0001c0002t0001g0091 | 2 | HG03209.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.10-11304G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133653 | ||||||
chr1:50133655
|
A | AAG | 4 | a0001c0001t0001g0186a0001c0001t0002g0037a0001c0001t0002g0187others(1): Show | 4 | HG00438.hp2 HG02647.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-11300_10-11299d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50133655 | |||||
chr1:50133655
|
A | G | 2 | a0001c0001t0002g0222a0001c0002t0001g0091 | 2 | HG03209.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.10-11302A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133655 | ||||||
chr1:50133746
|
A | G | 1 | a0001c0002t0001g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.10-11211A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133746 | ||||||
chr1:50133872
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.10-11085T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133872 | ||||||
chr1:50133905
|
A | G | 1 | a0001c0001t0009g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.10-11052A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50133905 | ||||||
chr1:50134320
|
G | A | 10 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0160others(7): Show | 10 | HG01069.hp1 HG01109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.10-10637G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50134320 | ||||||
chr1:50134663
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.10-10294G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50134663 | ||||||
chr1:50134911
|
G | T | 1 | a0001c0002t0005g0243 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.10-10046G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50134911 | ||||||
chr1:50134967
|
T | G | 1 | a0001c0001t0001g0017 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.10-9990T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50134967 | ||||||
chr1:50134972
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.10-9985A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50134972 | ||||||
chr1:50135209
|
C | T | 10 | a0001c0001t0001g0129a0001c0002t0001g0051a0001c0002t0001g0102others(7): Show | 10 | HG01167.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.10-9748C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50135209 | ||||||
chr1:50135595
|
T | G | 4 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0193others(1): Show | 4 | HG02280.hp2 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-9362T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50135595 | ||||||
chr1:50136064
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.10-8893G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136064 | ||||||
chr1:50136074
|
G | A | 1 | a0001c0002t0013g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.10-8883G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136074 | ||||||
chr1:50136452
|
T | C | 1 | a0001c0001t0002g0263 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.10-8505T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136452 | ||||||
chr1:50136748
|
A | G | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-8209A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136748 | ||||||
chr1:50136749
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0226a0001c0001t0001g0228 | 3 | HG00140.hp1 HG01361.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.10-8208T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136749 | ||||||
chr1:50136823
|
G | A | 82 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(79): Show | 82 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.10-8134G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50136823 | ||||||
chr1:50137006
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0001g0227 | 2 | HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.10-7951T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137006 | ||||||
chr1:50137078
|
A | G | 1 | a0001c0001t0011g0219 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.10-7879A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137078 | ||||||
chr1:50137112
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.10-7845G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137112 | ||||||
chr1:50137172
|
T | G | 1 | a0001c0002t0004g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.10-7785T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137172 | ||||||
chr1:50137390
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.10-7567T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137390 | ||||||
chr1:50137955
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.10-7002A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50137955 | ||||||
chr1:50138072
|
G | A | 1 | a0001c0001t0009g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.10-6885G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50138072 | ||||||
chr1:50138214
|
A | G | 1 | a0001c0002t0003g0166 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.10-6743A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50138214 | ||||||
chr1:50138323
|
A | C | 79 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(76): Show | 79 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.10-6634A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50138323 | ||||||
chr1:50138465
|
CT | C | 102 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(99): Show | 104 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.10-6480delT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 50138465 | |||||
chr1:50138546
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.10-6411G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50138546 | ||||||
chr1:50139565
|
C | G | 1 | a0001c0001t0001g0001 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.10-5392C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50139565 | ||||||
chr1:50139665
|
T | C | 157 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.10-5292T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50139665 | ||||||
chr1:50139689
|
G | A | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-5268G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50139689 | ||||||
chr1:50139805
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.10-5152G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50139805 | ||||||
chr1:50139976
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.10-4981T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50139976 | ||||||
chr1:50140072
|
C | T | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.10-4885C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50140072 | ||||||
chr1:50140245
|
G | C | 2 | a0001c0002t0001g0094a0001c0002t0001g0109 | 2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.10-4712G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50140245 | ||||||
chr1:50140255
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.10-4702T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50140255 | ||||||
chr1:50140801
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.10-4156T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50140801 | ||||||
chr1:50141204
|
A | G | 182 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(179): Show | 184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.10-3753A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50141204 | ||||||
chr1:50141357
|
T | G | 10 | a0001c0001t0001g0129a0001c0002t0001g0051a0001c0002t0001g0102others(7): Show | 10 | HG01167.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.10-3600T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50141357 | ||||||
chr1:50141688
|
G | T | 1 | a0001c0002t0001g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.10-3269G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50141688 | ||||||
chr1:50141958
|
C | T | 1 | a0001c0002t0003g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.10-2999C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50141958 | ||||||
chr1:50141998
|
T | G | 2 | a0001c0002t0001g0056a0001c0002t0001g0218 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.10-2959T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50141998 | ||||||
chr1:50142194
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.10-2763A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50142194 | ||||||
chr1:50142454
|
C | T | 2 | a0001c0001t0001g0118a0001c0002t0013g0090 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.10-2503C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50142454 | ||||||
chr1:50142493
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.10-2464G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50142493 | ||||||
chr1:50142665
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.10-2292G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50142665 | ||||||
chr1:50143492
|
T | A | 1 | a0001c0002t0013g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.10-1465T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143492 | ||||||
chr1:50143527
|
C | T | 1 | a0001c0001t0002g0262 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.10-1430C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143527 | ||||||
chr1:50143537
|
C | T | 1 | a0001c0002t0001g0251 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.10-1420C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143537 | ||||||
chr1:50143592
|
C | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0214others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-1365C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143592 | ||||||
chr1:50143779
|
G | T | 2 | a0001c0002t0001g0190a0001c0002t0001g0203 | 2 | HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.10-1178G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143779 | ||||||
chr1:50143811
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.10-1146T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143811 | ||||||
chr1:50143834
|
A | G | 1 | a0001c0002t0007g0242 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.10-1123A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50143834 | ||||||
chr1:50144437
|
G | A | 1 | a0001c0002t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.10-520G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 1/6 | chr1 | 50144437 | ||||||
chr1:50145326
|
T | G | 1 | a0001c0002t0001g0234 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.250+129T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50145326 | ||||||
chr1:50145366
|
T | C | 1 | a0001c0001t0001g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.250+169T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50145366 | ||||||
chr1:50145619
|
C | G | 1 | a0001c0002t0007g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.250+422C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50145619 | ||||||
chr1:50145866
|
T | A | 1 | a0001c0001t0002g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.250+669T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50145866 | ||||||
chr1:50146028
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.250+831G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50146028 | ||||||
chr1:50146154
|
GT | G | 153 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(150): Show | 155 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.250+970delT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50146154 | |||||
chr1:50146154
|
GTT | G | 5 | a0001c0001t0001g0126a0001c0001t0001g0139a0001c0002t0001g0091others(2): Show | 5 | HG01070.hp2 HG01168.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.250+969_250+970del others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50146154 | |||||
chr1:50146238
|
A | ATG | 3 | a0001c0001t0001g0067a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | NA18959.hp1 NA18985.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.250+1051_250+1052d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50146238 | |||||
chr1:50146248
|
G | A | 1 | a0001c0002t0004g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+1051G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50146248 | ||||||
chr1:50146506
|
A | G | 5 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0006g0101others(2): Show | 5 | HG01123.hp2 HG01358.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.250+1309A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50146506 | ||||||
chr1:50146578
|
A | G | 59 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(56): Show | 59 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.250+1381A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50146578 | ||||||
chr1:50147042
|
C | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0222 | 2 | HG00438.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.250+1845C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147042 | ||||||
chr1:50147203
|
A | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0250 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.250+2006A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147203 | ||||||
chr1:50147232
|
G | T | 1 | a0001c0002t0003g0166 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.250+2035G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147232 | ||||||
chr1:50147359
|
C | A | 1 | a0001c0002t0001g0071 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.250+2162C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147359 | ||||||
chr1:50147508
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.250+2311A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147508 | ||||||
chr1:50147587
|
G | A | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+2390G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147587 | ||||||
chr1:50147728
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.250+2531A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50147728 | ||||||
chr1:50148004
|
T | G | 102 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(99): Show | 104 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.250+2807T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50148004 | ||||||
chr1:50148017
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0213 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.250+2820G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50148017 | ||||||
chr1:50148100
|
G | A | 52 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.250+2903G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50148100 | ||||||
chr1:50148429
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.250+3232A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50148429 | ||||||
chr1:50148873
|
T | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0199 | 3 | HG02132.hp1 NA18965.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.250+3676T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50148873 | ||||||
chr1:50149062
|
G | A | 1 | a0001c0002t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.250+3865G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149062 | ||||||
chr1:50149136
|
G | A | 6 | a0001c0001t0001g0048a0001c0001t0001g0246a0001c0002t0004g0004others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+3939G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149136 | ||||||
chr1:50149303
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.250+4106C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149303 | ||||||
chr1:50149499
|
G | A | 15 | a0001c0001t0001g0076a0001c0001t0001g0129a0001c0002t0001g0051others(12): Show | 15 | HG01167.hp1 HG01243.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.250+4302G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149499 | ||||||
chr1:50149542
|
C | CT | 65 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0033others(62): Show | 65 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.250+4364dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50149542 | |||||
chr1:50149543
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250+4346T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149543 | ||||||
chr1:50149694
|
CCACCACG others(3): Show |
C | 1 | a0001c0002t0008g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.250+4498_250+4507d others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149694 | ||||||
chr1:50149705
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.250+4508G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149705 | ||||||
chr1:50149945
|
G | GT | 3 | a0001c0001t0001g0029a0001c0001t0001g0214a0001c0001t0001g0227 | 3 | HG01515.hp2 HG03942.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.250+4749dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50149945 | |||||
chr1:50149955
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.250+4758T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50149955 | ||||||
chr1:50150042
|
A | AAAAGC | 9 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0122others(6): Show | 9 | HG00735.hp1 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.250+4850_250+4854d others(7): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50150042 | |||||
chr1:50150055
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.250+4858T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50150055 | ||||||
chr1:50150189
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.250+4992C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50150189 | ||||||
chr1:50150266
|
G | A | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+5069G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50150266 | ||||||
chr1:50150293
|
G | A | 16 | a0001c0001t0001g0076a0001c0001t0001g0085a0001c0001t0001g0129others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.250+5096G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50150293 | ||||||
chr1:50150703
|
G | T | 2 | a0001c0002t0003g0002a0001c0002t0003g0027 | 3 | HG01168.hp1 HG01169.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.250+5506G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50150703 | ||||||
chr1:50151115
|
C | T | 1 | a0001c0002t0001g0273 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.250+5918C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50151115 | ||||||
chr1:50151303
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.250+6106G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50151303 | ||||||
chr1:50151618
|
G | C | 174 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(171): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.250+6421G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50151618 | ||||||
chr1:50151824
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0039 | 2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.250+6627G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50151824 | ||||||
chr1:50151878
|
G | A | 12 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258others(9): Show | 12 | HG02148.hp2 NA18948.hp1 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.250+6681G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50151878 | ||||||
chr1:50152021
|
CAG | C | 16 | a0001c0001t0001g0076a0001c0001t0001g0118a0001c0001t0001g0129others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.250+6828_250+6829d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50152021 | |||||
chr1:50152102
|
A | C | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+6905A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152102 | ||||||
chr1:50152182
|
G | T | 1 | a0001c0002t0004g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+6985G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152182 | ||||||
chr1:50152191
|
C | G | 4 | a0001c0001t0001g0076a0001c0002t0001g0086a0001c0002t0001g0087others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+6994C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152191 | ||||||
chr1:50152202
|
A | C | 1 | a0001c0002t0001g0071 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.250+7005A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152202 | ||||||
chr1:50152411
|
A | AAC | 5 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0002g0119others(2): Show | 5 | HG01256.hp1 HG02559.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.250+7233_250+7234d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50152411 | |||||
chr1:50152430
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.250+7233A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152430 | ||||||
chr1:50152556
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.250+7359C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152556 | ||||||
chr1:50152689
|
C | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0213 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.250+7492C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152689 | ||||||
chr1:50152766
|
G | A | 3 | a0001c0001t0002g0125a0001c0002t0001g0056a0001c0002t0001g0218 | 3 | HG02976.hp1 HG03139.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.250+7569G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152766 | ||||||
chr1:50152829
|
A | G | 6 | a0001c0001t0001g0048a0001c0001t0001g0246a0001c0002t0004g0004others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+7632A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50152829 | ||||||
chr1:50153095
|
C | T | 7 | a0001c0001t0001g0158a0001c0001t0001g0253a0001c0001t0001g0254others(4): Show | 7 | HG00642.hp1 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+7898C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153095 | ||||||
chr1:50153096
|
G | A | 55 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(52): Show | 55 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.250+7899G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153096 | ||||||
chr1:50153248
|
G | A | 2 | a0001c0001t0002g0015a0001c0001t0002g0115 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.250+8051G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153248 | ||||||
chr1:50153336
|
T | A | 1 | a0001c0001t0002g0217 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+8139T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153336 | ||||||
chr1:50153368
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.250+8171G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153368 | ||||||
chr1:50153403
|
A | T | 1 | a0001c0001t0002g0217 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+8206A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153403 | ||||||
chr1:50153453
|
G | A | 1 | a0001c0001t0006g0111 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.250+8256G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153453 | ||||||
chr1:50153677
|
T | C | 53 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.250+8480T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153677 | ||||||
chr1:50153918
|
A | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(8): Show | 11 | HG00140.hp1 HG00280.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.250+8721A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50153918 | ||||||
chr1:50154020
|
T | A | 1 | a0001c0001t0001g0012 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.250+8823T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154020 | ||||||
chr1:50154044
|
C | T | 1 | a0001c0002t0004g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+8847C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154044 | ||||||
chr1:50154056
|
A | C | 1 | a0001c0002t0004g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.250+8859A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154056 | ||||||
chr1:50154125
|
C | T | 1 | a0001c0002t0004g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.250+8928C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154125 | ||||||
chr1:50154312
|
G | A | 1 | a0001c0002t0004g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.250+9115G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154312 | ||||||
chr1:50154358
|
C | A | 1 | a0001c0001t0001g0200 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.250+9161C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154358 | ||||||
chr1:50154389
|
T | TAA | 157 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.250+9193_250+9194i others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50154389 | |||||
chr1:50154493
|
G | T | 1 | a0001c0002t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.250+9296G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154493 | ||||||
chr1:50154522
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.250+9325C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154522 | ||||||
chr1:50154523
|
G | A | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+9326G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154523 | ||||||
chr1:50154752
|
T | TTG | 28 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(25): Show | 28 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.250+9587_250+9588d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50154752 | |||||
chr1:50154752
|
T | TTGTG | 3 | a0001c0001t0001g0059a0001c0001t0001g0191a0001c0002t0004g0270 | 3 | HG00323.hp2 HG02145.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.250+9585_250+9588d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50154752 | |||||
chr1:50154752
|
TTG | T | 124 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.250+9587_250+9588d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50154752 | |||||
chr1:50154861
|
T | C | 1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+9664T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154861 | ||||||
chr1:50154908
|
T | A | 6 | a0001c0001t0001g0048a0001c0001t0001g0246a0001c0002t0004g0004others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.250+9711T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50154908 | ||||||
chr1:50155005
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.250+9808C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155005 | ||||||
chr1:50155034
|
T | C | 1 | a0001c0002t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.250+9837T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155034 | ||||||
chr1:50155058
|
A | C | 1 | a0001c0002t0004g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.250+9861A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155058 | ||||||
chr1:50155070
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.250+9873T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155070 | ||||||
chr1:50155172
|
C | T | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+9975C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155172 | ||||||
chr1:50155273
|
A | G | 22 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0069others(19): Show | 24 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.250+10076A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155273 | ||||||
chr1:50155440
|
ACATGGAA others(11): Show |
A | 1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+10244_250+1026 others(22): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155440 | ||||||
chr1:50155621
|
G | A | 53 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.250+10424G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155621 | ||||||
chr1:50155636
|
G | T | 1 | a0001c0001t0002g0217 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+10439G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155636 | ||||||
chr1:50155666
|
T | C | 1 | a0001c0001t0009g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.250+10469T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155666 | ||||||
chr1:50155785
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.250+10588C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155785 | ||||||
chr1:50155964
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.250+10767C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50155964 | ||||||
chr1:50156019
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0171 | 2 | HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.250+10822G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156019 | ||||||
chr1:50156027
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0002g0217 | 2 | HG01358.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.250+10830G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156027 | ||||||
chr1:50156031
|
G | A | 52 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.250+10834G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156031 | ||||||
chr1:50156031
|
G | GCA | 85 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(82): Show | 85 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.250+10853_250+1085 others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50156031 | |||||
chr1:50156302
|
A | C | 1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+11105A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156302 | ||||||
chr1:50156303
|
C | A | 1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+11106C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156303 | ||||||
chr1:50156614
|
G | A | 1 | a0001c0002t0013g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.250+11417G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156614 | ||||||
chr1:50156754
|
C | G | 1 | a0001c0001t0002g0217 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+11557C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156754 | ||||||
chr1:50156756
|
G | C | 1 | a0001c0001t0002g0217 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+11559G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156756 | ||||||
chr1:50156898
|
A | T | 1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+11701A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50156898 | ||||||
chr1:50157295
|
C | T | 1 | a0001c0002t0003g0166 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.250+12098C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50157295 | ||||||
chr1:50157652
|
A | G | 3 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0002t0001g0251 | 3 | HG00642.hp1 HG02818.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.250+12455A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50157652 | ||||||
chr1:50157838
|
C | G | 1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+12641C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50157838 | ||||||
chr1:50157839
|
A | C | 1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+12642A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50157839 | ||||||
chr1:50157840
|
C | A | 1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+12643C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50157840 | ||||||
chr1:50158042
|
T | G | 1 | a0001c0001t0002g0217 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+12845T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158042 | ||||||
chr1:50158068
|
T | C | 157 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.250+12871T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158068 | ||||||
chr1:50158191
|
A | G | 1 | a0001c0001t0002g0217 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.250+12994A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158191 | ||||||
chr1:50158464
|
T | A | 1 | a0001c0002t0001g0181 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.250+13267T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158464 | ||||||
chr1:50158594
|
C | T | 20 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0069others(17): Show | 22 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.250+13397C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158594 | ||||||
chr1:50158711
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.250+13514A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158711 | ||||||
chr1:50158776
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.250+13579C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158776 | ||||||
chr1:50158823
|
G | A | 1 | a0001c0001t0012g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.250+13626G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158823 | ||||||
chr1:50158916
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.250+13719T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50158916 | ||||||
chr1:50159039
|
C | CA | 34 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0069others(31): Show | 36 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.250+13860dupA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50159039 | |||||
chr1:50159054
|
A | AG | 76 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0038others(73): Show | 76 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.250+13857_250+1385 others(5): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159054 | ||||||
chr1:50159054
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0078a0001c0001t0001g0159 | 3 | HG02698.hp1 NA18962.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.250+13857A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159054 | ||||||
chr1:50159092
|
A | T | 1 | a0001c0002t0005g0240 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.250+13895A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159092 | ||||||
chr1:50159116
|
A | T | 2 | a0001c0001t0001g0096a0001c0002t0001g0123 | 2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.250+13919A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159116 | ||||||
chr1:50159242
|
T | A | 1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+14045T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159242 | ||||||
chr1:50159371
|
A | G | 174 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(171): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.250+14174A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159371 | ||||||
chr1:50159437
|
A | C | 2 | a0001c0001t0001g0202a0001c0001t0002g0143 | 2 | NA19010.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.250+14240A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159437 | ||||||
chr1:50159482
|
G | C | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.250+14285G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159482 | ||||||
chr1:50159508
|
C | G | 20 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0069others(17): Show | 22 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.250+14311C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159508 | ||||||
chr1:50159683
|
A | C | 1 | a0001c0002t0001g0056 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.250+14486A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159683 | ||||||
chr1:50159688
|
C | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.250+14491C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50159688 | ||||||
chr1:50160021
|
T | C | 1 | a0001c0002t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.250+14824T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160021 | ||||||
chr1:50160034
|
C | A | 1 | a0001c0002t0004g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.250+14837C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160034 | ||||||
chr1:50160307
|
C | T | 82 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(79): Show | 82 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.250+15110C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160307 | ||||||
chr1:50160317
|
A | G | 1 | a0001c0001t0002g0212 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.250+15120A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160317 | ||||||
chr1:50160352
|
T | G | 1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+15155T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160352 | ||||||
chr1:50160582
|
C | CAGATATT others(23): Show |
1 | a0001c0001t0002g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.250+15386_250+1541 others(34): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50160582 | |||||
chr1:50160720
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.250+15523A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160720 | ||||||
chr1:50160777
|
A | T | 1 | a0001c0002t0001g0190 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.250+15580A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160777 | ||||||
chr1:50160793
|
T | G | 1 | a0001c0001t0001g0189 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.250+15596T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50160793 | ||||||
chr1:50161122
|
C | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | NA18977.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.250+15925C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50161122 | ||||||
chr1:50161563
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.251-15526A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50161563 | ||||||
chr1:50161749
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.251-15340A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50161749 | ||||||
chr1:50161843
|
G | C | 6 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0160others(3): Show | 6 | HG01069.hp1 HG01109.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-15246G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50161843 | ||||||
chr1:50161952
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.251-15137G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50161952 | ||||||
chr1:50162430
|
G | A | 1 | a0001c0002t0013g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.251-14659G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50162430 | ||||||
chr1:50162554
|
T | G | 10 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0160others(7): Show | 10 | HG01069.hp1 HG01109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.251-14535T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50162554 | ||||||
chr1:50162587
|
C | T | 1 | a0001c0002t0005g0243 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.251-14502C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50162587 | ||||||
chr1:50162829
|
C | G | 3 | a0001c0002t0001g0063a0001c0002t0001g0071a0001c0002t0001g0234 | 3 | HG02572.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.251-14260C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50162829 | ||||||
chr1:50162852
|
AG | A | 8 | a0001c0001t0001g0048a0001c0001t0001g0246a0001c0002t0003g0225others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-14235delG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50162852 | |||||
chr1:50163098
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.251-13991C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163098 | ||||||
chr1:50163113
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.251-13976C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163113 | ||||||
chr1:50163179
|
G | A | 82 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(79): Show | 82 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.251-13910G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163179 | ||||||
chr1:50163451
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.251-13638G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163451 | ||||||
chr1:50163550
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.251-13539G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163550 | ||||||
chr1:50163565
|
G | A | 1 | a0001c0002t0003g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.251-13524G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163565 | ||||||
chr1:50163608
|
T | C | 1 | a0001c0002t0004g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.251-13481T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163608 | ||||||
chr1:50163719
|
G | A | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.251-13370G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163719 | ||||||
chr1:50163877
|
T | C | 1 | a0001c0002t0004g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.251-13212T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163877 | ||||||
chr1:50163929
|
C | T | 1 | a0001c0002t0003g0225 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.251-13160C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50163929 | ||||||
chr1:50164172
|
G | C | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.251-12917G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50164172 | ||||||
chr1:50164207
|
G | C | 1 | a0001c0001t0001g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.251-12882G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50164207 | ||||||
chr1:50164354
|
C | G | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.251-12735C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50164354 | ||||||
chr1:50164732
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.251-12357C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50164732 | ||||||
chr1:50165108
|
G | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG00609.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.251-11981G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165108 | ||||||
chr1:50165359
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.251-11730T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165359 | ||||||
chr1:50165377
|
T | C | 2 | a0001c0001t0002g0259a0001c0001t0002g0262 | 2 | NA18948.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.251-11712T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165377 | ||||||
chr1:50165427
|
G | GAT | 59 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0038others(56): Show | 59 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.251-11648_251-1164 others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50165427 | |||||
chr1:50165437
|
T | G | 6 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0174others(3): Show | 6 | HG02145.hp1 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-11652T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165437 | ||||||
chr1:50165437
|
TATATAG | T | 8 | a0001c0001t0001g0048a0001c0001t0001g0246a0001c0002t0003g0225others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.251-11636_251-1163 others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50165437 | |||||
chr1:50165439
|
T | G | 1 | a0001c0002t0001g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.251-11650T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165439 | ||||||
chr1:50165457
|
T | TAC | 4 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0193others(1): Show | 4 | HG02280.hp2 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-11617_251-1161 others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50165457 | |||||
chr1:50165521
|
G | A | 103 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(100): Show | 105 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.251-11568G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165521 | ||||||
chr1:50165529
|
A | T | 1 | a0001c0002t0013g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.251-11560A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165529 | ||||||
chr1:50165752
|
A | G | 51 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.251-11337A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165752 | ||||||
chr1:50165762
|
G | GTGTGTAT others(3): Show |
253 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.251-11318_251-1131 others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50165762 | |||||
chr1:50165762
|
G | GTGTGTAT others(73): Show |
2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.251-11318_251-1131 others(84): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50165762 | |||||
chr1:50165772
|
G | A | 1 | a0001c0002t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.251-11317G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165772 | ||||||
chr1:50165822
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.251-11267A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50165822 | ||||||
chr1:50166303
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.251-10786A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50166303 | ||||||
chr1:50166760
|
C | T | 3 | a0001c0002t0001g0195a0001c0002t0003g0196a0001c0002t0003g0252 | 3 | HG02809.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.251-10329C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50166760 | ||||||
chr1:50166930
|
A | G | 1 | a0001c0001t0001g0017 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.251-10159A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50166930 | ||||||
chr1:50166998
|
A | T | 1 | a0001c0002t0013g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.251-10091A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50166998 | ||||||
chr1:50167023
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.251-10066T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50167023 | ||||||
chr1:50167406
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.251-9683G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50167406 | ||||||
chr1:50167704
|
G | T | 53 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.251-9385G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50167704 | ||||||
chr1:50168682
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.251-8407G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50168682 | ||||||
chr1:50168724
|
C | T | 15 | a0001c0001t0001g0247a0001c0002t0003g0003a0001c0002t0003g0166others(12): Show | 16 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.251-8365C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50168724 | ||||||
chr1:50168946
|
G | GTA | 9 | a0001c0001t0001g0016a0001c0001t0001g0062a0001c0001t0001g0120others(6): Show | 9 | HG01167.hp1 HG02148.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.251-8126_251-8125d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50168946 | |||||
chr1:50168946
|
G | GTATA | 41 | a0001c0001t0001g0033a0001c0001t0001g0151a0001c0001t0001g0200others(38): Show | 41 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.251-8128_251-8125d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50168946 | |||||
chr1:50168946
|
G | GTATATA | 11 | a0001c0001t0001g0116a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG00609.hp1 HG02135.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.251-8130_251-8125d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50168946 | |||||
chr1:50168963
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.251-8126T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50168963 | ||||||
chr1:50168963
|
TAC | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0002t0001g0233 | 3 | HG01891.hp2 HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.251-8116_251-8115d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50168963 | |||||
chr1:50168984
|
G | GTA | 13 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0081others(10): Show | 13 | HG01891.hp1 HG02145.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.251-8090_251-8089d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50168984 | |||||
chr1:50169029
|
A | G | 1 | a0001c0001t0002g0210 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.251-8060A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50169029 | ||||||
chr1:50169101
|
G | A | 1 | a0001c0002t0008g0130 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.251-7988G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50169101 | ||||||
chr1:50169371
|
C | T | 1 | a0001c0001t0002g0082 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.251-7718C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50169371 | ||||||
chr1:50169849
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0075 | 2 | HG02040.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.251-7240A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50169849 | ||||||
chr1:50169859
|
T | C | 4 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0193others(1): Show | 4 | HG02280.hp2 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-7230T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50169859 | ||||||
chr1:50170109
|
G | A | 1 | a0001c0002t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.251-6980G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50170109 | ||||||
chr1:50170161
|
G | A | 1 | a0001c0002t0004g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.251-6928G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50170161 | ||||||
chr1:50170520
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.251-6569C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50170520 | ||||||
chr1:50170838
|
G | A | 52 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.251-6251G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50170838 | ||||||
chr1:50170999
|
C | G | 1 | a0001c0001t0001g0227 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.251-6090C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50170999 | ||||||
chr1:50171010
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.251-6079G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171010 | ||||||
chr1:50171039
|
A | G | 7 | a0001c0001t0001g0048a0001c0001t0001g0246a0001c0002t0003g0225others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.251-6050A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171039 | ||||||
chr1:50171418
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.251-5671T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171418 | ||||||
chr1:50171532
|
A | G | 94 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(91): Show | 95 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.251-5557A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171532 | ||||||
chr1:50171652
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.251-5437A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171652 | ||||||
chr1:50171670
|
A | G | 1 | a0001c0002t0004g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.251-5419A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171670 | ||||||
chr1:50171843
|
G | T | 1 | a0001c0001t0001g0024 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.251-5246G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171843 | ||||||
chr1:50171882
|
C | T | 157 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.251-5207C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50171882 | ||||||
chr1:50172013
|
A | G | 2 | a0001c0002t0001g0091a0001c0002t0001g0273 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.251-5076A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50172013 | ||||||
chr1:50172079
|
GAT | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0023others(8): Show | 12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.251-5009_251-5008d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50172079 | ||||||
chr1:50172179
|
AG | A | 4 | a0001c0001t0001g0247a0001c0002t0003g0175a0001c0002t0003g0249others(1): Show | 4 | HG02257.hp1 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.251-4908delG | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50172179 | |||||
chr1:50172350
|
C | T | 51 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.251-4739C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50172350 | ||||||
chr1:50172362
|
A | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.251-4727A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50172362 | ||||||
chr1:50172965
|
T | C | 1 | a0001c0002t0003g0196 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.251-4124T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50172965 | ||||||
chr1:50173303
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.251-3786G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173303 | ||||||
chr1:50173405
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.251-3684C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173405 | ||||||
chr1:50173668
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.251-3421T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173668 | ||||||
chr1:50173792
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.251-3297C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173792 | ||||||
chr1:50173877
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.251-3212G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173877 | ||||||
chr1:50173990
|
C | T | 1 | a0001c0002t0003g0027 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.251-3099C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173990 | ||||||
chr1:50173991
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.251-3098G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50173991 | ||||||
chr1:50174085
|
T | C | 7 | a0001c0002t0005g0237a0001c0002t0005g0239a0001c0002t0005g0240others(4): Show | 7 | HG02486.hp2 HG02922.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.251-3004T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50174085 | ||||||
chr1:50174449
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.251-2640C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50174449 | ||||||
chr1:50174488
|
G | GT | 88 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(85): Show | 90 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.251-2588dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50174488 | |||||
chr1:50174488
|
GT | G | 6 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0179others(3): Show | 6 | HG01074.hp1 HG01123.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-2588delT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50174488 | |||||
chr1:50174990
|
C | T | 51 | a0001c0001t0001g0033a0001c0001t0001g0116a0001c0001t0001g0144others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.251-2099C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50174990 | ||||||
chr1:50175066
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0250 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.251-2023A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175066 | ||||||
chr1:50175160
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0002g0198 | 2 | HG02056.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.251-1929A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175160 | ||||||
chr1:50175284
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.251-1805A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175284 | ||||||
chr1:50175311
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.251-1778T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175311 | ||||||
chr1:50175387
|
T | TAC | 17 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0069others(14): Show | 18 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.251-1667_251-1666d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | |||||
chr1:50175387
|
T | TACAC | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0009g0131others(2): Show | 5 | HG02559.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-1669_251-1666d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | |||||
chr1:50175387
|
TAC | T | 32 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0014others(29): Show | 32 | HG00280.hp2 HG01074.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.251-1667_251-1666d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | |||||
chr1:50175387
|
TACAC | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(90): Show | 94 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.251-1669_251-1666d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | |||||
chr1:50175387
|
TACACAC | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0023others(23): Show | 27 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(24): Show |
intron_variant | MODIFIER | c.251-1671_251-1666d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | |||||
chr1:50175387
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0059 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.251-1679_251-1666d others(16): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 50175387 | |||||
chr1:50175946
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.251-1143G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175946 | ||||||
chr1:50175984
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0150a0001c0001t0001g0154 | 3 | HG00741.hp2 HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.251-1105G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50175984 | ||||||
chr1:50176160
|
C | T | 1 | a0001c0002t0001g0234 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.251-929C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176160 | ||||||
chr1:50176272
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.251-817C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176272 | ||||||
chr1:50176295
|
C | T | 1 | a0001c0001t0010g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.251-794C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176295 | ||||||
chr1:50176411
|
C | A | 1 | a0001c0001t0001g0214 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.251-678C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176411 | ||||||
chr1:50176430
|
C | G | 1 | a0001c0001t0002g0037 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.251-659C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176430 | ||||||
chr1:50176450
|
G | T | 1 | a0001c0001t0001g0033 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.251-639G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176450 | ||||||
chr1:50176547
|
G | A | 1 | a0001c0002t0001g0063 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.251-542G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176547 | ||||||
chr1:50176557
|
C | T | 1 | a0001c0001t0002g0269 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.251-532C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176557 | ||||||
chr1:50176916
|
T | G | 1 | a0001c0001t0002g0073 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.251-173T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50176916 | ||||||
chr1:50177000
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.251-89A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 2/6 | chr1 | 50177000 | ||||||
chr1:50177829
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.354+637A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50177829 | ||||||
chr1:50177994
|
A | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(253): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.354+802A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50177994 | ||||||
chr1:50178019
|
G | A | 1 | a0001c0002t0004g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.354+827G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178019 | ||||||
chr1:50178062
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.354+870T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178062 | ||||||
chr1:50178378
|
G | A | 1 | a0001c0002t0013g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.354+1186G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178378 | ||||||
chr1:50178841
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.354+1649G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178841 | ||||||
chr1:50178962
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.354+1770T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178962 | ||||||
chr1:50178963
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.354+1771G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178963 | ||||||
chr1:50178964
|
C | CT | 146 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(143): Show | 147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.354+1784dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50178964 | |||||
chr1:50178964
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.354+1772C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50178964 | ||||||
chr1:50179148
|
G | A | 47 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0038others(44): Show | 47 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.354+1956G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179148 | ||||||
chr1:50179219
|
C | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(16): Show | 19 | HG00609.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.354+2027C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179219 | ||||||
chr1:50179506
|
A | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0022others(8): Show | 11 | HG00280.hp2 HG00323.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.354+2314A>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179506 | ||||||
chr1:50179594
|
A | C | 1 | a0001c0001t0010g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.354+2402A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179594 | ||||||
chr1:50179789
|
T | A | 1 | a0001c0002t0007g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.354+2597T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179789 | ||||||
chr1:50179925
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.354+2733T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50179925 | ||||||
chr1:50180219
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.354+3027A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50180219 | ||||||
chr1:50180403
|
A | G | 7 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0161others(4): Show | 7 | HG01069.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.354+3211A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50180403 | ||||||
chr1:50180463
|
C | A | 15 | a0001c0002t0001g0195a0001c0002t0003g0002a0001c0002t0003g0003others(12): Show | 17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.354+3271C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50180463 | ||||||
chr1:50180817
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.354+3625G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50180817 | ||||||
chr1:50180941
|
A | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.354+3749A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50180941 | ||||||
chr1:50181354
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.354+4162T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181354 | ||||||
chr1:50181568
|
G | T | 1 | a0001c0001t0001g0226 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.354+4376G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181568 | ||||||
chr1:50181675
|
G | GTTTGT | 232 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.354+4502_354+4506d others(7): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50181675 | |||||
chr1:50181803
|
C | A | 15 | a0001c0002t0001g0195a0001c0002t0003g0002a0001c0002t0003g0003others(12): Show | 17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.354+4611C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181803 | ||||||
chr1:50181841
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.354+4649G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181841 | ||||||
chr1:50181875
|
G | T | 7 | a0001c0002t0004g0004a0001c0002t0004g0054a0001c0002t0004g0055others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.354+4683G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181875 | ||||||
chr1:50181972
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0075 | 2 | HG02040.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.354+4780C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50181972 | ||||||
chr1:50182117
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0150a0001c0001t0001g0154 | 3 | HG00741.hp2 HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.354+4925C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182117 | ||||||
chr1:50182309
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.354+5117G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182309 | ||||||
chr1:50182360
|
A | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(246): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.354+5168A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182360 | ||||||
chr1:50182802
|
G | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.354+5610G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182802 | ||||||
chr1:50182870
|
CT | C | 18 | a0001c0001t0002g0211a0001c0001t0009g0131a0001c0002t0001g0195others(15): Show | 20 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.354+5690delT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50182870 | |||||
chr1:50182875
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.354+5683T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182875 | ||||||
chr1:50182982
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.354+5790C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50182982 | ||||||
chr1:50183085
|
T | G | 11 | a0001c0002t0001g0087a0001c0002t0001g0091a0001c0002t0001g0234others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.354+5893T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50183085 | ||||||
chr1:50183123
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.354+5931G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50183123 | ||||||
chr1:50183465
|
G | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0023others(8): Show | 12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.354+6273G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50183465 | ||||||
chr1:50183794
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.354+6602T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50183794 | ||||||
chr1:50183938
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.354+6746G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50183938 | ||||||
chr1:50184027
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(57): Show | 61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.354+6835C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184027 | ||||||
chr1:50184142
|
G | A | 1 | a0001c0002t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.354+6950G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184142 | ||||||
chr1:50184144
|
G | C | 1 | a0001c0002t0013g0090 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.354+6952G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184144 | ||||||
chr1:50184197
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.354+7005C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184197 | ||||||
chr1:50184226
|
C | T | 12 | a0001c0002t0001g0063a0001c0002t0001g0071a0001c0002t0001g0088others(9): Show | 12 | HG02486.hp2 HG02895.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.354+7034C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184226 | ||||||
chr1:50184257
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0001g0179others(1): Show | 4 | HG01074.hp1 HG01123.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+7065G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184257 | ||||||
chr1:50184346
|
C | T | 1 | a0001c0001t0001g0214 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.354+7154C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184346 | ||||||
chr1:50184398
|
C | CA | 226 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.354+7222dupA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50184398 | |||||
chr1:50184398
|
C | CAA | 13 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0096others(10): Show | 13 | HG00642.hp1 HG01243.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.354+7221_354+7222d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50184398 | |||||
chr1:50184527
|
G | A | 42 | a0001c0001t0001g0033a0001c0001t0001g0204a0001c0001t0002g0008others(39): Show | 42 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.354+7335G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50184527 | ||||||
chr1:50185284
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.354+8092C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50185284 | ||||||
chr1:50185522
|
T | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0192others(1): Show | 4 | HG01255.hp1 HG01261.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-8243T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50185522 | ||||||
chr1:50185616
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0180a0001c0001t0001g0182others(2): Show | 5 | HG00423.hp1 HG00438.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-8149A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50185616 | ||||||
chr1:50185731
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.355-8034G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50185731 | ||||||
chr1:50185958
|
C | T | 1 | a0001c0002t0005g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-7807C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50185958 | ||||||
chr1:50186107
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.355-7658A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186107 | ||||||
chr1:50186440
|
G | A | 6 | a0001c0002t0003g0003a0001c0002t0003g0005a0001c0002t0003g0166others(3): Show | 7 | HG02572.hp2 HG02630.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.355-7325G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186440 | ||||||
chr1:50186565
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.355-7200G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186565 | ||||||
chr1:50186627
|
CATAGAA | C | 15 | a0001c0002t0001g0195a0001c0002t0003g0002a0001c0002t0003g0003others(12): Show | 17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.355-7129_355-7124d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50186627 | |||||
chr1:50186646
|
T | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.355-7119T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186646 | ||||||
chr1:50186671
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.355-7094T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186671 | ||||||
chr1:50186697
|
G | A | 1 | a0001c0001t0002g0073 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.355-7068G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186697 | ||||||
chr1:50186800
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.355-6965G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186800 | ||||||
chr1:50186842
|
A | AAAG | 232 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.355-6921_355-6920i others(5): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50186842 | |||||
chr1:50186895
|
A | G | 1 | a0001c0001t0009g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.355-6870A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186895 | ||||||
chr1:50186919
|
A | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0136a0001c0001t0001g0142others(1): Show | 4 | HG02056.hp2 HG02135.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-6846A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186919 | ||||||
chr1:50186973
|
C | T | 6 | a0001c0002t0001g0056a0001c0002t0001g0086a0001c0002t0001g0190others(3): Show | 6 | HG00642.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.355-6792C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50186973 | ||||||
chr1:50187160
|
G | T | 1 | a0001c0001t0002g0222 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.355-6605G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50187160 | ||||||
chr1:50187260
|
A | G | 1 | a0001c0002t0004g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.355-6505A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50187260 | ||||||
chr1:50187371
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0226a0001c0001t0001g0228 | 3 | HG00140.hp1 HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.355-6394T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50187371 | ||||||
chr1:50187460
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.355-6305A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50187460 | ||||||
chr1:50188159
|
T | A | 1 | a0001c0002t0004g0244 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.355-5606T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50188159 | ||||||
chr1:50188460
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.355-5305G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50188460 | ||||||
chr1:50188487
|
T | C | 4 | a0001c0002t0003g0175a0001c0002t0003g0225a0001c0002t0003g0249others(1): Show | 4 | HG02257.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-5278T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50188487 | ||||||
chr1:50189167
|
G | A | 15 | a0001c0002t0001g0195a0001c0002t0003g0002a0001c0002t0003g0003others(12): Show | 17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.355-4598G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189167 | ||||||
chr1:50189249
|
C | T | 1 | a0001c0002t0004g0244 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.355-4516C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189249 | ||||||
chr1:50189305
|
C | G | 6 | a0001c0002t0001g0056a0001c0002t0001g0086a0001c0002t0001g0190others(3): Show | 6 | HG00642.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.355-4460C>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189305 | ||||||
chr1:50189329
|
G | A | 6 | a0001c0001t0001g0247a0001c0001t0001g0267a0001c0002t0001g0087others(3): Show | 6 | HG02572.hp1 HG02647.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-4436G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189329 | ||||||
chr1:50189535
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.355-4230G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189535 | ||||||
chr1:50189629
|
T | G | 1 | a0001c0002t0001g0251 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.355-4136T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189629 | ||||||
chr1:50189666
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.355-4099G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189666 | ||||||
chr1:50189992
|
G | T | 1 | a0001c0001t0010g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.355-3773G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50189992 | ||||||
chr1:50190034
|
G | C | 1 | a0001c0002t0004g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.355-3731G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190034 | ||||||
chr1:50190204
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0075 | 2 | HG02040.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.355-3561G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190204 | ||||||
chr1:50190319
|
CTTTCAGC others(14): Show |
C | 1 | a0001c0001t0001g0189 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.355-3445_355-3425d others(23): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190319 | ||||||
chr1:50190401
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.355-3364G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190401 | ||||||
chr1:50190469
|
C | T | 8 | a0001c0002t0001g0056a0001c0002t0001g0086a0001c0002t0001g0165others(5): Show | 8 | HG00642.hp1 HG02109.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.355-3296C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190469 | ||||||
chr1:50190574
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.355-3191T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190574 | ||||||
chr1:50190761
|
C | T | 5 | a0001c0002t0004g0004a0001c0002t0004g0054a0001c0002t0004g0236others(2): Show | 5 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-3004C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190761 | ||||||
chr1:50190787
|
A | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(57): Show | 61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.355-2978A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190787 | ||||||
chr1:50190921
|
T | A | 14 | a0001c0002t0003g0002a0001c0002t0003g0003a0001c0002t0003g0005others(11): Show | 16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.355-2844T>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190921 | ||||||
chr1:50190992
|
T | G | 1 | a0001c0001t0001g0057 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.355-2773T>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50190992 | ||||||
chr1:50191044
|
C | A | 7 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0160others(4): Show | 7 | HG01069.hp1 HG01109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.355-2721C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191044 | ||||||
chr1:50191249
|
A | G | 5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0174others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-2516A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191249 | ||||||
chr1:50191649
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.355-2116A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191649 | ||||||
chr1:50191656
|
A | G | 1 | a0001c0002t0001g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.355-2109A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191656 | ||||||
chr1:50191748
|
G | A | 1 | a0001c0002t0003g0196 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.355-2017G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191748 | ||||||
chr1:50191753
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.355-2012G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191753 | ||||||
chr1:50191754
|
G | C | 5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0174others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-2011G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191754 | ||||||
chr1:50191794
|
G | A | 1 | a0001c0002t0003g0248 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.355-1971G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191794 | ||||||
chr1:50191855
|
C | T | 14 | a0001c0002t0003g0002a0001c0002t0003g0003a0001c0002t0003g0005others(11): Show | 16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.355-1910C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50191855 | ||||||
chr1:50192178
|
C | T | 4 | a0001c0002t0001g0087a0001c0002t0001g0091a0001c0002t0001g0234others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-1587C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192178 | ||||||
chr1:50192245
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.355-1520G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192245 | ||||||
chr1:50192398
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG00280.hp2 HG00741.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.355-1367C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192398 | ||||||
chr1:50192519
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.355-1246G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192519 | ||||||
chr1:50192519
|
G | GCA | 36 | a0001c0001t0001g0019a0001c0001t0001g0050a0001c0001t0001g0057others(33): Show | 37 | HG00438.hp1 HG00642.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.355-1202_355-1201d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
G | GCACA | 47 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(44): Show | 47 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.355-1204_355-1201d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
G | GCACACA | 40 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0038others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.355-1206_355-1201d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
G | GCACACAC others(1): Show |
24 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0020others(21): Show | 24 | HG00609.hp1 HG00609.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.355-1208_355-1201d others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
G | GCACACAC others(3): Show |
9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0127others(6): Show | 9 | HG01071.hp2 HG02056.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.355-1210_355-1201d others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
G | GCACACAC others(5): Show |
3 | a0001c0001t0001g0065a0001c0001t0001g0141a0001c0001t0001g0158 | 3 | HG01346.hp1 HG01361.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.355-1212_355-1201d others(14): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
G | GCACGCAC others(3): Show |
1 | a0001c0001t0001g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.355-1243_355-1242i others(12): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
GCA | G | 15 | a0001c0001t0001g0085a0001c0001t0002g0008a0001c0001t0002g0045others(12): Show | 15 | HG00280.hp1 HG00673.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.355-1202_355-1201d others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
GCACA | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0023others(51): Show | 55 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.355-1204_355-1201d others(6): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
GCACACA | G | 6 | a0001c0001t0002g0015a0001c0002t0001g0071a0001c0002t0001g0087others(3): Show | 6 | HG00323.hp1 HG01243.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-1206_355-1201d others(8): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
GCACACAC others(1): Show |
G | 4 | a0001c0001t0001g0033a0001c0001t0002g0187a0001c0001t0002g0263others(1): Show | 4 | HG02922.hp2 NA18962.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-1208_355-1201d others(10): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
GCACACAC others(7): Show |
G | 1 | a0001c0002t0001g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.355-1214_355-1201d others(16): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
GCACACAC others(9): Show |
G | 1 | a0001c0001t0010g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.355-1216_355-1201d others(18): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192519
|
GCACACAC others(17): Show |
G | 1 | a0001c0001t0002g0072 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.355-1224_355-1201d others(26): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50192519 | |||||
chr1:50192523
|
A | G | 2 | a0001c0002t0003g0002a0001c0002t0013g0090 | 3 | HG01168.hp1 HG01169.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.355-1242A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192523 | ||||||
chr1:50192801
|
T | C | 1 | a0001c0001t0001g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.355-964T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192801 | ||||||
chr1:50192922
|
A | G | 5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0174others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-843A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50192922 | ||||||
chr1:50193114
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.355-651C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50193114 | ||||||
chr1:50193366
|
G | GT | 236 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.355-385dupT | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 50193366 | |||||
chr1:50193406
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.355-359G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50193406 | ||||||
chr1:50193407
|
T | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0039 | 2 | HG00140.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.355-358T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50193407 | ||||||
chr1:50193442
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.355-323G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50193442 | ||||||
chr1:50193744
|
G | A | 1 | a0001c0002t0001g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.355-21G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 3/6 | chr1 | 50193744 | ||||||
chr1:50194256
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0001g0048others(2): Show | 5 | HG01074.hp1 HG01123.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.508+338A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50194256 | ||||||
chr1:50194469
|
T | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.508+551T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50194469 | ||||||
chr1:50194960
|
G | T | 1 | a0001c0001t0001g0076 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.509-601G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50194960 | ||||||
chr1:50194974
|
A | G | 7 | a0001c0002t0005g0237a0001c0002t0005g0239a0001c0002t0005g0240others(4): Show | 7 | HG02486.hp2 HG02922.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.509-587A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50194974 | ||||||
chr1:50195071
|
TGTTA | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.509-489_509-486del others(4): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50195071 | ||||||
chr1:50195309
|
A | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(246): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.509-252A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50195309 | ||||||
chr1:50195352
|
G | C | 14 | a0001c0002t0003g0002a0001c0002t0003g0003a0001c0002t0003g0005others(11): Show | 16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.509-209G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50195352 | ||||||
chr1:50195466
|
C | T | 14 | a0001c0002t0003g0002a0001c0002t0003g0003a0001c0002t0003g0005others(11): Show | 16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.509-95C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 4/6 | chr1 | 50195466 | ||||||
chr1:50195857
|
T | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0002g0042 | 3 | NA18973.hp1 NA19057.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.734+71T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50195857 | ||||||
chr1:50195911
|
C | T | 7 | a0001c0002t0001g0056a0001c0002t0001g0086a0001c0002t0001g0190others(4): Show | 7 | HG00642.hp1 HG02109.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.734+125C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50195911 | ||||||
chr1:50196016
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.734+230T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196016 | ||||||
chr1:50196067
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.734+281C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196067 | ||||||
chr1:50196085
|
A | G | 1 | a0001c0001t0002g0211 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.734+299A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196085 | ||||||
chr1:50196168
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0001g0179others(1): Show | 4 | HG01074.hp1 HG01123.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.734+382G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196168 | ||||||
chr1:50196769
|
C | A | 1 | a0001c0001t0002g0037 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.735-660C>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196769 | ||||||
chr1:50196976
|
T | C | 5 | a0001c0002t0001g0087a0001c0002t0001g0091a0001c0002t0001g0146others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.735-453T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50196976 | ||||||
chr1:50197164
|
A | AAT | 6 | a0001c0002t0001g0087a0001c0002t0001g0091a0001c0002t0001g0146others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-265_735-264ins others(2): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197164 | ||||||
chr1:50197167
|
T | TATTAA | 6 | a0001c0002t0001g0087a0001c0002t0001g0091a0001c0002t0001g0146others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-262_735-261ins others(5): Show |
ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197167 | ||||||
chr1:50197168
|
G | T | 6 | a0001c0002t0001g0087a0001c0002t0001g0091a0001c0002t0001g0146others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-261G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197168 | ||||||
chr1:50197169
|
G | T | 6 | a0001c0002t0001g0087a0001c0002t0001g0091a0001c0002t0001g0146others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-260G>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197169 | ||||||
chr1:50197170
|
G | C | 6 | a0001c0002t0001g0087a0001c0002t0001g0091a0001c0002t0001g0146others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-259G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197170 | ||||||
chr1:50197171
|
G | A | 6 | a0001c0002t0001g0087a0001c0002t0001g0091a0001c0002t0001g0146others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.735-258G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197171 | ||||||
chr1:50197226
|
T | C | 1 | a0001c0002t0003g0245 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.735-203T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197226 | ||||||
chr1:50197283
|
G | A | 1 | a0001c0002t0004g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.735-146G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 5/6 | chr1 | 50197283 | ||||||
chr1:50197861
|
T | C | 1 | a0001c0001t0002g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.773+394T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50197861 | ||||||
chr1:50198179
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.773+712G>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50198179 | ||||||
chr1:50198193
|
C | T | 1 | a0001c0002t0003g0166 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.773+726C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50198193 | ||||||
chr1:50198435
|
C | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(266): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.773+968C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50198435 | ||||||
chr1:50198939
|
T | C | 6 | a0001c0002t0001g0087a0001c0002t0001g0091a0001c0002t0001g0146others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.773+1472T>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50198939 | ||||||
chr1:50199507
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.774-1344A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50199507 | ||||||
chr1:50199633
|
G | A | 14 | a0001c0002t0003g0002a0001c0002t0003g0003a0001c0002t0003g0005others(11): Show | 16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.774-1218G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50199633 | ||||||
chr1:50199734
|
G | GA | 14 | a0001c0002t0003g0002a0001c0002t0003g0003a0001c0002t0003g0005others(11): Show | 16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.774-1108dupA | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr1 | 50199734 | |||||
chr1:50200242
|
C | T | 14 | a0001c0002t0003g0002a0001c0002t0003g0003a0001c0002t0003g0005others(11): Show | 16 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.774-609C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200242 | ||||||
chr1:50200401
|
A | G | 1 | a0001c0002t0001g0233 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.774-450A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200401 | ||||||
chr1:50200495
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.774-356A>C | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200495 | ||||||
chr1:50200517
|
G | A | 15 | a0001c0001t0001g0117a0001c0002t0003g0002a0001c0002t0003g0003others(12): Show | 17 | HG01168.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.774-334G>A | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200517 | ||||||
chr1:50200548
|
A | G | 1 | a0001c0001t0002g0222 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.774-303A>G | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200548 | ||||||
chr1:50200843
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
splice_region_variant&intron_variant | LOW | c.774-8C>T | ELAVL4 | ENSG00000162374.18 | transcript | ENST00000371824.7 | protein_coding | 6/6 | chr1 | 50200843 |