Item | Value |
---|---|
geneid | 1994 |
ensemblid | ENSG00000066044.15 |
hgncid | 3312 |
symbol | ELAVL1 |
name | ELAV like RNA binding protein 1 |
refseq_nuc | NM_001419.3 |
refseq_prot | NP_001410.2 |
ensembl_nuc | ENST00000407627.7 |
ensembl_prot | ENSP00000385269.1 |
mane_status | MANE Select |
chr | chr19 |
start | 7958573 |
end | 8005641 |
strand | - |
ver | v1.2 |
region | chr19:7958573-8005641 |
region5000 | chr19:7953573-8010641 |
regionname0 | ELAVL1_chr19_7958573_8005641 |
regionname5000 | ELAVL1_chr19_7953573_8010641 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 326 | 276 | 82 | 58 | 88 | 16 | 30 | 66 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 981 | 223 | 66 | 43 | 75 | 10 | 27 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
c0002 | 0/0 | 981 | 49 | 14 | 15 | 11 | 6 | 3 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
c0003 | 0/0 | 981 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
c0004 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
c0005 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 5074 | 108 | 39 | 18 | 25 | 7 | 18 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0002 | 0/1 | 5073 | 32 | 2 | 6 | 14 | 2 | 7 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0003 | 0/0 | 5046 | 21 | 1 | 11 | 8 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0004 | 0/0 | 5074 | 19 | 2 | 10 | 0 | 4 | 3 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0005 | 0/0 | 5046 | 15 | 0 | 3 | 10 | 2 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0006 | 0/0 | 5074 | 11 | 10 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0007 | 0/0 | 5073 | 8 | 0 | 2 | 6 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0008 | 0/0 | 5074 | 7 | 0 | 0 | 7 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0009 | 0/0 | 5074 | 5 | 5 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0010 | 0/0 | 5073 | 5 | 0 | 0 | 5 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0011 | 0/0 | 5046 | 4 | 4 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0012 | 0/0 | 5073 | 3 | 1 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0013 | 0/0 | 5074 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0014 | 0/0 | 5074 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0015 | 0/0 | 5158 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0016 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0017 | 0/0 | 5074 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0018 | 0/0 | 5102 | 2 | 1 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0019 | 0/0 | 5074 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0020 | 0/0 | 5073 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0021 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0022 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0023 | 0/0 | 5074 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0024 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0025 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0026 | 0/0 | 5046 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0027 | 0/0 | 5046 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0028 | 0/0 | 5046 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0029 | 0/0 | 5046 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0030 | 0/0 | 5074 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0031 | 0/0 | 5046 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0032 | 0/0 | 5074 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0033 | 0/0 | 5074 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0034 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0035 | 0/0 | 5074 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0036 | 0/0 | 5102 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0037 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0038 | 0/0 | 5074 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0039 | 0/0 | 5097 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
t0040 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0002 | 0/0 | 5 | 0 | 0 | 1 | 0 | 4 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0003 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0004 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0006 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0008 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 981 | 223 | 66 | 43 | 75 | 10 | 27 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0002 | 0/0 | 981 | 49 | 14 | 15 | 11 | 6 | 3 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0003 | 0/0 | 981 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0004 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0005 | 0/0 | 981 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6054 | 104 | 37 | 18 | 23 | 7 | 18 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0002 | 0/1 | 6053 | 32 | 2 | 6 | 14 | 2 | 7 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0003 | 0/0 | 6026 | 21 | 1 | 11 | 8 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0006 | 0/0 | 6054 | 11 | 10 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0007 | 0/0 | 6053 | 8 | 0 | 2 | 6 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0008 | 0/0 | 6054 | 7 | 0 | 0 | 7 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0010 | 0/0 | 6053 | 5 | 0 | 0 | 5 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0012 | 0/0 | 6053 | 3 | 1 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0013 | 0/0 | 6054 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0014 | 0/0 | 6054 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0015 | 0/0 | 6138 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0017 | 0/0 | 6054 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0018 | 0/0 | 6082 | 2 | 1 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0019 | 0/0 | 6054 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0020 | 0/0 | 6053 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0021 | 0/0 | 6053 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0022 | 0/0 | 6054 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0023 | 0/0 | 6054 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0024 | 0/0 | 6054 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0025 | 0/0 | 6053 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0030 | 0/0 | 6054 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0031 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0032 | 0/0 | 6054 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0033 | 0/0 | 6054 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0034 | 0/0 | 6053 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0035 | 0/0 | 6054 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0036 | 0/0 | 6082 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0037 | 0/0 | 6110 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0038 | 0/0 | 6054 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0039 | 0/0 | 6077 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0001t0040 | 0/0 | 6053 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0002t0004 | 0/0 | 6054 | 19 | 2 | 10 | 0 | 4 | 3 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0002t0005 | 0/0 | 6026 | 15 | 0 | 3 | 10 | 2 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0002t0009 | 0/0 | 6054 | 5 | 5 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0002t0011 | 0/0 | 6026 | 4 | 4 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0002t0016 | 0/0 | 6054 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0002t0026 | 0/0 | 6026 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0002t0027 | 0/0 | 6026 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0002t0028 | 0/0 | 6026 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0002t0029 | 0/0 | 6026 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0003t0001 | 0/0 | 6054 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0004t0001 | 0/0 | 6054 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
a0001c0005t0001 | 0/0 | 6054 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | copy fasta | chr19 | 7953573 | 8010641 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 1 | 0 | 4 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0001 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0007g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0008g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0010g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0010g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0010g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0012g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0012g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0013g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0013g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0014g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0014g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0015g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0015g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0015g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0017g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0018g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0018g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0019g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0019g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0020g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0021g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0022g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0023g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0024g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0025g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0030g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0031g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0032g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0033g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0034g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0035g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0036g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0037g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0038g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0039g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0001t0040g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0004 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0009g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0009g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0016g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0016g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0026g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0027g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0028g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0002t0029g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0003t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
a0001c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00140 | hp1 | a0001 | c0002 | t0004 | g0020 | EUR | GBR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00280 | hp1 | a0001 | c0002 | t0005 | g0017 | EUR | FIN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00280 | hp2 | a0001 | c0002 | t0004 | g0238 | EUR | FIN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00408 | hp1 | a0001 | c0001 | t0021 | g0151 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00544 | hp2 | a0001 | c0001 | t0010 | g0193 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00609 | hp1 | a0001 | c0001 | t0007 | g0170 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00621 | hp2 | a0001 | c0001 | t0010 | g0154 | EAS | CHS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00642 | hp1 | a0001 | c0002 | t0026 | g0209 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0105 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00733 | hp1 | a0001 | c0002 | t0004 | g0225 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00733 | hp2 | a0001 | c0002 | t0005 | g0016 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG00738 | hp2 | a0001 | c0002 | t0004 | g0019 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01070 | hp1 | a0001 | c0002 | t0004 | g0004 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01071 | hp2 | a0001 | c0002 | t0004 | g0004 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01106 | hp1 | a0001 | c0001 | t0035 | g0060 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01109 | hp1 | a0001 | c0002 | t0004 | g0004 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01109 | hp2 | a0001 | c0002 | t0005 | g0017 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01168 | hp1 | a0001 | c0001 | t0033 | g0121 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01243 | hp1 | a0001 | c0002 | t0004 | g0223 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01256 | hp2 | a0001 | c0002 | t0004 | g0221 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01257 | hp1 | a0001 | c0002 | t0004 | g0222 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01261 | hp1 | a0001 | c0001 | t0007 | g0108 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01261 | hp2 | a0001 | c0001 | t0006 | g0199 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01346 | hp1 | a0001 | c0002 | t0028 | g0205 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01433 | hp1 | a0001 | c0001 | t0023 | g0177 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01433 | hp2 | a0001 | c0002 | t0004 | g0224 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01517 | hp2 | a0001 | c0002 | t0004 | g0020 | EUR | IBS | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01891 | hp1 | a0001 | c0002 | t0009 | g0232 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01928 | hp1 | a0001 | c0001 | t0007 | g0156 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01934 | hp1 | a0001 | c0001 | t0038 | g0084 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01981 | hp2 | a0001 | c0001 | t0020 | g0169 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02004 | hp1 | a0001 | c0002 | t0005 | g0207 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0194 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02055 | hp2 | a0001 | c0001 | t0015 | g0041 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02135 | hp1 | a0001 | c0001 | t0031 | g0073 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02135 | hp2 | a0001 | c0001 | t0007 | g0195 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0198 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02257 | hp2 | a0001 | c0002 | t0009 | g0231 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02280 | hp1 | a0001 | c0001 | t0013 | g0043 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0161 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02300 | hp2 | a0001 | c0002 | t0004 | g0019 | AMR | PEL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02523 | hp2 | a0001 | c0002 | t0005 | g0206 | EAS | KHV | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0203 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02602 | hp1 | a0001 | c0002 | t0004 | g0237 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02622 | hp1 | a0001 | c0002 | t0011 | g0024 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0200 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02647 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02698 | hp1 | a0001 | c0002 | t0004 | g0228 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02717 | hp2 | a0001 | c0002 | t0011 | g0027 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0202 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02723 | hp2 | a0001 | c0001 | t0014 | g0014 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02922 | hp1 | a0001 | c0002 | t0027 | g0204 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0162 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02976 | hp1 | a0001 | c0001 | t0017 | g0009 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03041 | hp1 | a0001 | c0002 | t0009 | g0230 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03041 | hp2 | a0001 | c0001 | t0012 | g0236 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03098 | hp1 | a0001 | c0001 | t0025 | g0038 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03130 | hp2 | a0001 | c0002 | t0011 | g0026 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03139 | hp1 | a0001 | c0002 | t0009 | g0021 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0044 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03195 | hp2 | a0001 | c0001 | t0014 | g0014 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03209 | hp1 | a0001 | c0002 | t0016 | g0233 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03486 | hp1 | a0001 | c0001 | t0017 | g0009 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03516 | hp2 | a0001 | c0002 | t0011 | g0025 | AFR | ESN | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03579 | hp1 | a0001 | c0001 | t0036 | g0040 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03579 | hp2 | a0001 | c0002 | t0016 | g0220 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | STU | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | STU | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03927 | hp1 | a0001 | c0002 | t0004 | g0004 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | STU | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18522 | hp2 | a0001 | c0001 | t0034 | g0143 | AFR | YRI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18612 | hp1 | a0001 | c0001 | t0010 | g0168 | EAS | CHB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18941 | hp2 | a0001 | c0001 | t0008 | g0100 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18946 | hp1 | a0001 | c0001 | t0024 | g0176 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18946 | hp2 | a0001 | c0004 | t0001 | g0107 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18952 | hp1 | a0001 | c0002 | t0005 | g0216 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18952 | hp2 | a0001 | c0001 | t0008 | g0080 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18953 | hp1 | a0001 | c0001 | t0007 | g0197 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18953 | hp2 | a0001 | c0001 | t0008 | g0079 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18959 | hp1 | a0001 | c0002 | t0005 | g0218 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18960 | hp1 | a0001 | c0002 | t0005 | g0217 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18961 | hp2 | a0001 | c0001 | t0012 | g0235 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18962 | hp2 | a0001 | c0002 | t0005 | g0215 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18964 | hp1 | a0001 | c0001 | t0032 | g0059 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18964 | hp2 | a0001 | c0002 | t0005 | g0018 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18966 | hp1 | a0001 | c0001 | t0037 | g0051 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18966 | hp2 | a0001 | c0001 | t0007 | g0174 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18968 | hp1 | a0001 | c0001 | t0039 | g0066 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18968 | hp2 | a0001 | c0001 | t0012 | g0234 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18969 | hp2 | a0001 | c0002 | t0005 | g0214 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18970 | hp2 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18971 | hp1 | a0001 | c0001 | t0007 | g0028 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18971 | hp2 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18973 | hp1 | a0001 | c0001 | t0040 | g0179 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18980 | hp2 | a0001 | c0002 | t0029 | g0213 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18982 | hp1 | a0001 | c0001 | t0008 | g0106 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19007 | hp1 | a0001 | c0001 | t0008 | g0137 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19009 | hp1 | a0001 | c0002 | t0005 | g0208 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19012 | hp1 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19012 | hp2 | a0001 | c0005 | t0001 | g0113 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19030 | hp1 | a0001 | c0001 | t0013 | g0045 | AFR | LWK | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19043 | hp2 | a0001 | c0002 | t0009 | g0021 | AFR | LWK | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19065 | hp2 | a0001 | c0002 | t0005 | g0018 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19077 | hp1 | a0001 | c0001 | t0022 | g0165 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19079 | hp2 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19082 | hp2 | a0001 | c0001 | t0019 | g0240 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19090 | hp1 | a0001 | c0002 | t0005 | g0212 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA19090 | hp2 | a0001 | c0001 | t0019 | g0239 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA20129 | hp1 | a0001 | c0002 | t0004 | g0229 | AFR | ASW | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA20129 | hp2 | a0001 | c0001 | t0014 | g0124 | AFR | ASW | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA20752 | hp1 | a0001 | c0001 | t0018 | g0119 | EUR | TSI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA20752 | hp2 | a0001 | c0002 | t0005 | g0016 | EUR | TSI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA20805 | hp2 | a0001 | c0002 | t0004 | g0227 | EUR | TSI | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA20905 | hp2 | a0001 | c0001 | t0030 | g0099 | SAS | GIH | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02486 | hp1 | a0001 | c0002 | t0004 | g0226 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03471 | hp1 | a0001 | c0001 | t0018 | g0039 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0166 | REF | REF | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0055 | REF | REF | ELAVL1_chr19_7953573_8010641 | ELAVL1 | chr19 | 7953573 | 8010641 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:7963660
|
A | G | 1 | a0001c0002 | 49 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
synonymous_variant | LOW | c.804T>C | p.Gly268Gly | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 967/6054 | 804/981 | 268/326 | chr19 | 7963660 | ||
chr19:7963696
|
G | A | 1 | a0001c0004 | 1 | NA18946.hp2 | synonymous_variant | LOW | c.768C>T | p.Asp256Asp | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 931/6054 | 768/981 | 256/326 | chr19 | 7963696 | ||
chr19:7963765
|
G | A | 1 | a0001c0005 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.699C>T | p.Gly233Gly | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 862/6054 | 699/981 | 233/326 | chr19 | 7963765 | ||
chr19:7991657
|
C | G | 1 | a0001c0003 | 2 | HG02622.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.159G>C | p.Arg53Arg | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/6 | 322/6054 | 159/981 | 53/326 | chr19 | 7991657 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:7958588
|
T | A | 1 | a0001c0001t0024 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4895A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4895 | chr19 | 7958588 | |||||
chr19:7959057
|
TA | T | 10 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(7): Show | 54 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*4425delT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4425 | chr19 | 7959057 | |||||
chr19:7959064
|
A | T | 2 | a0001c0001t0017a0001c0001t0031 | 3 | HG02135.hp1 HG02976.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4419T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4419 | chr19 | 7959064 | |||||
chr19:7959071
|
A | T | 1 | a0001c0001t0022 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4412T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4412 | chr19 | 7959071 | |||||
chr19:7959101
|
A | C | 1 | a0001c0001t0022 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4382T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4382 | chr19 | 7959101 | |||||
chr19:7959383
|
C | T | 1 | a0001c0001t0040 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4100G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4100 | chr19 | 7959383 | |||||
chr19:7959384
|
T | C | 1 | a0001c0001t0040 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4099A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4099 | chr19 | 7959384 | |||||
chr19:7959387
|
C | T | 1 | a0001c0001t0036 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4096G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4096 | chr19 | 7959387 | |||||
chr19:7959403
|
G | A | 1 | a0001c0002t0026 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4080C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4080 | chr19 | 7959403 | |||||
chr19:7959453
|
G | T | 1 | a0001c0001t0033 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4030C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 4030 | chr19 | 7959453 | |||||
chr19:7959554
|
A | T | 1 | a0001c0001t0014 | 3 | HG02723.hp2 HG03195.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3929T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3929 | chr19 | 7959554 | |||||
chr19:7959605
|
G | A | 1 | a0001c0002t0011 | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3878C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3878 | chr19 | 7959605 | |||||
chr19:7959715
|
G | A | 5 | a0001c0002t0005a0001c0002t0026a0001c0002t0027others(2): Show | 19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3768C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3768 | chr19 | 7959715 | |||||
chr19:7959800
|
A | C | 2 | a0001c0002t0004a0001c0002t0009 | 24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3683T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3683 | chr19 | 7959800 | |||||
chr19:7959998
|
G | T | 1 | a0001c0001t0032 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3485C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3485 | chr19 | 7959998 | |||||
chr19:7960127
|
G | A | 1 | a0001c0001t0012 | 3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3356C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 3356 | chr19 | 7960127 | |||||
chr19:7960607
|
T | C | 9 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(6): Show | 61 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2876A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2876 | chr19 | 7960607 | |||||
chr19:7961047
|
C | T | 1 | a0001c0002t0004 | 19 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2436G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2436 | chr19 | 7961047 | |||||
chr19:7961051
|
G | A | 1 | a0001c0001t0035 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2432C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2432 | chr19 | 7961051 | |||||
chr19:7961182
|
G | A | 1 | a0001c0002t0011 | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2301C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2301 | chr19 | 7961182 | |||||
chr19:7961286
|
T | C | 2 | a0001c0001t0012a0001c0001t0025 | 4 | HG03041.hp2 HG03098.hp1 NA18961.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2197A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2197 | chr19 | 7961286 | |||||
chr19:7961303
|
G | GCCTTCCA others(21): Show |
2 | a0001c0001t0018a0001c0001t0036 | 3 | HG03471.hp1 HG03579.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2152_*2179dupTGGG others(24): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2179 | chr19 | 7961303 | |||||
chr19:7961303
|
G | GCCTTCCA others(49): Show |
1 | a0001c0001t0037 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2124_*2179dupTGGG others(52): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2179 | chr19 | 7961303 | |||||
chr19:7961303
|
G | GCCTTCCA others(77): Show |
1 | a0001c0001t0015 | 3 | HG02055.hp2 HG02145.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2096_*2179dupTGGG others(80): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2179 | chr19 | 7961303 | |||||
chr19:7961303
|
GCCTTCCA others(21): Show |
G | 8 | a0001c0001t0003a0001c0001t0031a0001c0002t0005others(5): Show | 45 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2152_*2179delTGGG others(24): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2152 | chr19 | 7961303 | |||||
chr19:7961341
|
A | G | 4 | a0001c0002t0005a0001c0002t0026a0001c0002t0028others(1): Show | 18 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2142T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 2142 | chr19 | 7961341 | |||||
chr19:7961534
|
G | A | 5 | a0001c0002t0005a0001c0002t0026a0001c0002t0027others(2): Show | 19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1949C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1949 | chr19 | 7961534 | |||||
chr19:7961562
|
C | T | 1 | a0001c0001t0013 | 3 | HG02280.hp1 HG02647.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1921G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1921 | chr19 | 7961562 | |||||
chr19:7961665
|
A | G | 9 | a0001c0002t0004a0001c0002t0005a0001c0002t0009others(6): Show | 49 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1818T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1818 | chr19 | 7961665 | |||||
chr19:7961668
|
C | T | 1 | a0001c0001t0030 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1815G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1815 | chr19 | 7961668 | |||||
chr19:7961797
|
T | C | 1 | a0001c0001t0039 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1686 | chr19 | 7961797 | |||||
chr19:7961798
|
G | T | 1 | a0001c0001t0039 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1685 | chr19 | 7961798 | |||||
chr19:7962056
|
C | A | 1 | a0001c0002t0028 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1427G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1427 | chr19 | 7962056 | |||||
chr19:7962171
|
G | T | 9 | a0001c0002t0004a0001c0002t0005a0001c0002t0009others(6): Show | 49 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1312C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1312 | chr19 | 7962171 | |||||
chr19:7962181
|
T | C | 1 | a0001c0001t0038 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1302A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1302 | chr19 | 7962181 | |||||
chr19:7962295
|
T | TTAATGGT others(17): Show |
1 | a0001c0001t0039 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1164_*1187dupTTAC others(20): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 1187 | chr19 | 7962295 | |||||
chr19:7962648
|
G | A | 1 | a0001c0002t0029 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*835C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 835 | chr19 | 7962648 | |||||
chr19:7962719
|
G | T | 3 | a0001c0001t0010a0001c0001t0020a0001c0001t0040 | 7 | HG00544.hp2 HG00621.hp2 HG01981.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*764C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 764 | chr19 | 7962719 | |||||
chr19:7962870
|
C | A | 5 | a0001c0002t0005a0001c0002t0026a0001c0002t0027others(2): Show | 19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*613G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 613 | chr19 | 7962870 | |||||
chr19:7962878
|
A | G | 20 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(17): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*605T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 605 | chr19 | 7962878 | |||||
chr19:7962900
|
T | G | 4 | a0001c0001t0007a0001c0001t0010a0001c0001t0020others(1): Show | 15 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*583A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 583 | chr19 | 7962900 | |||||
chr19:7962923
|
C | T | 1 | a0001c0001t0020 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*560G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 560 | chr19 | 7962923 | |||||
chr19:7963058
|
G | A | 1 | a0001c0001t0008 | 7 | NA18941.hp2 NA18952.hp2 NA18953.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*425C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 6/6 | 425 | chr19 | 7963058 | |||||
chr19:8005534
|
G | A | 1 | a0001c0001t0019 | 2 | NA19082.hp2 NA19090.hp2 |
5_prime_UTR_variant | MODIFIER | c.-56C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/6 | 13719 | chr19 | 8005534 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:7963827
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.657-20G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7963827 | ||||||
chr19:7963897
|
T | C | 2 | a0001c0001t0018g0039a0001c0001t0036g0040 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.657-90A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7963897 | ||||||
chr19:7964004
|
G | C | 4 | a0001c0002t0009g0021a0001c0002t0009g0230a0001c0002t0009g0231others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-197C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964004 | ||||||
chr19:7964040
|
G | C | 3 | a0001c0002t0009g0021a0001c0002t0009g0230a0001c0002t0009g0232 | 4 | HG01891.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-233C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964040 | ||||||
chr19:7964043
|
C | T | 3 | a0001c0002t0009g0021a0001c0002t0009g0230a0001c0002t0009g0232 | 4 | HG01891.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-236G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964043 | ||||||
chr19:7964047
|
AC | A | 4 | a0001c0002t0009g0021a0001c0002t0009g0230a0001c0002t0009g0231others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.657-241delG | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964047 | ||||||
chr19:7964103
|
A | G | 4 | a0001c0002t0011g0024a0001c0002t0011g0025a0001c0002t0011g0026others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-296T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964103 | ||||||
chr19:7964435
|
T | C | 2 | a0001c0002t0016g0220a0001c0002t0016g0233 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.657-628A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964435 | ||||||
chr19:7964504
|
G | A | 8 | a0001c0001t0007g0028a0001c0001t0007g0108a0001c0001t0007g0155others(5): Show | 8 | HG00609.hp1 HG01261.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.657-697C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7964504 | ||||||
chr19:7965352
|
A | G | 4 | a0001c0002t0011g0024a0001c0002t0011g0025a0001c0002t0011g0026others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.657-1545T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7965352 | ||||||
chr19:7965638
|
G | A | 7 | a0001c0001t0010g0149a0001c0001t0010g0154a0001c0001t0010g0168others(4): Show | 7 | HG00544.hp2 HG00621.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-1831C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7965638 | ||||||
chr19:7965758
|
C | T | 4 | a0001c0001t0012g0234a0001c0001t0012g0235a0001c0001t0012g0236others(1): Show | 4 | HG03041.hp2 HG03098.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+1807G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7965758 | ||||||
chr19:7966013
|
G | A | 10 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0076others(7): Show | 18 | HG00408.hp2 HG01069.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.656+1552C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7966013 | ||||||
chr19:7966086
|
C | T | 3 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG02647.hp2 HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.656+1479G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7966086 | ||||||
chr19:7966708
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.656+857G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7966708 | ||||||
chr19:7966827
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.656+738G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7966827 | ||||||
chr19:7966883
|
G | C | 7 | a0001c0001t0010g0149a0001c0001t0010g0154a0001c0001t0010g0168others(4): Show | 7 | HG00544.hp2 HG00621.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.656+682C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7966883 | ||||||
chr19:7967025
|
CT | C | 5 | a0001c0001t0001g0031a0001c0001t0001g0110a0001c0001t0001g0122others(2): Show | 5 | HG00099.hp2 HG01069.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.656+539delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7967025 | ||||||
chr19:7967049
|
A | G | 1 | a0001c0005t0001g0113 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.656+516T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7967049 | ||||||
chr19:7967228
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.656+337A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7967228 | ||||||
chr19:7967373
|
A | C | 202 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(199): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.656+192T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7967373 | ||||||
chr19:7967548
|
G | A | 45 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0069others(42): Show | 50 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.656+17C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 5/5 | chr19 | 7967548 | ||||||
chr19:7967796
|
C | T | 56 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(53): Show | 65 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(62): Show |
splice_region_variant&intron_variant | LOW | c.431-6G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7967796 | ||||||
chr19:7968088
|
G | A | 18 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(15): Show | 24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.431-298C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968088 | ||||||
chr19:7968233
|
A | C | 1 | a0001c0002t0005g0016 | 2 | HG00733.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.431-443T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968233 | ||||||
chr19:7968349
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.431-559C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968349 | ||||||
chr19:7968464
|
A | G | 40 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(37): Show | 49 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.431-674T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968464 | ||||||
chr19:7968541
|
G | A | 2 | a0001c0002t0005g0212a0001c0002t0029g0213 | 2 | NA18980.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.431-751C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968541 | ||||||
chr19:7968616
|
C | A | 1 | a0001c0001t0006g0202 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.431-826G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968616 | ||||||
chr19:7968647
|
C | T | 15 | a0001c0002t0005g0016a0001c0002t0005g0017a0001c0002t0005g0018others(12): Show | 18 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.431-857G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968647 | ||||||
chr19:7968658
|
A | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048 | 3 | HG01891.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.431-868T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968658 | ||||||
chr19:7968674
|
A | G | 3 | a0001c0002t0004g0019a0001c0002t0004g0226a0001c0002t0004g0227 | 4 | HG00738.hp2 HG02300.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-884T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968674 | ||||||
chr19:7968690
|
A | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(230): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.431-900T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968690 | ||||||
chr19:7968805
|
G | A | 7 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-1015C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968805 | ||||||
chr19:7968849
|
C | T | 2 | a0001c0001t0015g0041a0001c0001t0015g0044 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.431-1059G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7968849 | ||||||
chr19:7969012
|
A | G | 40 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(37): Show | 49 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.431-1222T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969012 | ||||||
chr19:7969171
|
A | G | 4 | a0001c0002t0011g0024a0001c0002t0011g0025a0001c0002t0011g0026others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1381T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969171 | ||||||
chr19:7969623
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.431-1833G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969623 | ||||||
chr19:7969680
|
G | A | 1 | a0001c0001t0023g0177 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.431-1890C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969680 | ||||||
chr19:7969686
|
C | T | 4 | a0001c0001t0012g0234a0001c0001t0012g0235a0001c0001t0012g0236others(1): Show | 4 | HG03041.hp2 HG03098.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-1896G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969686 | ||||||
chr19:7969745
|
G | A | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.431-1955C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969745 | ||||||
chr19:7969980
|
A | G | 50 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0069others(47): Show | 55 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.431-2190T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969980 | ||||||
chr19:7969984
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431-2194A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7969984 | ||||||
chr19:7970012
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.431-2222C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970012 | ||||||
chr19:7970225
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.431-2435C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970225 | ||||||
chr19:7970258
|
C | T | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431-2468G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970258 | ||||||
chr19:7970397
|
C | T | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431-2607G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970397 | ||||||
chr19:7970527
|
C | T | 16 | a0001c0002t0005g0016a0001c0002t0005g0017a0001c0002t0005g0018others(13): Show | 19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.431-2737G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970527 | ||||||
chr19:7970614
|
C | T | 1 | a0001c0001t0038g0084 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.431-2824G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970614 | ||||||
chr19:7970664
|
G | C | 1 | a0001c0001t0001g0141 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.431-2874C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970664 | ||||||
chr19:7970738
|
T | TA | 5 | a0001c0002t0004g0238a0001c0002t0009g0021a0001c0002t0009g0230others(2): Show | 6 | HG00280.hp2 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-2949dupT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970738 | ||||||
chr19:7970820
|
C | T | 4 | a0001c0002t0011g0024a0001c0002t0011g0025a0001c0002t0011g0026others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2905G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970820 | ||||||
chr19:7970911
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.430+2814T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970911 | ||||||
chr19:7970957
|
T | C | 1 | a0001c0001t0030g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.430+2768A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7970957 | ||||||
chr19:7971162
|
T | A | 1 | a0001c0001t0014g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.430+2563A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7971162 | ||||||
chr19:7971227
|
T | G | 1 | a0001c0001t0006g0161 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.430+2498A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7971227 | ||||||
chr19:7971697
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.430+2028G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7971697 | ||||||
chr19:7971903
|
C | T | 16 | a0001c0002t0005g0016a0001c0002t0005g0017a0001c0002t0005g0018others(13): Show | 19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.430+1822G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7971903 | ||||||
chr19:7971904
|
A | G | 16 | a0001c0002t0005g0016a0001c0002t0005g0017a0001c0002t0005g0018others(13): Show | 19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.430+1821T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7971904 | ||||||
chr19:7972125
|
C | T | 16 | a0001c0002t0005g0016a0001c0002t0005g0017a0001c0002t0005g0018others(13): Show | 19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.430+1600G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972125 | ||||||
chr19:7972156
|
T | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(156): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.430+1569A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972156 | ||||||
chr19:7972160
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430+1565A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972160 | ||||||
chr19:7972352
|
C | T | 4 | a0001c0001t0012g0234a0001c0001t0012g0235a0001c0001t0012g0236others(1): Show | 4 | HG03041.hp2 HG03098.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+1373G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972352 | ||||||
chr19:7972617
|
CTTTTT | C | 11 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.430+1103_430+1107d others(7): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972617 | ||||||
chr19:7972633
|
CT | C | 41 | a0001c0001t0003g0077a0001c0002t0004g0004a0001c0002t0004g0019others(38): Show | 50 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.430+1091delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972633 | ||||||
chr19:7972689
|
C | T | 15 | a0001c0002t0005g0016a0001c0002t0005g0017a0001c0002t0005g0018others(12): Show | 18 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.430+1036G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972689 | ||||||
chr19:7972696
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.430+1029C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972696 | ||||||
chr19:7972708
|
C | G | 1 | a0001c0001t0001g0031 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.430+1017G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972708 | ||||||
chr19:7972800
|
C | CT | 72 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(69): Show | 89 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.430+924dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | ||||||
chr19:7972800
|
C | CTT | 48 | a0001c0001t0001g0013a0001c0001t0001g0049a0001c0001t0001g0074others(45): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.430+923_430+924dup others(2): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | ||||||
chr19:7972800
|
C | CTTT | 18 | a0001c0001t0001g0089a0001c0001t0001g0144a0001c0001t0002g0150others(15): Show | 18 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.430+922_430+924dup others(3): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | ||||||
chr19:7972800
|
C | T | 1 | a0001c0002t0004g0225 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.430+925G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | ||||||
chr19:7972800
|
CTT | C | 23 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0001g0063others(20): Show | 27 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.430+923_430+924del others(2): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | ||||||
chr19:7972800
|
CTTT | C | 23 | a0001c0001t0001g0007a0001c0001t0001g0036a0001c0001t0001g0050others(20): Show | 24 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.430+922_430+924del others(3): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | ||||||
chr19:7972800
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0012g0234a0001c0001t0025g0038 | 2 | HG03098.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.430+915_430+924del others(10): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | ||||||
chr19:7972800
|
CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0007g0108a0001c0001t0007g0155a0001c0001t0007g0156others(4): Show | 7 | HG00609.hp1 HG01261.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+914_430+924del others(11): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972800 | ||||||
chr19:7972898
|
G | A | 1 | a0001c0002t0005g0214 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.430+827C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972898 | ||||||
chr19:7972915
|
C | G | 3 | a0001c0002t0004g0223a0001c0002t0004g0224a0001c0002t0004g0225 | 3 | HG00733.hp1 HG01243.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.430+810G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972915 | ||||||
chr19:7972916
|
G | A | 1 | a0001c0002t0009g0021 | 2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.430+809C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7972916 | ||||||
chr19:7973025
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.430+700G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7973025 | ||||||
chr19:7973212
|
G | A | 1 | a0001c0002t0004g0004 | 4 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+513C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7973212 | ||||||
chr19:7973229
|
C | CT | 6 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0012g0234others(3): Show | 6 | HG02055.hp2 HG02572.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+495dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7973229 | ||||||
chr19:7973229
|
CTT | C | 12 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(9): Show | 17 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.430+494_430+495del others(2): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7973229 | ||||||
chr19:7973510
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.430+215C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 4/5 | chr19 | 7973510 | ||||||
chr19:7973930
|
T | C | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.277-52A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7973930 | ||||||
chr19:7974206
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0138 | 2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.277-328C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974206 | ||||||
chr19:7974207
|
G | A | 16 | a0001c0002t0005g0016a0001c0002t0005g0017a0001c0002t0005g0018others(13): Show | 19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-329C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974207 | ||||||
chr19:7974211
|
C | A | 4 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0002g0187others(1): Show | 4 | HG00639.hp1 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-333G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974211 | ||||||
chr19:7974212
|
AG | A | 20 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(17): Show | 26 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.277-335delC | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974212 | ||||||
chr19:7974283
|
G | A | 18 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(15): Show | 24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.277-405C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974283 | ||||||
chr19:7974800
|
G | A | 4 | a0001c0002t0011g0024a0001c0002t0011g0025a0001c0002t0011g0026others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-922C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974800 | ||||||
chr19:7974812
|
C | T | 2 | a0001c0002t0016g0220a0001c0002t0016g0233 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.277-934G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974812 | ||||||
chr19:7974813
|
G | A | 2 | a0001c0001t0002g0180a0001c0001t0002g0190 | 2 | NA18970.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.277-935C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974813 | ||||||
chr19:7974842
|
C | T | 4 | a0001c0001t0001g0042a0001c0001t0013g0037a0001c0001t0013g0043others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-964G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974842 | ||||||
chr19:7974843
|
G | A | 2 | a0001c0002t0016g0220a0001c0002t0016g0233 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.277-965C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7974843 | ||||||
chr19:7975038
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.277-1160C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975038 | ||||||
chr19:7975199
|
C | A | 1 | a0001c0001t0008g0137 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.277-1321G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975199 | ||||||
chr19:7975213
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02886.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.277-1335C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975213 | ||||||
chr19:7975222
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.277-1344G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975222 | ||||||
chr19:7975399
|
C | G | 1 | a0001c0001t0012g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.277-1521G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975399 | ||||||
chr19:7975529
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.277-1651C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975529 | ||||||
chr19:7975615
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0122 | 3 | HG00099.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.277-1737A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7975615 | ||||||
chr19:7976051
|
T | C | 105 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(102): Show | 119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.277-2173A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976051 | ||||||
chr19:7976294
|
C | T | 1 | a0001c0002t0005g0207 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.277-2416G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976294 | ||||||
chr19:7976334
|
G | A | 2 | a0001c0002t0016g0220a0001c0002t0016g0233 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.277-2456C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976334 | ||||||
chr19:7976489
|
T | G | 43 | a0001c0001t0001g0141a0001c0001t0001g0210a0001c0001t0001g0211others(40): Show | 52 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.277-2611A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976489 | ||||||
chr19:7976499
|
G | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(14): Show | 20 | HG00544.hp1 HG00558.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.277-2621C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976499 | ||||||
chr19:7976511
|
C | T | 2 | a0001c0002t0016g0220a0001c0002t0016g0233 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.277-2633G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976511 | ||||||
chr19:7976517
|
G | A | 1 | a0001c0002t0009g0231 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.277-2639C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976517 | ||||||
chr19:7976534
|
G | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(156): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.277-2656C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976534 | ||||||
chr19:7976637
|
T | C | 4 | a0001c0002t0011g0024a0001c0002t0011g0025a0001c0002t0011g0026others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-2759A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976637 | ||||||
chr19:7976650
|
T | G | 7 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.277-2772A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976650 | ||||||
chr19:7976816
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0035others(3): Show | 7 | HG00544.hp1 HG00558.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.277-2938C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976816 | ||||||
chr19:7976840
|
A | AT | 25 | a0001c0001t0001g0094a0001c0001t0001g0141a0001c0001t0001g0210others(22): Show | 29 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.277-2963dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976840 | ||||||
chr19:7976840
|
AT | A | 8 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0064others(5): Show | 8 | HG01168.hp2 HG01257.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-2963delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976840 | ||||||
chr19:7976860
|
GT | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0071others(11): Show | 16 | HG01884.hp1 HG02559.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.277-2983delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7976860 | ||||||
chr19:7977064
|
C | T | 4 | a0001c0002t0011g0024a0001c0002t0011g0025a0001c0002t0011g0026others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-3186G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977064 | ||||||
chr19:7977093
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0081others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.277-3215C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977093 | ||||||
chr19:7977139
|
C | T | 1 | a0001c0002t0028g0205 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.277-3261G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977139 | ||||||
chr19:7977156
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.277-3278C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977156 | ||||||
chr19:7977527
|
CAG | C | 11 | a0001c0001t0006g0139a0001c0001t0006g0145a0001c0001t0006g0159others(8): Show | 11 | HG01261.hp2 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+3554_276+3555d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977527 | ||||||
chr19:7977547
|
A | G | 102 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(99): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.276+3536T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977547 | ||||||
chr19:7977563
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.276+3520A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977563 | ||||||
chr19:7977886
|
G | T | 20 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(17): Show | 26 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.276+3197C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7977886 | ||||||
chr19:7978029
|
C | A | 1 | a0001c0001t0017g0009 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.276+3054G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978029 | ||||||
chr19:7978103
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.276+2980G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978103 | ||||||
chr19:7978154
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.276+2929G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978154 | ||||||
chr19:7978161
|
C | T | 21 | a0001c0001t0025g0038a0001c0002t0005g0016a0001c0002t0005g0017others(18): Show | 24 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.276+2922G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978161 | ||||||
chr19:7978238
|
T | C | 1 | a0001c0001t0002g0183 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.276+2845A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978238 | ||||||
chr19:7978293
|
A | G | 5 | a0001c0001t0025g0038a0001c0002t0011g0024a0001c0002t0011g0025others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.276+2790T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978293 | ||||||
chr19:7978341
|
G | A | 1 | a0001c0001t0040g0179 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.276+2742C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978341 | ||||||
chr19:7978355
|
G | A | 1 | a0001c0001t0018g0119 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.276+2728C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978355 | ||||||
chr19:7978357
|
G | A | 16 | a0001c0002t0005g0016a0001c0002t0005g0017a0001c0002t0005g0018others(13): Show | 19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+2726C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978357 | ||||||
chr19:7978672
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.276+2411T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978672 | ||||||
chr19:7978693
|
G | C | 25 | a0001c0001t0025g0038a0001c0002t0004g0004a0001c0002t0004g0019others(22): Show | 31 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.276+2390C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978693 | ||||||
chr19:7978721
|
A | G | 2 | a0001c0001t0002g0163a0001c0001t0002g0175 | 2 | NA18944.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.276+2362T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978721 | ||||||
chr19:7978852
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.276+2231A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978852 | ||||||
chr19:7978909
|
T | G | 1 | a0001c0002t0005g0216 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.276+2174A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7978909 | ||||||
chr19:7979092
|
C | A | 4 | a0001c0002t0009g0021a0001c0002t0009g0230a0001c0002t0009g0231others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.276+1991G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979092 | ||||||
chr19:7979241
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.276+1842C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979241 | ||||||
chr19:7979264
|
G | A | 1 | a0001c0001t0019g0239 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.276+1819C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979264 | ||||||
chr19:7979339
|
G | A | 2 | a0001c0002t0005g0206a0001c0002t0028g0205 | 2 | HG01346.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.276+1744C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979339 | ||||||
chr19:7979555
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 9 | HG01884.hp1 HG02559.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.276+1528C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979555 | ||||||
chr19:7979616
|
G | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.276+1467C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979616 | ||||||
chr19:7979627
|
C | T | 2 | a0001c0002t0016g0220a0001c0002t0016g0233 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.276+1456G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979627 | ||||||
chr19:7979673
|
C | T | 14 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(11): Show | 19 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.276+1410G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979673 | ||||||
chr19:7979726
|
C | T | 18 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(15): Show | 24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.276+1357G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979726 | ||||||
chr19:7979831
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.276+1252A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979831 | ||||||
chr19:7979855
|
G | C | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.276+1228C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979855 | ||||||
chr19:7979923
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.276+1160T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7979923 | ||||||
chr19:7980071
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.276+1012A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980071 | ||||||
chr19:7980163
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.276+920G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980163 | ||||||
chr19:7980269
|
G | A | 16 | a0001c0002t0005g0016a0001c0002t0005g0017a0001c0002t0005g0018others(13): Show | 19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.276+814C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980269 | ||||||
chr19:7980397
|
C | T | 1 | a0001c0002t0016g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.276+686G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980397 | ||||||
chr19:7980508
|
C | T | 1 | a0001c0001t0031g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.276+575G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980508 | ||||||
chr19:7980524
|
ACTATGGC others(1): Show |
A | 3 | a0001c0001t0012g0234a0001c0001t0012g0235a0001c0001t0012g0236 | 3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.276+551_276+558del others(8): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980524 | ||||||
chr19:7980653
|
G | C | 1 | a0001c0001t0001g0065 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.276+430C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980653 | ||||||
chr19:7980665
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.276+418C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980665 | ||||||
chr19:7980978
|
G | A | 17 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(14): Show | 22 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.276+105C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7980978 | ||||||
chr19:7981060
|
C | T | 3 | a0001c0001t0007g0028a0001c0001t0007g0174a0001c0001t0007g0197 | 3 | NA18953.hp1 NA18966.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.276+23G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 3/5 | chr19 | 7981060 | ||||||
chr19:7981314
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.173-128G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981314 | ||||||
chr19:7981355
|
C | CT | 5 | a0001c0001t0002g0167a0001c0001t0002g0180a0001c0001t0010g0154others(2): Show | 5 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.173-170dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981355 | ||||||
chr19:7981355
|
CT | C | 27 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0110others(24): Show | 32 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.173-170delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981355 | ||||||
chr19:7981355
|
CTT | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0005g0016others(15): Show | 21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.173-171_173-170del others(2): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981355 | ||||||
chr19:7981410
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0033g0121 | 2 | HG01168.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.173-224A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981410 | ||||||
chr19:7981415
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.173-229G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981415 | ||||||
chr19:7981561
|
T | C | 1 | a0001c0001t0002g0166 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.173-375A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981561 | ||||||
chr19:7981622
|
C | T | 1 | a0001c0002t0005g0207 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.173-436G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981622 | ||||||
chr19:7981673
|
G | A | 1 | a0001c0001t0002g0173 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.173-487C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981673 | ||||||
chr19:7981731
|
T | A | 215 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(212): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.173-545A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981731 | ||||||
chr19:7981795
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.173-609C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981795 | ||||||
chr19:7981835
|
GGACA | G | 11 | a0001c0001t0001g0210a0001c0002t0005g0016a0001c0002t0005g0017others(8): Show | 13 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.173-653_173-650del others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7981835 | ||||||
chr19:7982364
|
C | T | 20 | a0001c0001t0001g0096a0001c0001t0001g0138a0001c0001t0001g0210others(17): Show | 23 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.173-1178G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982364 | ||||||
chr19:7982465
|
G | A | 2 | a0001c0001t0002g0180a0001c0001t0002g0190 | 2 | NA18970.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.173-1279C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982465 | ||||||
chr19:7982787
|
C | T | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0005g0016others(15): Show | 21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.173-1601G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982787 | ||||||
chr19:7982812
|
G | A | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0009g0231 | 3 | HG02257.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.173-1626C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982812 | ||||||
chr19:7982836
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.173-1650C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982836 | ||||||
chr19:7982848
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.173-1662G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982848 | ||||||
chr19:7982892
|
C | T | 2 | a0001c0001t0015g0041a0001c0001t0015g0044 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.173-1706G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982892 | ||||||
chr19:7982902
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-1716C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7982902 | ||||||
chr19:7983040
|
G | A | 49 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0069others(46): Show | 54 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.173-1854C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983040 | ||||||
chr19:7983155
|
C | T | 1 | a0001c0001t0034g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.173-1969G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983155 | ||||||
chr19:7983197
|
T | G | 2 | a0001c0001t0002g0181a0001c0001t0002g0191 | 2 | HG01975.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.173-2011A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983197 | ||||||
chr19:7983258
|
C | T | 1 | a0001c0001t0006g0199 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.173-2072G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983258 | ||||||
chr19:7983478
|
C | A | 2 | a0001c0001t0015g0041a0001c0001t0015g0044 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.173-2292G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983478 | ||||||
chr19:7983489
|
G | C | 18 | a0001c0001t0001g0141a0001c0001t0001g0210a0001c0001t0001g0211others(15): Show | 21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.173-2303C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983489 | ||||||
chr19:7983995
|
C | T | 5 | a0001c0001t0025g0038a0001c0002t0011g0024a0001c0002t0011g0025others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-2809G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7983995 | ||||||
chr19:7984013
|
T | C | 5 | a0001c0001t0025g0038a0001c0002t0011g0024a0001c0002t0011g0025others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-2827A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984013 | ||||||
chr19:7984196
|
C | T | 1 | a0001c0002t0011g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.173-3010G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984196 | ||||||
chr19:7984254
|
C | T | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.173-3068G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984254 | ||||||
chr19:7984268
|
A | G | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0005g0016others(15): Show | 21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.173-3082T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984268 | ||||||
chr19:7984277
|
A | G | 92 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0002g0003others(89): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.173-3091T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984277 | ||||||
chr19:7984480
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.173-3294C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984480 | ||||||
chr19:7984558
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.173-3372C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984558 | ||||||
chr19:7984699
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0032others(24): Show | 34 | HG00099.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.173-3513G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984699 | ||||||
chr19:7984968
|
C | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0081others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.173-3782G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7984968 | ||||||
chr19:7985208
|
C | T | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0005g0016others(15): Show | 21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.173-4022G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985208 | ||||||
chr19:7985210
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.173-4024C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985210 | ||||||
chr19:7985212
|
G | A | 3 | a0001c0001t0012g0234a0001c0001t0012g0235a0001c0001t0012g0236 | 3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.173-4026C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985212 | ||||||
chr19:7985324
|
C | T | 7 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0079others(4): Show | 7 | NA18941.hp2 NA18952.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.173-4138G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985324 | ||||||
chr19:7985427
|
C | A | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.173-4241G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985427 | ||||||
chr19:7985597
|
G | C | 1 | a0001c0001t0013g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.173-4411C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985597 | ||||||
chr19:7985635
|
G | A | 2 | a0001c0001t0008g0079a0001c0001t0008g0106 | 2 | NA18953.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.173-4449C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985635 | ||||||
chr19:7985814
|
C | T | 1 | a0001c0001t0007g0028 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.173-4628G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985814 | ||||||
chr19:7985838
|
G | A | 1 | a0001c0001t0014g0014 | 2 | HG02723.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.173-4652C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985838 | ||||||
chr19:7985935
|
T | C | 1 | a0001c0001t0002g0182 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.173-4749A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7985935 | ||||||
chr19:7986203
|
G | A | 2 | a0001c0002t0016g0220a0001c0002t0016g0233 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.173-5017C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986203 | ||||||
chr19:7986370
|
G | C | 1 | a0001c0001t0006g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.173-5184C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986370 | ||||||
chr19:7986417
|
T | G | 15 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0071others(12): Show | 17 | HG01884.hp1 HG02559.hp2 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.172+5227A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986417 | ||||||
chr19:7986477
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.172+5167C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986477 | ||||||
chr19:7986525
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.172+5119A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986525 | ||||||
chr19:7986559
|
C | T | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.172+5085G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986559 | ||||||
chr19:7986570
|
G | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0071others(13): Show | 18 | HG01884.hp1 HG02559.hp2 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.172+5074C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986570 | ||||||
chr19:7986574
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.172+5070C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986574 | ||||||
chr19:7986582
|
G | A | 2 | a0001c0002t0016g0220a0001c0002t0016g0233 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.172+5062C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986582 | ||||||
chr19:7986590
|
C | T | 3 | a0001c0001t0012g0234a0001c0001t0012g0235a0001c0001t0012g0236 | 3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.172+5054G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986590 | ||||||
chr19:7986762
|
G | A | 18 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(15): Show | 24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.172+4882C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986762 | ||||||
chr19:7986983
|
C | A | 1 | a0001c0002t0004g0227 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.172+4661G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7986983 | ||||||
chr19:7987035
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.172+4609T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987035 | ||||||
chr19:7987116
|
C | CG | 73 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0054others(70): Show | 76 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.172+4527dupC | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987116 | ||||||
chr19:7987116
|
C | CGG | 36 | a0001c0001t0001g0005a0001c0001t0001g0042a0001c0001t0001g0046others(33): Show | 41 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.172+4526_172+4527d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987116 | ||||||
chr19:7987116
|
CG | C | 41 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0004g0004others(38): Show | 50 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.172+4527delC | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987116 | ||||||
chr19:7987120
|
G | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0146a0001c0001t0037g0051 | 3 | NA18966.hp1 NA18977.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.172+4524C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987120 | ||||||
chr19:7987137
|
C | T | 1 | a0001c0001t0003g0072 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.172+4507G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987137 | ||||||
chr19:7987171
|
C | T | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.172+4473G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987171 | ||||||
chr19:7987283
|
T | A | 1 | a0001c0001t0003g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.172+4361A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987283 | ||||||
chr19:7987425
|
A | G | 42 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0004g0004others(39): Show | 51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.172+4219T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987425 | ||||||
chr19:7987762
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(48): Show | 60 | HG00099.hp2 HG01069.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.172+3882G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987762 | ||||||
chr19:7987868
|
C | T | 2 | a0001c0002t0004g0221a0001c0002t0004g0222 | 2 | HG01256.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.172+3776G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987868 | ||||||
chr19:7987890
|
A | G | 4 | a0001c0002t0011g0024a0001c0002t0011g0025a0001c0002t0011g0026others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+3754T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987890 | ||||||
chr19:7987977
|
C | T | 3 | a0001c0001t0012g0234a0001c0001t0012g0235a0001c0001t0012g0236 | 3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.172+3667G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7987977 | ||||||
chr19:7988299
|
C | G | 1 | a0001c0002t0016g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.172+3345G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988299 | ||||||
chr19:7988431
|
A | T | 2 | a0001c0002t0005g0206a0001c0002t0028g0205 | 2 | HG01346.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.172+3213T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988431 | ||||||
chr19:7988479
|
A | G | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0005g0016others(15): Show | 21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.172+3165T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988479 | ||||||
chr19:7988537
|
AGAGGATG others(10): Show |
A | 8 | a0001c0002t0005g0018a0001c0002t0005g0212a0001c0002t0005g0214others(5): Show | 9 | NA18952.hp1 NA18959.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.172+3090_172+3106d others(19): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988537 | ||||||
chr19:7988645
|
G | T | 2 | a0001c0001t0001g0089a0001c0004t0001g0107 | 2 | HG00558.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.172+2999C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988645 | ||||||
chr19:7988877
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172+2767C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988877 | ||||||
chr19:7988897
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.172+2747G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988897 | ||||||
chr19:7988963
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.172+2681G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7988963 | ||||||
chr19:7989056
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.172+2588G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989056 | ||||||
chr19:7989226
|
G | A | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.172+2418C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989226 | ||||||
chr19:7989234
|
G | A | 3 | a0001c0002t0009g0021a0001c0002t0009g0230a0001c0002t0009g0232 | 4 | HG01891.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+2410C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989234 | ||||||
chr19:7989463
|
C | A | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.172+2181G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989463 | ||||||
chr19:7989551
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.172+2093T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989551 | ||||||
chr19:7989956
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0032others(22): Show | 31 | HG00099.hp2 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.172+1688C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7989956 | ||||||
chr19:7990098
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.172+1546A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7990098 | ||||||
chr19:7990338
|
G | GTT | 18 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(15): Show | 24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.172+1304_172+1305d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7990338 | ||||||
chr19:7990404
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.172+1240A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7990404 | ||||||
chr19:7990967
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.172+677C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7990967 | ||||||
chr19:7991174
|
G | A | 1 | a0001c0002t0005g0215 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.172+470C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7991174 | ||||||
chr19:7991225
|
G | A | 2 | a0001c0001t0002g0184a0001c0001t0002g0185 | 2 | HG01074.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.172+419C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7991225 | ||||||
chr19:7991264
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.172+380G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 2/5 | chr19 | 7991264 | ||||||
chr19:7991873
|
T | C | 3 | a0001c0002t0005g0214a0001c0002t0005g0215a0001c0002t0005g0216 | 3 | NA18952.hp1 NA18962.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-16-42A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7991873 | ||||||
chr19:7991898
|
T | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(1): Show | 4 | HG01884.hp1 HG02559.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-67A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7991898 | ||||||
chr19:7991932
|
C | CT | 100 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(97): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.-16-102dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7991932 | ||||||
chr19:7992183
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-16-352G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992183 | ||||||
chr19:7992221
|
A | G | 42 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0004g0004others(39): Show | 51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16-390T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992221 | ||||||
chr19:7992589
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-16-758C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992589 | ||||||
chr19:7992740
|
G | A | 4 | a0001c0001t0006g0159a0001c0001t0006g0160a0001c0001t0006g0161others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-909C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992740 | ||||||
chr19:7992829
|
C | T | 42 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0004g0004others(39): Show | 51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16-998G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992829 | ||||||
chr19:7992889
|
C | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-16-1058G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992889 | ||||||
chr19:7992915
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-16-1084C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992915 | ||||||
chr19:7992936
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0056 | 3 | HG03239.hp1 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-16-1105G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992936 | ||||||
chr19:7992937
|
G | A | 24 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(21): Show | 30 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-16-1106C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7992937 | ||||||
chr19:7993636
|
A | T | 1 | a0001c0001t0015g0041 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-16-1805T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7993636 | ||||||
chr19:7993794
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-16-1963C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7993794 | ||||||
chr19:7993801
|
C | T | 2 | a0001c0002t0016g0220a0001c0002t0016g0233 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-16-1970G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7993801 | ||||||
chr19:7993855
|
C | T | 1 | a0001c0001t0014g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-16-2024G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7993855 | ||||||
chr19:7993971
|
G | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(236): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-16-2140C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7993971 | ||||||
chr19:7993997
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-16-2166G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7993997 | ||||||
chr19:7994237
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-16-2406C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7994237 | ||||||
chr19:7994544
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-16-2713C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7994544 | ||||||
chr19:7994771
|
G | A | 1 | a0001c0001t0008g0137 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-16-2940C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7994771 | ||||||
chr19:7994907
|
T | G | 4 | a0001c0002t0011g0024a0001c0002t0011g0025a0001c0002t0011g0026others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-3076A>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7994907 | ||||||
chr19:7994915
|
C | T | 1 | a0001c0001t0002g0166 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-16-3084G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7994915 | ||||||
chr19:7994987
|
AC | A | 12 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(9): Show | 12 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-16-3157delG | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7994987 | ||||||
chr19:7995012
|
A | T | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-16-3181T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995012 | ||||||
chr19:7995462
|
C | T | 42 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0004g0004others(39): Show | 51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16-3631G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995462 | ||||||
chr19:7995536
|
T | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(212): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-16-3705A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995536 | ||||||
chr19:7995562
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-16-3731A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995562 | ||||||
chr19:7995662
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-16-3831G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995662 | ||||||
chr19:7995690
|
A | C | 2 | a0001c0002t0016g0220a0001c0002t0016g0233 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-16-3859T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995690 | ||||||
chr19:7995783
|
T | TA | 11 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0094others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-16-3953dupT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995783 | ||||||
chr19:7995783
|
TA | T | 43 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0054others(40): Show | 52 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.-16-3953delT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995783 | ||||||
chr19:7995818
|
C | T | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0005g0016others(15): Show | 21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-16-3987G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995818 | ||||||
chr19:7995916
|
C | CT | 16 | a0001c0001t0001g0030a0001c0001t0010g0154a0001c0002t0004g0004others(13): Show | 21 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-16-4086dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7995916 | ||||||
chr19:7996003
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-16-4172G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996003 | ||||||
chr19:7996126
|
T | C | 1 | a0001c0001t0015g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-16-4295A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996126 | ||||||
chr19:7996156
|
G | A | 1 | a0001c0001t0030g0099 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-16-4325C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996156 | ||||||
chr19:7996183
|
CT | C | 21 | a0001c0001t0001g0048a0001c0001t0001g0210a0001c0001t0001g0211others(18): Show | 25 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-16-4353delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996183 | ||||||
chr19:7996250
|
C | T | 3 | a0001c0001t0012g0234a0001c0001t0012g0235a0001c0001t0012g0236 | 3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-16-4419G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996250 | ||||||
chr19:7996374
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-16-4543C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996374 | ||||||
chr19:7996468
|
C | T | 2 | a0001c0001t0018g0039a0001c0001t0036g0040 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-16-4637G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996468 | ||||||
chr19:7996469
|
G | A | 24 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(21): Show | 30 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-16-4638C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996469 | ||||||
chr19:7996485
|
G | A | 1 | a0001c0002t0004g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-16-4654C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996485 | ||||||
chr19:7996671
|
G | A | 1 | a0001c0001t0008g0100 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-16-4840C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996671 | ||||||
chr19:7996694
|
T | C | 1 | a0001c0001t0014g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-16-4863A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996694 | ||||||
chr19:7996785
|
A | C | 42 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0004g0004others(39): Show | 51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16-4954T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996785 | ||||||
chr19:7996792
|
G | A | 3 | a0001c0001t0010g0154a0001c0001t0010g0193a0001c0001t0010g0194 | 3 | HG00544.hp2 HG00621.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-16-4961C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996792 | ||||||
chr19:7996854
|
A | C | 1 | a0001c0002t0027g0204 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-16-5023T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996854 | ||||||
chr19:7996969
|
G | A | 20 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(17): Show | 26 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16-5138C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7996969 | ||||||
chr19:7997031
|
C | G | 1 | a0001c0002t0009g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-16-5200G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997031 | ||||||
chr19:7997050
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-16-5219C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997050 | ||||||
chr19:7997120
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-16-5289G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997120 | ||||||
chr19:7997457
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-16-5626C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997457 | ||||||
chr19:7997468
|
C | T | 1 | a0001c0001t0037g0051 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-16-5637G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997468 | ||||||
chr19:7997672
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-16-5841C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997672 | ||||||
chr19:7997725
|
A | G | 1 | a0001c0001t0025g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-16-5894T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997725 | ||||||
chr19:7997881
|
G | A | 1 | a0001c0002t0016g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-16-6050C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7997881 | ||||||
chr19:7998177
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-16-6346T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998177 | ||||||
chr19:7998264
|
A | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG01884.hp1 HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-16-6433T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998264 | ||||||
chr19:7998305
|
G | A | 7 | a0001c0001t0006g0139a0001c0001t0006g0145a0001c0001t0006g0159others(4): Show | 7 | HG01261.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16-6474C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998305 | ||||||
chr19:7998308
|
G | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG01884.hp1 HG02559.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-16-6477C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998308 | ||||||
chr19:7998355
|
A | C | 42 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0004g0004others(39): Show | 51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16-6524T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998355 | ||||||
chr19:7998391
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-16-6560G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998391 | ||||||
chr19:7998413
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-16-6582C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998413 | ||||||
chr19:7998733
|
TTGGCCTC others(37): Show |
T | 1 | a0001c0002t0016g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-17+6718_-17+6761d others(46): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998733 | ||||||
chr19:7998796
|
C | T | 42 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0004g0004others(39): Show | 51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-17+6699G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998796 | ||||||
chr19:7998966
|
A | G | 1 | a0001c0001t0022g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-17+6529T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7998966 | ||||||
chr19:7999099
|
G | A | 1 | a0001c0001t0034g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-17+6396C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999099 | ||||||
chr19:7999190
|
T | C | 1 | a0001c0001t0002g0192 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-17+6305A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999190 | ||||||
chr19:7999386
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-17+6109T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999386 | ||||||
chr19:7999494
|
G | C | 2 | a0001c0001t0010g0193a0001c0001t0010g0194 | 2 | HG00544.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.-17+6001C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999494 | ||||||
chr19:7999740
|
G | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0007g0195others(16): Show | 22 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.-17+5755C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999740 | ||||||
chr19:7999978
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0032others(24): Show | 34 | HG00099.hp2 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-17+5517G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 7999978 | ||||||
chr19:8000054
|
A | G | 42 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0004g0004others(39): Show | 51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-17+5441T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000054 | ||||||
chr19:8000106
|
G | A | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0005g0016others(15): Show | 21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17+5389C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000106 | ||||||
chr19:8000301
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-17+5194A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000301 | ||||||
chr19:8000310
|
T | A | 3 | a0001c0002t0004g0228a0001c0002t0004g0229a0001c0002t0004g0237 | 3 | HG02602.hp1 HG02698.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-17+5185A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000310 | ||||||
chr19:8000345
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-17+5150C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000345 | ||||||
chr19:8000860
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-17+4635C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8000860 | ||||||
chr19:8001063
|
C | T | 6 | a0001c0001t0006g0145a0001c0001t0006g0159a0001c0001t0006g0160others(3): Show | 6 | HG01261.hp2 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+4432G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001063 | ||||||
chr19:8001113
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-17+4382C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001113 | ||||||
chr19:8001633
|
A | C | 20 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(17): Show | 26 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17+3862T>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001633 | ||||||
chr19:8001634
|
A | AT | 17 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0005g0016others(14): Show | 20 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-17+3860dupA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001634 | ||||||
chr19:8001634
|
A | T | 2 | a0001c0001t0001g0033a0001c0001t0002g0164 | 2 | HG03491.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-17+3861T>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001634 | ||||||
chr19:8001634
|
AT | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0144a0001c0001t0003g0105others(2): Show | 5 | HG00642.hp2 NA18942.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+3860delA | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001634 | ||||||
chr19:8001648
|
T | A | 2 | a0001c0001t0002g0196a0001c0001t0007g0197 | 2 | HG00639.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-17+3847A>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001648 | ||||||
chr19:8001648
|
T | TA | 49 | a0001c0001t0001g0152a0001c0001t0001g0188a0001c0001t0002g0003others(46): Show | 55 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.-17+3846dupT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001648 | ||||||
chr19:8001760
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17+3735G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001760 | ||||||
chr19:8001791
|
G | C | 1 | a0001c0001t0012g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-17+3704C>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8001791 | ||||||
chr19:8002066
|
C | G | 3 | a0001c0001t0007g0108a0001c0001t0007g0155a0001c0001t0007g0156 | 3 | HG01261.hp1 HG01928.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-17+3429G>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8002066 | ||||||
chr19:8002241
|
C | T | 13 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(10): Show | 13 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17+3254G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8002241 | ||||||
chr19:8003027
|
C | T | 1 | a0001c0001t0013g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-17+2468G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003027 | ||||||
chr19:8003113
|
C | T | 4 | a0001c0002t0011g0024a0001c0002t0011g0025a0001c0002t0011g0026others(1): Show | 4 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17+2382G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003113 | ||||||
chr19:8003355
|
C | CA | 97 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0013others(94): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-17+2139dupT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003355 | ||||||
chr19:8003355
|
CA | C | 28 | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0034others(25): Show | 34 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.-17+2139delT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003355 | ||||||
chr19:8003355
|
CAA | C | 21 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0004g0221others(18): Show | 24 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.-17+2138_-17+2139d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003355 | ||||||
chr19:8003371
|
A | G | 4 | a0001c0002t0009g0021a0001c0002t0009g0230a0001c0002t0009g0231others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+2124T>C | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003371 | ||||||
chr19:8003381
|
GA | G | 19 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(16): Show | 24 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.-17+2113delT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003381 | ||||||
chr19:8003381
|
GAA | G | 16 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0005g0016others(13): Show | 19 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17+2112_-17+2113d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003381 | ||||||
chr19:8003691
|
C | CA | 64 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0152others(61): Show | 70 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.-17+1803dupT | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003691 | ||||||
chr19:8003691
|
C | CAA | 7 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201others(4): Show | 7 | HG01261.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17+1802_-17+1803d others(4): Show |
ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003691 | ||||||
chr19:8003819
|
G | A | 42 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0004g0004others(39): Show | 51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-17+1676C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8003819 | ||||||
chr19:8004062
|
G | T | 18 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(15): Show | 24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-17+1433C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004062 | ||||||
chr19:8004066
|
C | T | 18 | a0001c0002t0004g0004a0001c0002t0004g0019a0001c0002t0004g0020others(15): Show | 24 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.-17+1429G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004066 | ||||||
chr19:8004435
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-17+1060C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004435 | ||||||
chr19:8004485
|
T | C | 3 | a0001c0001t0012g0234a0001c0001t0012g0235a0001c0001t0012g0236 | 3 | HG03041.hp2 NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-17+1010A>G | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004485 | ||||||
chr19:8004565
|
C | A | 1 | a0001c0002t0004g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-17+930G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004565 | ||||||
chr19:8004643
|
G | T | 1 | a0001c0001t0007g0028 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-17+852C>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004643 | ||||||
chr19:8004806
|
C | T | 5 | a0001c0002t0011g0024a0001c0002t0011g0025a0001c0002t0011g0026others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17+689G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004806 | ||||||
chr19:8004807
|
C | T | 2 | a0001c0001t0008g0022a0001c0001t0008g0023 | 2 | NA18970.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-17+688G>A | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8004807 | ||||||
chr19:8005265
|
C | A | 1 | a0001c0002t0004g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-17+230G>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8005265 | ||||||
chr19:8005285
|
G | A | 23 | a0001c0001t0012g0234a0001c0001t0012g0235a0001c0001t0012g0236others(20): Show | 29 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17+210C>T | ELAVL1 | ENSG00000066044.15 | transcript | ENST00000407627.7 | protein_coding | 1/5 | chr19 | 8005285 |