geneid | 22936 |
---|---|
ensemblid | ENSG00000118985.16 |
hgncid | 17064 |
symbol | ELL2 |
name | elongation factor for RNA polymerase II 2 |
refseq_nuc | NM_012081.6 |
refseq_prot | NP_036213.2 |
ensembl_nuc | ENST00000237853.9 |
ensembl_prot | ENSP00000237853.4 |
mane_status | MANE Select |
chr | chr5 |
start | 95885098 |
end | 95961851 |
strand | - |
ver | v1.2 |
region | chr5:95885098-95961851 |
region5000 | chr5:95880098-95966851 |
regionname0 | ELL2_chr5_95885098_95961851 |
regionname5000 | ELL2_chr5_95880098_95966851 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 640 | 195 | 45 | 39 | 87 | 3 | 19 | 72 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002 | 0/0 | 640 | 111 | 29 | 17 | 50 | 4 | 11 | 36 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0003 | 0/0 | 640 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0004 | 0/0 | 640 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0005 | 0/0 | 640 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0006 | 0/0 | 640 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0007 | 0/0 | 640 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1923 | 152 | 23 | 35 | 72 | 3 | 17 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0002 | 0/0 | 1923 | 109 | 28 | 16 | 50 | 4 | 11 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0003 | 0/0 | 1923 | 29 | 12 | 4 | 11 | 0 | 2 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0004 | 0/0 | 1923 | 5 | 5 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0005 | 0/0 | 1923 | 4 | 4 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0006 | 0/0 | 1923 | 4 | 0 | 0 | 4 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0007 | 0/0 | 1923 | 3 | 1 | 1 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0008 | 0/0 | 1923 | 2 | 1 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0009 | 0/0 | 1923 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0010 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0011 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0012 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
c0013 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3906 | 101 | 29 | 14 | 43 | 5 | 10 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0002 | 1/1 | 3904 | 82 | 17 | 22 | 28 | 3 | 10 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0003 | 0/0 | 3904 | 71 | 4 | 13 | 48 | 0 | 6 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0004 | 0/0 | 3906 | 16 | 0 | 2 | 12 | 0 | 2 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0005 | 0/0 | 3905 | 8 | 7 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0006 | 0/0 | 3907 | 6 | 2 | 1 | 3 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0007 | 0/0 | 3908 | 3 | 2 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0008 | 0/0 | 3906 | 3 | 3 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0009 | 0/0 | 3907 | 3 | 0 | 2 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0010 | 0/0 | 3906 | 3 | 3 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0011 | 0/0 | 3906 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0012 | 0/0 | 3905 | 2 | 2 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0013 | 0/0 | 3906 | 2 | 2 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0014 | 0/0 | 3904 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0015 | 0/0 | 3904 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0016 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0017 | 0/0 | 3904 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0018 | 0/0 | 3905 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0019 | 0/0 | 3906 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0020 | 0/0 | 3905 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0021 | 0/0 | 3906 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0022 | 0/0 | 3906 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0023 | 0/0 | 3906 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0024 | 0/0 | 3906 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
t0025 | 0/0 | 3904 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0251 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1923 | 152 | 23 | 35 | 72 | 3 | 17 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0003 | 0/0 | 1923 | 29 | 12 | 4 | 11 | 0 | 2 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0004 | 0/0 | 1923 | 5 | 5 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0005 | 0/0 | 1923 | 4 | 4 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0006 | 0/0 | 1923 | 4 | 0 | 0 | 4 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0012 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0002 | 0/0 | 1923 | 109 | 28 | 16 | 50 | 4 | 11 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0008 | 0/0 | 1923 | 2 | 1 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0003c0007 | 0/0 | 1923 | 3 | 1 | 1 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0004c0009 | 0/0 | 1923 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0005c0011 | 0/0 | 1923 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0006c0010 | 0/0 | 1923 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0007c0013 | 0/0 | 1923 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5828 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0001t0002 | 1/1 | 5826 | 77 | 16 | 22 | 24 | 3 | 10 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0001t0003 | 0/0 | 5826 | 69 | 4 | 13 | 46 | 0 | 6 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0001t0014 | 0/0 | 5826 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0001t0015 | 0/0 | 5826 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0001t0016 | 0/0 | 5826 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0001t0017 | 0/0 | 5826 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0001t0023 | 0/0 | 5828 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0003t0004 | 0/0 | 5828 | 14 | 0 | 2 | 10 | 0 | 2 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0003t0005 | 0/0 | 5827 | 8 | 7 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0003t0007 | 0/0 | 5830 | 3 | 2 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0003t0008 | 0/0 | 5828 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0003t0012 | 0/0 | 5827 | 2 | 2 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0003t0024 | 0/0 | 5828 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0004t0001 | 0/0 | 5828 | 5 | 5 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0005t0008 | 0/0 | 5828 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0005t0010 | 0/0 | 5828 | 3 | 3 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0006t0004 | 0/0 | 5828 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0006t0011 | 0/0 | 5828 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0001c0012t0002 | 0/0 | 5826 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0002t0001 | 0/0 | 5828 | 90 | 22 | 12 | 43 | 4 | 9 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0002t0002 | 0/0 | 5826 | 3 | 0 | 0 | 3 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0002t0006 | 0/0 | 5829 | 6 | 2 | 1 | 3 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0002t0009 | 0/0 | 5829 | 3 | 0 | 2 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0002t0013 | 0/0 | 5828 | 2 | 2 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0002t0018 | 0/0 | 5827 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0002t0019 | 0/0 | 5828 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0002t0020 | 0/0 | 5827 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0002t0021 | 0/0 | 5828 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0002t0022 | 0/0 | 5828 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0002c0008t0001 | 0/0 | 5828 | 2 | 1 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0003c0007t0001 | 0/0 | 5828 | 3 | 1 | 1 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0004c0009t0003 | 0/0 | 5826 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0005c0011t0008 | 0/0 | 5828 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0006c0010t0025 | 0/0 | 5826 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
a0007c0013t0002 | 0/0 | 5826 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | copy fasta | chr5 | 95880098 | 95966851 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0251 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0014g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0015g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0016g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0017g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0001t0023g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0004g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0007g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0003t0024g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0004t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0004t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0004t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0004t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0005t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0005t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0005t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0005t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0006t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0006t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0006t0011g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0006t0011g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0001c0012t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0006g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0009g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0009g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0009g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0013g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0018g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0019g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0020g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0021g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0002t0022g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0008t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0002c0008t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0003c0007t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0003c0007t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0003c0007t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0004c0009t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0004c0009t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0005c0011t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0006c0010t0025g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
a0007c0013t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0272 | EUR | GBR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0057 | EUR | GBR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0254 | EUR | GBR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0081 | EUR | GBR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0105 | EUR | FIN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0275 | EUR | FIN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | CHS | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | CHS | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00609 | hp1 | a0001 | c0006 | t0004 | g0042 | EAS | CHS | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | CHS | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0295 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | CHS | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00673 | hp2 | a0002 | c0002 | t0006 | g0108 | EAS | CHS | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01070 | hp2 | a0003 | c0007 | t0001 | g0104 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01106 | hp1 | a0002 | c0002 | t0009 | g0056 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01106 | hp2 | a0002 | c0002 | t0009 | g0118 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01109 | hp1 | a0001 | c0003 | t0007 | g0018 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0246 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01168 | hp1 | a0001 | c0003 | t0004 | g0029 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01255 | hp1 | a0006 | c0010 | t0025 | g0154 | AMR | CLM | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01255 | hp2 | a0002 | c0002 | t0022 | g0116 | AMR | CLM | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | CLM | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01346 | hp1 | a0002 | c0008 | t0001 | g0107 | AMR | CLM | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | CLM | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01496 | hp1 | a0001 | c0003 | t0005 | g0035 | AMR | CLM | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | CLM | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01891 | hp2 | a0002 | c0002 | t0018 | g0132 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01934 | hp2 | a0002 | c0002 | t0006 | g0055 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01975 | hp1 | a0001 | c0003 | t0004 | g0044 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0080 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02015 | hp1 | a0002 | c0002 | t0006 | g0059 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02055 | hp1 | a0001 | c0001 | t0015 | g0256 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02074 | hp2 | a0001 | c0001 | t0016 | g0158 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02135 | hp1 | a0004 | c0009 | t0003 | g0155 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02145 | hp2 | a0002 | c0008 | t0001 | g0106 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0069 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | CDX | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | CDX | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02258 | hp2 | a0001 | c0003 | t0005 | g0032 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02451 | hp2 | a0001 | c0001 | t0014 | g0025 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02523 | hp1 | a0002 | c0002 | t0006 | g0090 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02523 | hp2 | a0001 | c0003 | t0024 | g0037 | EAS | KHV | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02572 | hp1 | a0005 | c0011 | t0008 | g0012 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0079 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02622 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02622 | hp2 | a0001 | c0005 | t0010 | g0049 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02647 | hp1 | a0001 | c0003 | t0005 | g0039 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02723 | hp1 | a0001 | c0005 | t0008 | g0014 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02723 | hp2 | a0001 | c0003 | t0007 | g0019 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02818 | hp1 | a0002 | c0002 | t0013 | g0064 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02818 | hp2 | a0001 | c0003 | t0008 | g0013 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0144 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02896 | hp2 | a0001 | c0004 | t0001 | g0022 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0133 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02965 | hp1 | a0001 | c0003 | t0012 | g0015 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0121 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03041 | hp2 | a0001 | c0005 | t0010 | g0050 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0117 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03139 | hp1 | a0001 | c0004 | t0001 | g0232 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03139 | hp2 | a0001 | c0003 | t0005 | g0038 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03209 | hp1 | a0001 | c0003 | t0005 | g0031 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03209 | hp2 | a0002 | c0002 | t0021 | g0134 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03225 | hp2 | a0002 | c0002 | t0006 | g0123 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0096 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0146 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0205 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03491 | hp2 | a0001 | c0003 | t0004 | g0003 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03492 | hp2 | a0001 | c0003 | t0004 | g0003 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03516 | hp2 | a0001 | c0012 | t0002 | g0247 | AFR | ESN | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03540 | hp2 | a0002 | c0002 | t0013 | g0063 | AFR | GWD | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0024 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0127 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0289 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03710 | hp2 | a0002 | c0002 | t0019 | g0094 | SAS | PJL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | BEB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03834 | hp1 | a0002 | c0002 | t0009 | g0054 | SAS | BEB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0255 | SAS | BEB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0270 | SAS | BEB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | BEB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | STU | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | STU | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0199 | SAS | BEB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0296 | SAS | BEB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | STU | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0086 | SAS | STU | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0161 | SAS | STU | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | STU | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0113 | AFR | YRI | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0023 | AFR | YRI | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | CHB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | CHB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | CHB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | YRI | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18906 | hp2 | a0001 | c0005 | t0010 | g0048 | AFR | YRI | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18941 | hp1 | a0001 | c0006 | t0004 | g0047 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18951 | hp2 | a0001 | c0003 | t0004 | g0033 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18957 | hp1 | a0001 | c0003 | t0004 | g0040 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18961 | hp1 | a0007 | c0013 | t0002 | g0304 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18961 | hp2 | a0001 | c0003 | t0004 | g0046 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18962 | hp1 | a0002 | c0002 | t0020 | g0052 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18966 | hp2 | a0001 | c0003 | t0004 | g0045 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18975 | hp1 | a0001 | c0003 | t0004 | g0005 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18981 | hp1 | a0001 | c0003 | t0004 | g0041 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18985 | hp2 | a0001 | c0006 | t0011 | g0027 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18989 | hp1 | a0001 | c0003 | t0004 | g0043 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19009 | hp1 | a0001 | c0003 | t0004 | g0005 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19011 | hp2 | a0001 | c0003 | t0004 | g0004 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | LWK | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19030 | hp2 | a0001 | c0003 | t0005 | g0030 | AFR | LWK | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19043 | hp1 | a0001 | c0003 | t0012 | g0016 | AFR | LWK | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19043 | hp2 | a0001 | c0003 | t0007 | g0017 | AFR | LWK | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19063 | hp1 | a0001 | c0006 | t0011 | g0028 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19070 | hp1 | a0001 | c0003 | t0004 | g0004 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19072 | hp2 | a0004 | c0009 | t0003 | g0194 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA19090 | hp2 | a0001 | c0001 | t0023 | g0169 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA20129 | hp1 | a0001 | c0003 | t0005 | g0036 | AFR | ASW | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | ASW | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA20805 | hp1 | a0003 | c0007 | t0001 | g0110 | EUR | TSI | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0258 | EUR | TSI | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | GIH | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0068 | SAS | GIH | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | CLM | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | CLM | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02109 | hp2 | a0003 | c0007 | t0001 | g0111 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0126 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02559 | hp1 | a0001 | c0001 | t0017 | g0231 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | ACB | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03471 | hp1 | a0002 | c0002 | t0006 | g0122 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
HG03471 | hp2 | a0001 | c0003 | t0005 | g0034 | AFR | MSL | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0251 | REF | REF | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0271 | REF | REF | ELL2_chr5_95880098_95966851 | ELL2 | chr5 | 95880098 | 95966851 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:95885100
|
G | T | 1 | a0001 | 1 | HG02559.hp1 | splice_region_variant | LOW | c.*3771C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | chr5 | 95885100 | ||||||
chr5:95898447
|
G | C | 1 | a0005 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1318C>G | p.Pro440Ala | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/12 | 1448/5826 | 1318/1923 | 440/640 | chr5 | 95898447 | ||
chr5:95898781
|
A | T | 1 | a0004 | 2 | HG02135.hp1 NA19072.hp2 |
missense_variant | MODERATE | c.984T>A | p.Asp328Glu | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/12 | 1114/5826 | 984/1923 | 328/640 | chr5 | 95898781 | ||
chr5:95900755
|
C | T | 2 | a0002a0003 | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
missense_variant | MODERATE | c.892G>A | p.Ala298Thr | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/12 | 1022/5826 | 892/1923 | 298/640 | chr5 | 95900755 | ||
chr5:95900770
|
G | T | 1 | a0006 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.877C>A | p.Pro293Thr | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/12 | 1007/5826 | 877/1923 | 293/640 | chr5 | 95900770 | ||
chr5:95943025
|
T | C | 1 | a0003 | 3 | HG01070.hp2 HG02109.hp2 NA20805.hp1 |
missense_variant | MODERATE | c.172A>G | p.Ile58Val | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/12 | 302/5826 | 172/1923 | 58/640 | chr5 | 95943025 | ||
chr5:95961663
|
C | A | 1 | a0007 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.59G>T | p.Gly20Val | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/12 | 189/5826 | 59/1923 | 20/640 | chr5 | 95961663 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:95888949
|
T | C | 1 | a0001c0006 | 4 | HG00609.hp1 NA18941.hp1 NA18985.hp2 others(1): Show |
synonymous_variant | LOW | c.1845A>G | p.Glu615Glu | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 1975/5826 | 1845/1923 | 615/640 | chr5 | 95888949 | ||
chr5:95898646
|
A | G | 8 | a0001c0003a0001c0004a0001c0005others(5): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
synonymous_variant | LOW | c.1119T>C | p.Pro373Pro | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/12 | 1249/5826 | 1119/1923 | 373/640 | chr5 | 95898646 | ||
chr5:95898673
|
C | T | 4 | a0001c0004a0002c0002a0002c0008others(1): Show | 119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
synonymous_variant | LOW | c.1092G>A | p.Pro364Pro | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/12 | 1222/5826 | 1092/1923 | 364/640 | chr5 | 95898673 | ||
chr5:95898688
|
A | C | 5 | a0001c0004a0001c0005a0002c0002others(2): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
synonymous_variant | LOW | c.1077T>G | p.Ser359Ser | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/12 | 1207/5826 | 1077/1923 | 359/640 | chr5 | 95898688 | ||
chr5:95900711
|
G | A | 3 | a0002c0002a0002c0008a0003c0007 | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
synonymous_variant | LOW | c.936C>T | p.Asp312Asp | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/12 | 1066/5826 | 936/1923 | 312/640 | chr5 | 95900711 | ||
chr5:95900750
|
G | C | 1 | a0002c0008 | 2 | HG01346.hp1 HG02145.hp2 |
synonymous_variant | LOW | c.897C>G | p.Gly299Gly | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/12 | 1027/5826 | 897/1923 | 299/640 | chr5 | 95900750 | ||
chr5:95906640
|
G | A | 1 | a0001c0012 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.624C>T | p.Asp208Asp | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/12 | 754/5826 | 624/1923 | 208/640 | chr5 | 95906640 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:95885134
|
G | A | 1 | a0001c0001t0016 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3737C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 3737 | chr5 | 95885134 | |||||
chr5:95885633
|
C | T | 19 | a0001c0001t0001a0001c0003t0004a0001c0003t0005others(16): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*3238G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 3238 | chr5 | 95885633 | |||||
chr5:95886059
|
T | C | 1 | a0002c0002t0021 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2812A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2812 | chr5 | 95886059 | |||||
chr5:95886125
|
A | AG | 4 | a0001c0003t0004a0001c0003t0024a0001c0006t0004others(1): Show | 19 | HG00609.hp1 HG01168.hp1 HG01975.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2745dupC | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2745 | chr5 | 95886125 | |||||
chr5:95886149
|
C | T | 1 | a0002c0002t0013 | 2 | HG02818.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2722G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2722 | chr5 | 95886149 | |||||
chr5:95886173
|
G | A | 1 | a0002c0002t0022 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2698C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2698 | chr5 | 95886173 | |||||
chr5:95886452
|
C | T | 13 | a0001c0001t0001a0001c0004t0001a0002c0002t0001others(10): Show | 117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*2419G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2419 | chr5 | 95886452 | |||||
chr5:95886573
|
C | T | 30 | a0001c0001t0001a0001c0001t0003a0001c0001t0014others(27): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2298G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2298 | chr5 | 95886573 | |||||
chr5:95886659
|
T | TA | 16 | a0001c0001t0001a0001c0001t0023a0001c0003t0008others(13): Show | 116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*2211dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2211 | chr5 | 95886659 | |||||
chr5:95886659
|
T | TAA | 1 | a0002c0002t0006 | 6 | HG00673.hp2 HG01934.hp2 HG02015.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2210_*2211dupTT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2211 | chr5 | 95886659 | |||||
chr5:95886659
|
T | TTA | 1 | a0002c0002t0009 | 3 | HG01106.hp1 HG01106.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2211_*2212insTA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2211 | chr5 | 95886659 | |||||
chr5:95886669
|
A | T | 1 | a0001c0001t0016 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2202T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2202 | chr5 | 95886669 | |||||
chr5:95886694
|
T | G | 1 | a0001c0003t0012 | 2 | HG02965.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2177A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2177 | chr5 | 95886694 | |||||
chr5:95886807
|
T | C | 15 | a0001c0001t0001a0001c0001t0023a0001c0004t0001others(12): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2064A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 2064 | chr5 | 95886807 | |||||
chr5:95886982
|
C | G | 5 | a0001c0003t0004a0001c0003t0005a0001c0003t0024others(2): Show | 27 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1889G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 1889 | chr5 | 95886982 | |||||
chr5:95887377
|
A | G | 1 | a0002c0002t0019 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1494T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 1494 | chr5 | 95887377 | |||||
chr5:95887520
|
A | G | 1 | a0001c0001t0015 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1351T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 1351 | chr5 | 95887520 | |||||
chr5:95887727
|
G | GA | 22 | a0001c0001t0001a0001c0001t0023a0001c0003t0004others(19): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*1143dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 1143 | chr5 | 95887727 | |||||
chr5:95887923
|
C | T | 1 | a0001c0001t0014 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*948G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 948 | chr5 | 95887923 | |||||
chr5:95888493
|
G | GTTGT | 1 | a0001c0003t0007 | 3 | HG01109.hp1 HG02723.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*374_*377dupACAA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 377 | chr5 | 95888493 | |||||
chr5:95888515
|
C | G | 1 | a0001c0006t0011 | 2 | NA18985.hp2 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*356G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 356 | chr5 | 95888515 | |||||
chr5:95888599
|
T | C | 1 | a0001c0003t0024 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*272A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 272 | chr5 | 95888599 | |||||
chr5:95888775
|
G | A | 1 | a0006c0010t0025 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 12/12 | 96 | chr5 | 95888775 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:95888996
|
G | GA | 74 | a0001c0001t0002g0193a0001c0001t0003g0002a0001c0001t0003g0007others(71): Show | 77 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1807-10dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 11/11 | chr5 | 95888996 | ||||||
chr5:95888996
|
GA | G | 6 | a0001c0001t0002g0214a0001c0001t0002g0218a0001c0001t0002g0272others(3): Show | 6 | HG00099.hp1 HG01168.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1807-10delT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 11/11 | chr5 | 95888996 | ||||||
chr5:95888996
|
GAA | G | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 26 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.1807-11_1807-10del others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 11/11 | chr5 | 95888996 | ||||||
chr5:95889079
|
T | C | 9 | a0001c0003t0004g0004a0001c0003t0004g0005a0001c0003t0004g0033others(6): Show | 11 | HG01975.hp1 NA18951.hp2 NA18957.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1806+7A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 11/11 | chr5 | 95889079 | ||||||
chr5:95889246
|
T | C | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1762-116A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 10/11 | chr5 | 95889246 | ||||||
chr5:95889335
|
C | A | 51 | a0002c0002t0001g0006a0002c0002t0001g0053a0002c0002t0001g0057others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1762-205G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 10/11 | chr5 | 95889335 | ||||||
chr5:95889726
|
C | G | 2 | a0002c0002t0001g0020a0002c0002t0001g0026 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1762-596G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 10/11 | chr5 | 95889726 | ||||||
chr5:95889826
|
T | TA | 4 | a0001c0001t0002g0262a0001c0001t0002g0263a0001c0001t0002g0276others(1): Show | 4 | HG00738.hp1 HG01981.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762-697dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 10/11 | chr5 | 95889826 | ||||||
chr5:95889834
|
C | T | 1 | a0001c0001t0002g0284 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1762-704G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 10/11 | chr5 | 95889834 | ||||||
chr5:95889889
|
G | C | 1 | a0002c0002t0001g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1762-759C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 10/11 | chr5 | 95889889 | ||||||
chr5:95889913
|
G | A | 1 | a0001c0003t0005g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1762-783C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 10/11 | chr5 | 95889913 | ||||||
chr5:95890951
|
A | G | 118 | a0001c0001t0001g0267a0001c0001t0023g0169a0001c0004t0001g0021others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.1761+152T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 10/11 | chr5 | 95890951 | ||||||
chr5:95891357
|
G | T | 3 | a0003c0007t0001g0104a0003c0007t0001g0110a0003c0007t0001g0111 | 3 | HG01070.hp2 HG02109.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1590-83C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95891357 | ||||||
chr5:95891603
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1590-329T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95891603 | ||||||
chr5:95891758
|
T | C | 150 | a0001c0001t0001g0267a0001c0001t0023g0169a0001c0003t0004g0003others(147): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1590-484A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95891758 | ||||||
chr5:95891771
|
A | C | 8 | a0001c0003t0005g0030a0001c0003t0005g0031a0001c0003t0005g0032others(5): Show | 8 | HG01496.hp1 HG02258.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1590-497T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95891771 | ||||||
chr5:95891803
|
T | C | 101 | a0001c0001t0001g0267a0001c0001t0023g0169a0002c0002t0001g0001others(98): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.1590-529A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95891803 | ||||||
chr5:95891876
|
C | A | 2 | a0001c0003t0012g0015a0001c0003t0012g0016 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1590-602G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95891876 | ||||||
chr5:95892149
|
C | CT | 28 | a0001c0001t0003g0152a0001c0001t0003g0200a0001c0003t0004g0003others(25): Show | 31 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.1590-876dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95892149 | ||||||
chr5:95892185
|
C | T | 2 | a0001c0003t0012g0015a0001c0003t0012g0016 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1590-911G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95892185 | ||||||
chr5:95892186
|
G | A | 5 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0133others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1590-912C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95892186 | ||||||
chr5:95892206
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1590-932C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95892206 | ||||||
chr5:95892257
|
G | A | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1590-983C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95892257 | ||||||
chr5:95893032
|
G | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1590-1758C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95893032 | ||||||
chr5:95893044
|
T | TA | 3 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019 | 3 | HG01109.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1590-1771dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95893044 | ||||||
chr5:95893132
|
A | G | 118 | a0001c0001t0001g0267a0001c0001t0023g0169a0001c0004t0001g0021others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.1590-1858T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95893132 | ||||||
chr5:95893181
|
T | G | 4 | a0001c0006t0004g0042a0001c0006t0004g0047a0001c0006t0011g0027others(1): Show | 4 | HG00609.hp1 NA18941.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1590-1907A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95893181 | ||||||
chr5:95893426
|
C | A | 1 | a0001c0001t0002g0285 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1590-2152G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95893426 | ||||||
chr5:95893534
|
C | T | 1 | a0001c0004t0001g0232 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1589+2094G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95893534 | ||||||
chr5:95893725
|
T | C | 120 | a0001c0001t0001g0267a0001c0001t0023g0169a0001c0004t0001g0021others(117): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.1589+1903A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95893725 | ||||||
chr5:95893941
|
A | G | 1 | a0001c0001t0015g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1589+1687T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95893941 | ||||||
chr5:95894235
|
C | T | 1 | a0001c0001t0003g0213 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1589+1393G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95894235 | ||||||
chr5:95894247
|
A | C | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.1589+1381T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95894247 | ||||||
chr5:95894249
|
A | G | 1 | a0002c0002t0001g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1589+1379T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95894249 | ||||||
chr5:95894274
|
T | C | 2 | a0001c0003t0012g0015a0001c0003t0012g0016 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1589+1354A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95894274 | ||||||
chr5:95894976
|
A | G | 2 | a0001c0003t0012g0015a0001c0003t0012g0016 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1589+652T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95894976 | ||||||
chr5:95895062
|
A | G | 4 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0023others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1589+566T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95895062 | ||||||
chr5:95895316
|
C | G | 1 | a0001c0001t0002g0217 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1589+312G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95895316 | ||||||
chr5:95895392
|
C | T | 3 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019 | 3 | HG01109.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1589+236G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95895392 | ||||||
chr5:95895411
|
C | T | 51 | a0002c0002t0001g0006a0002c0002t0001g0053a0002c0002t0001g0057others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.1589+217G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 9/11 | chr5 | 95895411 | ||||||
chr5:95895731
|
A | G | 1 | a0002c0002t0001g0070 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1526-40T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95895731 | ||||||
chr5:95895849
|
T | C | 26 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(23): Show | 29 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.1526-158A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95895849 | ||||||
chr5:95896279
|
A | T | 2 | a0001c0001t0003g0157a0001c0001t0003g0159 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1526-588T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95896279 | ||||||
chr5:95896279
|
AT | A | 144 | a0001c0001t0001g0267a0001c0003t0004g0003a0001c0003t0004g0004others(141): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1526-589delA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95896279 | ||||||
chr5:95896374
|
C | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1526-683G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95896374 | ||||||
chr5:95896492
|
G | A | 8 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(5): Show | 8 | HG01109.hp1 HG02572.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1526-801C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95896492 | ||||||
chr5:95896506
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1526-815G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95896506 | ||||||
chr5:95896695
|
C | A | 4 | a0001c0001t0002g0262a0001c0001t0002g0263a0001c0001t0002g0276others(1): Show | 4 | HG00738.hp1 HG01981.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1526-1004G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95896695 | ||||||
chr5:95896734
|
C | A | 1 | a0001c0001t0016g0158 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1526-1043G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95896734 | ||||||
chr5:95896831
|
C | G | 4 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0133others(1): Show | 4 | HG02559.hp2 HG02922.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1526-1140G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95896831 | ||||||
chr5:95896837
|
G | A | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1526-1146C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95896837 | ||||||
chr5:95896847
|
G | A | 116 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0023others(113): Show | 119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1526-1156C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95896847 | ||||||
chr5:95897018
|
G | T | 1 | a0002c0002t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1525+1222C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95897018 | ||||||
chr5:95897366
|
A | T | 1 | a0001c0001t0003g0210 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1525+874T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95897366 | ||||||
chr5:95897400
|
TG | T | 116 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0023others(113): Show | 119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1525+839delC | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95897400 | ||||||
chr5:95897686
|
G | A | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1525+554C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95897686 | ||||||
chr5:95897690
|
G | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1525+550C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95897690 | ||||||
chr5:95897789
|
A | G | 2 | a0002c0002t0001g0070a0002c0002t0009g0118 | 2 | HG01106.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1525+451T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95897789 | ||||||
chr5:95897968
|
A | T | 1 | a0002c0002t0001g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1525+272T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95897968 | ||||||
chr5:95898091
|
GA | G | 181 | a0001c0001t0002g0269a0001c0001t0003g0007a0001c0001t0003g0008others(178): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1525+148delT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95898091 | ||||||
chr5:95898091
|
GAAA | G | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.1525+146_1525+148d others(5): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95898091 | ||||||
chr5:95898129
|
A | G | 1 | a0001c0001t0003g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1525+111T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 8/11 | chr5 | 95898129 | ||||||
chr5:95898926
|
G | T | 116 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0023others(113): Show | 119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.955-116C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95898926 | ||||||
chr5:95898940
|
C | T | 1 | a0002c0002t0001g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.955-130G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95898940 | ||||||
chr5:95898962
|
A | AAAAC | 148 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(145): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.955-156_955-153dup others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95898962 | ||||||
chr5:95899087
|
C | T | 116 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0023others(113): Show | 119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.955-277G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95899087 | ||||||
chr5:95899382
|
T | TA | 5 | a0002c0002t0001g0127a0002c0002t0001g0129a0002c0002t0001g0130others(2): Show | 5 | HG00673.hp1 HG02135.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-573dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95899382 | ||||||
chr5:95899409
|
A | T | 2 | a0001c0001t0002g0302a0001c0001t0002g0303 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.955-599T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95899409 | ||||||
chr5:95899437
|
G | C | 1 | a0001c0003t0007g0018 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.955-627C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95899437 | ||||||
chr5:95899453
|
A | AT | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.955-644dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95899453 | ||||||
chr5:95899489
|
T | C | 127 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(124): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.955-679A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95899489 | ||||||
chr5:95899785
|
T | C | 1 | a0001c0001t0003g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.954+908A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95899785 | ||||||
chr5:95899812
|
C | T | 6 | a0001c0001t0001g0267a0001c0001t0002g0250a0001c0001t0002g0260others(3): Show | 6 | HG00099.hp1 HG01346.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.954+881G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95899812 | ||||||
chr5:95899923
|
T | C | 152 | a0001c0001t0003g0195a0001c0003t0004g0003a0001c0003t0004g0004others(149): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.954+770A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95899923 | ||||||
chr5:95899968
|
T | C | 4 | a0002c0002t0001g0065a0002c0002t0001g0067a0002c0002t0001g0069others(1): Show | 4 | HG01928.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+725A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95899968 | ||||||
chr5:95900044
|
G | C | 127 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(124): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.954+649C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95900044 | ||||||
chr5:95900287
|
T | C | 10 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(7): Show | 10 | HG01109.hp1 HG02622.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.954+406A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95900287 | ||||||
chr5:95900301
|
T | G | 1 | a0001c0001t0002g0252 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.954+392A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95900301 | ||||||
chr5:95900306
|
A | C | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.954+387T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95900306 | ||||||
chr5:95900594
|
G | C | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.954+99C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95900594 | ||||||
chr5:95900636
|
C | T | 1 | a0001c0003t0007g0019 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.954+57G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 7/11 | chr5 | 95900636 | ||||||
chr5:95901336
|
C | T | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.742-256G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95901336 | ||||||
chr5:95901364
|
A | T | 9 | a0001c0001t0003g0165a0001c0001t0003g0173a0001c0001t0003g0174others(6): Show | 9 | HG01943.hp2 NA18940.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.742-284T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95901364 | ||||||
chr5:95901469
|
C | T | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(63): Show | 68 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.742-389G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95901469 | ||||||
chr5:95901518
|
T | C | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.742-438A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95901518 | ||||||
chr5:95901559
|
T | TAAC | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.742-482_742-480dup others(3): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95901559 | ||||||
chr5:95901661
|
A | C | 124 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(121): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.742-581T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95901661 | ||||||
chr5:95901682
|
C | G | 9 | a0001c0003t0004g0004a0001c0003t0004g0005a0001c0003t0004g0033others(6): Show | 11 | HG01975.hp1 NA18951.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.742-602G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95901682 | ||||||
chr5:95902076
|
C | A | 111 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.742-996G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902076 | ||||||
chr5:95902117
|
C | T | 1 | a0002c0002t0001g0086 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.742-1037G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902117 | ||||||
chr5:95902143
|
C | T | 1 | a0001c0001t0002g0252 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.742-1063G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902143 | ||||||
chr5:95902212
|
T | C | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.742-1132A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902212 | ||||||
chr5:95902394
|
G | T | 1 | a0001c0001t0003g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.742-1314C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902394 | ||||||
chr5:95902398
|
A | G | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.742-1318T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902398 | ||||||
chr5:95902456
|
A | C | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.742-1376T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902456 | ||||||
chr5:95902486
|
A | G | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.742-1406T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902486 | ||||||
chr5:95902543
|
A | G | 1 | a0001c0001t0002g0214 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.742-1463T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902543 | ||||||
chr5:95902878
|
C | G | 111 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.742-1798G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902878 | ||||||
chr5:95902917
|
GACTACAG others(9): Show |
G | 8 | a0002c0002t0001g0020a0002c0002t0001g0026a0002c0002t0001g0119others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.742-1853_742-1838d others(18): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902917 | ||||||
chr5:95902943
|
G | A | 1 | a0002c0002t0001g0092 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.742-1863C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95902943 | ||||||
chr5:95903017
|
G | A | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.742-1937C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903017 | ||||||
chr5:95903039
|
G | A | 10 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(7): Show | 10 | HG01109.hp1 HG02622.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.742-1959C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903039 | ||||||
chr5:95903208
|
C | CT | 95 | a0001c0001t0002g0009a0001c0001t0002g0193a0001c0001t0002g0206others(92): Show | 98 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.742-2129dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903208 | ||||||
chr5:95903208
|
C | CTT | 23 | a0001c0001t0001g0267a0001c0001t0002g0221a0001c0001t0002g0265others(20): Show | 23 | HG00642.hp2 HG00735.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.742-2130_742-2129d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903208 | ||||||
chr5:95903208
|
CT | C | 26 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0066others(23): Show | 26 | HG00673.hp1 HG01106.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.742-2129delA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903208 | ||||||
chr5:95903208
|
CTT | C | 94 | a0001c0003t0005g0034a0001c0003t0012g0015a0001c0003t0012g0016others(91): Show | 97 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.742-2130_742-2129d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903208 | ||||||
chr5:95903208
|
CTTT | C | 26 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(23): Show | 29 | HG00609.hp1 HG01109.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.742-2131_742-2129d others(5): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903208 | ||||||
chr5:95903208
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0005t0008g0014 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.742-2140_742-2129d others(14): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903208 | ||||||
chr5:95903464
|
C | T | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.742-2384G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903464 | ||||||
chr5:95903518
|
G | A | 1 | a0001c0001t0002g0245 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.742-2438C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903518 | ||||||
chr5:95903569
|
A | G | 1 | a0002c0002t0001g0096 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.742-2489T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903569 | ||||||
chr5:95903705
|
A | T | 1 | a0001c0001t0015g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.742-2625T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903705 | ||||||
chr5:95903869
|
C | T | 2 | a0001c0001t0002g0257a0001c0001t0002g0258 | 2 | HG02004.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.741+2654G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903869 | ||||||
chr5:95903956
|
ATTGTCTC | A | 5 | a0001c0001t0002g0193a0001c0001t0002g0291a0001c0001t0002g0292others(2): Show | 5 | HG00558.hp1 NA18940.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.741+2560_741+2566d others(9): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95903956 | ||||||
chr5:95904043
|
C | T | 1 | a0001c0001t0003g0160 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.741+2480G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904043 | ||||||
chr5:95904067
|
TTAAATGC others(4): Show |
T | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.741+2445_741+2455d others(13): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904067 | ||||||
chr5:95904218
|
T | C | 1 | a0002c0002t0001g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.741+2305A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904218 | ||||||
chr5:95904223
|
A | G | 2 | a0001c0001t0003g0162a0001c0001t0003g0205 | 2 | HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.741+2300T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904223 | ||||||
chr5:95904623
|
A | G | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(63): Show | 68 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+1900T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904623 | ||||||
chr5:95904783
|
T | C | 1 | a0001c0001t0002g0269 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.741+1740A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904783 | ||||||
chr5:95904785
|
A | AT | 10 | a0002c0002t0001g0121a0002c0002t0001g0124a0002c0002t0001g0125others(7): Show | 10 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.741+1737dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904785 | ||||||
chr5:95904794
|
T | G | 1 | a0001c0001t0002g0269 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.741+1729A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904794 | ||||||
chr5:95904902
|
C | G | 1 | a0001c0003t0008g0013 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.741+1621G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904902 | ||||||
chr5:95904902
|
C | T | 7 | a0002c0002t0001g0060a0002c0002t0001g0092a0002c0002t0001g0093others(4): Show | 7 | HG00673.hp2 HG02015.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.741+1621G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904902 | ||||||
chr5:95904926
|
G | A | 1 | a0001c0001t0003g0196 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.741+1597C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904926 | ||||||
chr5:95904955
|
G | A | 102 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(99): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.741+1568C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904955 | ||||||
chr5:95904968
|
T | G | 1 | a0002c0002t0001g0082 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.741+1555A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95904968 | ||||||
chr5:95905161
|
A | T | 124 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(121): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.741+1362T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905161 | ||||||
chr5:95905233
|
A | ACG | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.741+1288_741+1289d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905233 | ||||||
chr5:95905234
|
C | T | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(63): Show | 68 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+1289G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905234 | ||||||
chr5:95905237
|
G | GCA | 109 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(106): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.741+1284_741+1285d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905237 | ||||||
chr5:95905239
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.741+1284T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905239 | ||||||
chr5:95905255
|
G | A | 2 | a0002c0002t0009g0054a0002c0002t0009g0056 | 2 | HG01106.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.741+1268C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905255 | ||||||
chr5:95905292
|
C | T | 111 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.741+1231G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905292 | ||||||
chr5:95905423
|
C | T | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.741+1100G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905423 | ||||||
chr5:95905440
|
T | TGAC | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.741+1080_741+1082d others(5): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905440 | ||||||
chr5:95905501
|
T | TCTC | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.741+1021_741+1022i others(5): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905501 | ||||||
chr5:95905518
|
T | C | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.741+1005A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905518 | ||||||
chr5:95905538
|
T | C | 1 | a0001c0001t0002g0288 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.741+985A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905538 | ||||||
chr5:95905539
|
G | A | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(63): Show | 68 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+984C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905539 | ||||||
chr5:95905740
|
C | G | 1 | a0002c0002t0001g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.741+783G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905740 | ||||||
chr5:95905742
|
G | C | 1 | a0001c0001t0003g0188 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.741+781C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905742 | ||||||
chr5:95905747
|
G | GT | 118 | a0001c0001t0002g0239a0001c0003t0004g0045a0001c0003t0008g0013others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.741+775dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905747 | ||||||
chr5:95905747
|
GT | G | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(63): Show | 68 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+775delA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905747 | ||||||
chr5:95905891
|
G | A | 1 | a0002c0002t0001g0270 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.741+632C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905891 | ||||||
chr5:95905912
|
A | G | 1 | a0001c0001t0002g0251 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.741+611T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95905912 | ||||||
chr5:95906158
|
G | C | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(63): Show | 68 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+365C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95906158 | ||||||
chr5:95906164
|
T | C | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.741+359A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95906164 | ||||||
chr5:95906198
|
A | C | 1 | a0001c0003t0007g0019 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.741+325T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95906198 | ||||||
chr5:95906340
|
T | C | 7 | a0002c0002t0001g0102a0002c0002t0001g0113a0002c0002t0001g0114others(4): Show | 7 | HG00738.hp2 HG01255.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.741+183A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 5/11 | chr5 | 95906340 | ||||||
chr5:95906873
|
A | G | 2 | a0001c0001t0002g0260a0001c0001t0002g0272 | 2 | HG00099.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.482-91T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95906873 | ||||||
chr5:95907030
|
T | G | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.482-248A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907030 | ||||||
chr5:95907079
|
G | C | 1 | a0002c0002t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.482-297C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907079 | ||||||
chr5:95907112
|
C | G | 1 | a0001c0001t0002g0278 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.482-330G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907112 | ||||||
chr5:95907208
|
C | T | 7 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(4): Show | 7 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-426G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907208 | ||||||
chr5:95907227
|
T | C | 114 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050others(111): Show | 117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.482-445A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907227 | ||||||
chr5:95907270
|
C | T | 1 | a0002c0002t0001g0095 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.482-488G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907270 | ||||||
chr5:95907294
|
A | ATTTTTTT others(6): Show |
1 | a0002c0002t0021g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.482-513_482-512ins others(13): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907294 | ||||||
chr5:95907294
|
A | ATTTTTTT others(8): Show |
1 | a0002c0002t0001g0270 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.482-513_482-512ins others(15): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907294 | ||||||
chr5:95907294
|
A | ATTTTTTT others(9): Show |
1 | a0002c0002t0001g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.482-513_482-512ins others(16): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907294 | ||||||
chr5:95907294
|
A | T | 2 | a0001c0003t0008g0013a0001c0005t0008g0014 | 2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.482-512T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907294 | ||||||
chr5:95907296
|
A | ATATATAT others(38): Show |
1 | a0001c0003t0007g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.482-515_482-514ins others(45): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(21): Show |
1 | a0001c0003t0007g0018 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.482-515_482-514ins others(28): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(22): Show |
1 | a0001c0003t0007g0019 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.482-515_482-514ins others(29): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(27): Show |
1 | a0001c0003t0012g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.482-515_482-514ins others(34): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(17): Show |
1 | a0001c0003t0004g0043 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.482-515_482-514ins others(24): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(25): Show |
1 | a0001c0003t0012g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.482-515_482-514ins others(32): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(13): Show |
1 | a0001c0003t0004g0044 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.482-515_482-514ins others(20): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(14): Show |
2 | a0001c0003t0005g0034a0001c0003t0005g0035 | 2 | HG01496.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.482-515_482-514ins others(21): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(15): Show |
1 | a0001c0003t0024g0037 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.482-515_482-514ins others(22): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(21): Show |
1 | a0001c0005t0010g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.482-515_482-514ins others(28): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(22): Show |
2 | a0001c0005t0010g0048a0001c0005t0010g0049 | 2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.482-515_482-514ins others(29): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(12): Show |
6 | a0001c0003t0004g0029a0001c0003t0005g0030a0001c0003t0005g0031others(3): Show | 6 | HG01168.hp1 HG02258.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-515_482-514ins others(19): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(13): Show |
8 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(5): Show | 11 | HG03491.hp2 HG03492.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-515_482-514ins others(20): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(12): Show |
1 | a0001c0003t0005g0039 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.482-515_482-514ins others(19): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATAT others(13): Show |
4 | a0001c0006t0004g0042a0001c0006t0004g0047a0001c0006t0011g0027others(1): Show | 4 | HG00609.hp1 NA18941.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-515_482-514ins others(20): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATTT others(10): Show |
1 | a0002c0002t0001g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.482-515_482-514ins others(17): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATTT others(11): Show |
5 | a0002c0002t0001g0026a0002c0002t0001g0119a0002c0002t0001g0120others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-515_482-514ins others(18): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATATTT others(12): Show |
1 | a0002c0002t0001g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.482-515_482-514ins others(19): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATTTTT others(6): Show |
1 | a0001c0004t0001g0232 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.482-515_482-514ins others(13): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATTTTT others(8): Show |
5 | a0002c0002t0001g0082a0002c0002t0001g0102a0002c0002t0001g0114others(2): Show | 5 | HG00738.hp2 HG01891.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-515_482-514ins others(15): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATTTTT others(9): Show |
2 | a0002c0002t0001g0068a0002c0002t0001g0087 | 2 | HG02056.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.482-515_482-514ins others(16): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATTTTT others(10): Show |
1 | a0002c0002t0001g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.482-515_482-514ins others(17): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATATTTTT others(12): Show |
1 | a0002c0002t0001g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.482-515_482-514ins others(19): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATTTTTTT others(4): Show |
1 | a0001c0004t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.482-525_482-515dup others(11): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATTTTTTT others(5): Show |
3 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0024 | 3 | HG02622.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.482-526_482-515dup others(12): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATTTTTTT others(7): Show |
2 | a0002c0002t0001g0067a0002c0002t0001g0115 | 2 | HG02055.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.482-515_482-514ins others(14): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATTTTTTT others(8): Show |
69 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(66): Show | 72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.482-515_482-514ins others(15): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATTTTTTT others(9): Show |
18 | a0002c0002t0001g0069a0002c0002t0001g0070a0002c0002t0001g0086others(15): Show | 18 | HG00673.hp1 HG00741.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.482-515_482-514ins others(16): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | ATTTTTTT others(10): Show |
3 | a0002c0002t0001g0130a0002c0002t0006g0055a0002c0002t0006g0122 | 3 | HG01934.hp2 HG02135.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.482-515_482-514ins others(17): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907296
|
A | T | 10 | a0001c0001t0002g0214a0001c0001t0002g0219a0001c0001t0014g0025others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.482-514T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907296 | ||||||
chr5:95907297
|
T | TA | 61 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0058others(58): Show | 63 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.482-516_482-515ins others(1): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907297 | ||||||
chr5:95907298
|
T | A | 3 | a0001c0001t0002g0206a0001c0001t0003g0162a0001c0001t0003g0223 | 3 | HG02717.hp1 HG04115.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.482-516A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907298 | ||||||
chr5:95907314
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.482-532G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907314 | ||||||
chr5:95907455
|
C | G | 1 | a0001c0001t0002g0244 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.482-673G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907455 | ||||||
chr5:95907512
|
T | G | 1 | a0002c0002t0001g0151 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.482-730A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907512 | ||||||
chr5:95907538
|
G | A | 1 | a0001c0001t0003g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.482-756C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907538 | ||||||
chr5:95907650
|
A | G | 1 | a0001c0001t0002g0219 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.482-868T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907650 | ||||||
chr5:95907962
|
G | A | 1 | a0001c0001t0003g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.482-1180C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95907962 | ||||||
chr5:95908710
|
C | T | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.482-1928G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95908710 | ||||||
chr5:95908886
|
G | C | 2 | a0002c0002t0001g0057a0002c0002t0006g0055 | 2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.482-2104C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95908886 | ||||||
chr5:95909040
|
G | A | 1 | a0002c0002t0001g0140 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.482-2258C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95909040 | ||||||
chr5:95909134
|
G | A | 1 | a0002c0002t0001g0254 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.482-2352C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95909134 | ||||||
chr5:95909160
|
T | C | 3 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0011 | 4 | HG01243.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-2378A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95909160 | ||||||
chr5:95909532
|
G | GA | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.482-2751dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95909532 | ||||||
chr5:95909640
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.482-2858C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95909640 | ||||||
chr5:95909680
|
C | T | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.482-2898G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95909680 | ||||||
chr5:95909830
|
T | C | 1 | a0001c0001t0003g0205 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.482-3048A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95909830 | ||||||
chr5:95909943
|
G | GC | 303 | a0001c0001t0001g0267a0001c0001t0002g0009a0001c0001t0002g0193others(300): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.482-3162dupG | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95909943 | ||||||
chr5:95910165
|
C | CT | 10 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(7): Show | 10 | HG01109.hp1 HG02622.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.482-3384dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910165 | ||||||
chr5:95910263
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.482-3481T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910263 | ||||||
chr5:95910281
|
G | A | 1 | a0002c0002t0009g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.481+3490C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910281 | ||||||
chr5:95910348
|
T | C | 1 | a0002c0002t0001g0289 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.481+3423A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910348 | ||||||
chr5:95910392
|
A | T | 1 | a0001c0004t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.481+3379T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910392 | ||||||
chr5:95910430
|
T | G | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.481+3341A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910430 | ||||||
chr5:95910661
|
T | C | 1 | a0002c0002t0001g0091 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.481+3110A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910661 | ||||||
chr5:95910683
|
C | A | 2 | a0002c0002t0001g0102a0002c0002t0001g0128 | 2 | HG00738.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.481+3088G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910683 | ||||||
chr5:95910768
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.481+3003G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910768 | ||||||
chr5:95910845
|
T | C | 1 | a0001c0001t0003g0160 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.481+2926A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910845 | ||||||
chr5:95910947
|
C | CAATTTGG others(1): Show |
10 | a0002c0002t0001g0121a0002c0002t0001g0124a0002c0002t0001g0125others(7): Show | 10 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+2816_481+2823d others(10): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910947 | ||||||
chr5:95910977
|
A | G | 25 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(22): Show | 28 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.481+2794T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95910977 | ||||||
chr5:95911056
|
G | A | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.481+2715C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911056 | ||||||
chr5:95911163
|
G | A | 111 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.481+2608C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911163 | ||||||
chr5:95911224
|
A | G | 10 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(7): Show | 10 | HG01109.hp1 HG02622.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+2547T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911224 | ||||||
chr5:95911226
|
A | G | 1 | a0001c0001t0003g0212 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.481+2545T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911226 | ||||||
chr5:95911343
|
C | CT | 149 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(146): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.481+2427dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911343 | ||||||
chr5:95911401
|
A | G | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.481+2370T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911401 | ||||||
chr5:95911452
|
C | T | 4 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0023others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+2319G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911452 | ||||||
chr5:95911486
|
C | T | 1 | a0002c0002t0001g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.481+2285G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911486 | ||||||
chr5:95911581
|
C | T | 3 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019 | 3 | HG01109.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.481+2190G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911581 | ||||||
chr5:95911593
|
G | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.481+2178C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911593 | ||||||
chr5:95911692
|
C | T | 1 | a0001c0001t0003g0172 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.481+2079G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911692 | ||||||
chr5:95911705
|
G | A | 1 | a0001c0001t0003g0175 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.481+2066C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911705 | ||||||
chr5:95911812
|
G | A | 2 | a0001c0001t0003g0178a0001c0001t0003g0180 | 2 | NA18953.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.481+1959C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911812 | ||||||
chr5:95911872
|
C | T | 1 | a0002c0002t0001g0088 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.481+1899G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911872 | ||||||
chr5:95911929
|
G | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.481+1842C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911929 | ||||||
chr5:95911930
|
A | C | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.481+1841T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95911930 | ||||||
chr5:95912022
|
T | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.481+1749A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95912022 | ||||||
chr5:95912145
|
T | C | 1 | a0001c0001t0003g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.481+1626A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95912145 | ||||||
chr5:95912225
|
G | A | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.481+1546C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95912225 | ||||||
chr5:95912268
|
C | T | 111 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.481+1503G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95912268 | ||||||
chr5:95913072
|
GGT | G | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.481+697_481+698del others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95913072 | ||||||
chr5:95913206
|
T | A | 1 | a0001c0001t0002g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.481+565A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95913206 | ||||||
chr5:95913209
|
G | A | 1 | a0001c0001t0002g0292 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.481+562C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95913209 | ||||||
chr5:95913428
|
G | A | 1 | a0001c0001t0003g0185 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.481+343C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95913428 | ||||||
chr5:95913548
|
G | C | 2 | a0001c0001t0003g0162a0001c0001t0003g0205 | 2 | HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.481+223C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 4/11 | chr5 | 95913548 | ||||||
chr5:95914117
|
CAT | C | 6 | a0002c0002t0001g0246a0002c0002t0001g0254a0002c0002t0001g0255others(3): Show | 6 | HG00140.hp1 HG00639.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.318-185_318-184del others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95914117 | ||||||
chr5:95914569
|
A | T | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.318-635T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95914569 | ||||||
chr5:95914632
|
T | C | 2 | a0001c0003t0007g0018a0001c0003t0007g0019 | 2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.318-698A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95914632 | ||||||
chr5:95914665
|
G | A | 1 | a0002c0002t0009g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.318-731C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95914665 | ||||||
chr5:95914748
|
A | G | 1 | a0002c0002t0001g0097 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.318-814T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95914748 | ||||||
chr5:95914774
|
T | G | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.318-840A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95914774 | ||||||
chr5:95914949
|
G | C | 1 | a0001c0003t0007g0018 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.318-1015C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95914949 | ||||||
chr5:95915142
|
T | C | 1 | a0001c0001t0002g0261 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.318-1208A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915142 | ||||||
chr5:95915143
|
G | A | 1 | a0001c0001t0002g0261 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.318-1209C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915143 | ||||||
chr5:95915188
|
T | C | 223 | a0001c0001t0002g0228a0001c0001t0002g0275a0001c0001t0003g0002others(220): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.318-1254A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915188 | ||||||
chr5:95915268
|
A | T | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.318-1334T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915268 | ||||||
chr5:95915364
|
T | G | 1 | a0001c0001t0002g0228 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.318-1430A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915364 | ||||||
chr5:95915380
|
G | A | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.318-1446C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915380 | ||||||
chr5:95915398
|
C | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0120 | 2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.318-1464G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915398 | ||||||
chr5:95915440
|
T | C | 5 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0023others(2): Show | 5 | HG02622.hp1 HG02896.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.318-1506A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915440 | ||||||
chr5:95915510
|
G | A | 1 | a0001c0001t0003g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.318-1576C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915510 | ||||||
chr5:95915534
|
G | A | 125 | a0001c0001t0002g0228a0001c0001t0003g0185a0001c0003t0007g0017others(122): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.318-1600C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915534 | ||||||
chr5:95915609
|
GA | G | 5 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0133others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.318-1676delT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915609 | ||||||
chr5:95915642
|
G | A | 152 | a0001c0001t0002g0228a0001c0003t0004g0003a0001c0003t0004g0004others(149): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.318-1708C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915642 | ||||||
chr5:95915681
|
C | T | 2 | a0001c0001t0003g0178a0001c0001t0003g0180 | 2 | NA18953.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.318-1747G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915681 | ||||||
chr5:95915719
|
T | C | 1 | a0001c0001t0002g0275 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.318-1785A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95915719 | ||||||
chr5:95916131
|
T | C | 1 | a0001c0001t0003g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.318-2197A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95916131 | ||||||
chr5:95916144
|
GA | G | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.318-2211delT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95916144 | ||||||
chr5:95916207
|
G | C | 151 | a0001c0001t0002g0243a0001c0003t0004g0003a0001c0003t0004g0004others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.318-2273C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95916207 | ||||||
chr5:95916223
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0011 | 4 | HG01243.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-2289G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95916223 | ||||||
chr5:95916748
|
GA | G | 148 | a0001c0001t0002g0300a0001c0001t0003g0177a0001c0001t0017g0231others(145): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.317+2675delT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95916748 | ||||||
chr5:95916890
|
C | A | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(101): Show | 107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.317+2534G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95916890 | ||||||
chr5:95916947
|
C | T | 1 | a0001c0003t0007g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.317+2477G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95916947 | ||||||
chr5:95917015
|
T | G | 1 | a0001c0001t0002g0303 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.317+2409A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917015 | ||||||
chr5:95917096
|
G | A | 1 | a0001c0001t0002g0291 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.317+2328C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917096 | ||||||
chr5:95917142
|
A | C | 1 | a0002c0002t0001g0076 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.317+2282T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917142 | ||||||
chr5:95917300
|
G | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.317+2124C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917300 | ||||||
chr5:95917404
|
C | G | 124 | a0001c0003t0008g0013a0001c0003t0012g0015a0001c0003t0012g0016others(121): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.317+2020G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917404 | ||||||
chr5:95917478
|
A | G | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.317+1946T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917478 | ||||||
chr5:95917591
|
G | T | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.317+1833C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917591 | ||||||
chr5:95917632
|
C | T | 5 | a0002c0002t0001g0246a0002c0002t0001g0254a0002c0002t0001g0255others(2): Show | 5 | HG00140.hp1 HG00639.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+1792G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917632 | ||||||
chr5:95917754
|
C | CT | 218 | a0001c0001t0002g0275a0001c0001t0003g0007a0001c0001t0003g0008others(215): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.317+1669dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917754 | ||||||
chr5:95917785
|
A | G | 118 | a0001c0003t0005g0030a0001c0003t0005g0031a0001c0003t0005g0032others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.317+1639T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917785 | ||||||
chr5:95917823
|
T | C | 7 | a0002c0002t0001g0060a0002c0002t0001g0092a0002c0002t0001g0093others(4): Show | 7 | HG00673.hp2 HG02015.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.317+1601A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917823 | ||||||
chr5:95917997
|
G | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0120 | 2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.317+1427C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95917997 | ||||||
chr5:95918050
|
T | C | 67 | a0001c0001t0002g0275a0001c0001t0003g0007a0001c0001t0003g0008others(64): Show | 69 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.317+1374A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95918050 | ||||||
chr5:95918446
|
G | T | 8 | a0002c0002t0001g0020a0002c0002t0001g0026a0002c0002t0001g0119others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.317+978C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95918446 | ||||||
chr5:95918467
|
G | T | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.317+957C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95918467 | ||||||
chr5:95918510
|
G | T | 1 | a0001c0001t0003g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.317+914C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95918510 | ||||||
chr5:95918515
|
A | AT | 13 | a0001c0001t0003g0165a0001c0001t0003g0168a0001c0001t0003g0172others(10): Show | 13 | HG01943.hp2 NA18747.hp1 NA18940.hp1 others(10): Show |
intron_variant | MODIFIER | c.317+908dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95918515 | ||||||
chr5:95918627
|
G | A | 1 | a0001c0001t0003g0177 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.317+797C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95918627 | ||||||
chr5:95918798
|
T | C | 113 | a0001c0005t0010g0048a0001c0005t0010g0049a0002c0002t0001g0001others(110): Show | 116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.317+626A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95918798 | ||||||
chr5:95918826
|
C | T | 67 | a0001c0001t0002g0275a0001c0001t0003g0007a0001c0001t0003g0008others(64): Show | 69 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.317+598G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95918826 | ||||||
chr5:95918877
|
C | CTT | 148 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(145): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.317+545_317+546dup others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95918877 | ||||||
chr5:95918978
|
A | G | 1 | a0001c0001t0003g0203 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.317+446T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95918978 | ||||||
chr5:95919112
|
A | G | 13 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(10): Show | 13 | HG01109.hp1 HG02572.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.317+312T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95919112 | ||||||
chr5:95919274
|
T | A | 1 | a0002c0002t0001g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.317+150A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 3/11 | chr5 | 95919274 | ||||||
chr5:95919675
|
G | A | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.196-130C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95919675 | ||||||
chr5:95919827
|
A | C | 67 | a0001c0001t0002g0275a0001c0001t0003g0007a0001c0001t0003g0008others(64): Show | 69 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.196-282T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95919827 | ||||||
chr5:95919911
|
T | C | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.196-366A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95919911 | ||||||
chr5:95920020
|
A | G | 119 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(116): Show | 122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.196-475T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920020 | ||||||
chr5:95920148
|
C | T | 1 | a0001c0003t0007g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.196-603G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920148 | ||||||
chr5:95920247
|
G | T | 1 | a0007c0013t0002g0304 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.196-702C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920247 | ||||||
chr5:95920277
|
A | ATATT | 88 | a0001c0001t0001g0267a0001c0001t0002g0009a0001c0001t0002g0193others(85): Show | 92 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.196-736_196-733dup others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920277 | ||||||
chr5:95920277
|
A | ATATTTAT others(1): Show |
5 | a0001c0001t0002g0264a0001c0001t0002g0266a0001c0001t0002g0297others(2): Show | 5 | HG02559.hp2 HG04204.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-740_196-733dup others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920277 | ||||||
chr5:95920277
|
ATATT | A | 52 | a0001c0001t0002g0229a0001c0001t0002g0283a0001c0001t0003g0167others(49): Show | 54 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.196-736_196-733del others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920277 | ||||||
chr5:95920277
|
ATATTTAT others(1): Show |
A | 9 | a0001c0003t0007g0019a0001c0003t0012g0015a0001c0003t0012g0016others(6): Show | 9 | HG00280.hp1 HG02622.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-740_196-733del others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920277 | ||||||
chr5:95920277
|
ATATTTAT others(5): Show |
A | 3 | a0001c0001t0003g0203a0001c0003t0007g0017a0001c0003t0007g0018 | 3 | HG01109.hp1 NA18954.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196-744_196-733del others(12): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920277 | ||||||
chr5:95920277
|
ATATTTAT others(9): Show |
A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.196-748_196-733del others(16): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920277 | ||||||
chr5:95920277
|
ATATTTAT others(17): Show |
A | 1 | a0001c0006t0004g0047 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.196-756_196-733del others(24): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920277 | ||||||
chr5:95920333
|
C | T | 13 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(10): Show | 13 | HG01109.hp1 HG02572.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-788G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920333 | ||||||
chr5:95920433
|
C | T | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.196-888G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920433 | ||||||
chr5:95920646
|
G | A | 1 | a0006c0010t0025g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196-1101C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920646 | ||||||
chr5:95920689
|
A | G | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.196-1144T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920689 | ||||||
chr5:95920917
|
A | ACT | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.196-1373_196-1372i others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920917 | ||||||
chr5:95920960
|
G | C | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.196-1415C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95920960 | ||||||
chr5:95921057
|
TC | T | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.196-1513delG | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95921057 | ||||||
chr5:95921120
|
C | A | 1 | a0001c0001t0002g0272 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.196-1575G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95921120 | ||||||
chr5:95921203
|
T | C | 1 | a0001c0001t0002g0245 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.196-1658A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95921203 | ||||||
chr5:95921270
|
T | C | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.196-1725A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95921270 | ||||||
chr5:95921337
|
A | G | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.196-1792T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95921337 | ||||||
chr5:95921384
|
A | G | 4 | a0001c0001t0003g0156a0001c0001t0003g0189a0001c0001t0003g0199others(1): Show | 4 | HG01496.hp2 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-1839T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95921384 | ||||||
chr5:95921499
|
G | A | 1 | a0002c0002t0009g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.196-1954C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95921499 | ||||||
chr5:95921566
|
G | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.196-2021C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95921566 | ||||||
chr5:95921700
|
G | A | 7 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(4): Show | 7 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-2155C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95921700 | ||||||
chr5:95921742
|
G | A | 3 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019 | 3 | HG01109.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196-2197C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95921742 | ||||||
chr5:95922025
|
C | G | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.196-2480G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95922025 | ||||||
chr5:95922071
|
A | AT | 118 | a0001c0003t0007g0017a0001c0003t0012g0015a0001c0003t0012g0016others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.196-2527dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95922071 | ||||||
chr5:95922095
|
T | G | 4 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0023others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-2550A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95922095 | ||||||
chr5:95922103
|
G | A | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.196-2558C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95922103 | ||||||
chr5:95922121
|
T | A | 4 | a0001c0006t0004g0042a0001c0006t0004g0047a0001c0006t0011g0027others(1): Show | 4 | HG00609.hp1 NA18941.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-2576A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95922121 | ||||||
chr5:95922278
|
G | A | 13 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(10): Show | 13 | HG01109.hp1 HG02572.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-2733C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95922278 | ||||||
chr5:95922642
|
A | G | 1 | a0002c0002t0001g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.196-3097T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95922642 | ||||||
chr5:95922646
|
ATCTT | A | 7 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(4): Show | 7 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-3105_196-3102d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95922646 | ||||||
chr5:95922686
|
G | A | 5 | a0002c0002t0001g0127a0002c0002t0001g0129a0002c0002t0001g0130others(2): Show | 5 | HG00673.hp1 HG02135.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-3141C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95922686 | ||||||
chr5:95922743
|
T | C | 111 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.196-3198A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95922743 | ||||||
chr5:95922836
|
C | CT | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.196-3292dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95922836 | ||||||
chr5:95923050
|
T | G | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.196-3505A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95923050 | ||||||
chr5:95923240
|
G | GA | 110 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(107): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.196-3696dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95923240 | ||||||
chr5:95923240
|
G | GAA | 8 | a0002c0002t0001g0020a0002c0002t0001g0026a0002c0002t0001g0119others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-3697_196-3696d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95923240 | ||||||
chr5:95923346
|
A | T | 1 | a0002c0002t0001g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.196-3801T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95923346 | ||||||
chr5:95923434
|
T | C | 2 | a0002c0002t0001g0071a0002c0002t0001g0077 | 2 | NA18747.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.196-3889A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95923434 | ||||||
chr5:95923692
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.196-4147C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95923692 | ||||||
chr5:95924066
|
T | C | 2 | a0002c0002t0013g0063a0002c0002t0013g0064 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.196-4521A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95924066 | ||||||
chr5:95924113
|
A | G | 13 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(10): Show | 13 | HG01109.hp1 HG02572.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-4568T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95924113 | ||||||
chr5:95924128
|
G | A | 6 | a0002c0002t0001g0057a0002c0002t0006g0055a0002c0002t0009g0054others(3): Show | 6 | HG00099.hp2 HG01106.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-4583C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95924128 | ||||||
chr5:95924158
|
C | T | 124 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(121): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.196-4613G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95924158 | ||||||
chr5:95924310
|
G | T | 1 | a0002c0002t0001g0140 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.196-4765C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95924310 | ||||||
chr5:95924440
|
GA | G | 5 | a0002c0002t0001g0127a0002c0002t0001g0129a0002c0002t0001g0130others(2): Show | 5 | HG00673.hp1 HG02135.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-4896delT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95924440 | ||||||
chr5:95924556
|
T | C | 1 | a0001c0003t0005g0038 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.196-5011A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95924556 | ||||||
chr5:95924732
|
A | G | 3 | a0001c0003t0005g0030a0001c0003t0005g0031a0001c0003t0005g0032 | 3 | HG02258.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.196-5187T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95924732 | ||||||
chr5:95924968
|
C | T | 1 | a0002c0002t0021g0134 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196-5423G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95924968 | ||||||
chr5:95925693
|
AAG | A | 7 | a0001c0001t0002g0221a0001c0001t0002g0224a0001c0001t0002g0265others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-6150_196-6149d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95925693 | ||||||
chr5:95925806
|
C | T | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.196-6261G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95925806 | ||||||
chr5:95925834
|
C | G | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.196-6289G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95925834 | ||||||
chr5:95925930
|
T | C | 8 | a0002c0002t0001g0020a0002c0002t0001g0026a0002c0002t0001g0119others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-6385A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95925930 | ||||||
chr5:95926061
|
A | T | 1 | a0001c0001t0002g0244 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.196-6516T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95926061 | ||||||
chr5:95926176
|
GA | G | 7 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(4): Show | 7 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-6632delT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95926176 | ||||||
chr5:95926203
|
C | T | 5 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0133others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-6658G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95926203 | ||||||
chr5:95926340
|
G | C | 111 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.196-6795C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95926340 | ||||||
chr5:95926541
|
C | T | 1 | a0002c0002t0001g0093 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.196-6996G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95926541 | ||||||
chr5:95926809
|
C | T | 69 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(66): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.196-7264G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95926809 | ||||||
chr5:95926912
|
T | C | 78 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(75): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.196-7367A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95926912 | ||||||
chr5:95927150
|
T | C | 2 | a0001c0003t0005g0039a0002c0002t0001g0129 | 2 | HG02647.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.196-7605A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927150 | ||||||
chr5:95927362
|
T | G | 1 | a0001c0001t0002g0222 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.196-7817A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927362 | ||||||
chr5:95927364
|
T | G | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(63): Show | 68 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.196-7819A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927364 | ||||||
chr5:95927366
|
G | C | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(63): Show | 68 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.196-7821C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927366 | ||||||
chr5:95927368
|
C | CACACACA others(373): Show |
1 | a0001c0001t0015g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.196-7824_196-7823i others(382): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927368 | ||||||
chr5:95927370
|
T | C | 2 | a0001c0001t0015g0256a0001c0001t0017g0231 | 2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.196-7825A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927370 | ||||||
chr5:95927370
|
T | TAC | 3 | a0001c0001t0002g0229a0001c0001t0003g0196a0001c0001t0003g0202 | 3 | HG01928.hp2 HG01993.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.196-7827_196-7826d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927370 | ||||||
chr5:95927370
|
TACAC | T | 3 | a0001c0001t0002g0220a0001c0001t0002g0264a0007c0013t0002g0304 | 3 | HG01978.hp2 HG04228.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.196-7829_196-7826d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927370 | ||||||
chr5:95927372
|
C | T | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.196-7827G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927372 | ||||||
chr5:95927374
|
C | T | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.196-7829G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927374 | ||||||
chr5:95927374
|
CACACACA others(43): Show |
C | 2 | a0001c0001t0003g0002a0001c0001t0003g0223 | 3 | HG01243.hp2 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.196-7879_196-7830d others(52): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927374 | ||||||
chr5:95927376
|
C | CACATATG others(47): Show |
1 | a0002c0002t0001g0087 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.196-7832_196-7831i others(56): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927376 | ||||||
chr5:95927376
|
C | CACATATG others(19): Show |
16 | a0002c0002t0001g0006a0002c0002t0001g0053a0002c0002t0001g0060others(13): Show | 17 | HG00280.hp1 HG00673.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.196-7832_196-7831i others(28): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927376 | ||||||
chr5:95927376
|
C | CACATATG others(47): Show |
2 | a0003c0007t0001g0104a0003c0007t0001g0110 | 2 | HG01070.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.196-7832_196-7831i others(56): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927376 | ||||||
chr5:95927376
|
C | CACATATG others(103): Show |
1 | a0002c0002t0009g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.196-7832_196-7831i others(112): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927376 | ||||||
chr5:95927376
|
C | T | 35 | a0001c0003t0008g0013a0001c0003t0012g0015a0001c0003t0012g0016others(32): Show | 35 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.196-7831G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927376 | ||||||
chr5:95927376
|
CACACACG others(17): Show |
C | 2 | a0001c0001t0003g0010a0001c0001t0003g0011 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.196-7855_196-7832d others(26): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927376 | ||||||
chr5:95927378
|
C | T | 29 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(26): Show | 29 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.196-7833G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927378 | ||||||
chr5:95927380
|
C | T | 67 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(64): Show | 69 | HG00099.hp2 HG00140.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.196-7835G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927380 | ||||||
chr5:95927381
|
ACG | A | 67 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(64): Show | 69 | HG00099.hp2 HG00140.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.196-7838_196-7837d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927381 | ||||||
chr5:95927382
|
C | T | 84 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(81): Show | 88 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.196-7837G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927382 | ||||||
chr5:95927383
|
G | A | 85 | a0001c0001t0014g0025a0001c0003t0004g0003a0001c0003t0004g0004others(82): Show | 89 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.196-7838C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927383 | ||||||
chr5:95927384
|
T | C | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.196-7839A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927384 | ||||||
chr5:95927389
|
A | ATATATAG others(93): Show |
1 | a0001c0001t0002g0248 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.196-7845_196-7844i others(102): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927389 | ||||||
chr5:95927389
|
A | ATATATAG others(173): Show |
1 | a0001c0001t0002g0263 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.196-7845_196-7844i others(182): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927389 | ||||||
chr5:95927389
|
A | ATATATAG others(45): Show |
1 | a0001c0001t0002g0286 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.196-7845_196-7844i others(54): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927389 | ||||||
chr5:95927389
|
A | ATATATAG others(43): Show |
2 | a0001c0001t0002g0221a0001c0001t0002g0265 | 2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.196-7845_196-7844i others(52): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927389 | ||||||
chr5:95927389
|
A | G | 2 | a0001c0001t0002g0228a0001c0001t0014g0025 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.196-7844T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927389 | ||||||
chr5:95927389
|
ATATATAG others(297): Show |
A | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 26 | HG01168.hp1 HG01496.hp1 HG01975.hp1 others(23): Show |
intron_variant | MODIFIER | c.196-8148_196-7845d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927389 | ||||||
chr5:95927389
|
ATATATAG others(357): Show |
A | 4 | a0001c0006t0004g0042a0001c0006t0004g0047a0001c0006t0011g0027others(1): Show | 4 | HG00609.hp1 NA18941.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8208_196-7845d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927389 | ||||||
chr5:95927394
|
T | G | 69 | a0001c0001t0002g0222a0001c0001t0002g0262a0001c0001t0003g0007others(66): Show | 71 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.196-7849A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927394 | ||||||
chr5:95927396
|
G | C | 68 | a0001c0001t0002g0222a0001c0001t0003g0007a0001c0001t0003g0008others(65): Show | 70 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.196-7851C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927396 | ||||||
chr5:95927398
|
C | CATAT | 84 | a0001c0003t0007g0018a0001c0003t0007g0019a0001c0004t0001g0232others(81): Show | 87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.196-7854_196-7853i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927398 | ||||||
chr5:95927398
|
C | T | 2 | a0001c0001t0002g0222a0007c0013t0002g0304 | 2 | HG01943.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.196-7853G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927398 | ||||||
chr5:95927398
|
CATACACA others(15): Show |
C | 1 | a0001c0001t0003g0160 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.196-7875_196-7854d others(24): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927398 | ||||||
chr5:95927400
|
T | C | 6 | a0001c0001t0002g0222a0001c0001t0002g0229a0001c0001t0014g0025others(3): Show | 6 | HG01943.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-7855A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TAC | 85 | a0001c0001t0002g0214a0001c0001t0002g0216a0001c0001t0002g0217others(82): Show | 87 | HG00099.hp1 HG00544.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.196-7857_196-7856d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACAC | 4 | a0001c0001t0002g0236a0001c0001t0002g0269a0001c0001t0002g0280others(1): Show | 4 | HG01261.hp2 HG02273.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-7859_196-7856d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(25): Show |
1 | a0001c0001t0002g0244 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.196-7856_196-7855i others(34): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(53): Show |
2 | a0001c0001t0002g0206a0001c0001t0002g0292 | 2 | NA18943.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.196-7856_196-7855i others(62): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(211): Show |
1 | a0001c0001t0002g0193 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.196-7856_196-7855i others(220): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(23): Show |
1 | a0004c0009t0003g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.196-7856_196-7855i others(32): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(23): Show |
2 | a0001c0001t0003g0176a0004c0009t0003g0194 | 2 | HG00609.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.196-7856_196-7855i others(32): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(21): Show |
1 | a0001c0001t0002g0291 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.196-7856_196-7855i others(30): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(95): Show |
1 | a0001c0001t0002g0282 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.196-7856_196-7855i others(104): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(23): Show |
1 | a0001c0001t0002g0225 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.196-7856_196-7855i others(32): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(73): Show |
1 | a0001c0001t0002g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.196-7856_196-7855i others(82): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(77): Show |
1 | a0001c0012t0002g0247 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.196-7856_196-7855i others(86): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(79): Show |
1 | a0006c0010t0025g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196-7856_196-7855i others(88): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(19): Show |
1 | a0001c0001t0002g0233 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.196-7881_196-7856d others(28): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
T | TACACACA others(45): Show |
1 | a0001c0001t0002g0234 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.196-7907_196-7856d others(54): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
TACACACA others(113): Show |
T | 5 | a0002c0002t0001g0246a0002c0002t0001g0255a0002c0002t0001g0295others(2): Show | 5 | HG00639.hp2 HG01109.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-7975_196-7856d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
TACACACA others(139): Show |
T | 2 | a0002c0002t0001g0126a0002c0002t0001g0242 | 2 | HG00544.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.196-8001_196-7856d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
TACACACA others(165): Show |
T | 6 | a0001c0003t0008g0013a0002c0002t0001g0143a0002c0002t0001g0144others(3): Show | 6 | HG00741.hp2 HG01243.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-8027_196-7856d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
TACACACA others(191): Show |
T | 7 | a0001c0005t0008g0014a0002c0002t0001g0127a0002c0002t0001g0129others(4): Show | 7 | HG00673.hp1 HG02135.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-8053_196-7856d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
TACACACA others(217): Show |
T | 1 | a0001c0004t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196-8079_196-7856d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
TACACACA others(243): Show |
T | 3 | a0001c0003t0007g0017a0001c0003t0012g0015a0001c0003t0012g0016 | 3 | HG02965.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.196-8105_196-7856d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927400
|
TACACACA others(299): Show |
T | 1 | a0001c0004t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.196-8161_196-7856d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927400 | ||||||
chr5:95927401
|
ACACACAC others(5): Show |
A | 2 | a0002c0002t0001g0020a0002c0002t0001g0150 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.196-7868_196-7857d others(14): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927401 | ||||||
chr5:95927401
|
ACACACAC others(31): Show |
A | 2 | a0002c0002t0001g0119a0002c0002t0001g0133 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.196-7894_196-7857d others(40): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927401 | ||||||
chr5:95927401
|
ACACACAC others(105): Show |
A | 5 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0124others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-7968_196-7857d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927401 | ||||||
chr5:95927401
|
ACACACAC others(129): Show |
A | 4 | a0002c0002t0001g0121a0002c0002t0001g0125a0002c0002t0006g0123others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-7992_196-7857d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927401 | ||||||
chr5:95927401
|
ACACACAC others(207): Show |
A | 2 | a0001c0004t0001g0021a0001c0004t0001g0022 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.196-8070_196-7857d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927401 | ||||||
chr5:95927402
|
CACACACG others(115): Show |
C | 1 | a0001c0001t0003g0204 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.196-7979_196-7858d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927402 | ||||||
chr5:95927406
|
C | T | 84 | a0001c0003t0007g0018a0001c0003t0007g0019a0001c0004t0001g0232others(81): Show | 87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.196-7861G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927406 | ||||||
chr5:95927408
|
C | CACACGT | 6 | a0001c0001t0002g0259a0001c0001t0002g0261a0001c0001t0002g0283others(3): Show | 6 | HG00558.hp1 HG03704.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-7864_196-7863i others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927408 | ||||||
chr5:95927408
|
C | CACACGTG others(27): Show |
2 | a0001c0001t0002g0260a0001c0001t0002g0276 | 2 | HG01346.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.196-7864_196-7863i others(36): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927408 | ||||||
chr5:95927408
|
C | CACGT | 8 | a0001c0001t0001g0267a0001c0001t0002g0226a0001c0001t0002g0228others(5): Show | 8 | HG00280.hp2 HG01993.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-7864_196-7863i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927408 | ||||||
chr5:95927408
|
C | CACGTGTG others(25): Show |
1 | a0001c0001t0002g0009 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.196-7864_196-7863i others(34): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927408 | ||||||
chr5:95927408
|
C | T | 84 | a0001c0003t0007g0018a0001c0003t0007g0019a0001c0004t0001g0232others(81): Show | 87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.196-7863G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927408 | ||||||
chr5:95927409
|
G | A | 1 | a0001c0001t0002g0219 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.196-7864C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927409 | ||||||
chr5:95927410
|
T | C | 1 | a0001c0001t0002g0219 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.196-7865A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927410 | ||||||
chr5:95927413
|
G | A | 100 | a0001c0001t0001g0267a0001c0001t0002g0009a0001c0001t0002g0226others(97): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.196-7868C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927413 | ||||||
chr5:95927420
|
G | GAC | 54 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(51): Show | 56 | HG00544.hp1 HG00642.hp1 HG01496.hp2 others(53): Show |
intron_variant | MODIFIER | c.196-7877_196-7876d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927420 | ||||||
chr5:95927420
|
G | T | 2 | a0002c0002t0001g0020a0002c0002t0001g0150 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.196-7875C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927420 | ||||||
chr5:95927422
|
C | CAT | 80 | a0001c0003t0007g0018a0001c0003t0007g0019a0001c0004t0001g0232others(77): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.196-7879_196-7878d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927422 | ||||||
chr5:95927424
|
T | C | 7 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0157others(4): Show | 7 | HG01069.hp1 HG01074.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-7879A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927424 | ||||||
chr5:95927424
|
TAC | T | 3 | a0001c0001t0002g0235a0001c0001t0002g0248a0001c0001t0002g0274 | 3 | HG03490.hp2 NA19001.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.196-7881_196-7880d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927424 | ||||||
chr5:95927424
|
TACACACA others(89): Show |
T | 4 | a0002c0002t0001g0096a0002c0002t0001g0254a0002c0002t0001g0289others(1): Show | 4 | HG00140.hp1 HG01255.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-7975_196-7880d others(98): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927424 | ||||||
chr5:95927426
|
C | CACACACA others(15): Show |
1 | a0001c0001t0002g0251 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196-7882_196-7881i others(24): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927426 | ||||||
chr5:95927426
|
C | CACACACA others(17): Show |
1 | a0001c0001t0002g0258 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.196-7905_196-7882d others(26): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927426 | ||||||
chr5:95927426
|
C | CACACACG others(39): Show |
1 | a0001c0001t0002g0239 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.196-7882_196-7881i others(48): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927426 | ||||||
chr5:95927426
|
C | CACACACG others(63): Show |
1 | a0001c0001t0002g0216 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.196-7882_196-7881i others(72): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927426 | ||||||
chr5:95927426
|
C | T | 82 | a0001c0001t0003g0157a0001c0001t0003g0159a0001c0003t0007g0018others(79): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.196-7881G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927426 | ||||||
chr5:95927428
|
CACACACG others(89): Show |
C | 2 | a0001c0001t0003g0157a0001c0001t0003g0159 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.196-7979_196-7884d others(98): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927428 | ||||||
chr5:95927432
|
C | T | 80 | a0001c0003t0007g0018a0001c0003t0007g0019a0001c0004t0001g0232others(77): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.196-7887G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927432 | ||||||
chr5:95927434
|
C | T | 82 | a0001c0003t0007g0018a0001c0003t0007g0019a0001c0004t0001g0232others(79): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.196-7889G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927434 | ||||||
chr5:95927439
|
G | A | 82 | a0001c0003t0007g0018a0001c0003t0007g0019a0001c0004t0001g0232others(79): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.196-7894C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927439 | ||||||
chr5:95927446
|
G | GAC | 10 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0001t0003g0161others(7): Show | 10 | HG01928.hp2 HG01993.hp2 HG04228.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-7903_196-7902d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927446 | ||||||
chr5:95927446
|
G | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0133 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.196-7901C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927446 | ||||||
chr5:95927448
|
C | CAT | 64 | a0001c0003t0007g0018a0001c0003t0007g0019a0002c0002t0001g0001others(61): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.196-7905_196-7904d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927448 | ||||||
chr5:95927450
|
T | C | 10 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0011others(7): Show | 11 | HG01243.hp2 HG01496.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-7905A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927450 | ||||||
chr5:95927450
|
TAC | T | 23 | a0001c0001t0002g0216a0001c0001t0002g0217a0001c0001t0002g0224others(20): Show | 23 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.196-7907_196-7906d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927450 | ||||||
chr5:95927450
|
TACACACA others(63): Show |
T | 3 | a0001c0004t0001g0232a0002c0002t0001g0138a0002c0002t0001g0147 | 3 | HG03041.hp1 HG03139.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.196-7975_196-7906d others(72): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927450 | ||||||
chr5:95927452
|
C | CACACACA others(91): Show |
1 | a0001c0001t0002g0236 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.196-7908_196-7907i others(100): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927452 | ||||||
chr5:95927452
|
C | CACACACG others(15): Show |
2 | a0001c0001t0002g0214a0001c0001t0002g0218 | 2 | HG01168.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.196-7908_196-7907i others(24): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927452 | ||||||
chr5:95927452
|
C | CACACACG others(111): Show |
1 | a0001c0001t0002g0222 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.196-7908_196-7907i others(120): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927452 | ||||||
chr5:95927452
|
C | T | 79 | a0001c0003t0007g0018a0001c0003t0007g0019a0002c0002t0001g0001others(76): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.196-7907G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927452 | ||||||
chr5:95927452
|
CACACACA others(17): Show |
C | 1 | a0001c0001t0002g0219 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.196-7931_196-7908d others(26): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927452 | ||||||
chr5:95927452
|
CACACACA others(65): Show |
C | 1 | a0001c0001t0003g0180 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.196-7979_196-7908d others(74): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927452 | ||||||
chr5:95927454
|
C | T | 15 | a0002c0002t0001g0020a0002c0002t0001g0076a0002c0002t0001g0077others(12): Show | 15 | HG02040.hp2 HG02615.hp1 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-7909G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927454 | ||||||
chr5:95927458
|
C | T | 64 | a0001c0003t0007g0018a0001c0003t0007g0019a0002c0002t0001g0001others(61): Show | 67 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.196-7913G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927458 | ||||||
chr5:95927460
|
C | T | 81 | a0001c0003t0007g0018a0001c0003t0007g0019a0002c0002t0001g0001others(78): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.196-7915G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927460 | ||||||
chr5:95927461
|
G | A | 15 | a0002c0002t0001g0020a0002c0002t0001g0076a0002c0002t0001g0077others(12): Show | 15 | HG02040.hp2 HG02615.hp1 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-7916C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927461 | ||||||
chr5:95927465
|
G | A | 66 | a0001c0003t0007g0018a0001c0003t0007g0019a0002c0002t0001g0001others(63): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.196-7920C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927465 | ||||||
chr5:95927467
|
A | ATATAGAC others(117): Show |
1 | a0001c0001t0002g0284 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.196-7923_196-7922i others(126): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927467 | ||||||
chr5:95927470
|
TAGAC | T | 15 | a0002c0002t0001g0020a0002c0002t0001g0076a0002c0002t0001g0077others(12): Show | 15 | HG02040.hp2 HG02615.hp1 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-7929_196-7926d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927470 | ||||||
chr5:95927472
|
G | C | 1 | a0001c0001t0017g0231 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.196-7927C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927472 | ||||||
chr5:95927472
|
G | GAC | 4 | a0001c0001t0002g0229a0001c0001t0003g0223a0001c0001t0014g0025others(1): Show | 4 | HG02055.hp1 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-7929_196-7928d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927472 | ||||||
chr5:95927474
|
C | CATAT | 56 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(53): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.196-7930_196-7929i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927474 | ||||||
chr5:95927474
|
CATACACA others(39): Show |
C | 2 | a0001c0001t0003g0156a0001c0001t0003g0189 | 2 | HG01496.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.196-7975_196-7930d others(48): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927474 | ||||||
chr5:95927476
|
T | C | 9 | a0001c0001t0002g0206a0001c0001t0002g0229a0001c0001t0003g0002others(6): Show | 10 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-7931A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927476 | ||||||
chr5:95927476
|
T | TAC | 51 | a0001c0001t0002g0193a0001c0001t0002g0215a0001c0001t0002g0218others(48): Show | 51 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.196-7933_196-7932d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927476 | ||||||
chr5:95927476
|
T | TACACACA others(21): Show |
2 | a0001c0001t0002g0264a0001c0001t0002g0294 | 2 | HG04228.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.196-7932_196-7931i others(30): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927476 | ||||||
chr5:95927476
|
TACACACA others(37): Show |
T | 6 | a0002c0002t0001g0071a0002c0002t0001g0073a0002c0002t0001g0074others(3): Show | 6 | HG01106.hp2 HG02155.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-7975_196-7932d others(46): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927476 | ||||||
chr5:95927476
|
TACACACA others(191): Show |
T | 2 | a0001c0003t0007g0018a0001c0003t0007g0019 | 2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.196-8129_196-7932d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927476 | ||||||
chr5:95927477
|
ACACACAC others(5): Show |
A | 2 | a0002c0002t0001g0119a0002c0002t0001g0133 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.196-7944_196-7933d others(14): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927477 | ||||||
chr5:95927478
|
C | G | 15 | a0002c0002t0001g0020a0002c0002t0001g0076a0002c0002t0001g0077others(12): Show | 15 | HG02040.hp2 HG02615.hp1 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-7933G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927478 | ||||||
chr5:95927478
|
CACACACG others(15): Show |
C | 11 | a0001c0001t0002g0243a0001c0001t0003g0051a0001c0001t0003g0173others(8): Show | 11 | HG01261.hp1 HG01943.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-7955_196-7934d others(24): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927478 | ||||||
chr5:95927478
|
CACACACG others(39): Show |
C | 19 | a0001c0001t0002g0220a0001c0001t0003g0007a0001c0001t0003g0008others(16): Show | 21 | HG00544.hp1 HG01928.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.196-7979_196-7934d others(48): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927478 | ||||||
chr5:95927480
|
CACACGTG others(3): Show |
C | 15 | a0002c0002t0001g0020a0002c0002t0001g0076a0002c0002t0001g0077others(12): Show | 15 | HG02040.hp2 HG02615.hp1 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-7945_196-7936d others(12): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927480 | ||||||
chr5:95927480
|
CACACGTG others(13): Show |
C | 1 | a0001c0001t0002g0226 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.196-7955_196-7936d others(22): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927480 | ||||||
chr5:95927482
|
C | T | 56 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(53): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.196-7937G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927482 | ||||||
chr5:95927484
|
C | T | 56 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(53): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.196-7939G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927484 | ||||||
chr5:95927489
|
G | A | 56 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(53): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.196-7944C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927489 | ||||||
chr5:95927494
|
TAGAC | T | 15 | a0002c0002t0001g0020a0002c0002t0001g0076a0002c0002t0001g0077others(12): Show | 15 | HG02040.hp2 HG02615.hp1 HG02922.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-7953_196-7950d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927494 | ||||||
chr5:95927496
|
G | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0133 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.196-7951C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927496 | ||||||
chr5:95927498
|
C | CATAT | 56 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(53): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.196-7954_196-7953i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927498 | ||||||
chr5:95927500
|
T | C | 8 | a0001c0001t0002g0206a0001c0001t0002g0229a0001c0001t0003g0002others(5): Show | 9 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-7955A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927500 | ||||||
chr5:95927500
|
T | TAC | 48 | a0001c0001t0002g0193a0001c0001t0002g0221a0001c0001t0002g0224others(45): Show | 48 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.196-7957_196-7956d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927500 | ||||||
chr5:95927500
|
T | TACACACA others(17): Show |
1 | a0001c0001t0002g0299 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.196-7956_196-7955i others(26): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927500 | ||||||
chr5:95927500
|
TACACACA others(43): Show |
T | 1 | a0001c0001t0003g0197 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.196-8005_196-7956d others(52): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927500 | ||||||
chr5:95927506
|
C | T | 71 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(68): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.196-7961G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927506 | ||||||
chr5:95927508
|
C | T | 72 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(69): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.196-7963G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927508 | ||||||
chr5:95927509
|
G | A | 1 | a0006c0010t0025g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196-7964C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927509 | ||||||
chr5:95927510
|
T | C | 1 | a0006c0010t0025g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196-7965A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927510 | ||||||
chr5:95927513
|
G | A | 73 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(70): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.196-7968C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927513 | ||||||
chr5:95927520
|
G | GACACACA others(67): Show |
1 | a0001c0001t0002g0206 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.196-7976_196-7975i others(76): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927520 | ||||||
chr5:95927520
|
G | T | 5 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0124others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-7975C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927520 | ||||||
chr5:95927522
|
C | CACACACA others(21): Show |
1 | a0001c0001t0002g0217 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.196-7978_196-7977i others(30): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927522 | ||||||
chr5:95927522
|
C | CATAT | 73 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(70): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.196-7978_196-7977i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927522 | ||||||
chr5:95927522
|
C | T | 18 | a0001c0004t0001g0232a0002c0002t0001g0071a0002c0002t0001g0073others(15): Show | 18 | HG00140.hp1 HG00639.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.196-7977G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927522 | ||||||
chr5:95927524
|
T | C | 12 | a0001c0001t0002g0206a0001c0001t0002g0217a0001c0001t0002g0229others(9): Show | 13 | HG00733.hp2 HG01243.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-7979A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
T | TAC | 35 | a0001c0001t0002g0193a0001c0001t0002g0221a0001c0001t0002g0224others(32): Show | 35 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.196-7981_196-7980d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
T | TACACACA others(19): Show |
1 | a0001c0001t0002g0272 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.196-7980_196-7979i others(28): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
T | TACACACA others(47): Show |
1 | a0001c0001t0002g0293 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.196-7980_196-7979i others(56): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
T | TACACACA others(71): Show |
2 | a0001c0001t0002g0253a0001c0001t0002g0261 | 2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.196-8057_196-7980d others(80): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
T | TACACACA others(97): Show |
1 | a0001c0001t0002g0250 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.196-8083_196-7980d others(106): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
T | TACACACA others(123): Show |
1 | a0001c0001t0002g0292 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.196-8109_196-7980d others(132): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
T | TACACACA others(69): Show |
1 | a0001c0001t0002g0259 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.196-7980_196-7979i others(78): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
T | TACACACA others(95): Show |
3 | a0001c0001t0002g0009a0001c0001t0002g0277a0001c0001t0002g0297 | 4 | HG00642.hp2 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-7980_196-7979i others(104): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
T | TACACACA others(121): Show |
1 | a0001c0001t0002g0273 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.196-7980_196-7979i others(130): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
T | TACACACA others(93): Show |
1 | a0001c0001t0002g0275 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.196-7980_196-7979i others(102): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
T | TACACACA others(119): Show |
1 | a0001c0001t0002g0262 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.196-7980_196-7979i others(128): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
TACACAC | T | 5 | a0002c0002t0001g0026a0002c0002t0001g0120a0002c0002t0001g0124others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-7985_196-7980d others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927524
|
TACACACA others(19): Show |
T | 1 | a0001c0001t0002g0288 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.196-8005_196-7980d others(28): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927524 | ||||||
chr5:95927530
|
C | T | 91 | a0001c0004t0001g0232a0002c0002t0001g0001a0002c0002t0001g0006others(88): Show | 94 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.196-7985G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927530 | ||||||
chr5:95927532
|
C | T | 96 | a0001c0004t0001g0232a0002c0002t0001g0001a0002c0002t0001g0006others(93): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.196-7987G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927532 | ||||||
chr5:95927533
|
G | A | 1 | a0006c0010t0025g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196-7988C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927533 | ||||||
chr5:95927534
|
T | C | 1 | a0006c0010t0025g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196-7989A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927534 | ||||||
chr5:95927537
|
G | A | 96 | a0001c0004t0001g0232a0002c0002t0001g0001a0002c0002t0001g0006others(93): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.196-7992C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927537 | ||||||
chr5:95927544
|
G | T | 4 | a0002c0002t0001g0121a0002c0002t0001g0125a0002c0002t0006g0123others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-7999C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927544 | ||||||
chr5:95927546
|
C | CAT | 94 | a0001c0004t0001g0232a0002c0002t0001g0001a0002c0002t0001g0006others(91): Show | 97 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.196-8003_196-8002d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927546 | ||||||
chr5:95927546
|
CAT | C | 4 | a0001c0001t0003g0002a0001c0001t0003g0011a0001c0001t0014g0025others(1): Show | 5 | HG01243.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-8003_196-8002d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927546 | ||||||
chr5:95927548
|
T | C | 4 | a0001c0001t0002g0229a0001c0001t0015g0256a0004c0009t0003g0155others(1): Show | 4 | HG02055.hp1 HG02135.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-8003A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927548 | ||||||
chr5:95927548
|
TAC | T | 24 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0238others(21): Show | 25 | HG00544.hp1 HG01496.hp2 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.196-8005_196-8004d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927548 | ||||||
chr5:95927548
|
TACACACA others(1): Show |
T | 4 | a0002c0002t0001g0121a0002c0002t0001g0125a0002c0002t0006g0123others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8011_196-8004d others(10): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927548 | ||||||
chr5:95927548
|
TACACACA others(21): Show |
T | 1 | a0001c0001t0003g0208 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.196-8031_196-8004d others(30): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927548 | ||||||
chr5:95927550
|
C | CACACACG others(15): Show |
2 | a0001c0001t0002g0237a0001c0001t0002g0241 | 2 | HG01069.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.196-8006_196-8005i others(24): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927550 | ||||||
chr5:95927550
|
C | CACACACG others(63): Show |
1 | a0001c0001t0002g0276 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.196-8006_196-8005i others(72): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927550 | ||||||
chr5:95927550
|
C | T | 99 | a0001c0001t0003g0207a0001c0004t0001g0232a0002c0002t0001g0001others(96): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.196-8005G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927550 | ||||||
chr5:95927552
|
C | T | 2 | a0002c0002t0001g0071a0002c0002t0001g0077 | 2 | NA18747.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.196-8007G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927552 | ||||||
chr5:95927556
|
C | CAT | 3 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0191 | 3 | NA18973.hp2 NA18994.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.196-8012_196-8011i others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927556 | ||||||
chr5:95927556
|
C | T | 96 | a0001c0004t0001g0232a0002c0002t0001g0001a0002c0002t0001g0006others(93): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.196-8011G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927556 | ||||||
chr5:95927558
|
C | T | 105 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0191others(102): Show | 108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.196-8013G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927558 | ||||||
chr5:95927559
|
G | A | 2 | a0002c0002t0001g0071a0002c0002t0001g0077 | 2 | NA18747.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.196-8014C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927559 | ||||||
chr5:95927560
|
T | TGTATATA others(13): Show |
1 | a0001c0001t0003g0175 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.196-8016_196-8015i others(22): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927560 | ||||||
chr5:95927563
|
G | A | 100 | a0001c0004t0001g0232a0002c0002t0001g0001a0002c0002t0001g0006others(97): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.196-8018C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927563 | ||||||
chr5:95927572
|
C | CAT | 95 | a0001c0004t0001g0232a0002c0002t0001g0001a0002c0002t0001g0006others(92): Show | 98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.196-8029_196-8028d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927572 | ||||||
chr5:95927572
|
C | CATATATA others(51): Show |
1 | a0002c0002t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-8028_196-8027i others(60): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927572 | ||||||
chr5:95927574
|
T | C | 5 | a0001c0001t0002g0229a0001c0001t0003g0170a0001c0001t0014g0025others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-8029A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927574 | ||||||
chr5:95927574
|
TAC | T | 30 | a0001c0001t0002g0235a0001c0001t0003g0008a0001c0001t0003g0160others(27): Show | 31 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.196-8031_196-8030d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927574 | ||||||
chr5:95927574
|
TACACACA others(21): Show |
T | 1 | a0001c0001t0003g0058 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.196-8057_196-8030d others(30): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927574 | ||||||
chr5:95927576
|
C | T | 112 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0191others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.196-8031G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927576 | ||||||
chr5:95927578
|
C | T | 6 | a0002c0002t0001g0060a0002c0002t0001g0071a0002c0002t0001g0077others(3): Show | 6 | HG00673.hp2 HG02074.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-8033G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927578 | ||||||
chr5:95927582
|
C | CAT | 4 | a0001c0001t0003g0163a0001c0001t0003g0172a0001c0001t0003g0192others(1): Show | 4 | NA18747.hp1 NA18940.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8038_196-8037i others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927582 | ||||||
chr5:95927582
|
C | T | 102 | a0001c0003t0008g0013a0001c0004t0001g0232a0002c0002t0001g0001others(99): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.196-8037G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927582 | ||||||
chr5:95927584
|
C | CATAT | 4 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0191others(1): Show | 4 | NA18965.hp1 NA18973.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8040_196-8039i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927584 | ||||||
chr5:95927584
|
C | T | 112 | a0001c0001t0003g0163a0001c0001t0003g0172a0001c0001t0003g0192others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.196-8039G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927584 | ||||||
chr5:95927585
|
G | A | 6 | a0002c0002t0001g0060a0002c0002t0001g0071a0002c0002t0001g0077others(3): Show | 6 | HG00673.hp2 HG02074.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-8040C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927585 | ||||||
chr5:95927589
|
G | A | 102 | a0001c0003t0008g0013a0001c0004t0001g0232a0002c0002t0001g0001others(99): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.196-8044C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927589 | ||||||
chr5:95927596
|
G | T | 2 | a0002c0002t0006g0090a0002c0002t0006g0108 | 2 | HG00673.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.196-8051C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927596 | ||||||
chr5:95927597
|
A | T | 1 | a0002c0002t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.196-8052T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927597 | ||||||
chr5:95927598
|
C | CAT | 101 | a0001c0003t0008g0013a0001c0004t0001g0232a0002c0002t0001g0001others(98): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.196-8055_196-8054d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927598 | ||||||
chr5:95927598
|
C | T | 2 | a0002c0002t0006g0090a0002c0002t0006g0108 | 2 | HG00673.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.196-8053G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927598 | ||||||
chr5:95927600
|
T | C | 3 | a0001c0001t0002g0229a0001c0001t0015g0256a0001c0001t0017g0231 | 3 | HG02055.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.196-8055A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927600 | ||||||
chr5:95927600
|
TAC | T | 26 | a0001c0001t0003g0007a0001c0001t0003g0051a0001c0001t0003g0152others(23): Show | 27 | HG00544.hp1 HG00609.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.196-8057_196-8056d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927600 | ||||||
chr5:95927602
|
C | CACACACG others(63): Show |
1 | a0001c0001t0003g0186 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.196-8058_196-8057i others(72): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927602 | ||||||
chr5:95927602
|
C | T | 120 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0191others(117): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.196-8057G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927602 | ||||||
chr5:95927604
|
C | T | 5 | a0002c0002t0001g0060a0002c0002t0001g0071a0002c0002t0001g0077others(2): Show | 5 | HG02074.hp1 HG02647.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-8059G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927604 | ||||||
chr5:95927608
|
C | CAT | 21 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0163others(18): Show | 21 | HG00642.hp1 HG00735.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.196-8064_196-8063i others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927608 | ||||||
chr5:95927608
|
C | T | 110 | a0001c0003t0008g0013a0001c0004t0001g0232a0001c0005t0008g0014others(107): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.196-8063G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927608 | ||||||
chr5:95927610
|
C | CAT | 3 | a0001c0001t0003g0168a0001c0001t0003g0171a0001c0001t0003g0205 | 3 | HG03491.hp1 HG03654.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.196-8066_196-8065i others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927610 | ||||||
chr5:95927610
|
C | CATAT | 5 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0191others(2): Show | 5 | NA18965.hp1 NA18973.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-8066_196-8065i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927610 | ||||||
chr5:95927610
|
C | T | 136 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0163others(133): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.196-8065G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927610 | ||||||
chr5:95927611
|
G | A | 4 | a0002c0002t0001g0060a0002c0002t0001g0071a0002c0002t0001g0077others(1): Show | 4 | HG02074.hp1 NA18747.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8066C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927611 | ||||||
chr5:95927615
|
G | A | 111 | a0001c0003t0008g0013a0001c0004t0001g0232a0001c0005t0008g0014others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.196-8070C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927615 | ||||||
chr5:95927620
|
T | G | 1 | a0002c0002t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.196-8075A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927620 | ||||||
chr5:95927622
|
G | C | 1 | a0002c0002t0001g0060 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.196-8077C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927622 | ||||||
chr5:95927622
|
G | T | 3 | a0001c0004t0001g0021a0001c0004t0001g0022a0002c0002t0001g0093 | 3 | HG02622.hp1 HG02896.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.196-8077C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927622 | ||||||
chr5:95927624
|
C | CAT | 111 | a0001c0003t0008g0013a0001c0004t0001g0232a0001c0005t0008g0014others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.196-8081_196-8080d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927624 | ||||||
chr5:95927624
|
C | T | 2 | a0002c0002t0001g0060a0002c0002t0001g0093 | 2 | HG02074.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.196-8079G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927624 | ||||||
chr5:95927626
|
T | C | 2 | a0001c0001t0015g0256a0001c0001t0017g0231 | 2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.196-8081A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927626 | ||||||
chr5:95927626
|
TAC | T | 10 | a0001c0001t0003g0008a0001c0001t0003g0058a0001c0001t0003g0157others(7): Show | 11 | HG00558.hp2 HG01069.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-8083_196-8082d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927626 | ||||||
chr5:95927628
|
C | T | 143 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0163others(140): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.196-8083G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927628 | ||||||
chr5:95927630
|
C | T | 1 | a0002c0002t0006g0059 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.196-8085G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927630 | ||||||
chr5:95927630
|
CACACACG others(41): Show |
C | 4 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0191others(1): Show | 4 | NA18973.hp2 NA18994.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8133_196-8086d others(50): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927630 | ||||||
chr5:95927634
|
C | CAT | 25 | a0001c0001t0003g0007a0001c0001t0003g0051a0001c0001t0003g0152others(22): Show | 26 | HG00544.hp1 HG00609.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-8090_196-8089i others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927634 | ||||||
chr5:95927634
|
C | T | 115 | a0001c0003t0008g0013a0001c0004t0001g0024a0001c0004t0001g0232others(112): Show | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.196-8089G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927634 | ||||||
chr5:95927636
|
C | CATAT | 22 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0168others(19): Show | 22 | HG00642.hp1 HG00735.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.196-8092_196-8091i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927636 | ||||||
chr5:95927636
|
C | T | 144 | a0001c0001t0003g0007a0001c0001t0003g0051a0001c0001t0003g0152others(141): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.196-8091G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927636 | ||||||
chr5:95927637
|
G | A | 2 | a0001c0001t0003g0163a0002c0002t0006g0059 | 2 | HG02015.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.196-8092C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927637 | ||||||
chr5:95927639
|
G | A | 1 | a0001c0001t0003g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.196-8094C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927639 | ||||||
chr5:95927641
|
G | A | 117 | a0001c0003t0008g0013a0001c0004t0001g0021a0001c0004t0001g0022others(114): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.196-8096C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927641 | ||||||
chr5:95927643
|
A | ATATAGAC others(41): Show |
1 | a0001c0001t0002g0217 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.196-8099_196-8098i others(50): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927643 | ||||||
chr5:95927643
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.196-8098T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927643 | ||||||
chr5:95927645
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.196-8100T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927645 | ||||||
chr5:95927648
|
G | T | 1 | a0002c0002t0006g0059 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.196-8103C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927648 | ||||||
chr5:95927650
|
C | CAT | 106 | a0001c0001t0003g0186a0001c0001t0003g0189a0001c0003t0008g0013others(103): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.196-8107_196-8106d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927650 | ||||||
chr5:95927650
|
C | CATAT | 10 | a0002c0002t0001g0070a0002c0002t0001g0079a0002c0002t0001g0096others(7): Show | 10 | HG01106.hp2 HG01123.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-8106_196-8105i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927650 | ||||||
chr5:95927650
|
C | T | 1 | a0002c0002t0006g0059 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.196-8105G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927650 | ||||||
chr5:95927652
|
T | C | 5 | a0001c0001t0002g0229a0001c0001t0003g0157a0001c0001t0003g0159others(2): Show | 5 | HG01069.hp1 HG01074.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-8107A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927652 | ||||||
chr5:95927652
|
TACACACA others(137): Show |
T | 3 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0011 | 4 | HG01243.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-8251_196-8108d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927652 | ||||||
chr5:95927654
|
C | T | 169 | a0001c0001t0003g0007a0001c0001t0003g0051a0001c0001t0003g0152others(166): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.196-8109G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927654 | ||||||
chr5:95927656
|
C | T | 6 | a0001c0003t0012g0015a0001c0003t0012g0016a0002c0002t0001g0087others(3): Show | 6 | HG00544.hp2 HG02056.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-8111G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927656 | ||||||
chr5:95927660
|
C | CAT | 5 | a0001c0001t0003g0166a0001c0001t0003g0184a0001c0001t0003g0196others(2): Show | 5 | HG01928.hp2 HG01993.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-8116_196-8115i others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927660 | ||||||
chr5:95927660
|
C | T | 118 | a0001c0001t0003g0186a0001c0003t0007g0017a0001c0003t0008g0013others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.196-8115G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927660 | ||||||
chr5:95927661
|
A | ATATG | 2 | a0001c0001t0003g0008a0001c0001t0003g0058 | 3 | NA18983.hp2 NA18998.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.196-8117_196-8116i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927661 | ||||||
chr5:95927662
|
C | CATAT | 39 | a0001c0001t0003g0007a0001c0001t0003g0051a0001c0001t0003g0152others(36): Show | 40 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.196-8118_196-8117i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927662 | ||||||
chr5:95927662
|
C | T | 130 | a0001c0001t0003g0008a0001c0001t0003g0058a0001c0001t0003g0166others(127): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.196-8117G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927662 | ||||||
chr5:95927662
|
CGTGTGT | C | 8 | a0001c0001t0003g0161a0001c0001t0003g0168a0001c0001t0003g0171others(5): Show | 8 | HG00642.hp1 HG02074.hp2 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-8123_196-8118d others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927662 | ||||||
chr5:95927662
|
CGTGTGTA others(109): Show |
C | 1 | a0001c0001t0003g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.196-8233_196-8118d others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927662 | ||||||
chr5:95927663
|
G | A | 4 | a0001c0001t0003g0163a0002c0002t0001g0087a0002c0002t0001g0095others(1): Show | 4 | HG00544.hp2 HG02056.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8118C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927663 | ||||||
chr5:95927665
|
G | A | 1 | a0001c0001t0003g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.196-8120C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927665 | ||||||
chr5:95927667
|
G | A | 118 | a0001c0003t0007g0017a0001c0003t0008g0013a0001c0003t0012g0015others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.196-8122C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927667 | ||||||
chr5:95927669
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.196-8124T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927669 | ||||||
chr5:95927671
|
A | G | 1 | a0001c0001t0003g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.196-8126T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927671 | ||||||
chr5:95927672
|
TAGACATA others(9): Show |
T | 8 | a0001c0001t0003g0161a0001c0001t0003g0168a0001c0001t0003g0171others(5): Show | 8 | HG00642.hp1 HG02074.hp2 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-8143_196-8128d others(18): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927672 | ||||||
chr5:95927674
|
G | T | 1 | a0002c0002t0001g0095 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.196-8129C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927674 | ||||||
chr5:95927676
|
C | CAT | 26 | a0001c0001t0003g0203a0001c0003t0007g0017a0001c0005t0008g0014others(23): Show | 26 | HG00099.hp2 HG00673.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-8133_196-8132d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927676 | ||||||
chr5:95927676
|
C | CATAT | 47 | a0001c0004t0001g0232a0002c0002t0001g0001a0002c0002t0001g0020others(44): Show | 49 | HG00673.hp2 HG00733.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.196-8132_196-8131i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927676 | ||||||
chr5:95927676
|
C | T | 3 | a0001c0003t0007g0018a0001c0003t0007g0019a0002c0002t0001g0095 | 3 | HG01109.hp1 HG02723.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.196-8131G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927676 | ||||||
chr5:95927678
|
T | C | 3 | a0001c0001t0002g0229a0001c0001t0015g0256a0001c0001t0017g0231 | 3 | HG02055.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.196-8133A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927678 | ||||||
chr5:95927678
|
TAC | T | 4 | a0001c0001t0003g0157a0001c0001t0003g0159a0001c0001t0003g0204others(1): Show | 4 | HG00558.hp2 HG01069.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-8135_196-8134d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927678 | ||||||
chr5:95927680
|
C | CACACACA others(117): Show |
1 | a0001c0001t0002g0302 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196-8136_196-8135i others(126): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927680 | ||||||
chr5:95927680
|
C | T | 171 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(168): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.196-8135G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927680 | ||||||
chr5:95927682
|
C | T | 52 | a0001c0003t0008g0013a0001c0003t0012g0015a0001c0003t0012g0016others(49): Show | 53 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.196-8137G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927682 | ||||||
chr5:95927686
|
C | CACGTGTG others(135): Show |
1 | a0001c0001t0002g0281 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.196-8142_196-8141i others(144): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927686 | ||||||
chr5:95927686
|
C | T | 76 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0191others(73): Show | 78 | HG00099.hp2 HG00673.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.196-8141G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927686 | ||||||
chr5:95927688
|
C | CATAT | 49 | a0001c0001t0002g0243a0001c0001t0003g0007a0001c0001t0003g0008others(46): Show | 51 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.196-8144_196-8143i others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CATATGTG others(57): Show |
1 | a0001c0001t0002g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.196-8144_196-8143i others(66): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(23): Show |
5 | a0001c0001t0002g0259a0001c0001t0002g0261a0001c0001t0002g0273others(2): Show | 5 | HG01123.hp1 HG03225.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-8173_196-8144d others(32): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(53): Show |
5 | a0001c0001t0002g0216a0001c0001t0002g0221a0001c0001t0002g0225others(2): Show | 5 | HG01070.hp1 HG01074.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-8203_196-8144d others(62): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(83): Show |
2 | a0001c0001t0002g0226a0001c0001t0002g0265 | 2 | HG01993.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.196-8233_196-8144d others(92): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(113): Show |
1 | a0001c0001t0002g0286 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.196-8263_196-8144d others(122): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(95): Show |
1 | a0001c0001t0002g0244 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.196-8144_196-8143i others(104): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(103): Show |
1 | a0001c0001t0002g0245 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.196-8144_196-8143i others(112): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(109): Show |
1 | a0001c0001t0002g0278 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.196-8144_196-8143i others(118): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(109): Show |
1 | a0001c0001t0002g0269 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.196-8144_196-8143i others(118): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(75): Show |
1 | a0001c0001t0002g0248 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.196-8144_196-8143i others(84): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(105): Show |
1 | a0001c0001t0002g0222 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.196-8144_196-8143i others(114): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(213): Show |
1 | a0001c0001t0002g0285 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.196-8144_196-8143i others(222): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(153): Show |
1 | a0001c0001t0002g0280 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.196-8144_196-8143i others(162): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(125): Show |
1 | a0001c0001t0002g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.196-8144_196-8143i others(134): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(105): Show |
1 | a0001c0001t0002g0299 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.196-8144_196-8143i others(114): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(21): Show |
1 | a0001c0001t0002g0257 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.196-8144_196-8143i others(30): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | CGTGTGTA others(71): Show |
1 | a0001c0001t0002g0284 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.196-8144_196-8143i others(80): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
C | T | 130 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0187others(127): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.196-8143G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927688
|
CGTGTGTA others(23): Show |
C | 2 | a0001c0001t0002g0219a0001c0001t0002g0220 | 2 | HG01978.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.196-8173_196-8144d others(32): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927688 | ||||||
chr5:95927689
|
G | A | 50 | a0001c0003t0008g0013a0001c0003t0012g0015a0001c0003t0012g0016others(47): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.196-8144C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927689 | ||||||
chr5:95927693
|
G | A | 73 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(70): Show | 75 | HG00099.hp2 HG00673.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.196-8148C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927693 | ||||||
chr5:95927700
|
G | C | 2 | a0002c0002t0001g0071a0002c0002t0001g0077 | 2 | NA18747.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.196-8155C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927700 | ||||||
chr5:95927700
|
G | T | 47 | a0001c0003t0008g0013a0001c0003t0012g0015a0001c0003t0012g0016others(44): Show | 48 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.196-8155C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927700 | ||||||
chr5:95927702
|
C | CACACACA others(13): Show |
1 | a0001c0001t0015g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.196-8158_196-8157i others(22): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927702 | ||||||
chr5:95927702
|
C | G | 49 | a0001c0003t0008g0013a0001c0003t0012g0015a0001c0003t0012g0016others(46): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.196-8157G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927702 | ||||||
chr5:95927702
|
C | T | 1 | a0002c0002t0001g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.196-8157G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927702 | ||||||
chr5:95927704
|
T | C | 51 | a0001c0001t0002g0229a0001c0001t0017g0231a0001c0003t0008g0013others(48): Show | 52 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.196-8159A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927704 | ||||||
chr5:95927704
|
T | G | 2 | a0001c0001t0015g0256a0002c0002t0001g0146 | 2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196-8159A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927704 | ||||||
chr5:95927704
|
TAC | T | 50 | a0001c0001t0002g0250a0001c0001t0003g0172a0001c0001t0003g0187others(47): Show | 52 | HG00558.hp2 HG00673.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.196-8161_196-8160d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927704 | ||||||
chr5:95927704
|
TACACACA others(25): Show |
T | 1 | a0001c0001t0002g0287 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.196-8191_196-8160d others(34): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927704 | ||||||
chr5:95927704
|
TACACACA others(55): Show |
T | 2 | a0001c0001t0003g0157a0001c0001t0003g0159 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.196-8221_196-8160d others(64): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927704 | ||||||
chr5:95927706
|
C | CACACACA others(17): Show |
1 | a0001c0001t0002g0252 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.196-8162_196-8161i others(26): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927706 | ||||||
chr5:95927706
|
C | CACACACA others(95): Show |
1 | a0001c0001t0001g0267 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.196-8162_196-8161i others(104): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927706 | ||||||
chr5:95927706
|
C | CACACACA others(121): Show |
1 | a0001c0001t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.196-8162_196-8161i others(130): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927706 | ||||||
chr5:95927706
|
C | CACACACA others(147): Show |
1 | a0001c0001t0002g0291 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.196-8162_196-8161i others(156): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927706 | ||||||
chr5:95927706
|
C | CACACACA others(149): Show |
1 | a0001c0001t0002g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.196-8162_196-8161i others(158): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927706 | ||||||
chr5:95927706
|
C | T | 160 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(157): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.196-8161G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927706 | ||||||
chr5:95927708
|
C | CACACACG others(41): Show |
5 | a0001c0001t0002g0214a0001c0001t0002g0233a0001c0001t0002g0241others(2): Show | 5 | HG02300.hp2 HG04228.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-8164_196-8163i others(50): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927708 | ||||||
chr5:95927708
|
C | CACACACG others(93): Show |
1 | a0001c0001t0002g0276 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.196-8164_196-8163i others(102): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927708 | ||||||
chr5:95927708
|
C | CACACACG others(171): Show |
1 | a0001c0001t0002g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.196-8164_196-8163i others(180): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927708 | ||||||
chr5:95927708
|
C | CACACACG others(117): Show |
1 | a0001c0001t0002g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196-8164_196-8163i others(126): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927708 | ||||||
chr5:95927708
|
C | T | 150 | a0001c0001t0003g0172a0001c0001t0003g0187a0001c0001t0003g0195others(147): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.196-8163G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927708 | ||||||
chr5:95927710
|
C | T | 118 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.196-8165G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927710 | ||||||
chr5:95927712
|
C | T | 10 | a0002c0002t0001g0121a0002c0002t0001g0124a0002c0002t0001g0125others(7): Show | 10 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-8167G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927712 | ||||||
chr5:95927712
|
CACAT | C | 6 | a0002c0002t0001g0079a0002c0002t0001g0150a0002c0002t0009g0054others(3): Show | 6 | HG01070.hp2 HG01106.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-8171_196-8168d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927712 | ||||||
chr5:95927714
|
C | CGTGTGT | 4 | a0001c0001t0002g0234a0001c0001t0002g0237a0001c0001t0002g0268others(1): Show | 4 | HG01069.hp2 HG02109.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-8170_196-8169i others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927714 | ||||||
chr5:95927714
|
CATAT | C | 10 | a0001c0001t0002g0215a0001c0001t0002g0235a0001c0001t0002g0236others(7): Show | 10 | HG00099.hp1 HG01346.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-8173_196-8170d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927714 | ||||||
chr5:95927716
|
T | C | 10 | a0001c0001t0002g0214a0001c0001t0002g0217a0001c0001t0002g0230others(7): Show | 10 | HG00733.hp2 HG02055.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-8171A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927716 | ||||||
chr5:95927717
|
ATG | A | 5 | a0002c0002t0001g0121a0002c0002t0001g0124a0002c0002t0001g0125others(2): Show | 5 | HG01891.hp2 HG02896.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-8174_196-8173d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927717 | ||||||
chr5:95927718
|
T | C | 10 | a0001c0001t0002g0214a0001c0001t0002g0217a0001c0001t0002g0230others(7): Show | 10 | HG00733.hp2 HG02055.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-8173A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927718 | ||||||
chr5:95927718
|
T | TAGACATA others(9): Show |
4 | a0001c0001t0002g0234a0001c0001t0002g0237a0001c0001t0002g0268others(1): Show | 4 | HG01069.hp2 HG02109.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-8174_196-8173i others(18): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927718 | ||||||
chr5:95927723
|
G | A | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.196-8178C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927723 | ||||||
chr5:95927729
|
A | G | 1 | a0001c0003t0007g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.196-8184T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927729 | ||||||
chr5:95927730
|
G | T | 1 | a0001c0003t0007g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.196-8185C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927730 | ||||||
chr5:95927732
|
C | T | 1 | a0001c0003t0007g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.196-8187G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927732 | ||||||
chr5:95927734
|
T | C | 5 | a0001c0001t0002g0229a0001c0001t0015g0256a0001c0001t0017g0231others(2): Show | 5 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-8189A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927734 | ||||||
chr5:95927734
|
TAC | T | 58 | a0001c0001t0002g0252a0001c0001t0002g0268a0001c0001t0003g0164others(55): Show | 59 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.196-8191_196-8190d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927734 | ||||||
chr5:95927736
|
C | CACACACA others(43): Show |
1 | a0001c0001t0002g0260 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.196-8192_196-8191i others(52): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927736 | ||||||
chr5:95927736
|
C | CACACACA others(119): Show |
1 | a0001c0001t0002g0272 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.196-8192_196-8191i others(128): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927736 | ||||||
chr5:95927736
|
C | T | 154 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(151): Show | 161 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.196-8191G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927736 | ||||||
chr5:95927738
|
C | CACACGTG others(61): Show |
1 | a0001c0001t0002g0303 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.196-8194_196-8193i others(70): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927738 | ||||||
chr5:95927738
|
C | T | 153 | a0001c0001t0003g0164a0001c0001t0003g0182a0001c0001t0003g0183others(150): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.196-8193G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927738 | ||||||
chr5:95927740
|
C | T | 67 | a0001c0003t0007g0018a0001c0003t0007g0019a0001c0003t0012g0015others(64): Show | 68 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.196-8195G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927740 | ||||||
chr5:95927742
|
CACAT | C | 57 | a0001c0005t0010g0048a0001c0005t0010g0049a0002c0002t0001g0001others(54): Show | 59 | HG00140.hp2 HG00280.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.196-8201_196-8198d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927742 | ||||||
chr5:95927744
|
CAT | C | 23 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0003t0004g0003others(20): Show | 26 | HG01168.hp1 HG01496.hp1 HG01975.hp1 others(23): Show |
intron_variant | MODIFIER | c.196-8201_196-8200d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927744 | ||||||
chr5:95927744
|
CATAT | C | 4 | a0001c0001t0002g0235a0001c0001t0002g0300a0001c0001t0015g0256others(1): Show | 4 | HG02055.hp1 HG02559.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-8203_196-8200d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927744 | ||||||
chr5:95927746
|
T | C | 2 | a0001c0001t0002g0217a0001c0001t0002g0303 | 2 | HG00733.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.196-8201A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927746 | ||||||
chr5:95927748
|
T | C | 3 | a0001c0001t0002g0217a0001c0001t0002g0230a0001c0001t0002g0303 | 3 | HG00733.hp2 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.196-8203A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927748 | ||||||
chr5:95927753
|
G | A | 147 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(144): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.196-8208C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927753 | ||||||
chr5:95927755
|
A | ATATAGAC others(53): Show |
1 | a0001c0001t0002g0249 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.196-8211_196-8210i others(62): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927755 | ||||||
chr5:95927762
|
C | CACACACA others(67): Show |
1 | a0001c0001t0017g0231 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.196-8218_196-8217i others(76): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927762 | ||||||
chr5:95927764
|
T | C | 1 | a0001c0001t0015g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.196-8219A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927764 | ||||||
chr5:95927764
|
T | G | 1 | a0001c0001t0017g0231 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.196-8219A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927764 | ||||||
chr5:95927764
|
TAC | T | 74 | a0001c0001t0002g0233a0001c0001t0002g0268a0001c0001t0003g0007others(71): Show | 75 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.196-8221_196-8220d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927764 | ||||||
chr5:95927766
|
C | CACACACA others(111): Show |
1 | a0001c0001t0002g0206 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.196-8222_196-8221i others(120): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927766 | ||||||
chr5:95927766
|
C | T | 143 | a0001c0001t0003g0008a0001c0001t0003g0058a0001c0001t0003g0152others(140): Show | 150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.196-8221G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927766 | ||||||
chr5:95927768
|
C | CACACACA others(51): Show |
1 | a0001c0001t0003g0187 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.196-8224_196-8223i others(60): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927768 | ||||||
chr5:95927768
|
C | T | 204 | a0001c0001t0003g0007a0001c0001t0003g0051a0001c0001t0003g0156others(201): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.196-8223G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927768 | ||||||
chr5:95927770
|
C | T | 24 | a0001c0003t0005g0030a0001c0003t0005g0031a0001c0003t0005g0032others(21): Show | 25 | HG01109.hp1 HG01891.hp1 HG02004.hp1 others(22): Show |
intron_variant | MODIFIER | c.196-8225G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927770 | ||||||
chr5:95927772
|
C | CATATGTG others(45): Show |
1 | a0002c0002t0001g0128 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.196-8228_196-8227i others(54): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927772 | ||||||
chr5:95927772
|
C | CATATGTG others(71): Show |
1 | a0002c0002t0001g0053 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.196-8228_196-8227i others(80): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927772 | ||||||
chr5:95927772
|
C | CATATGTG others(43): Show |
8 | a0002c0002t0001g0066a0002c0002t0001g0067a0002c0002t0001g0069others(5): Show | 8 | HG02015.hp1 HG02027.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-8228_196-8227i others(52): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927772 | ||||||
chr5:95927772
|
C | CATGTGTA others(15): Show |
3 | a0002c0002t0001g0072a0002c0002t0001g0093a0002c0002t0013g0064 | 3 | HG02818.hp1 NA18986.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.196-8228_196-8227i others(24): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927772 | ||||||
chr5:95927772
|
C | CATGTGTA others(41): Show |
1 | a0003c0007t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196-8228_196-8227i others(50): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927772 | ||||||
chr5:95927772
|
CACAT | C | 91 | a0002c0002t0001g0001a0002c0002t0001g0020a0002c0002t0001g0026others(88): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.196-8231_196-8228d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927772 | ||||||
chr5:95927774
|
CAT | C | 19 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(16): Show | 22 | HG01168.hp1 HG01496.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.196-8231_196-8230d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927774 | ||||||
chr5:95927776
|
T | C | 14 | a0002c0002t0001g0053a0002c0002t0001g0066a0002c0002t0001g0067others(11): Show | 14 | HG00738.hp2 HG02015.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.196-8231A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927776 | ||||||
chr5:95927777
|
A | G | 1 | a0001c0001t0002g0303 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.196-8232T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927777 | ||||||
chr5:95927783
|
G | A | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.196-8238C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927783 | ||||||
chr5:95927794
|
T | C | 1 | a0001c0001t0015g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.196-8249A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927794 | ||||||
chr5:95927794
|
TAC | T | 5 | a0001c0001t0003g0152a0001c0001t0003g0153a0002c0002t0001g0006others(2): Show | 6 | HG02004.hp1 NA18944.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-8251_196-8250d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927794 | ||||||
chr5:95927796
|
C | T | 212 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(209): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.196-8251G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927796 | ||||||
chr5:95927798
|
C | T | 153 | a0001c0001t0003g0152a0001c0001t0003g0153a0001c0003t0004g0003others(150): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.196-8253G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927798 | ||||||
chr5:95927800
|
C | T | 124 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(121): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.196-8255G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927800 | ||||||
chr5:95927802
|
CACAT | C | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 26 | HG01168.hp1 HG01496.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.196-8261_196-8258d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927802 | ||||||
chr5:95927804
|
CAT | C | 4 | a0001c0006t0004g0042a0001c0006t0004g0047a0001c0006t0011g0027others(1): Show | 4 | HG00609.hp1 NA18941.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8261_196-8260d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927804 | ||||||
chr5:95927807
|
A | G | 1 | a0006c0010t0025g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196-8262T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927807 | ||||||
chr5:95927809
|
G | A | 21 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(18): Show | 24 | HG01168.hp1 HG01496.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.196-8264C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927809 | ||||||
chr5:95927813
|
G | A | 24 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(21): Show | 25 | HG00609.hp1 HG01109.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.196-8268C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927813 | ||||||
chr5:95927818
|
TAGAC | T | 116 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(113): Show | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.196-8277_196-8274d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927818 | ||||||
chr5:95927820
|
G | T | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG01168.hp1 HG01496.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.196-8275C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927820 | ||||||
chr5:95927822
|
C | CATATATA others(71): Show |
3 | a0002c0002t0001g0006a0002c0002t0001g0065a0002c0002t0001g0095 | 4 | HG02004.hp1 NA18944.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-8278_196-8277i others(80): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927822 | ||||||
chr5:95927822
|
C | T | 26 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(23): Show | 29 | HG01168.hp1 HG01496.hp1 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.196-8277G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927822 | ||||||
chr5:95927824
|
T | C | 1 | a0001c0001t0015g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.196-8279A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927824 | ||||||
chr5:95927826
|
C | T | 192 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(189): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.196-8281G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927826 | ||||||
chr5:95927828
|
C | T | 6 | a0001c0006t0004g0042a0001c0006t0004g0047a0001c0006t0011g0027others(3): Show | 6 | HG00609.hp1 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-8283G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927828 | ||||||
chr5:95927830
|
C | T | 2 | a0002c0002t0001g0102a0002c0002t0001g0114 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.196-8285G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927830 | ||||||
chr5:95927834
|
C | T | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG01168.hp1 HG01496.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.196-8289G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927834 | ||||||
chr5:95927836
|
T | C | 4 | a0001c0006t0004g0042a0001c0006t0004g0047a0001c0006t0011g0027others(1): Show | 4 | HG00609.hp1 NA18941.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8291A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927836 | ||||||
chr5:95927837
|
ATG | A | 121 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(118): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.196-8294_196-8293d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927837 | ||||||
chr5:95927837
|
ATGTG | A | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG01168.hp1 HG01496.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.196-8296_196-8293d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927837 | ||||||
chr5:95927839
|
G | A | 4 | a0001c0006t0004g0042a0001c0006t0004g0047a0001c0006t0011g0027others(1): Show | 4 | HG00609.hp1 NA18941.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8294C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927839 | ||||||
chr5:95927841
|
G | A | 125 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(122): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.196-8296C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927841 | ||||||
chr5:95927843
|
G | A | 149 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(146): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.196-8298C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927843 | ||||||
chr5:95927843
|
G | GTATATAT others(17): Show |
2 | a0002c0002t0001g0102a0002c0002t0001g0114 | 2 | HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.196-8299_196-8298i others(26): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927843 | ||||||
chr5:95927953
|
C | T | 7 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(4): Show | 7 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-8408G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95927953 | ||||||
chr5:95928031
|
G | A | 111 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.196-8486C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95928031 | ||||||
chr5:95928034
|
C | G | 25 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(22): Show | 28 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.196-8489G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95928034 | ||||||
chr5:95928048
|
T | A | 111 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0020others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.196-8503A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95928048 | ||||||
chr5:95928276
|
A | G | 3 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0011 | 4 | HG01243.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-8731T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95928276 | ||||||
chr5:95928309
|
C | T | 2 | a0001c0001t0003g0171a0001c0001t0003g0190 | 2 | HG00642.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.196-8764G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95928309 | ||||||
chr5:95928601
|
G | C | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.196-9056C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95928601 | ||||||
chr5:95928948
|
A | C | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.196-9403T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95928948 | ||||||
chr5:95928997
|
A | G | 4 | a0002c0002t0001g0065a0002c0002t0001g0067a0002c0002t0001g0069others(1): Show | 4 | HG01928.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-9452T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95928997 | ||||||
chr5:95929261
|
A | AT | 119 | a0001c0001t0002g0222a0001c0001t0002g0228a0001c0001t0002g0229others(116): Show | 125 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.196-9717dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929261 | ||||||
chr5:95929317
|
G | A | 3 | a0003c0007t0001g0104a0003c0007t0001g0110a0003c0007t0001g0111 | 3 | HG01070.hp2 HG02109.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.196-9772C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929317 | ||||||
chr5:95929352
|
G | A | 66 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0051others(63): Show | 68 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.196-9807C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929352 | ||||||
chr5:95929364
|
TTC | T | 7 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(4): Show | 7 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-9821_196-9820d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929364 | ||||||
chr5:95929383
|
C | T | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.196-9838G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929383 | ||||||
chr5:95929568
|
C | G | 1 | a0001c0001t0002g0269 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.196-10023G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929568 | ||||||
chr5:95929586
|
A | G | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.196-10041T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929586 | ||||||
chr5:95929781
|
T | TA | 13 | a0001c0001t0002g0222a0001c0001t0002g0228a0001c0001t0002g0229others(10): Show | 13 | HG01943.hp1 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-10237dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929781 | ||||||
chr5:95929792
|
A | C | 2 | a0001c0003t0012g0015a0001c0003t0012g0016 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.196-10247T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929792 | ||||||
chr5:95929827
|
C | T | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.196-10282G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929827 | ||||||
chr5:95929828
|
C | G | 3 | a0001c0001t0001g0267a0001c0001t0002g0250a0001c0001t0002g0266 | 3 | HG03831.hp1 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.196-10283G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929828 | ||||||
chr5:95929852
|
G | A | 151 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(148): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.196-10307C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95929852 | ||||||
chr5:95930026
|
G | A | 24 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0058others(21): Show | 26 | HG00544.hp1 HG00558.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-10481C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95930026 | ||||||
chr5:95930270
|
G | T | 1 | a0001c0001t0002g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.196-10725C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95930270 | ||||||
chr5:95930350
|
T | C | 2 | a0002c0002t0001g0053a0002c0002t0020g0052 | 2 | NA18962.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.196-10805A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95930350 | ||||||
chr5:95930364
|
G | T | 6 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-10819C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95930364 | ||||||
chr5:95930492
|
C | G | 1 | a0001c0001t0002g0277 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.196-10947G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95930492 | ||||||
chr5:95930778
|
T | C | 1 | a0001c0001t0002g0300 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.196-11233A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95930778 | ||||||
chr5:95930871
|
C | T | 1 | a0001c0001t0003g0170 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.196-11326G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95930871 | ||||||
chr5:95930909
|
AT | A | 147 | a0001c0001t0002g0221a0001c0001t0002g0224a0001c0001t0002g0265others(144): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.196-11365delA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95930909 | ||||||
chr5:95931108
|
C | A | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.196-11563G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931108 | ||||||
chr5:95931241
|
T | C | 1 | a0001c0001t0002g0241 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.196-11696A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931241 | ||||||
chr5:95931321
|
C | T | 4 | a0002c0002t0001g0143a0002c0002t0001g0144a0002c0002t0001g0145others(1): Show | 4 | HG00741.hp2 HG01243.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+11681G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931321 | ||||||
chr5:95931370
|
A | G | 1 | a0001c0003t0007g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.195+11632T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931370 | ||||||
chr5:95931371
|
A | G | 1 | a0001c0001t0003g0160 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.195+11631T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931371 | ||||||
chr5:95931645
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.195+11357T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931645 | ||||||
chr5:95931775
|
G | A | 1 | a0002c0002t0001g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.195+11227C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931775 | ||||||
chr5:95931796
|
T | TA | 113 | a0001c0001t0001g0267a0001c0001t0002g0009a0001c0001t0002g0206others(110): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.195+11205dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931796 | ||||||
chr5:95931796
|
T | TAA | 16 | a0001c0001t0002g0193a0001c0001t0002g0217a0001c0001t0002g0221others(13): Show | 17 | HG00642.hp2 HG00733.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.195+11204_195+1120 others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931796 | ||||||
chr5:95931796
|
T | TAAA | 7 | a0001c0001t0002g0240a0002c0002t0001g0135a0002c0002t0001g0143others(4): Show | 7 | HG00741.hp2 HG01243.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+11203_195+1120 others(7): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931796 | ||||||
chr5:95931796
|
T | TAAAA | 78 | a0001c0003t0008g0013a0002c0002t0001g0001a0002c0002t0001g0053others(75): Show | 80 | HG00140.hp2 HG00280.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.195+11202_195+1120 others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931796 | ||||||
chr5:95931796
|
T | TAAAAA | 17 | a0001c0005t0008g0014a0002c0002t0001g0006a0002c0002t0001g0057others(14): Show | 18 | HG00099.hp2 HG00673.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.195+11201_195+1120 others(9): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931796 | ||||||
chr5:95931796
|
T | TAAAAAAA others(3): Show |
2 | a0001c0003t0012g0016a0002c0002t0001g0026 | 2 | HG02280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.195+11196_195+1120 others(14): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931796 | ||||||
chr5:95931796
|
T | TAAAAAAA others(6): Show |
3 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019 | 3 | HG01109.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.195+11193_195+1120 others(17): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931796 | ||||||
chr5:95931978
|
G | GT | 77 | a0001c0001t0003g0212a0001c0003t0007g0017a0001c0003t0007g0018others(74): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.195+11023dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931978 | ||||||
chr5:95931978
|
G | GTT | 32 | a0002c0002t0001g0062a0002c0002t0001g0082a0002c0002t0001g0087others(29): Show | 32 | HG00673.hp1 HG00738.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.195+11022_195+1102 others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931978 | ||||||
chr5:95931978
|
GT | G | 26 | a0001c0001t0002g0293a0001c0003t0004g0003a0001c0003t0004g0004others(23): Show | 29 | HG00558.hp1 HG00609.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.195+11023delA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95931978 | ||||||
chr5:95932313
|
T | C | 1 | a0001c0001t0003g0188 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.195+10689A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95932313 | ||||||
chr5:95932679
|
G | A | 2 | a0002c0008t0001g0106a0002c0008t0001g0107 | 2 | HG01346.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.195+10323C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95932679 | ||||||
chr5:95932826
|
T | C | 1 | a0001c0001t0003g0290 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.195+10176A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95932826 | ||||||
chr5:95932931
|
T | C | 1 | a0001c0003t0008g0013 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.195+10071A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95932931 | ||||||
chr5:95933003
|
T | G | 16 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(13): Show | 19 | HG00609.hp1 HG01168.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.195+9999A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95933003 | ||||||
chr5:95933064
|
G | A | 101 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.195+9938C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95933064 | ||||||
chr5:95933539
|
A | T | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.195+9463T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95933539 | ||||||
chr5:95933595
|
CTG | C | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+9405_195+9406d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95933595 | ||||||
chr5:95933630
|
T | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.195+9372A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95933630 | ||||||
chr5:95933769
|
T | A | 1 | a0002c0002t0001g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.195+9233A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95933769 | ||||||
chr5:95933795
|
A | AT | 44 | a0001c0001t0002g0222a0001c0001t0015g0256a0001c0003t0004g0003others(41): Show | 47 | HG00609.hp1 HG01109.hp1 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.195+9206dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95933795 | ||||||
chr5:95933804
|
T | C | 6 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0133others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+9198A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95933804 | ||||||
chr5:95933897
|
C | T | 2 | a0002c0002t0001g0079a0002c0002t0001g0112 | 2 | HG00733.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.195+9105G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95933897 | ||||||
chr5:95933898
|
A | G | 94 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(91): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.195+9104T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95933898 | ||||||
chr5:95934284
|
GC | G | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+8717delG | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95934284 | ||||||
chr5:95934537
|
C | T | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.195+8465G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95934537 | ||||||
chr5:95934688
|
G | A | 7 | a0001c0001t0002g0221a0001c0001t0002g0224a0001c0001t0002g0265others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+8314C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95934688 | ||||||
chr5:95934977
|
T | C | 1 | a0004c0009t0003g0194 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.195+8025A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95934977 | ||||||
chr5:95935016
|
C | G | 1 | a0002c0002t0009g0056 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.195+7986G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935016 | ||||||
chr5:95935065
|
C | T | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.195+7937G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935065 | ||||||
chr5:95935161
|
A | C | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.195+7841T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935161 | ||||||
chr5:95935168
|
A | G | 128 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(125): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.195+7834T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935168 | ||||||
chr5:95935205
|
T | C | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.195+7797A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935205 | ||||||
chr5:95935315
|
C | A | 1 | a0006c0010t0025g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.195+7687G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935315 | ||||||
chr5:95935469
|
A | T | 101 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.195+7533T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935469 | ||||||
chr5:95935584
|
T | C | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.195+7418A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935584 | ||||||
chr5:95935620
|
T | C | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+7382A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935620 | ||||||
chr5:95935651
|
T | C | 3 | a0001c0003t0005g0030a0001c0003t0005g0031a0001c0003t0005g0032 | 3 | HG02258.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.195+7351A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935651 | ||||||
chr5:95935774
|
C | T | 77 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(74): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.195+7228G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935774 | ||||||
chr5:95935786
|
C | T | 1 | a0002c0002t0001g0087 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.195+7216G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935786 | ||||||
chr5:95935829
|
C | T | 1 | a0001c0001t0003g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.195+7173G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935829 | ||||||
chr5:95935902
|
T | TA | 94 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(91): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.195+7099dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935902 | ||||||
chr5:95935908
|
G | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.195+7094C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935908 | ||||||
chr5:95935945
|
T | C | 6 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0133others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+7057A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95935945 | ||||||
chr5:95936058
|
A | G | 1 | a0001c0001t0023g0169 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.195+6944T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95936058 | ||||||
chr5:95936227
|
T | A | 3 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019 | 3 | HG01109.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.195+6775A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95936227 | ||||||
chr5:95936308
|
G | C | 9 | a0001c0003t0004g0004a0001c0003t0004g0005a0001c0003t0004g0033others(6): Show | 11 | HG01975.hp1 NA18951.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+6694C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95936308 | ||||||
chr5:95936357
|
C | A | 2 | a0001c0001t0003g0157a0001c0001t0003g0159 | 2 | HG01069.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.195+6645G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95936357 | ||||||
chr5:95936523
|
C | T | 1 | a0001c0001t0003g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.195+6479G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95936523 | ||||||
chr5:95936653
|
C | T | 101 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.195+6349G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95936653 | ||||||
chr5:95936724
|
G | C | 101 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.195+6278C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95936724 | ||||||
chr5:95936725
|
A | C | 101 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.195+6277T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95936725 | ||||||
chr5:95936729
|
AGTAAGG | A | 101 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.195+6267_195+6272d others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95936729 | ||||||
chr5:95936834
|
G | A | 1 | a0001c0001t0003g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.195+6168C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95936834 | ||||||
chr5:95937003
|
C | T | 1 | a0001c0001t0003g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.195+5999G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95937003 | ||||||
chr5:95937006
|
G | A | 2 | a0002c0002t0001g0073a0002c0002t0001g0074 | 2 | NA19002.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.195+5996C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95937006 | ||||||
chr5:95937033
|
G | A | 7 | a0001c0001t0002g0221a0001c0001t0002g0224a0001c0001t0002g0265others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+5969C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95937033 | ||||||
chr5:95937273
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.195+5729G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95937273 | ||||||
chr5:95937450
|
G | A | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.195+5552C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95937450 | ||||||
chr5:95937503
|
C | CA | 109 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(106): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.195+5498dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95937503 | ||||||
chr5:95937503
|
C | CAA | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+5497_195+5498d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95937503 | ||||||
chr5:95937706
|
T | A | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.195+5296A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95937706 | ||||||
chr5:95937904
|
G | A | 14 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(11): Show | 14 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.195+5098C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95937904 | ||||||
chr5:95938078
|
T | G | 11 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(8): Show | 11 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+4924A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938078 | ||||||
chr5:95938190
|
T | C | 14 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(11): Show | 14 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.195+4812A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938190 | ||||||
chr5:95938211
|
G | C | 143 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(140): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.195+4791C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938211 | ||||||
chr5:95938283
|
G | A | 14 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(11): Show | 14 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.195+4719C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938283 | ||||||
chr5:95938286
|
T | C | 1 | a0001c0003t0004g0029 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.195+4716A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938286 | ||||||
chr5:95938434
|
A | G | 6 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0133others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+4568T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938434 | ||||||
chr5:95938503
|
T | C | 2 | a0001c0001t0002g0216a0001c0001t0002g0251 | 2 | HG01074.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.195+4499A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938503 | ||||||
chr5:95938664
|
G | A | 44 | a0002c0002t0001g0001a0002c0002t0001g0057a0002c0002t0001g0060others(41): Show | 46 | HG00099.hp2 HG00673.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.195+4338C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938664 | ||||||
chr5:95938787
|
T | C | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.195+4215A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938787 | ||||||
chr5:95938928
|
T | C | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.195+4074A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938928 | ||||||
chr5:95938941
|
T | C | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.195+4061A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938941 | ||||||
chr5:95938998
|
A | G | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.195+4004T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95938998 | ||||||
chr5:95939091
|
C | T | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.195+3911G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95939091 | ||||||
chr5:95939215
|
G | A | 2 | a0001c0003t0007g0018a0001c0003t0007g0019 | 2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.195+3787C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95939215 | ||||||
chr5:95939364
|
AT | A | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.195+3637delA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95939364 | ||||||
chr5:95939505
|
T | C | 1 | a0001c0001t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.195+3497A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95939505 | ||||||
chr5:95939529
|
G | A | 2 | a0001c0001t0002g0268a0001c0003t0004g0046 | 2 | HG02109.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.195+3473C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95939529 | ||||||
chr5:95939597
|
G | T | 4 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0023others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+3405C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95939597 | ||||||
chr5:95939598
|
TGAA | T | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.195+3401_195+3403d others(5): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95939598 | ||||||
chr5:95939699
|
A | G | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+3303T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95939699 | ||||||
chr5:95939932
|
G | A | 1 | a0001c0001t0003g0201 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.195+3070C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95939932 | ||||||
chr5:95940060
|
A | T | 1 | a0002c0002t0001g0242 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.195+2942T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95940060 | ||||||
chr5:95940313
|
T | C | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.195+2689A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95940313 | ||||||
chr5:95940359
|
G | A | 126 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(123): Show | 132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.195+2643C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95940359 | ||||||
chr5:95940556
|
C | A | 138 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(135): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.195+2446G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95940556 | ||||||
chr5:95940628
|
A | T | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 26 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.195+2374T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95940628 | ||||||
chr5:95940733
|
A | G | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 26 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.195+2269T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95940733 | ||||||
chr5:95940770
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.195+2232A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95940770 | ||||||
chr5:95940816
|
T | C | 7 | a0001c0003t0004g0004a0001c0003t0004g0005a0001c0003t0004g0033others(4): Show | 9 | HG01975.hp1 NA18951.hp2 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+2186A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95940816 | ||||||
chr5:95940843
|
T | C | 1 | a0002c0002t0001g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.195+2159A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95940843 | ||||||
chr5:95940875
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.195+2127C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95940875 | ||||||
chr5:95941418
|
A | G | 1 | a0002c0002t0001g0096 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.195+1584T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95941418 | ||||||
chr5:95941506
|
G | C | 3 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0024 | 3 | HG02622.hp1 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.195+1496C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95941506 | ||||||
chr5:95941648
|
A | T | 1 | a0001c0001t0003g0168 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.195+1354T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95941648 | ||||||
chr5:95941851
|
A | G | 110 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(107): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.195+1151T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95941851 | ||||||
chr5:95942072
|
C | T | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.195+930G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95942072 | ||||||
chr5:95942271
|
T | C | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.195+731A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95942271 | ||||||
chr5:95942315
|
A | G | 141 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(138): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.195+687T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95942315 | ||||||
chr5:95942527
|
T | A | 1 | a0001c0001t0003g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.195+475A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95942527 | ||||||
chr5:95942674
|
C | T | 1 | a0001c0004t0001g0232 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.195+328G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95942674 | ||||||
chr5:95942930
|
A | G | 1 | a0001c0001t0003g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.195+72T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95942930 | ||||||
chr5:95942975
|
G | A | 109 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(106): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.195+27C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95942975 | ||||||
chr5:95942988
|
A | G | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.195+14T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95942988 | ||||||
chr5:95942994
|
G | A | 1 | a0001c0001t0003g0298 | 1 | NA19004.hp1 | splice_region_variant&intron_variant | LOW | c.195+8C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 2/11 | chr5 | 95942994 | ||||||
chr5:95943131
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.148-82C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95943131 | ||||||
chr5:95943266
|
T | TA | 112 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(109): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.148-218dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95943266 | ||||||
chr5:95943357
|
T | C | 1 | a0001c0001t0002g0269 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.148-308A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95943357 | ||||||
chr5:95943529
|
A | C | 115 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(112): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.148-480T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95943529 | ||||||
chr5:95943574
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.148-525C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95943574 | ||||||
chr5:95943682
|
T | C | 1 | a0002c0002t0001g0075 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.148-633A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95943682 | ||||||
chr5:95943687
|
G | A | 6 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-638C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95943687 | ||||||
chr5:95943819
|
G | T | 1 | a0001c0001t0002g0248 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.148-770C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95943819 | ||||||
chr5:95943889
|
T | G | 1 | a0002c0002t0001g0255 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.148-840A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95943889 | ||||||
chr5:95943997
|
A | G | 6 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-948T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95943997 | ||||||
chr5:95944053
|
T | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.148-1004A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95944053 | ||||||
chr5:95944109
|
T | C | 2 | a0001c0003t0007g0018a0001c0003t0007g0019 | 2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.148-1060A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95944109 | ||||||
chr5:95944270
|
A | G | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.148-1221T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95944270 | ||||||
chr5:95944329
|
T | C | 115 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(112): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.148-1280A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95944329 | ||||||
chr5:95944464
|
G | A | 1 | a0001c0004t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.148-1415C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95944464 | ||||||
chr5:95944610
|
C | T | 2 | a0002c0002t0001g0020a0002c0002t0001g0026 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.148-1561G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95944610 | ||||||
chr5:95944735
|
T | C | 1 | a0002c0002t0001g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.148-1686A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95944735 | ||||||
chr5:95944849
|
A | G | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.148-1800T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95944849 | ||||||
chr5:95944864
|
C | A | 1 | a0001c0001t0002g0252 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.148-1815G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95944864 | ||||||
chr5:95944874
|
C | A | 1 | a0002c0002t0001g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.148-1825G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95944874 | ||||||
chr5:95945098
|
C | A | 1 | a0001c0004t0001g0232 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.148-2049G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95945098 | ||||||
chr5:95945144
|
T | A | 115 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(112): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.148-2095A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95945144 | ||||||
chr5:95945343
|
G | A | 1 | a0001c0003t0007g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-2294C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95945343 | ||||||
chr5:95945649
|
C | T | 94 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(91): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.148-2600G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95945649 | ||||||
chr5:95945848
|
A | T | 5 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0011others(2): Show | 6 | HG01243.hp2 HG02055.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-2799T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95945848 | ||||||
chr5:95945882
|
G | A | 6 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-2833C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95945882 | ||||||
chr5:95946032
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.148-2983G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95946032 | ||||||
chr5:95946276
|
G | A | 1 | a0001c0003t0004g0029 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.148-3227C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95946276 | ||||||
chr5:95946387
|
A | C | 143 | a0001c0001t0014g0025a0001c0003t0004g0003a0001c0003t0004g0004others(140): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.148-3338T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95946387 | ||||||
chr5:95946415
|
A | T | 1 | a0002c0002t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.148-3366T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95946415 | ||||||
chr5:95946444
|
G | T | 1 | a0001c0001t0003g0167 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.148-3395C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95946444 | ||||||
chr5:95946465
|
A | T | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.148-3416T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95946465 | ||||||
chr5:95946678
|
A | T | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.148-3629T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95946678 | ||||||
chr5:95946785
|
T | C | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.148-3736A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95946785 | ||||||
chr5:95946923
|
GGAGTGGT | G | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.148-3881_148-3875d others(9): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95946923 | ||||||
chr5:95947267
|
A | G | 115 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(112): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.148-4218T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95947267 | ||||||
chr5:95947270
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.148-4221C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95947270 | ||||||
chr5:95947420
|
T | C | 3 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0011 | 4 | HG01243.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-4371A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95947420 | ||||||
chr5:95947603
|
T | C | 1 | a0001c0003t0007g0019 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.148-4554A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95947603 | ||||||
chr5:95947650
|
G | C | 1 | a0001c0001t0003g0207 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.148-4601C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95947650 | ||||||
chr5:95947836
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.148-4787A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95947836 | ||||||
chr5:95947875
|
GT | G | 212 | a0001c0001t0002g0193a0001c0001t0002g0206a0001c0001t0003g0002others(209): Show | 221 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.148-4827delA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95947875 | ||||||
chr5:95947954
|
A | C | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.148-4905T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95947954 | ||||||
chr5:95947974
|
T | C | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.148-4925A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95947974 | ||||||
chr5:95948258
|
C | T | 3 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019 | 3 | HG01109.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.148-5209G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948258 | ||||||
chr5:95948267
|
T | TA | 74 | a0001c0001t0002g0294a0002c0002t0001g0001a0002c0002t0001g0006others(71): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.148-5219dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948267 | ||||||
chr5:95948302
|
C | T | 1 | a0002c0002t0001g0270 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.148-5253G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948302 | ||||||
chr5:95948377
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.148-5328G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948377 | ||||||
chr5:95948378
|
C | T | 4 | a0001c0004t0001g0021a0001c0004t0001g0022a0001c0004t0001g0023others(1): Show | 4 | HG02622.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-5329G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948378 | ||||||
chr5:95948429
|
C | CA | 28 | a0001c0001t0001g0267a0001c0001t0002g0221a0001c0001t0002g0224others(25): Show | 28 | HG00140.hp1 HG00558.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.148-5381dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAA | 58 | a0001c0001t0002g0206a0001c0001t0002g0292a0001c0001t0002g0297others(55): Show | 60 | HG00544.hp1 HG00609.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.148-5382_148-5381d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAA | 9 | a0001c0001t0002g0193a0001c0001t0003g0163a0001c0001t0003g0164others(6): Show | 9 | HG00558.hp2 HG00642.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-5383_148-5381d others(5): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAAAAA | 10 | a0001c0003t0007g0017a0001c0003t0012g0015a0001c0003t0012g0016others(7): Show | 10 | HG02647.hp2 HG02896.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.148-5386_148-5381d others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAAAAAA | 7 | a0001c0003t0004g0041a0001c0003t0007g0019a0001c0003t0008g0013others(4): Show | 7 | HG02559.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-5387_148-5381d others(9): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAAAAAA others(1): Show |
17 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0029others(14): Show | 19 | HG00609.hp1 HG01109.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.148-5388_148-5381d others(10): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAAAAAA others(2): Show |
44 | a0001c0003t0004g0005a0001c0003t0004g0040a0001c0003t0005g0030others(41): Show | 47 | HG01070.hp2 HG01123.hp2 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.148-5389_148-5381d others(11): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAAAAAA others(3): Show |
33 | a0002c0002t0001g0069a0002c0002t0001g0074a0002c0002t0001g0077others(30): Show | 33 | HG00280.hp1 HG00673.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.148-5390_148-5381d others(12): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAAAAAA others(4): Show |
14 | a0001c0003t0005g0034a0002c0002t0001g0006a0002c0002t0001g0057others(11): Show | 15 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.148-5391_148-5381d others(13): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAAAAAA others(5): Show |
3 | a0002c0002t0001g0102a0002c0002t0001g0114a0002c0002t0001g0115 | 3 | HG01891.hp1 HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.148-5392_148-5381d others(14): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAAAAAA others(6): Show |
1 | a0001c0005t0010g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.148-5393_148-5381d others(15): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAAAAAA others(7): Show |
5 | a0001c0005t0010g0049a0001c0005t0010g0050a0002c0002t0001g0126others(2): Show | 5 | HG00741.hp2 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.148-5394_148-5381d others(16): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAAAAAA others(8): Show |
1 | a0002c0002t0001g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.148-5395_148-5381d others(17): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948429
|
C | CAAAAAAA others(9): Show |
1 | a0002c0002t0001g0146 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.148-5396_148-5381d others(18): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948429 | ||||||
chr5:95948636
|
T | C | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.148-5587A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948636 | ||||||
chr5:95948637
|
C | T | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.148-5588G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95948637 | ||||||
chr5:95949696
|
A | G | 1 | a0001c0001t0003g0210 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.148-6647T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95949696 | ||||||
chr5:95949700
|
C | CA | 6 | a0001c0001t0002g0193a0001c0001t0002g0282a0001c0001t0002g0299others(3): Show | 6 | HG00738.hp1 HG02451.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.148-6652dupT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95949700 | ||||||
chr5:95949700
|
CA | C | 11 | a0001c0001t0002g0225a0001c0001t0003g0208a0001c0003t0012g0015others(8): Show | 11 | HG01070.hp1 HG02056.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.148-6652delT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95949700 | ||||||
chr5:95949700
|
CAA | C | 133 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(130): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.148-6653_148-6652d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95949700 | ||||||
chr5:95950067
|
G | A | 115 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(112): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.148-7018C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950067 | ||||||
chr5:95950085
|
C | T | 6 | a0001c0001t0002g0225a0001c0001t0002g0226a0001c0001t0002g0257others(3): Show | 6 | HG01070.hp1 HG01261.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-7036G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950085 | ||||||
chr5:95950313
|
A | G | 209 | a0001c0001t0002g0193a0001c0001t0002g0206a0001c0001t0003g0007others(206): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.148-7264T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950313 | ||||||
chr5:95950816
|
C | A | 1 | a0002c0002t0009g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.148-7767G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950816 | ||||||
chr5:95950830
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.148-7781T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950830 | ||||||
chr5:95950886
|
A | G | 114 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(111): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.148-7837T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950886 | ||||||
chr5:95950896
|
ATGTATG | A | 8 | a0001c0003t0007g0018a0002c0002t0001g0020a0002c0002t0001g0121others(5): Show | 8 | HG00741.hp2 HG01109.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.148-7853_148-7848d others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950896 | ||||||
chr5:95950898
|
GTATGTGT others(1): Show |
G | 13 | a0002c0002t0001g0026a0002c0002t0001g0065a0002c0002t0001g0066others(10): Show | 13 | HG01243.hp1 HG02004.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.148-7857_148-7850d others(10): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950898 | ||||||
chr5:95950898
|
GTATGTGT others(3): Show |
G | 10 | a0002c0002t0001g0070a0002c0002t0001g0071a0002c0002t0001g0072others(7): Show | 10 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.148-7859_148-7850d others(12): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950898 | ||||||
chr5:95950898
|
GTATGTGT others(5): Show |
G | 15 | a0002c0002t0001g0006a0002c0002t0001g0053a0002c0002t0001g0057others(12): Show | 16 | HG00099.hp2 HG00140.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.148-7861_148-7850d others(14): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950898 | ||||||
chr5:95950898
|
GTATGTGT others(7): Show |
G | 34 | a0001c0003t0007g0017a0002c0002t0001g0001a0002c0002t0001g0060others(31): Show | 36 | HG00673.hp1 HG01891.hp1 HG01928.hp1 others(33): Show |
intron_variant | MODIFIER | c.148-7863_148-7850d others(16): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950898 | ||||||
chr5:95950898
|
GTATGTGT others(9): Show |
G | 13 | a0001c0003t0007g0019a0002c0002t0001g0103a0002c0002t0001g0105others(10): Show | 13 | HG00280.hp1 HG00673.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.148-7865_148-7850d others(18): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950898 | ||||||
chr5:95950898
|
GTATGTGT others(11): Show |
G | 7 | a0001c0003t0008g0013a0002c0002t0001g0113a0002c0002t0001g0114others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.148-7867_148-7850d others(20): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950898 | ||||||
chr5:95950898
|
GTATGTGT others(13): Show |
G | 6 | a0001c0005t0008g0014a0002c0002t0001g0117a0002c0002t0001g0120others(3): Show | 6 | HG01255.hp2 HG02559.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-7869_148-7850d others(22): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950898 | ||||||
chr5:95950898
|
GTATGTGT others(17): Show |
G | 2 | a0002c0002t0001g0135a0002c0002t0009g0118 | 2 | HG01106.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.148-7873_148-7850d others(26): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950898 | ||||||
chr5:95950898
|
GTATGTGT others(27): Show |
G | 6 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-7883_148-7850d others(36): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950898 | ||||||
chr5:95950902
|
GTGTATAT others(3): Show |
G | 4 | a0001c0003t0005g0031a0001c0003t0005g0032a0001c0003t0005g0038others(1): Show | 4 | HG02258.hp2 HG02523.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-7863_148-7854d others(12): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950902 | ||||||
chr5:95950902
|
GTGTATAT others(5): Show |
G | 4 | a0001c0003t0004g0029a0001c0003t0004g0040a0001c0003t0005g0039others(1): Show | 4 | HG01168.hp1 HG02647.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-7865_148-7854d others(14): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950902 | ||||||
chr5:95950902
|
GTGTATAT others(7): Show |
G | 15 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(12): Show | 18 | HG00609.hp1 HG01975.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.148-7867_148-7854d others(16): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950902 | ||||||
chr5:95950904
|
G | A | 2 | a0001c0003t0005g0034a0002c0002t0001g0062 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.148-7855C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
G | GTA | 9 | a0001c0001t0002g0221a0001c0001t0002g0283a0001c0001t0002g0284others(6): Show | 9 | HG00741.hp1 HG01934.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.148-7857_148-7856d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
G | GTATA | 3 | a0001c0001t0002g0288a0002c0002t0001g0289a0002c0002t0001g0296 | 3 | HG03710.hp1 HG04184.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.148-7859_148-7856d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
G | GTATATA | 3 | a0001c0001t0002g0293a0001c0001t0002g0299a0001c0001t0003g0223 | 3 | HG00558.hp1 HG02717.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.148-7861_148-7856d others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTA | G | 15 | a0001c0001t0001g0267a0001c0001t0002g0218a0001c0001t0002g0257others(12): Show | 15 | HG01168.hp2 HG01255.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.148-7857_148-7856d others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATA | G | 14 | a0001c0001t0002g0214a0001c0001t0002g0220a0001c0001t0002g0248others(11): Show | 14 | HG00140.hp1 HG00639.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.148-7859_148-7856d others(6): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATATA | G | 11 | a0001c0001t0002g0217a0001c0001t0002g0244a0001c0001t0002g0245others(8): Show | 12 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.148-7861_148-7856d others(8): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATATAT others(1): Show |
G | 7 | a0001c0001t0002g0243a0001c0001t0003g0195a0001c0001t0003g0196others(4): Show | 7 | HG00544.hp2 HG01993.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-7863_148-7856d others(10): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATATAT others(3): Show |
G | 50 | a0001c0001t0002g0193a0001c0001t0002g0206a0001c0001t0002g0236others(47): Show | 52 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.148-7865_148-7856d others(12): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATATAT others(5): Show |
G | 13 | a0001c0001t0002g0219a0001c0001t0002g0233a0001c0001t0002g0234others(10): Show | 13 | HG00735.hp1 HG02056.hp2 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.148-7867_148-7856d others(14): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATATAT others(7): Show |
G | 4 | a0001c0001t0002g0303a0001c0001t0003g0157a0001c0001t0003g0159others(1): Show | 4 | HG01069.hp1 HG01074.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.148-7869_148-7856d others(16): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATATAT others(9): Show |
G | 1 | a0001c0001t0002g0302 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.148-7871_148-7856d others(18): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATATAT others(11): Show |
G | 1 | a0001c0004t0001g0232 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.148-7873_148-7856d others(20): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATATAT others(13): Show |
G | 7 | a0001c0001t0002g0222a0001c0001t0002g0228a0001c0001t0002g0229others(4): Show | 7 | HG01943.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.148-7875_148-7856d others(22): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATATAT others(25): Show |
G | 1 | a0001c0001t0003g0227 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.148-7887_148-7856d others(34): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATATAT others(29): Show |
G | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | HG01070.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.148-7891_148-7856d others(38): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950904
|
GTATATAT others(31): Show |
G | 1 | a0001c0001t0002g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.148-7893_148-7856d others(40): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950904 | ||||||
chr5:95950905
|
T | C | 2 | a0001c0003t0005g0034a0002c0002t0001g0062 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.148-7856A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950905 | ||||||
chr5:95950906
|
A | G | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.148-7857T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950906 | ||||||
chr5:95950907
|
T | C | 8 | a0001c0003t0007g0018a0002c0002t0001g0020a0002c0002t0001g0121others(5): Show | 8 | HG00741.hp2 HG01109.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.148-7858A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950907 | ||||||
chr5:95950909
|
T | C | 14 | a0001c0003t0005g0030a0002c0002t0001g0026a0002c0002t0001g0065others(11): Show | 14 | HG01243.hp1 HG02004.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.148-7860A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950909 | ||||||
chr5:95950911
|
T | C | 11 | a0001c0003t0005g0035a0002c0002t0001g0070a0002c0002t0001g0071others(8): Show | 11 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.148-7862A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950911 | ||||||
chr5:95950913
|
T | C | 16 | a0001c0003t0005g0036a0002c0002t0001g0006a0002c0002t0001g0053others(13): Show | 17 | HG00099.hp2 HG00140.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.148-7864A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950913 | ||||||
chr5:95950915
|
T | C | 38 | a0001c0003t0005g0031a0001c0003t0005g0032a0001c0003t0005g0038others(35): Show | 40 | HG00673.hp1 HG01891.hp1 HG01928.hp1 others(37): Show |
intron_variant | MODIFIER | c.148-7866A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950915 | ||||||
chr5:95950917
|
T | C | 17 | a0001c0003t0004g0029a0001c0003t0004g0040a0001c0003t0005g0039others(14): Show | 17 | HG00280.hp1 HG00673.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.148-7868A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950917 | ||||||
chr5:95950919
|
T | C | 22 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(19): Show | 25 | HG00609.hp1 HG01975.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.148-7870A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950919 | ||||||
chr5:95950921
|
T | C | 6 | a0001c0005t0008g0014a0002c0002t0001g0117a0002c0002t0001g0120others(3): Show | 6 | HG01255.hp2 HG02559.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-7872A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950921 | ||||||
chr5:95950925
|
T | C | 2 | a0002c0002t0001g0135a0002c0002t0009g0118 | 2 | HG01106.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.148-7876A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950925 | ||||||
chr5:95950935
|
T | C | 6 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-7886A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950935 | ||||||
chr5:95950937
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.148-7906_148-7889d others(20): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950937 | ||||||
chr5:95950948
|
A | T | 66 | a0001c0001t0002g0193a0001c0001t0002g0206a0001c0001t0003g0007others(63): Show | 68 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.148-7899T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950948 | ||||||
chr5:95950952
|
A | G | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.148-7903T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950952 | ||||||
chr5:95950955
|
A | T | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.148-7906T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95950955 | ||||||
chr5:95951022
|
A | C | 115 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(112): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.148-7973T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951022 | ||||||
chr5:95951031
|
C | G | 1 | a0001c0001t0003g0211 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.148-7982G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951031 | ||||||
chr5:95951135
|
C | T | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.148-8086G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951135 | ||||||
chr5:95951246
|
G | A | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.148-8197C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951246 | ||||||
chr5:95951364
|
G | A | 1 | a0001c0001t0003g0203 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.148-8315C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951364 | ||||||
chr5:95951380
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.148-8347_148-8332d others(18): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951380 | ||||||
chr5:95951385
|
A | T | 2 | a0002c0002t0001g0119a0002c0002t0001g0120 | 2 | HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.148-8336T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951385 | ||||||
chr5:95951409
|
C | A | 77 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(74): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.148-8360G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951409 | ||||||
chr5:95951411
|
A | AT | 75 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0053others(72): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.148-8363_148-8362i others(3): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951411 | ||||||
chr5:95951440
|
T | C | 1 | a0001c0003t0007g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.148-8391A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951440 | ||||||
chr5:95951610
|
A | T | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.148-8561T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951610 | ||||||
chr5:95951616
|
A | G | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.148-8567T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951616 | ||||||
chr5:95951675
|
G | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.148-8626C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951675 | ||||||
chr5:95951712
|
A | G | 1 | a0001c0001t0003g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.148-8663T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951712 | ||||||
chr5:95951863
|
G | A | 6 | a0001c0003t0012g0015a0001c0003t0012g0016a0001c0004t0001g0021others(3): Show | 6 | HG02622.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.148-8814C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951863 | ||||||
chr5:95951876
|
C | G | 1 | a0001c0001t0003g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.148-8827G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95951876 | ||||||
chr5:95952033
|
G | A | 1 | a0001c0001t0003g0204 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.148-8984C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95952033 | ||||||
chr5:95952035
|
G | A | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 27 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.148-8986C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95952035 | ||||||
chr5:95952461
|
G | A | 115 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(112): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.147+9114C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95952461 | ||||||
chr5:95952566
|
G | A | 3 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019 | 3 | HG01109.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.147+9009C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95952566 | ||||||
chr5:95952872
|
T | C | 143 | a0001c0001t0014g0025a0001c0003t0004g0003a0001c0003t0004g0004others(140): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.147+8703A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95952872 | ||||||
chr5:95952914
|
G | A | 115 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(112): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.147+8661C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95952914 | ||||||
chr5:95953087
|
C | T | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.147+8488G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953087 | ||||||
chr5:95953344
|
GA | G | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.147+8230delT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953344 | ||||||
chr5:95953396
|
C | A | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.147+8179G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953396 | ||||||
chr5:95953587
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.147+7988G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953587 | ||||||
chr5:95953629
|
A | G | 143 | a0001c0001t0014g0025a0001c0003t0004g0003a0001c0003t0004g0004others(140): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.147+7946T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953629 | ||||||
chr5:95953680
|
C | CTTTTG | 143 | a0001c0001t0014g0025a0001c0003t0004g0003a0001c0003t0004g0004others(140): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.147+7890_147+7894d others(7): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953680 | ||||||
chr5:95953694
|
A | G | 143 | a0001c0001t0014g0025a0001c0003t0004g0003a0001c0003t0004g0004others(140): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.147+7881T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953694 | ||||||
chr5:95953736
|
A | G | 1 | a0002c0002t0001g0062 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.147+7839T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953736 | ||||||
chr5:95953775
|
T | G | 1 | a0002c0002t0001g0138 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.147+7800A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953775 | ||||||
chr5:95953798
|
C | T | 143 | a0001c0001t0014g0025a0001c0003t0004g0003a0001c0003t0004g0004others(140): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.147+7777G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953798 | ||||||
chr5:95953838
|
G | A | 143 | a0001c0001t0014g0025a0001c0003t0004g0003a0001c0003t0004g0004others(140): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.147+7737C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953838 | ||||||
chr5:95953878
|
G | A | 1 | a0002c0002t0001g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.147+7697C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953878 | ||||||
chr5:95953930
|
A | T | 66 | a0001c0001t0002g0193a0001c0001t0002g0206a0001c0001t0003g0007others(63): Show | 68 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.147+7645T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95953930 | ||||||
chr5:95954040
|
T | G | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.147+7535A>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954040 | ||||||
chr5:95954403
|
C | CT | 8 | a0001c0001t0002g0219a0001c0001t0002g0220a0001c0001t0002g0221others(5): Show | 8 | HG01978.hp2 HG02074.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+7171dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954403 | ||||||
chr5:95954403
|
CT | C | 14 | a0001c0001t0002g0206a0001c0001t0002g0291a0001c0001t0002g0292others(11): Show | 14 | HG00558.hp1 HG02572.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.147+7171delA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954403 | ||||||
chr5:95954446
|
G | A | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.147+7129C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954446 | ||||||
chr5:95954467
|
T | C | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.147+7108A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954467 | ||||||
chr5:95954583
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0003t0008g0013a0001c0005t0008g0014a0005c0011t0008g0012 | 3 | HG02572.hp1 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.147+6978_147+6991d others(16): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954583 | ||||||
chr5:95954583
|
CTTTTTTT others(8): Show |
C | 4 | a0002c0002t0001g0143a0002c0002t0001g0144a0002c0002t0001g0145others(1): Show | 4 | HG00741.hp2 HG01243.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+6977_147+6991d others(17): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954583 | ||||||
chr5:95954583
|
CTTTTTTT others(13): Show |
C | 3 | a0001c0005t0010g0048a0001c0005t0010g0049a0001c0005t0010g0050 | 3 | HG02622.hp2 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.147+6972_147+6991d others(22): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954583 | ||||||
chr5:95954595
|
TC | T | 128 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(125): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.147+6979delG | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954595 | ||||||
chr5:95954596
|
C | CT | 67 | a0001c0001t0002g0193a0001c0001t0002g0206a0001c0001t0002g0217others(64): Show | 69 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.147+6978dupA | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954596 | ||||||
chr5:95954596
|
C | T | 5 | a0001c0001t0002g0294a0001c0001t0014g0025a0001c0003t0004g0033others(2): Show | 5 | HG02074.hp1 HG02451.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+6979G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954596 | ||||||
chr5:95954597
|
T | C | 5 | a0001c0001t0002g0294a0001c0001t0014g0025a0001c0003t0004g0033others(2): Show | 5 | HG02074.hp1 HG02451.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.147+6978A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954597 | ||||||
chr5:95954598
|
T | C | 128 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(125): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.147+6977A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954598 | ||||||
chr5:95954599
|
T | C | 1 | a0002c0002t0001g0147 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.147+6976A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954599 | ||||||
chr5:95954641
|
C | A | 2 | a0002c0002t0001g0148a0002c0002t0001g0149 | 2 | HG02080.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.147+6934G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954641 | ||||||
chr5:95954673
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.147+6902G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954673 | ||||||
chr5:95954683
|
G | A | 1 | a0001c0001t0003g0210 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.147+6892C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954683 | ||||||
chr5:95954715
|
C | T | 2 | a0001c0001t0003g0152a0001c0001t0003g0153 | 2 | NA19060.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.147+6860G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95954715 | ||||||
chr5:95955057
|
G | C | 1 | a0001c0001t0003g0211 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.147+6518C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955057 | ||||||
chr5:95955119
|
A | T | 1 | a0002c0002t0006g0059 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.147+6456T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955119 | ||||||
chr5:95955331
|
T | C | 1 | a0002c0002t0001g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.147+6244A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955331 | ||||||
chr5:95955352
|
G | C | 112 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(109): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.147+6223C>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955352 | ||||||
chr5:95955396
|
A | G | 3 | a0001c0003t0005g0030a0001c0003t0005g0031a0001c0003t0005g0032 | 3 | HG02258.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.147+6179T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955396 | ||||||
chr5:95955445
|
T | C | 1 | a0002c0002t0001g0151 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.147+6130A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955445 | ||||||
chr5:95955555
|
T | C | 3 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019 | 3 | HG01109.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.147+6020A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955555 | ||||||
chr5:95955626
|
G | A | 1 | a0001c0001t0003g0212 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.147+5949C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955626 | ||||||
chr5:95955721
|
G | A | 115 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019others(112): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.147+5854C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955721 | ||||||
chr5:95955868
|
C | G | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.147+5707G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955868 | ||||||
chr5:95955876
|
G | A | 1 | a0001c0001t0003g0213 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.147+5699C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955876 | ||||||
chr5:95955888
|
T | C | 2 | a0001c0003t0007g0018a0001c0003t0007g0019 | 2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.147+5687A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955888 | ||||||
chr5:95955937
|
G | T | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.147+5638C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955937 | ||||||
chr5:95955987
|
C | A | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.147+5588G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95955987 | ||||||
chr5:95956319
|
C | T | 3 | a0001c0003t0007g0017a0001c0003t0007g0018a0001c0003t0007g0019 | 3 | HG01109.hp1 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.147+5256G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95956319 | ||||||
chr5:95956517
|
C | T | 3 | a0001c0001t0002g0214a0001c0001t0002g0215a0007c0013t0002g0304 | 3 | NA18961.hp1 NA18993.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.147+5058G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95956517 | ||||||
chr5:95956525
|
T | C | 1 | a0001c0001t0014g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.147+5050A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95956525 | ||||||
chr5:95956563
|
C | T | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.147+5012G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95956563 | ||||||
chr5:95957557
|
C | T | 209 | a0001c0001t0002g0193a0001c0001t0002g0206a0001c0001t0003g0007others(206): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.147+4018G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95957557 | ||||||
chr5:95957612
|
C | G | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.147+3963G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95957612 | ||||||
chr5:95957708
|
G | A | 142 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(139): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.147+3867C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95957708 | ||||||
chr5:95957759
|
G | T | 4 | a0002c0002t0001g0057a0002c0002t0006g0055a0002c0002t0009g0054others(1): Show | 4 | HG00099.hp2 HG01106.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.147+3816C>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95957759 | ||||||
chr5:95957954
|
A | T | 1 | a0002c0002t0020g0052 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.147+3621T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95957954 | ||||||
chr5:95958145
|
C | T | 1 | a0006c0010t0025g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.147+3430G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95958145 | ||||||
chr5:95958361
|
A | G | 2 | a0001c0003t0012g0015a0001c0003t0012g0016 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.147+3214T>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95958361 | ||||||
chr5:95958362
|
C | G | 2 | a0001c0001t0003g0152a0001c0001t0003g0153 | 2 | NA19060.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.147+3213G>C | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95958362 | ||||||
chr5:95958758
|
G | A | 2 | a0002c0002t0001g0295a0002c0002t0001g0296 | 2 | HG00639.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.147+2817C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95958758 | ||||||
chr5:95958908
|
T | A | 1 | a0001c0001t0002g0297 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.147+2667A>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95958908 | ||||||
chr5:95958915
|
TA | T | 110 | a0001c0001t0003g0058a0001c0003t0007g0017a0001c0003t0007g0018others(107): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.147+2659delT | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95958915 | ||||||
chr5:95958916
|
A | T | 32 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(29): Show | 35 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.147+2659T>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95958916 | ||||||
chr5:95958978
|
C | T | 1 | a0001c0003t0004g0029 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.147+2597G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95958978 | ||||||
chr5:95959123
|
A | C | 2 | a0001c0006t0011g0027a0001c0006t0011g0028 | 2 | NA18985.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.147+2452T>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95959123 | ||||||
chr5:95959680
|
T | C | 1 | a0001c0001t0003g0298 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.147+1895A>G | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95959680 | ||||||
chr5:95959983
|
G | A | 27 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(24): Show | 30 | HG00609.hp1 HG01168.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.147+1592C>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95959983 | ||||||
chr5:95960809
|
C | T | 1 | a0001c0001t0003g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.147+766G>A | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95960809 | ||||||
chr5:95961070
|
G | GGTGT | 42 | a0001c0001t0014g0025a0001c0003t0004g0003a0001c0003t0004g0004others(39): Show | 45 | HG00609.hp1 HG01109.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.147+504_147+505ins others(4): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95961070 | ||||||
chr5:95961200
|
C | A | 1 | a0001c0001t0002g0299 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.147+375G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95961200 | ||||||
chr5:95961209
|
C | A | 3 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0011 | 4 | HG01243.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+366G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95961209 | ||||||
chr5:95961274
|
C | A | 4 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(1): Show | 4 | HG02717.hp2 HG02886.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+301G>T | ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95961274 | ||||||
chr5:95961552
|
A | AGCCT | 3 | a0001c0001t0003g0002a0001c0001t0003g0010a0001c0001t0003g0011 | 4 | HG01243.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.147+19_147+22dupAG others(2): Show |
ELL2 | ENSG00000118985.16 | transcript | ENST00000237853.9 | protein_coding | 1/11 | chr5 | 95961552 |