geneid | 8178 |
---|---|
ensemblid | ENSG00000105656.13 |
hgncid | 23114 |
symbol | ELL |
name | elongation factor for RNA polymerase II |
refseq_nuc | NM_006532.4 |
refseq_prot | NP_006523.1 |
ensembl_nuc | ENST00000262809.9 |
ensembl_prot | ENSP00000262809.3 |
mane_status | MANE Select |
chr | chr19 |
start | 18442663 |
end | 18522070 |
strand | - |
ver | v1.2 |
region | chr19:18442663-18522070 |
region5000 | chr19:18437663-18527070 |
regionname0 | ELL_chr19_18442663_18522070 |
regionname5000 | ELL_chr19_18437663_18527070 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 621 | 195 | 68 | 60 | 38 | 8 | 19 | 30 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0002 | 0/0 | 621 | 43 | 22 | 6 | 5 | 2 | 8 | 3 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0003 | 0/0 | 621 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0004 | 0/0 | 621 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0005 | 0/0 | 621 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0006 | 0/0 | 621 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0007 | 0/0 | 621 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1866 | 181 | 55 | 60 | 38 | 8 | 18 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0002 | 0/0 | 1866 | 43 | 22 | 6 | 5 | 2 | 8 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0003 | 0/0 | 1866 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0004 | 0/0 | 1866 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0005 | 0/0 | 1866 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0006 | 0/0 | 1866 | 2 | 0 | 1 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0007 | 0/0 | 1866 | 2 | 2 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0008 | 0/0 | 1866 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0009 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0010 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0011 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0012 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0013 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
c0014 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2102 | 121 | 56 | 26 | 21 | 5 | 13 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0002 | 1/1 | 2105 | 87 | 9 | 34 | 23 | 4 | 15 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0003 | 0/0 | 2105 | 7 | 6 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0004 | 0/0 | 2102 | 5 | 3 | 2 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0005 | 0/0 | 2102 | 4 | 4 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0006 | 0/0 | 2102 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0007 | 0/0 | 2102 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0008 | 0/0 | 2102 | 2 | 0 | 2 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0009 | 0/0 | 2102 | 2 | 2 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0010 | 0/0 | 2102 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0011 | 0/0 | 2103 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0012 | 0/0 | 2102 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0013 | 0/0 | 2102 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0014 | 0/0 | 2102 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0015 | 0/0 | 2105 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0016 | 0/0 | 2102 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0017 | 0/0 | 2102 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0018 | 0/0 | 2102 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
t0019 | 0/0 | 2102 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1866 | 181 | 55 | 60 | 38 | 8 | 18 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0003 | 0/0 | 1866 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0004 | 0/0 | 1866 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0005 | 0/0 | 1866 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0007 | 0/0 | 1866 | 2 | 2 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0010 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0012 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0013 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0002c0002 | 0/0 | 1866 | 43 | 22 | 6 | 5 | 2 | 8 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0003c0006 | 0/0 | 1866 | 2 | 0 | 1 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0004c0009 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0005c0014 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0006c0011 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0007c0008 | 0/0 | 1866 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3967 | 78 | 34 | 22 | 16 | 3 | 3 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0001t0002 | 1/1 | 3970 | 84 | 8 | 33 | 22 | 4 | 15 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0001t0003 | 0/0 | 3970 | 7 | 6 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0001t0004 | 0/0 | 3967 | 5 | 3 | 2 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0001t0011 | 0/0 | 3968 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0001t0012 | 0/0 | 3967 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0001t0014 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0001t0015 | 0/0 | 3970 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0001t0016 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0001t0017 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0001t0018 | 0/0 | 3967 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0003t0001 | 0/0 | 3967 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0004t0006 | 0/0 | 3967 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0005t0007 | 0/0 | 3967 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0007t0009 | 0/0 | 3967 | 2 | 2 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0010t0002 | 0/0 | 3970 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0012t0010 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0001c0013t0001 | 0/0 | 3967 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0002c0002t0001 | 0/0 | 3967 | 35 | 17 | 3 | 5 | 2 | 8 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0002c0002t0005 | 0/0 | 3967 | 4 | 4 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0002c0002t0008 | 0/0 | 3967 | 2 | 0 | 2 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0002c0002t0013 | 0/0 | 3967 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0002c0002t0019 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0003c0006t0001 | 0/0 | 3967 | 2 | 0 | 1 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0004c0009t0002 | 0/0 | 3970 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0005c0014t0001 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0006c0011t0001 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
a0007c0008t0002 | 0/0 | 3970 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | copy fasta | chr19 | 18437663 | 18527070 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0012g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0014g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0015g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0016g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0017g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0001t0018g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0004t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0004t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0004t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0005t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0005t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0005t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0007t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0007t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0010t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0012t0010g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0001c0013t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0008g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0013g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0002c0002t0019g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0003c0006t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0003c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0004c0009t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0005c0014t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0006c0011t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
a0007c0008t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0002 | g0058 | EUR | FIN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0052 | EUR | FIN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0240 | EUR | FIN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00639 | hp2 | a0007 | c0008 | t0002 | g0066 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00642 | hp2 | a0001 | c0001 | t0012 | g0228 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0112 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0153 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01346 | hp2 | a0002 | c0002 | t0008 | g0119 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01496 | hp1 | a0002 | c0002 | t0013 | g0113 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | IBS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | IBS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01516 | hp1 | a0001 | c0001 | t0018 | g0207 | EUR | IBS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0088 | EUR | IBS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01884 | hp2 | a0002 | c0002 | t0019 | g0131 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01975 | hp1 | a0001 | c0001 | t0015 | g0041 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02004 | hp1 | a0002 | c0002 | t0008 | g0116 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02004 | hp2 | a0003 | c0006 | t0001 | g0221 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | CDX | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CDX | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02572 | hp2 | a0002 | c0002 | t0005 | g0117 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02615 | hp1 | a0002 | c0002 | t0005 | g0128 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02622 | hp1 | a0001 | c0005 | t0007 | g0174 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02647 | hp1 | a0001 | c0005 | t0007 | g0175 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02647 | hp2 | a0002 | c0002 | t0005 | g0120 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0127 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0137 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02738 | hp2 | a0001 | c0013 | t0001 | g0220 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02886 | hp1 | a0001 | c0004 | t0006 | g0158 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02896 | hp1 | a0001 | c0005 | t0007 | g0176 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0167 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0242 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03041 | hp1 | a0001 | c0001 | t0016 | g0159 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03041 | hp2 | a0001 | c0004 | t0006 | g0156 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0166 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03139 | hp2 | a0001 | c0001 | t0017 | g0194 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03486 | hp1 | a0001 | c0012 | t0010 | g0172 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0118 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0115 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0134 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03654 | hp1 | a0003 | c0006 | t0001 | g0226 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0138 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | STU | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0241 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18522 | hp2 | a0001 | c0007 | t0009 | g0006 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | CHB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18906 | hp1 | a0006 | c0011 | t0001 | g0171 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18906 | hp2 | a0001 | c0004 | t0006 | g0157 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19030 | hp2 | a0001 | c0010 | t0002 | g0031 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0132 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19060 | hp2 | a0004 | c0009 | t0002 | g0038 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19240 | hp1 | a0001 | c0007 | t0009 | g0007 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ASW | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ASW | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0126 | EUR | TSI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | TSI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | GIH | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02109 | hp2 | a0001 | c0001 | t0014 | g0208 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03471 | hp1 | a0002 | c0002 | t0005 | g0123 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | USA | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0165 | AFR | USA | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA20300 | hp1 | a0005 | c0014 | t0001 | g0011 | AFR | USA | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0056 | REF | REF | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0075 | REF | REF | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:18446370
|
C | T | 1 | a0006 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1643G>A | p.Arg548Gln | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/12 | 1658/3970 | 1643/1866 | 548/621 | chr19 | 18446370 | ||
chr19:18450785
|
G | A | 1 | a0005 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1157C>T | p.Pro386Leu | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/12 | 1172/3970 | 1157/1866 | 386/621 | chr19 | 18450785 | ||
chr19:18451628
|
C | T | 1 | a0002 | 43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
missense_variant | MODERATE | c.890G>A | p.Ser297Asn | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/12 | 905/3970 | 890/1866 | 297/621 | chr19 | 18451628 | ||
chr19:18461595
|
C | T | 1 | a0003 | 2 | HG02004.hp2 HG03654.hp1 |
missense_variant | MODERATE | c.727G>A | p.Asp243Asn | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/12 | 742/3970 | 727/1866 | 243/621 | chr19 | 18461595 | ||
chr19:18461669
|
C | T | 1 | a0004 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.653G>A | p.Arg218Gln | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/12 | 668/3970 | 653/1866 | 218/621 | chr19 | 18461669 | ||
chr19:18465511
|
C | T | 1 | a0007 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.370G>A | p.Asp124Asn | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/12 | 385/3970 | 370/1866 | 124/621 | chr19 | 18465511 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:18446405
|
G | A | 1 | a0001c0003 | 3 | HG02965.hp2 HG03098.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.1608C>T | p.Tyr536Tyr | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/12 | 1623/3970 | 1608/1866 | 536/621 | chr19 | 18446405 | ||
chr19:18446771
|
C | T | 1 | a0001c0010 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1509G>A | p.Thr503Thr | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 9/12 | 1524/3970 | 1509/1866 | 503/621 | chr19 | 18446771 | ||
chr19:18446807
|
G | A | 1 | a0001c0012 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1473C>T | p.Asn491Asn | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 9/12 | 1488/3970 | 1473/1866 | 491/621 | chr19 | 18446807 | ||
chr19:18450499
|
G | A | 1 | a0001c0013 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1443C>T | p.Pro481Pro | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/12 | 1458/3970 | 1443/1866 | 481/621 | chr19 | 18450499 | ||
chr19:18450610
|
C | T | 2 | a0001c0004a0001c0005 | 6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
synonymous_variant | LOW | c.1332G>A | p.Ser444Ser | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/12 | 1347/3970 | 1332/1866 | 444/621 | chr19 | 18450610 | ||
chr19:18450663
|
G | A | 2 | a0001c0004a0001c0005 | 6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
synonymous_variant | LOW | c.1279C>T | p.Leu427Leu | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/12 | 1294/3970 | 1279/1866 | 427/621 | chr19 | 18450663 | ||
chr19:18451582
|
G | A | 1 | a0001c0007 | 2 | NA18522.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.936C>T | p.Gly312Gly | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/12 | 951/3970 | 936/1866 | 312/621 | chr19 | 18451582 | ||
chr19:18461806
|
C | A | 1 | a0001c0005 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
synonymous_variant | LOW | c.516G>T | p.Ala172Ala | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/12 | 531/3970 | 516/1866 | 172/621 | chr19 | 18461806 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:18442676
|
A | G | 1 | a0001c0001t0015 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2076T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 2076 | chr19 | 18442676 | |||||
chr19:18442770
|
CAGAT | C | 22 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(19): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1978_*1981delATCT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1978 | chr19 | 18442770 | |||||
chr19:18442875
|
GA | G | 21 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(18): Show | 148 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1876delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1876 | chr19 | 18442875 | |||||
chr19:18443394
|
G | GAC | 22 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(19): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1356_*1357dupGT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1357 | chr19 | 18443394 | |||||
chr19:18443489
|
T | C | 1 | a0001c0001t0015 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1263A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1263 | chr19 | 18443489 | |||||
chr19:18443493
|
C | T | 1 | a0001c0001t0012 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1259G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1259 | chr19 | 18443493 | |||||
chr19:18443567
|
C | T | 2 | a0001c0004t0006a0001c0005t0007 | 6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1185G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1185 | chr19 | 18443567 | |||||
chr19:18443751
|
C | G | 1 | a0002c0002t0008 | 2 | HG01346.hp2 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1001G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1001 | chr19 | 18443751 | |||||
chr19:18443795
|
T | C | 1 | a0002c0002t0013 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*957A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 957 | chr19 | 18443795 | |||||
chr19:18443804
|
T | C | 2 | a0002c0002t0005a0002c0002t0019 | 5 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*948A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 948 | chr19 | 18443804 | |||||
chr19:18443855
|
C | T | 2 | a0001c0001t0004a0001c0001t0011 | 6 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*897G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 897 | chr19 | 18443855 | |||||
chr19:18443975
|
C | G | 1 | a0001c0005t0007 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*777G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 777 | chr19 | 18443975 | |||||
chr19:18443997
|
C | A | 1 | a0001c0001t0014 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*755G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 755 | chr19 | 18443997 | |||||
chr19:18444162
|
A | G | 22 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(19): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*590T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 590 | chr19 | 18444162 | |||||
chr19:18444178
|
G | A | 1 | a0001c0007t0009 | 2 | NA18522.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*574C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 574 | chr19 | 18444178 | |||||
chr19:18444195
|
C | T | 1 | a0001c0001t0003 | 7 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*557G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 557 | chr19 | 18444195 | |||||
chr19:18444234
|
C | A | 1 | a0001c0001t0016 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*518G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 518 | chr19 | 18444234 | |||||
chr19:18444238
|
G | A | 1 | a0001c0001t0017 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*514C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 514 | chr19 | 18444238 | |||||
chr19:18444303
|
G | A | 1 | a0001c0001t0018 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*449C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 449 | chr19 | 18444303 | |||||
chr19:18444463
|
G | A | 1 | a0001c0005t0007 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*289C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 289 | chr19 | 18444463 | |||||
chr19:18444639
|
G | A | 1 | a0002c0002t0019 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 113 | chr19 | 18444639 | |||||
chr19:18444717
|
C | T | 1 | a0001c0012t0010 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*35G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 35 | chr19 | 18444717 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:18444947
|
C | T | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1750-79G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 11/11 | chr19 | 18444947 | ||||||
chr19:18445535
|
CGTGGGGG others(12): Show |
C | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1705-286_1705-268d others(21): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/11 | chr19 | 18445535 | ||||||
chr19:18445607
|
A | C | 42 | a0001c0001t0002g0060a0002c0002t0001g0012a0002c0002t0001g0015others(39): Show | 42 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1705-339T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/11 | chr19 | 18445607 | ||||||
chr19:18445939
|
T | C | 123 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(120): Show | 123 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1704+370A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/11 | chr19 | 18445939 | ||||||
chr19:18446031
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1704+278A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/11 | chr19 | 18446031 | ||||||
chr19:18446225
|
A | AGCAGGCC others(5): Show |
124 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(121): Show | 124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1704+83_1704+84ins others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/11 | chr19 | 18446225 | ||||||
chr19:18446502
|
A | G | 4 | a0001c0001t0002g0001a0001c0001t0002g0037a0001c0001t0002g0108others(1): Show | 5 | NA18975.hp1 NA19060.hp2 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.1533-22T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 9/11 | chr19 | 18446502 | ||||||
chr19:18446561
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1533-81C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 9/11 | chr19 | 18446561 | ||||||
chr19:18446847
|
C | T | 81 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1466-33G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18446847 | ||||||
chr19:18446863
|
C | T | 40 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(37): Show | 40 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1466-49G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18446863 | ||||||
chr19:18447014
|
G | A | 2 | a0002c0002t0001g0240a0002c0002t0001g0241 | 2 | HG00323.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1466-200C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447014 | ||||||
chr19:18447059
|
C | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1466-245G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447059 | ||||||
chr19:18447375
|
T | C | 2 | a0001c0001t0002g0035a0001c0001t0002g0036 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1466-561A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447375 | ||||||
chr19:18447528
|
G | A | 2 | a0001c0004t0006g0157a0001c0004t0006g0158 | 2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1466-714C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447528 | ||||||
chr19:18447615
|
A | C | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1466-801T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447615 | ||||||
chr19:18447707
|
G | A | 2 | a0002c0002t0008g0116a0002c0002t0008g0119 | 2 | HG01346.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1466-893C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447707 | ||||||
chr19:18447785
|
CT | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0181others(6): Show | 9 | HG01069.hp1 HG01515.hp2 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.1466-972delA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447785 | ||||||
chr19:18448009
|
C | T | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1466-1195G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448009 | ||||||
chr19:18448066
|
A | G | 124 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(121): Show | 124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1466-1252T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448066 | ||||||
chr19:18448087
|
AT | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0186others(15): Show | 18 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1466-1274delA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448087 | ||||||
chr19:18448133
|
C | A | 1 | a0001c0001t0002g0074 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1466-1319G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448133 | ||||||
chr19:18448257
|
C | T | 1 | a0002c0002t0001g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1466-1443G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448257 | ||||||
chr19:18448281
|
AG | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 23 | HG00280.hp2 HG01081.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1466-1468delC | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448281 | ||||||
chr19:18448287
|
C | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0206 | 2 | HG01952.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1466-1473G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448287 | ||||||
chr19:18448489
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1466-1675G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448489 | ||||||
chr19:18448538
|
C | T | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1466-1724G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448538 | ||||||
chr19:18448600
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1466-1786C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448600 | ||||||
chr19:18448703
|
CA | C | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1465+1773delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448703 | ||||||
chr19:18448844
|
C | T | 1 | a0001c0001t0003g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1465+1633G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448844 | ||||||
chr19:18448847
|
G | C | 124 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(121): Show | 124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1465+1630C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448847 | ||||||
chr19:18448853
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1465+1624C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448853 | ||||||
chr19:18449006
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1465+1471G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449006 | ||||||
chr19:18449039
|
T | G | 1 | a0006c0011t0001g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1465+1438A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449039 | ||||||
chr19:18449472
|
T | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1465+1005A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449472 | ||||||
chr19:18449491
|
A | G | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1465+986T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449491 | ||||||
chr19:18449753
|
G | A | 4 | a0001c0001t0002g0045a0001c0001t0002g0070a0001c0001t0002g0079others(1): Show | 4 | HG00642.hp1 HG01515.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465+724C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449753 | ||||||
chr19:18449822
|
C | T | 5 | a0001c0001t0002g0018a0001c0001t0002g0026a0001c0001t0002g0028others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465+655G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449822 | ||||||
chr19:18449892
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0206 | 2 | HG01952.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1465+585C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449892 | ||||||
chr19:18449974
|
C | CG | 43 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(40): Show | 43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.1465+502dupC | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449974 | ||||||
chr19:18450991
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.967-16C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18450991 | ||||||
chr19:18451182
|
G | A | 6 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(3): Show | 6 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-207C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451182 | ||||||
chr19:18451292
|
G | C | 6 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158others(3): Show | 6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+260C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451292 | ||||||
chr19:18451303
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.966+249T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451303 | ||||||
chr19:18451340
|
G | A | 2 | a0001c0001t0002g0046a0001c0001t0002g0053 | 2 | HG02132.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.966+212C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451340 | ||||||
chr19:18451429
|
G | C | 1 | a0001c0001t0001g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.966+123C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451429 | ||||||
chr19:18451449
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.966+103A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451449 | ||||||
chr19:18451498
|
C | T | 1 | a0001c0001t0012g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.966+54G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451498 | ||||||
chr19:18451517
|
G | A | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.966+35C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451517 | ||||||
chr19:18451535
|
A | C | 9 | a0001c0001t0002g0034a0001c0001t0002g0050a0001c0001t0002g0051others(6): Show | 9 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+17T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451535 | ||||||
chr19:18451814
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.870-166G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18451814 | ||||||
chr19:18451823
|
G | A | 9 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0189others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.870-175C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18451823 | ||||||
chr19:18451937
|
C | T | 1 | a0001c0001t0012g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.870-289G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18451937 | ||||||
chr19:18452141
|
T | A | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.870-493A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452141 | ||||||
chr19:18452143
|
C | A | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.870-495G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452143 | ||||||
chr19:18452151
|
T | A | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.870-503A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452151 | ||||||
chr19:18452195
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.870-547G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452195 | ||||||
chr19:18452249
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.870-601G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452249 | ||||||
chr19:18452278
|
GCGC | G | 11 | a0001c0001t0001g0009a0001c0001t0001g0155a0001c0001t0001g0163others(8): Show | 11 | HG01081.hp1 HG02886.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.870-633_870-631del others(3): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452278 | ||||||
chr19:18452286
|
C | G | 11 | a0001c0001t0001g0009a0001c0001t0001g0155a0001c0001t0001g0163others(8): Show | 11 | HG01081.hp1 HG02886.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.870-638G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452286 | ||||||
chr19:18452600
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-952G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452600 | ||||||
chr19:18452726
|
G | A | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.870-1078C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452726 | ||||||
chr19:18452874
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.870-1226G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452874 | ||||||
chr19:18452891
|
C | G | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.870-1243G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452891 | ||||||
chr19:18452904
|
G | A | 43 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(40): Show | 43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.870-1256C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452904 | ||||||
chr19:18453070
|
G | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.870-1422C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453070 | ||||||
chr19:18453160
|
A | C | 43 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(40): Show | 43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.870-1512T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453160 | ||||||
chr19:18453225
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.870-1577C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453225 | ||||||
chr19:18453563
|
G | A | 6 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158others(3): Show | 6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-1915C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453563 | ||||||
chr19:18453573
|
A | G | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.870-1925T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453573 | ||||||
chr19:18453590
|
G | A | 1 | a0001c0001t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.870-1942C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453590 | ||||||
chr19:18453608
|
C | T | 6 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158others(3): Show | 6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-1960G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453608 | ||||||
chr19:18453895
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.870-2247T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453895 | ||||||
chr19:18454097
|
G | A | 1 | a0001c0001t0011g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.870-2449C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454097 | ||||||
chr19:18454229
|
A | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.870-2581T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454229 | ||||||
chr19:18454412
|
T | C | 1 | a0002c0002t0001g0139 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.870-2764A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454412 | ||||||
chr19:18454493
|
G | A | 1 | a0001c0001t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.870-2845C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454493 | ||||||
chr19:18454510
|
G | T | 7 | a0001c0001t0002g0043a0001c0001t0002g0049a0001c0001t0002g0068others(4): Show | 7 | HG00408.hp1 HG01975.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.870-2862C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454510 | ||||||
chr19:18454698
|
G | A | 1 | a0001c0001t0004g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.870-3050C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454698 | ||||||
chr19:18454747
|
A | G | 1 | a0001c0010t0002g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.870-3099T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454747 | ||||||
chr19:18454784
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.870-3136A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454784 | ||||||
chr19:18454840
|
C | CA | 5 | a0001c0001t0001g0161a0001c0001t0002g0049a0001c0001t0002g0092others(2): Show | 5 | HG02055.hp2 HG02056.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-3193dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAA | 9 | a0001c0001t0001g0213a0002c0002t0001g0012a0002c0002t0001g0013others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.870-3195_870-3193d others(5): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAA | 11 | a0001c0001t0001g0180a0001c0001t0001g0209a0001c0001t0001g0212others(8): Show | 11 | HG02145.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.870-3196_870-3193d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAA | 22 | a0002c0002t0001g0109a0002c0002t0001g0110a0002c0002t0001g0112others(19): Show | 22 | HG00733.hp2 HG01081.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.870-3197_870-3193d others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.870-3202_870-3193d others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0001g0182a0001c0001t0001g0200a0001c0001t0001g0201others(3): Show | 6 | HG01255.hp1 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.870-3203_870-3193d others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(5): Show |
7 | a0001c0001t0001g0178a0001c0001t0001g0189a0001c0001t0001g0190others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-3204_870-3193d others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0188a0001c0001t0001g0192a0001c0001t0001g0227others(1): Show | 4 | HG01109.hp1 HG01943.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-3205_870-3193d others(15): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0219 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.870-3206_870-3193d others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0187a0001c0013t0001g0220 | 2 | HG02738.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.870-3207_870-3193d others(17): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0222a0003c0006t0001g0226 | 2 | HG01433.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.870-3208_870-3193d others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.870-3209_870-3193d others(19): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0185a0001c0001t0001g0236 | 2 | HG02132.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.870-3210_870-3193d others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0237a0001c0001t0004g0154 | 2 | HG00408.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(21): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(13): Show |
3 | a0001c0001t0001g0195a0001c0001t0001g0204a0001c0001t0004g0153 | 3 | HG01123.hp1 HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(14): Show |
3 | a0001c0001t0001g0205a0001c0001t0004g0150a0001c0001t0004g0152 | 3 | HG02145.hp1 HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(23): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0203others(1): Show | 4 | HG01891.hp2 HG02451.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-3193_870-3192i others(24): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(17): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0179a0001c0001t0001g0218 | 3 | HG02300.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(26): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(18): Show |
2 | a0001c0001t0001g0149a0001c0001t0001g0215 | 2 | HG00280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(27): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.870-3193_870-3192i others(29): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(21): Show |
4 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0199others(1): Show | 4 | HG01167.hp1 HG01952.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-3193_870-3192i others(30): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(24): Show |
2 | a0001c0001t0001g0225a0001c0001t0001g0235 | 2 | HG01928.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(33): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0001g0186a0001c0001t0001g0202 | 2 | HG01074.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(34): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(26): Show |
2 | a0001c0001t0001g0198a0001c0001t0012g0228 | 2 | HG00642.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(35): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(27): Show |
1 | a0001c0001t0001g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.870-3193_870-3192i others(36): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0018g0207 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.870-3193_870-3192i others(37): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(30): Show |
4 | a0001c0001t0001g0216a0001c0001t0001g0231a0001c0001t0001g0234others(1): Show | 4 | HG00735.hp2 HG01261.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-3193_870-3192i others(39): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(31): Show |
1 | a0003c0006t0001g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.870-3193_870-3192i others(40): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(33): Show |
1 | a0001c0001t0001g0177 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.870-3193_870-3192i others(42): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(38): Show |
1 | a0001c0001t0001g0224 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.870-3193_870-3192i others(47): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
C | CAAAAAAA others(53): Show |
1 | a0001c0001t0001g0217 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.870-3193_870-3192i others(62): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454840
|
CA | C | 13 | a0001c0001t0001g0144a0001c0001t0002g0034a0001c0001t0002g0050others(10): Show | 13 | HG00323.hp1 HG00639.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.870-3193delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | ||||||
chr19:18454938
|
G | C | 1 | a0001c0001t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.869+3267C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454938 | ||||||
chr19:18454998
|
G | A | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.869+3207C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454998 | ||||||
chr19:18455065
|
G | A | 4 | a0002c0002t0005g0117a0002c0002t0005g0120a0002c0002t0005g0123others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.869+3140C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455065 | ||||||
chr19:18455122
|
T | C | 6 | a0001c0001t0004g0150a0001c0001t0004g0151a0001c0001t0004g0152others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.869+3083A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455122 | ||||||
chr19:18455141
|
CA | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 140 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.869+3063delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455141 | ||||||
chr19:18455153
|
A | G | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.869+3052T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455153 | ||||||
chr19:18455226
|
ATCACGCC others(599): Show |
A | 2 | a0001c0001t0002g0025a0001c0001t0002g0064 | 2 | HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.869+2373_869+2978d others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455226 | ||||||
chr19:18455359
|
C | T | 1 | a0002c0002t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.869+2846G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455359 | ||||||
chr19:18455537
|
G | A | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.869+2668C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455537 | ||||||
chr19:18455585
|
T | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.869+2620A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455585 | ||||||
chr19:18455826
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.869+2379G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455826 | ||||||
chr19:18455827
|
G | A | 57 | a0001c0001t0001g0144a0001c0001t0003g0019a0001c0001t0003g0020others(54): Show | 57 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.869+2378C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455827 | ||||||
chr19:18455994
|
T | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.869+2211A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455994 | ||||||
chr19:18456097
|
CA | C | 6 | a0001c0001t0001g0149a0001c0001t0003g0020a0001c0004t0006g0156others(3): Show | 6 | HG02451.hp2 HG02886.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.869+2107delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456097 | ||||||
chr19:18456180
|
G | C | 1 | a0001c0001t0001g0211 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.869+2025C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456180 | ||||||
chr19:18456183
|
G | A | 6 | a0001c0001t0004g0150a0001c0001t0004g0151a0001c0001t0004g0152others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.869+2022C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456183 | ||||||
chr19:18456229
|
C | T | 60 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(57): Show | 61 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.869+1976G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456229 | ||||||
chr19:18456379
|
A | G | 45 | a0001c0001t0001g0223a0001c0001t0004g0151a0002c0002t0001g0012others(42): Show | 45 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.869+1826T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456379 | ||||||
chr19:18456745
|
C | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.869+1460G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456745 | ||||||
chr19:18456763
|
CAGCT | C | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.869+1438_869+1441d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456763 | ||||||
chr19:18456772
|
T | C | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.869+1433A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456772 | ||||||
chr19:18456946
|
T | C | 1 | a0002c0002t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.869+1259A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456946 | ||||||
chr19:18456961
|
G | GA | 15 | a0001c0001t0001g0010a0001c0001t0001g0163a0001c0001t0002g0057others(12): Show | 15 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.869+1243dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456961 | ||||||
chr19:18456961
|
GA | G | 70 | a0001c0001t0001g0149a0001c0001t0001g0177a0001c0001t0001g0178others(67): Show | 70 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.869+1243delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456961 | ||||||
chr19:18457091
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.869+1114G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457091 | ||||||
chr19:18457225
|
G | A | 2 | a0001c0001t0001g0219a0001c0013t0001g0220 | 2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.869+980C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457225 | ||||||
chr19:18457370
|
C | A | 1 | a0003c0006t0001g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.869+835G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457370 | ||||||
chr19:18457753
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.869+452G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457753 | ||||||
chr19:18457779
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.869+426C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457779 | ||||||
chr19:18457788
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.869+417C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457788 | ||||||
chr19:18457806
|
C | CT | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.869+398dupA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457806 | ||||||
chr19:18457984
|
C | T | 2 | a0001c0001t0002g0035a0001c0001t0002g0036 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.869+221G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457984 | ||||||
chr19:18457985
|
G | A | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.869+220C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457985 | ||||||
chr19:18458141
|
C | G | 43 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(40): Show | 43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.869+64G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18458141 | ||||||
chr19:18458343
|
C | T | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.745-14G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458343 | ||||||
chr19:18458402
|
T | C | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.745-73A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458402 | ||||||
chr19:18458485
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01891.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.745-156C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458485 | ||||||
chr19:18458601
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.745-272C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458601 | ||||||
chr19:18458624
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.745-295T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458624 | ||||||
chr19:18458672
|
G | A | 2 | a0001c0001t0002g0073a0001c0001t0002g0090 | 2 | HG01257.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.745-343C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458672 | ||||||
chr19:18458682
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.745-353G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458682 | ||||||
chr19:18458800
|
A | T | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-471T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458800 | ||||||
chr19:18458943
|
C | CAGTG | 10 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0072others(7): Show | 10 | HG00639.hp2 HG01069.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.745-618_745-615dup others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458943 | ||||||
chr19:18459023
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.745-694C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459023 | ||||||
chr19:18459100
|
G | A | 3 | a0001c0001t0002g0070a0001c0001t0002g0079a0001c0001t0002g0088 | 3 | HG00642.hp1 HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.745-771C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459100 | ||||||
chr19:18459144
|
G | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.745-815C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459144 | ||||||
chr19:18459147
|
G | A | 43 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(40): Show | 43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.745-818C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459147 | ||||||
chr19:18459225
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.745-896C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459225 | ||||||
chr19:18459258
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.745-929C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459258 | ||||||
chr19:18459521
|
AT | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0199a0001c0001t0001g0206others(10): Show | 13 | HG01167.hp2 HG01169.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.745-1193delA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459521 | ||||||
chr19:18459564
|
G | A | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-1235C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459564 | ||||||
chr19:18459565
|
GCT | G | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-1238_745-1237d others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459565 | ||||||
chr19:18459566
|
C | A | 1 | a0001c0001t0002g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.745-1237G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459566 | ||||||
chr19:18459569
|
G | T | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-1240C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459569 | ||||||
chr19:18459613
|
G | C | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-1284C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459613 | ||||||
chr19:18459669
|
G | C | 1 | a0002c0002t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.745-1340C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459669 | ||||||
chr19:18459716
|
T | TG | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.745-1388dupC | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459716 | ||||||
chr19:18459777
|
C | T | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.745-1448G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459777 | ||||||
chr19:18459809
|
A | G | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.745-1480T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459809 | ||||||
chr19:18459822
|
G | A | 63 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(60): Show | 63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.745-1493C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459822 | ||||||
chr19:18459847
|
T | C | 1 | a0003c0006t0001g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.745-1518A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459847 | ||||||
chr19:18460172
|
C | G | 2 | a0002c0002t0001g0112a0002c0002t0013g0113 | 2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.744+1406G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460172 | ||||||
chr19:18460179
|
T | G | 1 | a0001c0001t0002g0043 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.744+1399A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460179 | ||||||
chr19:18460187
|
A | AG | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+1390_744+1391i others(3): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460187 | ||||||
chr19:18460190
|
T | A | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+1388A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460190 | ||||||
chr19:18460191
|
C | CAG | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+1386_744+1387i others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460191 | ||||||
chr19:18460293
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.744+1285C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460293 | ||||||
chr19:18460331
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.744+1247T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460331 | ||||||
chr19:18460340
|
G | A | 43 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(40): Show | 43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.744+1238C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460340 | ||||||
chr19:18460357
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.744+1221C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460357 | ||||||
chr19:18460417
|
T | A | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.744+1161A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460417 | ||||||
chr19:18460590
|
C | A | 1 | a0002c0002t0001g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.744+988G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460590 | ||||||
chr19:18460834
|
G | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+744C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460834 | ||||||
chr19:18460923
|
C | T | 1 | a0001c0001t0004g0154 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.744+655G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460923 | ||||||
chr19:18460926
|
A | T | 1 | a0002c0002t0019g0131 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.744+652T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460926 | ||||||
chr19:18461022
|
G | A | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+556C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461022 | ||||||
chr19:18461058
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.744+520G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461058 | ||||||
chr19:18461168
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.744+410C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461168 | ||||||
chr19:18461231
|
C | T | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.744+347G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461231 | ||||||
chr19:18461267
|
C | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0155a0001c0001t0001g0163others(8): Show | 11 | HG01081.hp1 HG02886.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.744+311G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461267 | ||||||
chr19:18461291
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.744+287G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461291 | ||||||
chr19:18461403
|
T | G | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.744+175A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461403 | ||||||
chr19:18461482
|
G | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0155a0001c0001t0001g0163others(8): Show | 11 | HG01081.hp1 HG02886.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.744+96C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461482 | ||||||
chr19:18461545
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0100a0001c0001t0002g0101 | 3 | HG01243.hp1 HG01496.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.744+33G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461545 | ||||||
chr19:18461950
|
A | G | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | HG02055.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.470-98T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18461950 | ||||||
chr19:18462024
|
C | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.470-172G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462024 | ||||||
chr19:18462179
|
A | AGT | 23 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0026others(20): Show | 23 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.470-329_470-328dup others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462179 | ||||||
chr19:18462179
|
A | AGTGT | 10 | a0001c0001t0001g0144a0001c0001t0002g0035a0001c0001t0002g0036others(7): Show | 10 | HG01928.hp1 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.470-331_470-328dup others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462179 | ||||||
chr19:18462179
|
A | AGTGTGT | 4 | a0001c0001t0002g0062a0001c0001t0002g0074a0001c0001t0015g0041others(1): Show | 4 | HG00408.hp1 HG00741.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-333_470-328dup others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462179 | ||||||
chr19:18462204
|
GTGTGTGT others(11): Show |
G | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-370_470-353del others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462204 | ||||||
chr19:18462210
|
GTGTGTGT others(5): Show |
G | 5 | a0001c0001t0001g0181a0001c0001t0001g0196a0001c0001t0001g0210others(2): Show | 5 | HG01515.hp2 HG01884.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-370_470-359del others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462210 | ||||||
chr19:18462212
|
GTGTGTGT others(3): Show |
G | 11 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0189others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.470-370_470-361del others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462212 | ||||||
chr19:18462214
|
GTGTGTGT others(1): Show |
G | 14 | a0001c0001t0001g0161a0001c0001t0001g0179a0001c0001t0001g0187others(11): Show | 14 | HG01884.hp2 HG02055.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.470-370_470-363del others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462214 | ||||||
chr19:18462216
|
GTGTGTA | G | 37 | a0001c0001t0001g0162a0001c0001t0001g0173a0001c0001t0001g0177others(34): Show | 37 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.470-370_470-365del others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462216 | ||||||
chr19:18462218
|
GTGTA | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0155others(39): Show | 42 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.470-370_470-367del others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462218 | ||||||
chr19:18462220
|
GTA | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(21): Show | 24 | HG01109.hp1 HG01433.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.470-370_470-369del others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462220 | ||||||
chr19:18462222
|
A | G | 11 | a0001c0001t0001g0144a0001c0001t0001g0169a0001c0001t0001g0237others(8): Show | 11 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.470-370T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462222 | ||||||
chr19:18462232
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.470-380G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462232 | ||||||
chr19:18462253
|
A | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 236 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.470-401T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462253 | ||||||
chr19:18462334
|
G | GGT | 20 | a0002c0002t0001g0109a0002c0002t0001g0112a0002c0002t0001g0114others(17): Show | 20 | HG01081.hp2 HG01258.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.470-483_470-482ins others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462334 | ||||||
chr19:18462334
|
G | GGTGT | 8 | a0001c0001t0011g0115a0002c0002t0001g0110a0002c0002t0001g0129others(5): Show | 8 | HG00323.hp2 HG01884.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-483_470-482ins others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462334 | ||||||
chr19:18462334
|
G | GGTGTGTG others(3): Show |
2 | a0002c0002t0001g0141a0002c0002t0001g0142 | 2 | HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.470-483_470-482ins others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462334 | ||||||
chr19:18462334
|
G | GGTGTGTG others(7): Show |
1 | a0002c0002t0001g0143 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.470-483_470-482ins others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462334 | ||||||
chr19:18462334
|
GCT | G | 5 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-484_470-483del others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462334 | ||||||
chr19:18462335
|
C | CTGTGTG | 11 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0184others(8): Show | 11 | HG00408.hp2 HG02886.hp2 HG03540.hp1 others(8): Show |
intron_variant | MODIFIER | c.470-489_470-484dup others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | ||||||
chr19:18462335
|
C | CTGTGTGT others(1): Show |
16 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(13): Show | 16 | HG00280.hp2 HG00642.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.470-491_470-484dup others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | ||||||
chr19:18462335
|
C | CTGTGTGT others(3): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0196a0001c0001t0001g0203others(4): Show | 7 | HG02451.hp1 HG02965.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.470-493_470-484dup others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | ||||||
chr19:18462335
|
C | CTGTGTGT others(5): Show |
2 | a0001c0001t0001g0173a0001c0001t0001g0210 | 2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.470-495_470-484dup others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | ||||||
chr19:18462335
|
C | G | 39 | a0001c0001t0011g0115a0002c0002t0001g0109a0002c0002t0001g0110others(36): Show | 39 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.470-483G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | ||||||
chr19:18462335
|
CTG | C | 14 | a0001c0001t0002g0005a0001c0001t0002g0018a0001c0001t0002g0026others(11): Show | 14 | HG01361.hp2 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.470-485_470-484del others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | ||||||
chr19:18462337
|
G | C | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.470-485C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462337 | ||||||
chr19:18462352
|
T | G | 1 | a0001c0001t0001g0192 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.470-500A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462352 | ||||||
chr19:18462353
|
GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0192 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.470-514_470-502del others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462353 | ||||||
chr19:18462362
|
T | G | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.470-510A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462362 | ||||||
chr19:18462364
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.470-513_470-512ins others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462364 | ||||||
chr19:18462365
|
T | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(100): Show | 103 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.470-513A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462365 | ||||||
chr19:18462366
|
T | C | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.470-514A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0219 | 2 | HG01891.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.470-514A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGGG others(1): Show |
3 | a0001c0001t0001g0161a0001c0001t0001g0191a0001c0001t0001g0206 | 3 | HG01346.hp1 HG02055.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.470-515_470-514ins others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGGG others(3): Show |
1 | a0001c0001t0001g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.470-515_470-514ins others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGGG others(4): Show |
1 | a0001c0001t0001g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.470-515_470-514ins others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGTG others(3): Show |
5 | a0001c0001t0001g0146a0001c0001t0001g0170a0001c0001t0001g0218others(2): Show | 5 | HG01516.hp1 HG01928.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-515_470-514ins others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGTG others(4): Show |
2 | a0001c0001t0001g0224a0001c0003t0001g0166 | 2 | HG03098.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.470-515_470-514ins others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGTG others(6): Show |
2 | a0001c0001t0001g0188a0001c0001t0001g0229 | 2 | HG01261.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.470-515_470-514ins others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGTG others(5): Show |
6 | a0001c0001t0001g0179a0001c0001t0001g0185a0001c0001t0001g0189others(3): Show | 6 | HG00735.hp2 HG01069.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-515_470-514ins others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGTG others(6): Show |
4 | a0001c0001t0001g0190a0001c0001t0004g0150a0001c0001t0004g0152others(1): Show | 4 | HG01071.hp1 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-515_470-514ins others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0001g0200a0001c0001t0004g0153 | 2 | HG01167.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.470-515_470-514ins others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGTG others(8): Show |
1 | a0001c0001t0001g0202 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.470-515_470-514ins others(15): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGTG others(8): Show |
1 | a0001c0001t0017g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.470-515_470-514ins others(15): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGTG others(9): Show |
3 | a0001c0001t0001g0232a0001c0001t0004g0154a0003c0006t0001g0226 | 3 | HG01099.hp2 HG01169.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.470-515_470-514ins others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0204 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.470-515_470-514ins others(19): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462366
|
T | TGTGTGTG others(21): Show |
1 | a0002c0002t0001g0140 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.470-515_470-514ins others(28): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | ||||||
chr19:18462367
|
G | C | 1 | a0001c0001t0001g0192 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.470-515C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | ||||||
chr19:18462367
|
G | GT | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.470-516_470-515ins others(1): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | ||||||
chr19:18462367
|
G | GTGTGTGG others(2): Show |
6 | a0001c0001t0001g0155a0001c0001t0001g0168a0001c0001t0001g0183others(3): Show | 6 | HG01167.hp1 HG01943.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-516_470-515ins others(9): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | ||||||
chr19:18462367
|
G | GTGTGTGT others(4): Show |
4 | a0001c0001t0001g0187a0001c0001t0001g0198a0001c0001t0001g0214others(1): Show | 4 | HG01433.hp2 HG02293.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-516_470-515ins others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | ||||||
chr19:18462367
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0014g0208 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.470-516_470-515ins others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | ||||||
chr19:18462367
|
G | GTGTGTGT others(6): Show |
3 | a0001c0001t0001g0163a0001c0001t0001g0201a0005c0014t0001g0011 | 3 | HG01081.hp1 HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.470-516_470-515ins others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | ||||||
chr19:18462367
|
G | GTGTGTGT others(10): Show |
1 | a0001c0001t0001g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.470-516_470-515ins others(17): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | ||||||
chr19:18462368
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.470-516C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462368 | ||||||
chr19:18462368
|
G | T | 8 | a0001c0001t0001g0144a0001c0001t0001g0177a0001c0001t0001g0182others(5): Show | 8 | HG01074.hp2 HG01255.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.470-516C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462368 | ||||||
chr19:18462369
|
G | T | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.470-517C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462369 | ||||||
chr19:18462370
|
C | CG | 18 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 18 | HG01891.hp1 HG02004.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.470-519dupC | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462370 | ||||||
chr19:18462370
|
C | CGG | 33 | a0001c0001t0001g0162a0001c0001t0001g0164a0001c0001t0001g0173others(30): Show | 33 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.470-520_470-519dup others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462370 | ||||||
chr19:18462370
|
C | CGGGGGGG others(3): Show |
1 | a0002c0002t0001g0121 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.470-519_470-518ins others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462370 | ||||||
chr19:18462370
|
C | G | 55 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(52): Show | 55 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.470-518G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462370 | ||||||
chr19:18462370
|
C | T | 11 | a0001c0001t0001g0144a0001c0001t0001g0177a0001c0001t0001g0182others(8): Show | 11 | HG01074.hp2 HG01255.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.470-518G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462370 | ||||||
chr19:18462371
|
G | GTTT | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.470-520_470-519ins others(3): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462371 | ||||||
chr19:18462371
|
G | T | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.470-519C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462371 | ||||||
chr19:18462372
|
G | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0211 | 2 | NA18951.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.470-520C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462372 | ||||||
chr19:18462373
|
G | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0186 | 2 | HG01074.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.470-521C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462373 | ||||||
chr19:18462374
|
G | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0211 | 2 | NA18951.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.470-522C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462374 | ||||||
chr19:18462375
|
G | C | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.470-523C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462375 | ||||||
chr19:18462376
|
G | T | 1 | a0001c0001t0001g0211 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.470-524C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462376 | ||||||
chr19:18462377
|
C | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 145 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.470-525G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462377 | ||||||
chr19:18462378
|
G | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0211 | 2 | NA18951.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.470-526C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462378 | ||||||
chr19:18462379
|
G | T | 1 | a0001c0001t0002g0059 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.470-527C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462379 | ||||||
chr19:18462385
|
G | GGGGGGGG others(7): Show |
1 | a0002c0002t0001g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470-534_470-533ins others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462385 | ||||||
chr19:18462391
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.470-539A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462391 | ||||||
chr19:18462451
|
A | G | 1 | a0001c0010t0002g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.470-599T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462451 | ||||||
chr19:18462865
|
A | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.470-1013T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462865 | ||||||
chr19:18463217
|
G | C | 9 | a0001c0001t0001g0177a0001c0001t0001g0182a0001c0001t0001g0183others(6): Show | 9 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.470-1365C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463217 | ||||||
chr19:18463268
|
G | A | 6 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0148others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.470-1416C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463268 | ||||||
chr19:18463325
|
C | CT | 15 | a0001c0001t0001g0218a0001c0001t0001g0235a0001c0001t0002g0032others(12): Show | 15 | HG00642.hp1 HG01109.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.470-1474dupA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463325 | ||||||
chr19:18463325
|
CT | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(89): Show | 92 | HG00280.hp2 HG00408.hp2 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.470-1474delA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463325 | ||||||
chr19:18463325
|
CTT | C | 42 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0001g0219others(39): Show | 42 | HG00323.hp2 HG00733.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.470-1475_470-1474d others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463325 | ||||||
chr19:18463325
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0223 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.470-1487_470-1474d others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463325 | ||||||
chr19:18463425
|
T | C | 44 | a0001c0001t0011g0115a0002c0002t0001g0012a0002c0002t0001g0013others(41): Show | 44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.470-1573A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463425 | ||||||
chr19:18463444
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.470-1592G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463444 | ||||||
chr19:18463731
|
C | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.469+1681G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463731 | ||||||
chr19:18463749
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.469+1663A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463749 | ||||||
chr19:18463775
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.469+1637C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463775 | ||||||
chr19:18463968
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.469+1444T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463968 | ||||||
chr19:18463985
|
C | CA | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(94): Show | 97 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.469+1426dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463985 | ||||||
chr19:18463998
|
C | A | 1 | a0002c0002t0001g0121 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.469+1414G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463998 | ||||||
chr19:18464297
|
T | G | 1 | a0001c0001t0012g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.469+1115A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464297 | ||||||
chr19:18464375
|
A | G | 1 | a0002c0002t0001g0121 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.469+1037T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464375 | ||||||
chr19:18464383
|
A | G | 4 | a0001c0001t0002g0033a0001c0001t0002g0040a0001c0001t0002g0054others(1): Show | 4 | HG01123.hp2 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.469+1029T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464383 | ||||||
chr19:18464490
|
TACA | T | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.469+919_469+921del others(3): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464490 | ||||||
chr19:18464640
|
C | T | 68 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.469+772G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464640 | ||||||
chr19:18464719
|
C | T | 3 | a0001c0001t0002g0017a0001c0001t0002g0048a0001c0001t0002g0061 | 3 | HG00735.hp1 HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.469+693G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464719 | ||||||
chr19:18464770
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.469+642A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464770 | ||||||
chr19:18464889
|
G | A | 2 | a0001c0001t0002g0094a0001c0001t0002g0095 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.469+523C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464889 | ||||||
chr19:18464979
|
G | A | 5 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+433C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464979 | ||||||
chr19:18464998
|
G | A | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+414C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464998 | ||||||
chr19:18465053
|
G | A | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+359C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18465053 | ||||||
chr19:18465339
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.469+73C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18465339 | ||||||
chr19:18465344
|
G | A | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.469+68C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18465344 | ||||||
chr19:18465674
|
T | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.306-99A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 3/11 | chr19 | 18465674 | ||||||
chr19:18465704
|
T | A | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.305+93A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 3/11 | chr19 | 18465704 | ||||||
chr19:18465791
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.305+6G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 3/11 | chr19 | 18465791 | ||||||
chr19:18465957
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.184-39C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18465957 | ||||||
chr19:18466072
|
C | T | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-154G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466072 | ||||||
chr19:18466118
|
G | T | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-200C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466118 | ||||||
chr19:18466123
|
AGGCACC | A | 5 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-211_184-206del others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466123 | ||||||
chr19:18466130
|
T | G | 1 | a0001c0001t0002g0043 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.184-212A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466130 | ||||||
chr19:18466475
|
C | T | 6 | a0001c0001t0011g0115a0002c0002t0005g0117a0002c0002t0005g0120others(3): Show | 6 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-557G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466475 | ||||||
chr19:18466514
|
T | C | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-596A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466514 | ||||||
chr19:18466588
|
C | T | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-670G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466588 | ||||||
chr19:18466635
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.184-717C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466635 | ||||||
chr19:18467063
|
G | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 98 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.184-1145C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467063 | ||||||
chr19:18467272
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.184-1354G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467272 | ||||||
chr19:18467308
|
C | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0186 | 2 | HG01074.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.184-1390G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467308 | ||||||
chr19:18467368
|
G | A | 41 | a0001c0001t0011g0115a0002c0002t0001g0012a0002c0002t0001g0013others(38): Show | 41 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.184-1450C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467368 | ||||||
chr19:18467552
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.184-1634G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467552 | ||||||
chr19:18467631
|
C | CCA | 3 | a0001c0001t0002g0039a0001c0001t0002g0062a0001c0001t0002g0080 | 3 | HG00741.hp1 HG00741.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.184-1715_184-1714d others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
C | CCACA | 4 | a0001c0001t0002g0032a0001c0001t0002g0060a0001c0001t0002g0085others(1): Show | 4 | HG01069.hp2 HG04115.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1717_184-1714d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
C | CCACACA | 4 | a0001c0001t0002g0072a0001c0001t0002g0084a0001c0001t0002g0087others(1): Show | 4 | HG00639.hp2 HG01074.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1719_184-1714d others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
C | CCACACAC others(3): Show |
1 | a0001c0001t0002g0077 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.184-1723_184-1714d others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
CCACA | C | 15 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0045others(12): Show | 15 | HG00642.hp1 HG00738.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.184-1717_184-1714d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
CCACACA | C | 31 | a0001c0001t0002g0018a0001c0001t0002g0025a0001c0001t0002g0026others(28): Show | 31 | HG00639.hp1 HG00733.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-1719_184-1714d others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
CCACACAC others(1): Show |
C | 6 | a0001c0001t0001g0149a0001c0001t0004g0150a0001c0001t0004g0152others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-1721_184-1714d others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
CCACACAC others(3): Show |
C | 61 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(58): Show | 61 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.184-1723_184-1714d others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
CCACACAC others(5): Show |
C | 32 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(29): Show | 32 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.184-1725_184-1714d others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
CCACACAC others(7): Show |
C | 9 | a0001c0001t0001g0144a0001c0001t0001g0195a0001c0001t0001g0203others(6): Show | 9 | HG01123.hp1 HG02004.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-1727_184-1714d others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
CCACACAC others(9): Show |
C | 41 | a0001c0001t0002g0005a0001c0001t0011g0115a0002c0002t0001g0012others(38): Show | 41 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.184-1729_184-1714d others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
CCACACAC others(11): Show |
C | 1 | a0002c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184-1731_184-1714d others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467631
|
CCACACAC others(13): Show |
C | 1 | a0002c0002t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.184-1733_184-1714d others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | ||||||
chr19:18467674
|
A | C | 1 | a0001c0001t0002g0039 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.184-1756T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467674 | ||||||
chr19:18467701
|
CCACA | C | 4 | a0001c0001t0002g0047a0001c0001t0002g0065a0001c0001t0002g0071others(1): Show | 4 | HG00738.hp1 HG01071.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1787_184-1784d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467701 | ||||||
chr19:18467732
|
CCACA | C | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.184-1818_184-1815d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467732 | ||||||
chr19:18467734
|
A | C | 4 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0233others(1): Show | 4 | HG01109.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1816T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467734 | ||||||
chr19:18467762
|
C | T | 1 | a0001c0001t0018g0207 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.184-1844G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467762 | ||||||
chr19:18467807
|
A | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 98 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.184-1889T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467807 | ||||||
chr19:18467844
|
T | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.184-1926A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467844 | ||||||
chr19:18467879
|
A | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 98 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.184-1961T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467879 | ||||||
chr19:18467941
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.184-2023G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467941 | ||||||
chr19:18468027
|
A | C | 2 | a0001c0001t0002g0026a0001c0001t0002g0029 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.184-2109T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468027 | ||||||
chr19:18468087
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.184-2169T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468087 | ||||||
chr19:18468102
|
C | A | 1 | a0002c0002t0001g0129 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.184-2184G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468102 | ||||||
chr19:18468174
|
C | T | 41 | a0001c0001t0011g0115a0002c0002t0001g0012a0002c0002t0001g0013others(38): Show | 41 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.184-2256G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468174 | ||||||
chr19:18468214
|
CACAA | C | 12 | a0001c0001t0002g0018a0001c0001t0002g0026a0001c0001t0002g0028others(9): Show | 12 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.184-2300_184-2297d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468214 | ||||||
chr19:18468219
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.184-2301T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468219 | ||||||
chr19:18468221
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.184-2303T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468221 | ||||||
chr19:18468227
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.184-2309A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468227 | ||||||
chr19:18468227
|
T | TAC | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 110 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(107): Show |
intron_variant | MODIFIER | c.184-2311_184-2310d others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468227 | ||||||
chr19:18468227
|
T | TACAC | 40 | a0001c0001t0001g0162a0001c0001t0001g0173a0002c0002t0001g0012others(37): Show | 40 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.184-2313_184-2310d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468227 | ||||||
chr19:18468339
|
C | A | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | HG02055.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.184-2421G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468339 | ||||||
chr19:18468698
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.184-2780G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468698 | ||||||
chr19:18468967
|
A | G | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.184-3049T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468967 | ||||||
chr19:18469141
|
G | A | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.184-3223C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469141 | ||||||
chr19:18469329
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.184-3411C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469329 | ||||||
chr19:18469386
|
G | A | 1 | a0001c0001t0003g0020 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.183+3449C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469386 | ||||||
chr19:18469772
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.183+3063A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469772 | ||||||
chr19:18469818
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.183+3017A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469818 | ||||||
chr19:18469821
|
C | T | 9 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0189others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.183+3014G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469821 | ||||||
chr19:18469988
|
C | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.183+2847G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469988 | ||||||
chr19:18470143
|
C | T | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.183+2692G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18470143 | ||||||
chr19:18470204
|
C | T | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2631G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18470204 | ||||||
chr19:18470207
|
G | A | 2 | a0002c0002t0001g0240a0002c0002t0001g0241 | 2 | HG00323.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.183+2628C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18470207 | ||||||
chr19:18470417
|
T | C | 44 | a0001c0001t0011g0115a0002c0002t0001g0012a0002c0002t0001g0013others(41): Show | 44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.183+2418A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18470417 | ||||||
chr19:18470453
|
G | A | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.183+2382C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18470453 | ||||||
chr19:18471024
|
A | AGAGC | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.183+1807_183+1810d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18471024 | ||||||
chr19:18471091
|
A | T | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.183+1744T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18471091 | ||||||
chr19:18471106
|
C | T | 44 | a0001c0001t0011g0115a0002c0002t0001g0012a0002c0002t0001g0013others(41): Show | 44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.183+1729G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18471106 | ||||||
chr19:18471565
|
G | A | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.183+1270C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18471565 | ||||||
chr19:18471986
|
G | C | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+849C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18471986 | ||||||
chr19:18472006
|
G | A | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.183+829C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472006 | ||||||
chr19:18472279
|
A | G | 1 | a0002c0002t0019g0131 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.183+556T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472279 | ||||||
chr19:18472376
|
C | T | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+459G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472376 | ||||||
chr19:18472433
|
T | C | 2 | a0002c0002t0008g0116a0002c0002t0008g0119 | 2 | HG01346.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.183+402A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472433 | ||||||
chr19:18472657
|
C | T | 2 | a0001c0007t0009g0006a0001c0007t0009g0007 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.183+178G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472657 | ||||||
chr19:18472658
|
G | A | 5 | a0001c0001t0004g0150a0001c0001t0004g0151a0001c0001t0004g0152others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+177C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472658 | ||||||
chr19:18472886
|
T | TA | 28 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0209others(25): Show | 28 | HG00408.hp2 HG01109.hp1 HG01346.hp2 others(25): Show |
splice_region_variant&intron_variant | LOW | c.136-5dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18472886 | ||||||
chr19:18472886
|
TA | T | 21 | a0001c0001t0001g0155a0001c0001t0001g0162a0001c0001t0001g0186others(18): Show | 21 | HG00323.hp1 HG01069.hp1 HG01069.hp2 others(18): Show |
splice_region_variant&intron_variant | LOW | c.136-5delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18472886 | ||||||
chr19:18472986
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.136-104A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18472986 | ||||||
chr19:18473060
|
T | C | 1 | a0001c0001t0002g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.136-178A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473060 | ||||||
chr19:18473153
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-271C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473153 | ||||||
chr19:18473421
|
C | G | 2 | a0002c0002t0001g0112a0002c0002t0013g0113 | 2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.136-539G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473421 | ||||||
chr19:18473494
|
C | A | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096 | 3 | HG01175.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.136-612G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473494 | ||||||
chr19:18473590
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.136-708A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473590 | ||||||
chr19:18473668
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(97): Show | 100 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.136-786G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473668 | ||||||
chr19:18473810
|
T | C | 2 | a0001c0001t0003g0022a0001c0001t0003g0023 | 2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.136-928A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473810 | ||||||
chr19:18473893
|
A | AC | 4 | a0001c0001t0001g0212a0001c0001t0001g0239a0001c0001t0002g0081others(1): Show | 4 | HG01978.hp2 NA18985.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1012dupG | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473893 | ||||||
chr19:18473910
|
G | A | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-1028C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473910 | ||||||
chr19:18473934
|
C | T | 4 | a0001c0001t0001g0144a0001c0005t0007g0174a0001c0005t0007g0175others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1052G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473934 | ||||||
chr19:18473971
|
G | A | 63 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(60): Show | 63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-1089C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473971 | ||||||
chr19:18474041
|
G | A | 1 | a0001c0001t0002g0056 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.136-1159C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474041 | ||||||
chr19:18474184
|
CA | C | 4 | a0002c0002t0001g0240a0002c0002t0001g0241a0002c0002t0001g0242others(1): Show | 4 | HG00323.hp2 HG03017.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1303delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474184 | ||||||
chr19:18474197
|
G | A | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-1315C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474197 | ||||||
chr19:18474297
|
G | A | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-1415C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474297 | ||||||
chr19:18474349
|
C | A | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-1467G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474349 | ||||||
chr19:18474349
|
C | T | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-1467G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474349 | ||||||
chr19:18474515
|
A | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.136-1633T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474515 | ||||||
chr19:18474519
|
G | A | 24 | a0002c0002t0001g0109a0002c0002t0001g0110a0002c0002t0001g0112others(21): Show | 24 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.136-1637C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474519 | ||||||
chr19:18474546
|
A | C | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0230others(2): Show | 5 | HG01109.hp1 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-1664T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474546 | ||||||
chr19:18474572
|
G | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG02451.hp1 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.136-1690C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474572 | ||||||
chr19:18474600
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-1718G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474600 | ||||||
chr19:18474736
|
G | A | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.136-1854C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474736 | ||||||
chr19:18475024
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.136-2142G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475024 | ||||||
chr19:18475072
|
T | A | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-2190A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475072 | ||||||
chr19:18475075
|
G | T | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-2193C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475075 | ||||||
chr19:18475126
|
C | G | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-2244G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475126 | ||||||
chr19:18475159
|
G | C | 1 | a0003c0006t0001g0226 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.136-2277C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475159 | ||||||
chr19:18475330
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.136-2448C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475330 | ||||||
chr19:18475355
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-2473G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475355 | ||||||
chr19:18475403
|
G | A | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-2521C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475403 | ||||||
chr19:18475489
|
C | CT | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.136-2608_136-2607i others(3): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475489 | ||||||
chr19:18475669
|
T | C | 3 | a0001c0001t0001g0196a0001c0001t0001g0210a0001c0001t0014g0208 | 3 | HG01884.hp1 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.136-2787A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475669 | ||||||
chr19:18475709
|
T | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.136-2827A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475709 | ||||||
chr19:18475791
|
G | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0225 | 2 | HG01928.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.136-2909C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475791 | ||||||
chr19:18475949
|
G | T | 63 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(60): Show | 63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-3067C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475949 | ||||||
chr19:18475981
|
C | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.136-3099G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475981 | ||||||
chr19:18476020
|
G | A | 3 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139 | 3 | HG02735.hp2 HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.136-3138C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476020 | ||||||
chr19:18476130
|
G | C | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-3248C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476130 | ||||||
chr19:18476222
|
G | A | 1 | a0002c0002t0001g0109 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.136-3340C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476222 | ||||||
chr19:18476347
|
C | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-3465G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476347 | ||||||
chr19:18476362
|
G | T | 3 | a0001c0001t0002g0017a0001c0001t0002g0048a0001c0001t0002g0061 | 3 | HG00735.hp1 HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.136-3480C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476362 | ||||||
chr19:18476430
|
T | A | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-3548A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476430 | ||||||
chr19:18476535
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.136-3653C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476535 | ||||||
chr19:18476882
|
C | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.136-4000G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476882 | ||||||
chr19:18477052
|
G | A | 2 | a0002c0002t0001g0109a0002c0002t0001g0124 | 2 | NA18964.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.136-4170C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477052 | ||||||
chr19:18477334
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.136-4452C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477334 | ||||||
chr19:18477334
|
G | C | 1 | a0001c0001t0001g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.136-4452C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477334 | ||||||
chr19:18477484
|
G | T | 1 | a0001c0001t0001g0217 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.136-4602C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477484 | ||||||
chr19:18477519
|
G | A | 1 | a0003c0006t0001g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.136-4637C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477519 | ||||||
chr19:18477572
|
C | T | 1 | a0001c0001t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.136-4690G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477572 | ||||||
chr19:18477941
|
G | C | 1 | a0001c0001t0002g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.136-5059C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477941 | ||||||
chr19:18477990
|
A | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(90): Show | 93 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.136-5108T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477990 | ||||||
chr19:18478191
|
G | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0051 | 2 | HG01243.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.136-5309C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478191 | ||||||
chr19:18478206
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.136-5324G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478206 | ||||||
chr19:18478235
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-5353G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478235 | ||||||
chr19:18478278
|
T | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.136-5396A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478278 | ||||||
chr19:18478280
|
T | TA | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-5399dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478280 | ||||||
chr19:18478551
|
G | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-5669C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478551 | ||||||
chr19:18478683
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.136-5801C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478683 | ||||||
chr19:18478686
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136-5804G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478686 | ||||||
chr19:18478722
|
CCAGACCC others(10): Show |
C | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-5857_136-5841d others(19): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478722 | ||||||
chr19:18478815
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-5933G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478815 | ||||||
chr19:18478836
|
A | T | 1 | a0001c0001t0002g0078 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.136-5954T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478836 | ||||||
chr19:18478847
|
G | A | 1 | a0002c0002t0001g0121 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.136-5965C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478847 | ||||||
chr19:18478976
|
G | A | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-6094C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478976 | ||||||
chr19:18479004
|
C | T | 2 | a0001c0007t0009g0006a0001c0007t0009g0007 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.136-6122G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479004 | ||||||
chr19:18479133
|
C | T | 4 | a0001c0001t0002g0033a0001c0001t0002g0040a0001c0001t0002g0054others(1): Show | 4 | HG01123.hp2 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-6251G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479133 | ||||||
chr19:18479134
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-6252C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479134 | ||||||
chr19:18479300
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-6418G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479300 | ||||||
chr19:18479413
|
C | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.136-6531G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479413 | ||||||
chr19:18479441
|
C | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.136-6559G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479441 | ||||||
chr19:18479708
|
C | CA | 33 | a0001c0001t0001g0144a0001c0001t0002g0052a0001c0001t0002g0061others(30): Show | 33 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.136-6827dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479708 | ||||||
chr19:18479708
|
C | CAAA | 7 | a0001c0001t0001g0146a0001c0001t0001g0203a0001c0001t0001g0211others(4): Show | 7 | HG01167.hp2 HG02451.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-6829_136-6827d others(5): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479708 | ||||||
chr19:18479708
|
C | CAAAA | 63 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0148others(60): Show | 63 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-6830_136-6827d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479708 | ||||||
chr19:18479708
|
C | CAAAAA | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(31): Show | 34 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.136-6831_136-6827d others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479708 | ||||||
chr19:18480019
|
T | C | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.136-7137A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480019 | ||||||
chr19:18480059
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.136-7177A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480059 | ||||||
chr19:18480159
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.136-7277G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480159 | ||||||
chr19:18480182
|
G | A | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-7300C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480182 | ||||||
chr19:18480192
|
C | A | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-7310G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480192 | ||||||
chr19:18480911
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.136-8029C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480911 | ||||||
chr19:18480923
|
C | T | 7 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(4): Show | 7 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-8041G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480923 | ||||||
chr19:18480928
|
C | T | 5 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0230others(2): Show | 5 | HG01109.hp1 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-8046G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480928 | ||||||
chr19:18480935
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.136-8053C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480935 | ||||||
chr19:18481201
|
T | C | 1 | a0002c0002t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.136-8319A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481201 | ||||||
chr19:18481314
|
G | A | 3 | a0001c0001t0002g0070a0001c0001t0002g0079a0001c0001t0002g0088 | 3 | HG00642.hp1 HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.136-8432C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481314 | ||||||
chr19:18481431
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136-8549G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481431 | ||||||
chr19:18481441
|
C | A | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | HG01433.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.136-8559G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481441 | ||||||
chr19:18481457
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.136-8575C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481457 | ||||||
chr19:18481514
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.136-8632C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481514 | ||||||
chr19:18481743
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.136-8861C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481743 | ||||||
chr19:18481971
|
G | A | 4 | a0001c0001t0001g0144a0001c0005t0007g0174a0001c0005t0007g0175others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-9089C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481971 | ||||||
chr19:18482032
|
T | C | 1 | a0002c0002t0001g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.136-9150A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482032 | ||||||
chr19:18482240
|
T | A | 2 | a0002c0002t0001g0013a0002c0002t0001g0014 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.136-9358A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482240 | ||||||
chr19:18482307
|
CCTTTTTT others(3): Show |
C | 4 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(1): Show | 4 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-9435_136-9426d others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482307 | ||||||
chr19:18482307
|
CCTTTTTT others(4): Show |
C | 1 | a0002c0002t0001g0143 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.136-9436_136-9426d others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482307 | ||||||
chr19:18482308
|
C | CT | 15 | a0001c0001t0002g0039a0001c0001t0002g0044a0001c0001t0002g0047others(12): Show | 15 | HG00738.hp1 HG01071.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.136-9427dupA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | ||||||
chr19:18482308
|
C | CTT | 7 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0182others(4): Show | 7 | HG01074.hp2 HG01255.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-9428_136-9427d others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | ||||||
chr19:18482308
|
C | CTTT | 46 | a0001c0001t0001g0162a0001c0001t0001g0173a0001c0001t0001g0177others(43): Show | 46 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.136-9429_136-9427d others(5): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | ||||||
chr19:18482308
|
C | CTTTT | 25 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(22): Show | 25 | HG00280.hp2 HG01081.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.136-9430_136-9427d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | ||||||
chr19:18482308
|
C | CTTTTT | 14 | a0001c0001t0001g0008a0001c0001t0001g0147a0001c0001t0001g0160others(11): Show | 14 | HG01109.hp1 HG01169.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.136-9431_136-9427d others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | ||||||
chr19:18482308
|
C | CTTTTTT | 5 | a0001c0001t0001g0010a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG02451.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-9432_136-9427d others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | ||||||
chr19:18482308
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0209a0001c0001t0002g0018a0001c0001t0002g0028others(5): Show | 8 | HG01361.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-9434_136-9427d others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | ||||||
chr19:18482308
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.136-9439_136-9427d others(15): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | ||||||
chr19:18482308
|
CTTTTTT | C | 33 | a0002c0002t0001g0012a0002c0002t0001g0014a0002c0002t0001g0015others(30): Show | 33 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.136-9432_136-9427d others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | ||||||
chr19:18482308
|
CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-9435_136-9427d others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | ||||||
chr19:18482322
|
T | C | 1 | a0002c0002t0001g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.136-9440A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482322 | ||||||
chr19:18482343
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.136-9461C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482343 | ||||||
chr19:18482349
|
G | A | 1 | a0001c0001t0002g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.136-9467C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482349 | ||||||
chr19:18482427
|
C | CCTGCCT | 3 | a0001c0001t0004g0151a0001c0007t0009g0006a0002c0002t0019g0131 | 3 | HG01884.hp2 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.136-9551_136-9546d others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482427 | ||||||
chr19:18482427
|
C | CCTGCCTC others(5): Show |
4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-9557_136-9546d others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482427 | ||||||
chr19:18482526
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.136-9644G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482526 | ||||||
chr19:18482537
|
C | G | 1 | a0001c0001t0001g0211 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.136-9655G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482537 | ||||||
chr19:18482598
|
G | A | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-9716C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482598 | ||||||
chr19:18482690
|
T | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0202 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.136-9808A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482690 | ||||||
chr19:18482743
|
T | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.136-9861A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482743 | ||||||
chr19:18482762
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-9880A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482762 | ||||||
chr19:18482763
|
T | G | 4 | a0001c0001t0001g0144a0001c0005t0007g0174a0001c0005t0007g0175others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-9881A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482763 | ||||||
chr19:18482763
|
T | TTTGTTGT others(2): Show |
16 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(13): Show | 16 | HG00323.hp2 HG01081.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.136-9890_136-9882d others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482763 | ||||||
chr19:18482763
|
T | TTTGTTGT others(5): Show |
18 | a0002c0002t0001g0109a0002c0002t0001g0110a0002c0002t0001g0114others(15): Show | 18 | HG00733.hp2 HG01258.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.136-9893_136-9882d others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482763 | ||||||
chr19:18482763
|
T | TTTGTTGT others(8): Show |
9 | a0001c0001t0011g0115a0002c0002t0001g0015a0002c0002t0001g0125others(6): Show | 9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-9896_136-9882d others(17): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482763 | ||||||
chr19:18482794
|
T | TTGCTGCT others(2): Show |
3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.136-9913_136-9912i others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | ||||||
chr19:18482794
|
T | TTGTTGCT others(2): Show |
6 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0160others(3): Show | 6 | HG02055.hp2 HG02148.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-9913_136-9912i others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | ||||||
chr19:18482794
|
T | TTGTTGCT others(5): Show |
1 | a0001c0001t0001g0223 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-9913_136-9912i others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | ||||||
chr19:18482794
|
T | TTGTTGTT others(5): Show |
86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(83): Show | 86 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.136-9913_136-9912i others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | ||||||
chr19:18482794
|
T | TTGTTGTT others(8): Show |
9 | a0001c0001t0001g0003a0001c0001t0001g0149a0001c0001t0001g0173others(6): Show | 9 | HG02886.hp1 HG03471.hp2 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-9913_136-9912i others(17): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | ||||||
chr19:18482794
|
T | TTGTTGTT others(11): Show |
2 | a0001c0004t0006g0156a0003c0006t0001g0226 | 2 | HG03041.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.136-9913_136-9912i others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | ||||||
chr19:18482797
|
C | T | 1 | a0002c0002t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.136-9915G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482797 | ||||||
chr19:18482914
|
A | C | 1 | a0002c0002t0001g0242 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.136-10032T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482914 | ||||||
chr19:18482916
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.136-10034G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482916 | ||||||
chr19:18483328
|
A | G | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-10446T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18483328 | ||||||
chr19:18483438
|
G | A | 1 | a0001c0004t0006g0156 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.136-10556C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18483438 | ||||||
chr19:18483487
|
C | T | 4 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(1): Show | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-10605G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18483487 | ||||||
chr19:18483865
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-10983C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18483865 | ||||||
chr19:18483904
|
C | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-11022G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18483904 | ||||||
chr19:18484026
|
G | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-11144C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484026 | ||||||
chr19:18484031
|
C | T | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-11149G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484031 | ||||||
chr19:18484172
|
G | A | 1 | a0002c0002t0001g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.136-11290C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484172 | ||||||
chr19:18484229
|
C | T | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-11347G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484229 | ||||||
chr19:18484279
|
C | T | 44 | a0001c0001t0011g0115a0002c0002t0001g0012a0002c0002t0001g0013others(41): Show | 44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.136-11397G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484279 | ||||||
chr19:18484339
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-11457G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484339 | ||||||
chr19:18484354
|
A | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136-11472T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484354 | ||||||
chr19:18484538
|
G | A | 5 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-11656C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484538 | ||||||
chr19:18484568
|
C | T | 4 | a0001c0001t0001g0144a0001c0005t0007g0174a0001c0005t0007g0175others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-11686G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484568 | ||||||
chr19:18484641
|
A | G | 2 | a0002c0002t0005g0117a0002c0002t0005g0120 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.136-11759T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484641 | ||||||
chr19:18484710
|
T | C | 1 | a0002c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.136-11828A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484710 | ||||||
chr19:18484825
|
C | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.136-11943G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484825 | ||||||
chr19:18484837
|
G | A | 1 | a0002c0002t0001g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.136-11955C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484837 | ||||||
chr19:18484881
|
C | T | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-11999G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484881 | ||||||
chr19:18484904
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136-12022G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484904 | ||||||
chr19:18485012
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.136-12130G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485012 | ||||||
chr19:18485089
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-12207C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485089 | ||||||
chr19:18485802
|
C | G | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.136-12920G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485802 | ||||||
chr19:18485818
|
C | T | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-12936G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485818 | ||||||
chr19:18485847
|
G | A | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-12965C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485847 | ||||||
chr19:18485847
|
G | T | 1 | a0001c0001t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.136-12965C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485847 | ||||||
chr19:18485985
|
CA | C | 6 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0060others(3): Show | 6 | HG01099.hp1 HG01516.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-13104delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485985 | ||||||
chr19:18486001
|
A | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0212 | 2 | NA19080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.136-13119T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486001 | ||||||
chr19:18486174
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-13292C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486174 | ||||||
chr19:18486203
|
T | A | 2 | a0002c0002t0001g0240a0002c0002t0001g0241 | 2 | HG00323.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.136-13321A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486203 | ||||||
chr19:18486216
|
T | C | 5 | a0001c0001t0004g0150a0001c0001t0004g0151a0001c0001t0004g0152others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-13334A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486216 | ||||||
chr19:18486386
|
G | A | 28 | a0001c0001t0001g0180a0001c0001t0001g0185a0001c0001t0001g0199others(25): Show | 28 | HG00280.hp2 HG00408.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.136-13504C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486386 | ||||||
chr19:18486387
|
G | A | 3 | a0001c0001t0002g0042a0001c0001t0002g0046a0001c0001t0002g0053 | 3 | HG02132.hp1 NA18951.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.136-13505C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486387 | ||||||
chr19:18486390
|
G | T | 2 | a0001c0001t0002g0025a0001c0001t0002g0064 | 2 | HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.136-13508C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486390 | ||||||
chr19:18486556
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.136-13674C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486556 | ||||||
chr19:18486608
|
G | A | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-13726C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486608 | ||||||
chr19:18486649
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.136-13767C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486649 | ||||||
chr19:18486651
|
A | G | 1 | a0002c0002t0001g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136-13769T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486651 | ||||||
chr19:18486763
|
G | C | 1 | a0001c0001t0001g0196 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136-13881C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486763 | ||||||
chr19:18487021
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162 | 3 | HG02055.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.136-14139G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18487021 | ||||||
chr19:18487164
|
G | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0063 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.136-14282C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18487164 | ||||||
chr19:18487363
|
C | T | 5 | a0001c0001t0004g0150a0001c0001t0004g0151a0001c0001t0004g0152others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-14481G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18487363 | ||||||
chr19:18487403
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0011g0115a0002c0002t0001g0012others(42): Show | 45 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.136-14521A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18487403 | ||||||
chr19:18488170
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-15288A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488170 | ||||||
chr19:18488531
|
C | T | 2 | a0002c0002t0005g0123a0002c0002t0005g0128 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.136-15649G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488531 | ||||||
chr19:18488557
|
G | A | 2 | a0001c0001t0001g0219a0001c0013t0001g0220 | 2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.136-15675C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488557 | ||||||
chr19:18488620
|
C | T | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-15738G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488620 | ||||||
chr19:18488647
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.136-15765A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488647 | ||||||
chr19:18488759
|
A | AG | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-15878dupC | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488759 | ||||||
chr19:18488929
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.136-16047G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488929 | ||||||
chr19:18488947
|
A | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-16065T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488947 | ||||||
chr19:18488982
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-16100C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488982 | ||||||
chr19:18489006
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-16124A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489006 | ||||||
chr19:18489120
|
G | A | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.136-16238C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489120 | ||||||
chr19:18489148
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.136-16266A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489148 | ||||||
chr19:18489151
|
G | C | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.136-16269C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489151 | ||||||
chr19:18489198
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.136-16316C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489198 | ||||||
chr19:18489246
|
G | A | 46 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0011g0115others(43): Show | 46 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.136-16364C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489246 | ||||||
chr19:18489251
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.136-16369G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489251 | ||||||
chr19:18489260
|
G | A | 1 | a0001c0001t0011g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-16378C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489260 | ||||||
chr19:18489372
|
G | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-16490C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489372 | ||||||
chr19:18489461
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.136-16579G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489461 | ||||||
chr19:18489645
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-16763C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489645 | ||||||
chr19:18489663
|
C | T | 1 | a0001c0005t0007g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.136-16781G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489663 | ||||||
chr19:18490206
|
C | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-17324G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490206 | ||||||
chr19:18490211
|
C | G | 1 | a0001c0001t0003g0024 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136-17329G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490211 | ||||||
chr19:18490310
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136-17428G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490310 | ||||||
chr19:18490360
|
G | C | 1 | a0002c0002t0001g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.136-17478C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490360 | ||||||
chr19:18490361
|
G | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-17479C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490361 | ||||||
chr19:18490449
|
G | T | 4 | a0001c0001t0001g0144a0001c0005t0007g0174a0001c0005t0007g0175others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-17567C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490449 | ||||||
chr19:18490456
|
C | A | 2 | a0001c0001t0002g0046a0001c0001t0002g0053 | 2 | HG02132.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.136-17574G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490456 | ||||||
chr19:18490722
|
C | T | 5 | a0001c0001t0002g0018a0001c0001t0002g0026a0001c0001t0002g0028others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-17840G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490722 | ||||||
chr19:18490743
|
G | C | 1 | a0001c0001t0002g0032 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.136-17861C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490743 | ||||||
chr19:18491249
|
ATT | A | 6 | a0001c0001t0002g0032a0001c0001t0002g0055a0001c0001t0002g0085others(3): Show | 6 | HG00639.hp2 HG01069.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-18369_136-1836 others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTT | A | 7 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0029others(4): Show | 8 | HG01975.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-18370_136-1836 others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTT | A | 22 | a0001c0001t0002g0018a0001c0001t0002g0028a0001c0001t0002g0037others(19): Show | 22 | HG00741.hp1 HG00741.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.136-18371_136-1836 others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTT | A | 17 | a0001c0001t0002g0017a0001c0001t0002g0030a0001c0001t0002g0046others(14): Show | 17 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.136-18372_136-1836 others(9): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTT | A | 14 | a0001c0001t0002g0027a0001c0001t0002g0050a0001c0001t0002g0058others(11): Show | 14 | HG00280.hp1 HG00642.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.136-18373_136-1836 others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT | A | 13 | a0001c0001t0002g0025a0001c0001t0002g0045a0001c0001t0002g0047others(10): Show | 13 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.136-18374_136-1836 others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT others(6): Show |
A | 1 | a0002c0002t0001g0143 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.136-18380_136-1836 others(17): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT others(7): Show |
A | 4 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(1): Show | 4 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-18381_136-1836 others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT others(8): Show |
A | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-18382_136-1836 others(19): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT others(10): Show |
A | 14 | a0001c0001t0001g0177a0001c0001t0001g0180a0001c0001t0001g0182others(11): Show | 14 | HG01074.hp2 HG01099.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.136-18384_136-1836 others(21): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT others(11): Show |
A | 53 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(50): Show | 53 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.136-18385_136-1836 others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT others(12): Show |
A | 16 | a0001c0001t0001g0144a0001c0001t0001g0149a0001c0001t0001g0162others(13): Show | 16 | HG01109.hp1 HG01167.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-18386_136-1836 others(23): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT others(13): Show |
A | 1 | a0002c0002t0001g0013 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.136-18387_136-1836 others(24): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT others(14): Show |
A | 34 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0011g0115others(31): Show | 34 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.136-18388_136-1836 others(25): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT others(15): Show |
A | 7 | a0001c0001t0002g0033a0001c0001t0002g0040a0001c0001t0002g0054others(4): Show | 7 | HG01123.hp2 HG02735.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-18389_136-1836 others(26): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT others(17): Show |
A | 22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(19): Show | 22 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.136-18391_136-1836 others(28): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491249
|
ATTTTTTT others(18): Show |
A | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136-18392_136-1836 others(29): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | ||||||
chr19:18491403
|
C | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-18521G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491403 | ||||||
chr19:18491444
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-18562G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491444 | ||||||
chr19:18491654
|
C | T | 4 | a0001c0001t0001g0144a0001c0005t0007g0174a0001c0005t0007g0175others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-18772G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491654 | ||||||
chr19:18491751
|
C | CA | 5 | a0001c0001t0001g0222a0001c0001t0001g0238a0002c0002t0001g0137others(2): Show | 5 | HG00735.hp2 HG01433.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-18870dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491751 | ||||||
chr19:18491986
|
T | G | 5 | a0001c0001t0002g0027a0001c0001t0002g0080a0001c0001t0002g0081others(2): Show | 5 | HG00741.hp1 HG01243.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-19104A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491986 | ||||||
chr19:18491992
|
G | C | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-19110C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491992 | ||||||
chr19:18492493
|
A | C | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-19611T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18492493 | ||||||
chr19:18492494
|
C | T | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-19612G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18492494 | ||||||
chr19:18492651
|
A | C | 5 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-19769T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18492651 | ||||||
chr19:18493131
|
C | T | 1 | a0001c0001t0003g0024 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136-20249G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493131 | ||||||
chr19:18493211
|
TGGGGCTG others(17): Show |
T | 1 | a0001c0001t0002g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.136-20353_136-2033 others(28): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493211 | ||||||
chr19:18493270
|
C | T | 12 | a0001c0001t0002g0018a0001c0001t0002g0026a0001c0001t0002g0028others(9): Show | 12 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-20388G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493270 | ||||||
chr19:18493275
|
C | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.136-20393G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493275 | ||||||
chr19:18493344
|
C | T | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-20462G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493344 | ||||||
chr19:18493560
|
C | G | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-20678G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493560 | ||||||
chr19:18493635
|
C | T | 2 | a0002c0002t0005g0117a0002c0002t0005g0120 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.136-20753G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493635 | ||||||
chr19:18493645
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0210 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.136-20763C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493645 | ||||||
chr19:18493816
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136-20934G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493816 | ||||||
chr19:18493895
|
T | C | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-21013A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493895 | ||||||
chr19:18494068
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-21186T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494068 | ||||||
chr19:18494132
|
T | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.136-21250A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494132 | ||||||
chr19:18494175
|
T | C | 3 | a0001c0001t0001g0196a0001c0001t0001g0210a0001c0001t0014g0208 | 3 | HG01884.hp1 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.136-21293A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494175 | ||||||
chr19:18494249
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.136-21367C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494249 | ||||||
chr19:18494264
|
G | A | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-21382C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494264 | ||||||
chr19:18494400
|
G | GT | 5 | a0001c0001t0002g0105a0001c0001t0004g0150a0001c0001t0004g0152others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-21519dupA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494400 | ||||||
chr19:18494643
|
G | C | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-21761C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494643 | ||||||
chr19:18494913
|
T | C | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-22031A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494913 | ||||||
chr19:18495139
|
C | T | 1 | a0002c0002t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.136-22257G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495139 | ||||||
chr19:18495206
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-22324C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495206 | ||||||
chr19:18495456
|
A | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 147 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.136-22574T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495456 | ||||||
chr19:18495559
|
G | T | 28 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0011g0115others(25): Show | 28 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.136-22677C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495559 | ||||||
chr19:18495605
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.136-22723C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495605 | ||||||
chr19:18495646
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.136-22764C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495646 | ||||||
chr19:18495662
|
G | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.136-22780C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495662 | ||||||
chr19:18495712
|
C | A | 12 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(9): Show | 12 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-22830G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495712 | ||||||
chr19:18495716
|
T | G | 38 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0011g0115others(35): Show | 38 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.136-22834A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495716 | ||||||
chr19:18495784
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0239 | 3 | HG01891.hp1 HG02922.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.136-22902G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495784 | ||||||
chr19:18495846
|
G | A | 38 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0011g0115others(35): Show | 38 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.136-22964C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495846 | ||||||
chr19:18496134
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01891.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.136-23252A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496134 | ||||||
chr19:18496448
|
T | TTCCTCTA others(1): Show |
3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-23574_136-2356 others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496448 | ||||||
chr19:18496527
|
CT | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 148 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.136-23646delA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496527 | ||||||
chr19:18496583
|
C | G | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-23701G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496583 | ||||||
chr19:18496787
|
A | G | 1 | a0002c0002t0001g0127 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.136-23905T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496787 | ||||||
chr19:18496913
|
G | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(17): Show | 20 | HG01081.hp1 HG01891.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.136-24031C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496913 | ||||||
chr19:18496970
|
C | T | 63 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(60): Show | 63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-24088G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496970 | ||||||
chr19:18496985
|
C | G | 1 | a0001c0001t0011g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-24103G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496985 | ||||||
chr19:18497337
|
A | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.136-24455T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497337 | ||||||
chr19:18497353
|
G | A | 1 | a0006c0011t0001g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.136-24471C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497353 | ||||||
chr19:18497384
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0229 | 2 | HG01255.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.136-24502A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497384 | ||||||
chr19:18497409
|
G | A | 4 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0095others(1): Show | 4 | HG00733.hp1 HG01175.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+24512C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497409 | ||||||
chr19:18497473
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.135+24448G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497473 | ||||||
chr19:18497557
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.135+24364G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497557 | ||||||
chr19:18497708
|
C | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+24213G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497708 | ||||||
chr19:18497769
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+24152C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497769 | ||||||
chr19:18497815
|
C | CA | 44 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(41): Show | 44 | HG00323.hp2 HG00639.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.135+24105dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497815 | ||||||
chr19:18497815
|
CA | C | 16 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0160others(13): Show | 16 | HG00738.hp1 HG01167.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+24105delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497815 | ||||||
chr19:18497815
|
CAA | C | 76 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(73): Show | 76 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.135+24104_135+2410 others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497815 | ||||||
chr19:18497815
|
CAAA | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0184a0001c0001t0001g0197others(2): Show | 5 | HG01109.hp1 HG02293.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+24103_135+2410 others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497815 | ||||||
chr19:18498280
|
T | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+23641A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18498280 | ||||||
chr19:18498552
|
A | T | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.135+23369T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18498552 | ||||||
chr19:18498563
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.135+23358C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18498563 | ||||||
chr19:18498651
|
A | G | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+23270T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18498651 | ||||||
chr19:18498954
|
AAAC | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+22964_135+2296 others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18498954 | ||||||
chr19:18499706
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.135+22215T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18499706 | ||||||
chr19:18499721
|
C | T | 2 | a0001c0001t0002g0035a0001c0001t0002g0036 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.135+22200G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18499721 | ||||||
chr19:18500006
|
A | T | 10 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0072others(7): Show | 10 | HG00639.hp2 HG01069.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+21915T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500006 | ||||||
chr19:18500210
|
T | C | 2 | a0002c0002t0001g0242a0002c0002t0001g0243 | 2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.135+21711A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500210 | ||||||
chr19:18500234
|
C | G | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+21687G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500234 | ||||||
chr19:18500261
|
C | CA | 14 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0233others(11): Show | 14 | HG01109.hp1 HG01175.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.135+21659dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500261 | ||||||
chr19:18500310
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+21611C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500310 | ||||||
chr19:18500321
|
T | C | 1 | a0001c0001t0002g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.135+21600A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500321 | ||||||
chr19:18500337
|
A | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+21584T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500337 | ||||||
chr19:18500372
|
A | C | 1 | a0001c0001t0002g0037 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.135+21549T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500372 | ||||||
chr19:18500446
|
C | T | 1 | a0001c0003t0001g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.135+21475G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500446 | ||||||
chr19:18500556
|
G | A | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+21365C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500556 | ||||||
chr19:18500689
|
G | A | 1 | a0001c0010t0002g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.135+21232C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500689 | ||||||
chr19:18500735
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+21186G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500735 | ||||||
chr19:18500740
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+21181A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500740 | ||||||
chr19:18500816
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0210 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.135+21105G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500816 | ||||||
chr19:18501011
|
C | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+20910G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501011 | ||||||
chr19:18501085
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+20836G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501085 | ||||||
chr19:18501382
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+20539G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501382 | ||||||
chr19:18501387
|
G | A | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+20534C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501387 | ||||||
chr19:18501447
|
G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.135+20474C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501447 | ||||||
chr19:18501541
|
G | C | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+20380C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501541 | ||||||
chr19:18501542
|
G | A | 1 | a0002c0002t0001g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.135+20379C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501542 | ||||||
chr19:18501819
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+20102G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501819 | ||||||
chr19:18501827
|
G | A | 6 | a0001c0001t0011g0115a0002c0002t0005g0117a0002c0002t0005g0120others(3): Show | 6 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+20094C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501827 | ||||||
chr19:18501938
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+19983C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501938 | ||||||
chr19:18501948
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+19973C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501948 | ||||||
chr19:18502042
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.135+19879G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502042 | ||||||
chr19:18502112
|
T | C | 1 | a0001c0001t0012g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.135+19809A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502112 | ||||||
chr19:18502180
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.135+19741C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502180 | ||||||
chr19:18502222
|
C | G | 2 | a0001c0007t0009g0006a0001c0007t0009g0007 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.135+19699G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502222 | ||||||
chr19:18502673
|
C | T | 1 | a0002c0002t0001g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.135+19248G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502673 | ||||||
chr19:18502833
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.135+19088G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502833 | ||||||
chr19:18502842
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.135+19079G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502842 | ||||||
chr19:18503079
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.135+18842G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503079 | ||||||
chr19:18503107
|
C | T | 3 | a0001c0001t0002g0017a0001c0001t0002g0061a0001c0001t0002g0099 | 3 | HG00735.hp1 HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.135+18814G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503107 | ||||||
chr19:18503125
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.135+18796C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503125 | ||||||
chr19:18503383
|
C | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.135+18538G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503383 | ||||||
chr19:18503613
|
A | G | 46 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0011g0115others(43): Show | 46 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.135+18308T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503613 | ||||||
chr19:18503620
|
C | A | 1 | a0001c0001t0002g0062 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.135+18301G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503620 | ||||||
chr19:18503751
|
C | G | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+18170G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503751 | ||||||
chr19:18503780
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.135+18141G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503780 | ||||||
chr19:18504045
|
G | A | 3 | a0001c0001t0002g0017a0001c0001t0002g0061a0001c0001t0002g0099 | 3 | HG00735.hp1 HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.135+17876C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504045 | ||||||
chr19:18504125
|
T | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(98): Show | 101 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.135+17796A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504125 | ||||||
chr19:18504187
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.135+17734G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504187 | ||||||
chr19:18504460
|
C | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+17461G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504460 | ||||||
chr19:18504552
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.135+17369A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504552 | ||||||
chr19:18504615
|
C | T | 4 | a0001c0001t0002g0018a0001c0001t0002g0026a0001c0001t0002g0028others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+17306G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504615 | ||||||
chr19:18504634
|
C | T | 1 | a0002c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+17287G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504634 | ||||||
chr19:18504660
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.135+17261G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504660 | ||||||
chr19:18504690
|
T | A | 1 | a0001c0001t0003g0024 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.135+17231A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504690 | ||||||
chr19:18504852
|
G | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+17069C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504852 | ||||||
chr19:18505091
|
G | A | 2 | a0002c0002t0001g0111a0002c0002t0001g0134 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.135+16830C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18505091 | ||||||
chr19:18505097
|
G | A | 1 | a0002c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+16824C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18505097 | ||||||
chr19:18505202
|
C | G | 2 | a0002c0002t0001g0111a0002c0002t0001g0134 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.135+16719G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18505202 | ||||||
chr19:18505589
|
T | C | 63 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(60): Show | 63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.135+16332A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18505589 | ||||||
chr19:18505714
|
G | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+16207C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18505714 | ||||||
chr19:18506163
|
C | T | 3 | a0001c0001t0001g0219a0001c0001t0018g0207a0001c0013t0001g0220 | 3 | HG01516.hp1 HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.135+15758G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506163 | ||||||
chr19:18506339
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.135+15582G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506339 | ||||||
chr19:18506341
|
G | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+15580C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506341 | ||||||
chr19:18506544
|
C | T | 1 | a0001c0001t0002g0042 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.135+15377G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506544 | ||||||
chr19:18506575
|
A | C | 4 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0065others(1): Show | 4 | HG00738.hp2 HG01071.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+15346T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506575 | ||||||
chr19:18506983
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.135+14938C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506983 | ||||||
chr19:18507007
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.135+14914T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507007 | ||||||
chr19:18507026
|
C | A | 1 | a0001c0001t0002g0062 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.135+14895G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507026 | ||||||
chr19:18507302
|
T | C | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+14619A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507302 | ||||||
chr19:18507415
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+14506G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507415 | ||||||
chr19:18507507
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | HG01433.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.135+14414G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507507 | ||||||
chr19:18507634
|
G | A | 1 | a0002c0002t0001g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.135+14287C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507634 | ||||||
chr19:18507638
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+14283T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507638 | ||||||
chr19:18507755
|
T | C | 9 | a0001c0001t0002g0034a0001c0001t0002g0050a0001c0001t0002g0051others(6): Show | 9 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+14166A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507755 | ||||||
chr19:18507759
|
T | C | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.135+14162A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507759 | ||||||
chr19:18507770
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+14151G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507770 | ||||||
chr19:18508057
|
G | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+13864C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508057 | ||||||
chr19:18508213
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.135+13708G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508213 | ||||||
chr19:18508246
|
C | T | 2 | a0001c0001t0002g0025a0001c0001t0002g0064 | 2 | HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.135+13675G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508246 | ||||||
chr19:18508247
|
T | C | 44 | a0001c0001t0011g0115a0002c0002t0001g0012a0002c0002t0001g0013others(41): Show | 44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.135+13674A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508247 | ||||||
chr19:18508354
|
A | G | 4 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(1): Show | 4 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13567T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508354 | ||||||
chr19:18508391
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.135+13530A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508391 | ||||||
chr19:18508524
|
G | T | 3 | a0001c0001t0002g0042a0001c0001t0002g0046a0001c0001t0002g0053 | 3 | HG02132.hp1 NA18951.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.135+13397C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508524 | ||||||
chr19:18508587
|
G | A | 1 | a0001c0001t0011g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+13334C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508587 | ||||||
chr19:18508841
|
C | T | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+13080G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508841 | ||||||
chr19:18508927
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+12994G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508927 | ||||||
chr19:18509058
|
C | T | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.135+12863G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509058 | ||||||
chr19:18509120
|
T | A | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.135+12801A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509120 | ||||||
chr19:18509373
|
T | G | 1 | a0001c0001t0002g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.135+12548A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509373 | ||||||
chr19:18509440
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.135+12481C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509440 | ||||||
chr19:18509575
|
ATGCACG | A | 5 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+12340_135+1234 others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509575 | ||||||
chr19:18509582
|
T | TGC | 3 | a0002c0002t0001g0112a0002c0002t0001g0114a0002c0002t0013g0113 | 3 | HG01081.hp2 HG01496.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.135+12337_135+1233 others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509582 | ||||||
chr19:18509582
|
T | TGCGCGCG others(3): Show |
1 | a0002c0002t0001g0129 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.135+12329_135+1233 others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509582 | ||||||
chr19:18509582
|
T | TGCGCGCG others(5): Show |
2 | a0002c0002t0001g0111a0002c0002t0001g0130 | 2 | HG02559.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.135+12327_135+1233 others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509582 | ||||||
chr19:18509582
|
T | TGCGCGCG others(9): Show |
1 | a0002c0002t0001g0139 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.135+12338_135+1233 others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509582 | ||||||
chr19:18509582
|
T | TGTGCGCA others(11): Show |
1 | a0001c0001t0001g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.135+12338_135+1233 others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509582 | ||||||
chr19:18509584
|
C | T | 1 | a0002c0002t0005g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.135+12337G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509584 | ||||||
chr19:18509585
|
G | A | 4 | a0001c0001t0001g0144a0001c0005t0007g0174a0001c0005t0007g0175others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+12336C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509585 | ||||||
chr19:18509590
|
C | T | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.135+12331G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509590 | ||||||
chr19:18509591
|
GCGCACAT others(7): Show |
G | 3 | a0001c0001t0001g0183a0001c0001t0001g0225a0003c0006t0001g0226 | 3 | HG01167.hp1 HG01928.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.135+12316_135+1232 others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | ||||||
chr19:18509591
|
GCGCACAT others(9): Show |
G | 6 | a0001c0001t0001g0219a0001c0001t0001g0222a0001c0001t0001g0232others(3): Show | 6 | HG01099.hp2 HG01433.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+12314_135+1232 others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | ||||||
chr19:18509591
|
GCGCACAT others(11): Show |
G | 8 | a0001c0001t0001g0185a0001c0001t0001g0215a0001c0001t0001g0216others(5): Show | 8 | HG00280.hp2 HG00408.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+12312_135+1232 others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | ||||||
chr19:18509591
|
GCGCACAT others(13): Show |
G | 4 | a0001c0001t0001g0147a0001c0001t0001g0177a0001c0001t0001g0210others(1): Show | 4 | HG01884.hp1 NA18951.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+12310_135+1232 others(24): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | ||||||
chr19:18509591
|
GCGCACAT others(15): Show |
G | 16 | a0001c0001t0001g0145a0001c0001t0001g0178a0001c0001t0001g0181others(13): Show | 16 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.135+12308_135+1232 others(26): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | ||||||
chr19:18509591
|
GCGCACAT others(17): Show |
G | 8 | a0001c0001t0001g0184a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG01109.hp1 HG01952.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+12306_135+1232 others(28): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | ||||||
chr19:18509591
|
GCGCACAT others(19): Show |
G | 2 | a0001c0001t0011g0115a0001c0001t0017g0194 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.135+12304_135+1232 others(30): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | ||||||
chr19:18509591
|
GCGCACAT others(21): Show |
G | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.135+12302_135+1232 others(32): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | ||||||
chr19:18509592
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+12329G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509592 | ||||||
chr19:18509593
|
GCACATAC others(1): Show |
G | 8 | a0001c0001t0001g0161a0001c0001t0004g0153a0002c0002t0001g0012others(5): Show | 8 | HG01167.hp2 HG01258.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+12320_135+1232 others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(3): Show |
G | 3 | a0002c0002t0001g0118a0002c0002t0001g0134a0002c0002t0008g0119 | 3 | HG01346.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.135+12318_135+1232 others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(5): Show |
G | 7 | a0001c0001t0016g0159a0001c0004t0006g0157a0001c0004t0006g0158others(4): Show | 7 | HG02004.hp1 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+12316_135+1232 others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(7): Show |
G | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0004t0006g0156others(1): Show | 4 | HG02970.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+12314_135+1232 others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(9): Show |
G | 4 | a0001c0001t0001g0180a0001c0001t0001g0218a0001c0001t0001g0239others(1): Show | 4 | HG02300.hp2 HG02572.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+12312_135+1232 others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(11): Show |
G | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG00733.hp2 HG01891.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.135+12310_135+1232 others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(13): Show |
G | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0209others(4): Show | 7 | HG00642.hp2 HG02572.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+12308_135+1232 others(24): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(15): Show |
G | 17 | a0001c0001t0001g0155a0001c0001t0001g0164a0001c0001t0001g0168others(14): Show | 17 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.135+12306_135+1232 others(26): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(17): Show |
G | 5 | a0001c0001t0001g0146a0001c0001t0001g0195a0001c0001t0004g0152others(2): Show | 5 | HG01123.hp1 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+12304_135+1232 others(28): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(19): Show |
G | 6 | a0001c0001t0001g0004a0001c0001t0001g0144a0001c0001t0001g0160others(3): Show | 6 | HG01081.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+12302_135+1232 others(30): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(21): Show |
G | 2 | a0001c0005t0007g0176a0002c0002t0001g0140 | 2 | HG02257.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.135+12300_135+1232 others(32): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(23): Show |
G | 2 | a0001c0005t0007g0174a0001c0005t0007g0175 | 2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.135+12298_135+1232 others(34): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509593
|
GCACATAC others(25): Show |
G | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.135+12296_135+1232 others(36): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | ||||||
chr19:18509594
|
CACAT | C | 4 | a0002c0002t0001g0014a0002c0002t0001g0109a0002c0002t0001g0124others(1): Show | 4 | HG02896.hp2 HG03471.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+12323_135+1232 others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509594 | ||||||
chr19:18509595
|
A | C | 1 | a0002c0002t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.135+12326T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509595 | ||||||
chr19:18509595
|
A | G | 11 | a0001c0001t0004g0150a0002c0002t0001g0110a0002c0002t0001g0112others(8): Show | 11 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+12326T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509595 | ||||||
chr19:18509596
|
C | G | 1 | a0002c0002t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.135+12325G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509596 | ||||||
chr19:18509597
|
A | C | 1 | a0002c0002t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.135+12324T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509597 | ||||||
chr19:18509597
|
A | G | 12 | a0001c0001t0004g0150a0002c0002t0001g0110a0002c0002t0001g0112others(9): Show | 12 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.135+12324T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509597 | ||||||
chr19:18509598
|
T | C | 15 | a0001c0001t0001g0162a0001c0001t0004g0150a0002c0002t0001g0015others(12): Show | 15 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.135+12323A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
T | TAC | 10 | a0001c0001t0002g0032a0001c0001t0002g0077a0001c0001t0002g0078others(7): Show | 10 | HG00642.hp1 HG00741.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.135+12321_135+1232 others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
T | TACAC | 8 | a0001c0001t0002g0082a0001c0001t0002g0083a0001c0001t0002g0084others(5): Show | 8 | HG01069.hp2 HG01074.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+12319_135+1232 others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
T | TACACAC | 3 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0002g0095 | 3 | HG01257.hp1 HG02148.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.135+12317_135+1232 others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
T | TACACACA others(5): Show |
2 | a0001c0001t0002g0091a0001c0001t0002g0096 | 2 | HG01175.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.135+12311_135+1232 others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
T | TACACACA others(9): Show |
1 | a0001c0001t0002g0092 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.135+12307_135+1232 others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
TAC | T | 10 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0064others(7): Show | 10 | HG00639.hp2 HG01515.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+12321_135+1232 others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
TACAC | T | 7 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0060others(4): Show | 7 | HG00639.hp1 HG00741.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+12319_135+1232 others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
TACACAC | T | 10 | a0001c0001t0002g0033a0001c0001t0002g0053a0001c0001t0002g0054others(7): Show | 10 | HG00280.hp1 HG00738.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+12317_135+1232 others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
TACACACA others(1): Show |
T | 9 | a0001c0001t0002g0017a0001c0001t0002g0046a0001c0001t0002g0047others(6): Show | 9 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+12315_135+1232 others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
TACACACA others(3): Show |
T | 11 | a0001c0001t0002g0018a0001c0001t0002g0026a0001c0001t0002g0028others(8): Show | 11 | HG02300.hp1 HG02559.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+12313_135+1232 others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
TACACACA others(5): Show |
T | 2 | a0001c0001t0003g0024a0001c0001t0015g0041 | 2 | HG01975.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.135+12311_135+1232 others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
TACACACA others(7): Show |
T | 3 | a0001c0001t0002g0040a0001c0001t0003g0022a0001c0001t0003g0023 | 3 | HG02818.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.135+12309_135+1232 others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
TACACACA others(9): Show |
T | 4 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(1): Show | 4 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+12307_135+1232 others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
TACACACA others(11): Show |
T | 2 | a0001c0001t0002g0039a0001c0001t0002g0093 | 2 | HG00733.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.135+12305_135+1232 others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509598
|
TACACACA others(33): Show |
T | 4 | a0001c0001t0002g0001a0001c0001t0002g0037a0001c0001t0002g0108others(1): Show | 5 | NA18975.hp1 NA19060.hp2 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+12283_135+1232 others(44): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | ||||||
chr19:18509599
|
A | G | 13 | a0001c0001t0004g0150a0002c0002t0001g0109a0002c0002t0001g0112others(10): Show | 13 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.135+12322T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509599 | ||||||
chr19:18509601
|
A | G | 15 | a0001c0001t0004g0150a0001c0001t0004g0154a0002c0002t0001g0109others(12): Show | 15 | HG01081.hp2 HG01169.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+12320T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509601 | ||||||
chr19:18509603
|
A | G | 16 | a0001c0001t0001g0161a0001c0001t0004g0150a0001c0001t0004g0153others(13): Show | 16 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+12318T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509603 | ||||||
chr19:18509605
|
A | G | 16 | a0001c0001t0001g0161a0001c0001t0004g0150a0001c0001t0004g0153others(13): Show | 16 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.135+12316T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509605 | ||||||
chr19:18509607
|
A | G | 21 | a0001c0001t0004g0150a0001c0001t0004g0153a0001c0001t0004g0154others(18): Show | 21 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+12314T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509607 | ||||||
chr19:18509609
|
A | G | 21 | a0001c0001t0004g0150a0001c0001t0004g0153a0001c0001t0004g0154others(18): Show | 21 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+12312T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509609 | ||||||
chr19:18509611
|
A | G | 20 | a0001c0001t0004g0150a0001c0001t0004g0153a0001c0001t0004g0154others(17): Show | 20 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+12310T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509611 | ||||||
chr19:18509613
|
A | G | 23 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(20): Show | 23 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.135+12308T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509613 | ||||||
chr19:18509615
|
A | G | 17 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0149others(14): Show | 17 | HG01346.hp2 HG02004.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.135+12306T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509615 | ||||||
chr19:18509617
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0002g0005others(8): Show | 11 | HG02004.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+12304T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509617 | ||||||
chr19:18509619
|
A | G | 20 | a0001c0001t0001g0149a0001c0001t0001g0178a0001c0001t0001g0188others(17): Show | 20 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+12302T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509619 | ||||||
chr19:18509621
|
A | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0144a0001c0001t0001g0160others(5): Show | 8 | HG02717.hp2 HG02738.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+12300T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509621 | ||||||
chr19:18509623
|
A | G | 5 | a0001c0001t0001g0144a0001c0001t0001g0160a0001c0001t0001g0173others(2): Show | 5 | HG02738.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+12298T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509623 | ||||||
chr19:18509625
|
A | G | 4 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+12296T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509625 | ||||||
chr19:18509627
|
A | G | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0002c0002t0001g0137 | 3 | HG02622.hp1 HG02647.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.135+12294T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509627 | ||||||
chr19:18509629
|
A | G | 1 | a0002c0002t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.135+12292T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509629 | ||||||
chr19:18509631
|
A | G | 1 | a0002c0002t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.135+12290T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509631 | ||||||
chr19:18509916
|
A | T | 1 | a0002c0002t0001g0114 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.135+12005T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509916 | ||||||
chr19:18509975
|
G | T | 4 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(1): Show | 4 | HG02809.hp2 HG02886.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+11946C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509975 | ||||||
chr19:18510057
|
C | A | 1 | a0001c0001t0002g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.135+11864G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510057 | ||||||
chr19:18510239
|
G | A | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+11682C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510239 | ||||||
chr19:18510536
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+11385A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510536 | ||||||
chr19:18510612
|
G | A | 4 | a0001c0001t0002g0093a0001c0001t0002g0094a0001c0001t0002g0095others(1): Show | 4 | HG00733.hp1 HG01175.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+11309C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510612 | ||||||
chr19:18510732
|
C | T | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+11189G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510732 | ||||||
chr19:18510769
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.135+11152T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510769 | ||||||
chr19:18510809
|
T | C | 11 | a0001c0001t0001g0155a0001c0001t0001g0163a0001c0001t0001g0164others(8): Show | 11 | HG01081.hp1 HG02886.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+11112A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510809 | ||||||
chr19:18510860
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+11061T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510860 | ||||||
chr19:18510869
|
C | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.135+11052G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510869 | ||||||
chr19:18511184
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+10737T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511184 | ||||||
chr19:18511193
|
G | C | 3 | a0002c0002t0001g0111a0002c0002t0001g0134a0002c0002t0001g0135 | 3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+10728C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511193 | ||||||
chr19:18511303
|
G | A | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.135+10618C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511303 | ||||||
chr19:18511383
|
T | C | 44 | a0001c0001t0011g0115a0002c0002t0001g0012a0002c0002t0001g0013others(41): Show | 44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.135+10538A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511383 | ||||||
chr19:18511405
|
C | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+10516G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511405 | ||||||
chr19:18511541
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.135+10380C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511541 | ||||||
chr19:18511614
|
C | T | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+10307G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511614 | ||||||
chr19:18511633
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+10288G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511633 | ||||||
chr19:18511873
|
A | AT | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG01891.hp2 HG02717.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+10047_135+1004 others(5): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511873 | ||||||
chr19:18511873
|
A | T | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 146 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.135+10048T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511873 | ||||||
chr19:18511889
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+10032T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511889 | ||||||
chr19:18511996
|
A | G | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+9925T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511996 | ||||||
chr19:18512029
|
C | T | 63 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(60): Show | 63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.135+9892G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512029 | ||||||
chr19:18512149
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+9772G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512149 | ||||||
chr19:18512154
|
C | CA | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+9766dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512154 | ||||||
chr19:18512322
|
G | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+9599C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512322 | ||||||
chr19:18512388
|
G | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+9533C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512388 | ||||||
chr19:18512635
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.135+9286G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512635 | ||||||
chr19:18512647
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.135+9274G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512647 | ||||||
chr19:18512951
|
G | A | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+8970C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512951 | ||||||
chr19:18513041
|
G | A | 1 | a0002c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+8880C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513041 | ||||||
chr19:18513108
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.135+8813A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513108 | ||||||
chr19:18513271
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.135+8650C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513271 | ||||||
chr19:18513279
|
G | A | 1 | a0001c0001t0012g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.135+8642C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513279 | ||||||
chr19:18513361
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+8560C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513361 | ||||||
chr19:18513479
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG01891.hp1 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.135+8442T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513479 | ||||||
chr19:18513523
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.135+8398T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513523 | ||||||
chr19:18513580
|
T | G | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+8341A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513580 | ||||||
chr19:18513590
|
T | C | 1 | a0001c0001t0002g0099 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.135+8331A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513590 | ||||||
chr19:18513669
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+8252G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513669 | ||||||
chr19:18513796
|
T | C | 7 | a0001c0001t0001g0144a0001c0004t0006g0156a0001c0004t0006g0157others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+8125A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513796 | ||||||
chr19:18514154
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+7767C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514154 | ||||||
chr19:18514341
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+7580T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514341 | ||||||
chr19:18514370
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.135+7551G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514370 | ||||||
chr19:18514383
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0100a0001c0001t0002g0101 | 3 | HG01243.hp1 HG01496.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.135+7538C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514383 | ||||||
chr19:18514500
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+7421A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514500 | ||||||
chr19:18514513
|
C | CA | 16 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(13): Show | 16 | HG01261.hp1 HG01261.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.135+7407dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514513 | ||||||
chr19:18514513
|
CA | C | 15 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(12): Show | 15 | HG01099.hp1 HG01167.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+7407delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514513 | ||||||
chr19:18515128
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.135+6793G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18515128 | ||||||
chr19:18515146
|
C | T | 2 | a0001c0007t0009g0006a0001c0007t0009g0007 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.135+6775G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18515146 | ||||||
chr19:18515566
|
G | A | 1 | a0001c0001t0004g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.135+6355C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18515566 | ||||||
chr19:18515713
|
T | C | 1 | a0001c0001t0016g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.135+6208A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18515713 | ||||||
chr19:18515922
|
C | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+5999G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18515922 | ||||||
chr19:18516109
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0002g0005 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.135+5812G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516109 | ||||||
chr19:18516257
|
T | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+5664A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516257 | ||||||
chr19:18516310
|
A | T | 1 | a0001c0001t0002g0032 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.135+5611T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516310 | ||||||
chr19:18516323
|
C | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+5598G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516323 | ||||||
chr19:18516331
|
C | A | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+5590G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516331 | ||||||
chr19:18516424
|
C | G | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.135+5497G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516424 | ||||||
chr19:18516561
|
G | GC | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+5359dupG | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516561 | ||||||
chr19:18516667
|
C | G | 2 | a0002c0002t0001g0112a0002c0002t0013g0113 | 2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.135+5254G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516667 | ||||||
chr19:18516859
|
G | A | 1 | a0001c0005t0007g0176 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.135+5062C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516859 | ||||||
chr19:18516910
|
C | G | 1 | a0001c0001t0001g0180 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.135+5011G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516910 | ||||||
chr19:18516989
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.135+4932C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516989 | ||||||
chr19:18517143
|
A | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.135+4778T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517143 | ||||||
chr19:18517165
|
G | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(17): Show | 20 | HG01081.hp1 HG01891.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+4756C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517165 | ||||||
chr19:18517263
|
C | T | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+4658G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517263 | ||||||
chr19:18517267
|
T | C | 1 | a0005c0014t0001g0011 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.135+4654A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517267 | ||||||
chr19:18517334
|
T | C | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.135+4587A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517334 | ||||||
chr19:18517395
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+4526A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517395 | ||||||
chr19:18517433
|
T | C | 3 | a0001c0004t0006g0156a0001c0004t0006g0157a0001c0004t0006g0158 | 3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+4488A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517433 | ||||||
chr19:18517445
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.135+4476A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517445 | ||||||
chr19:18517465
|
G | A | 4 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0153others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+4456C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517465 | ||||||
chr19:18517544
|
C | T | 5 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+4377G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517544 | ||||||
chr19:18517636
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.135+4285C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517636 | ||||||
chr19:18517706
|
A | T | 41 | a0001c0001t0011g0115a0002c0002t0001g0012a0002c0002t0001g0013others(38): Show | 41 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.135+4215T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517706 | ||||||
chr19:18517707
|
T | A | 2 | a0001c0001t0001g0232a0001c0001t0002g0103 | 2 | HG01099.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.135+4214A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517707 | ||||||
chr19:18517808
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.135+4113C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517808 | ||||||
chr19:18517886
|
C | CA | 44 | a0001c0001t0011g0115a0001c0005t0007g0174a0001c0005t0007g0175others(41): Show | 44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.135+4034dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517886 | ||||||
chr19:18517886
|
CA | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0235a0001c0001t0002g0025others(2): Show | 5 | HG01169.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+4034delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517886 | ||||||
chr19:18518019
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+3902C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518019 | ||||||
chr19:18518079
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+3842C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518079 | ||||||
chr19:18518110
|
T | C | 3 | a0001c0005t0007g0174a0001c0005t0007g0175a0001c0005t0007g0176 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.135+3811A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518110 | ||||||
chr19:18518137
|
A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+3784T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518137 | ||||||
chr19:18518302
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+3619A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518302 | ||||||
chr19:18518323
|
G | A | 5 | a0002c0002t0001g0136a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+3598C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518323 | ||||||
chr19:18518425
|
G | A | 1 | a0001c0001t0002g0104 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.135+3496C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518425 | ||||||
chr19:18518465
|
G | A | 3 | a0002c0002t0001g0137a0002c0002t0001g0138a0002c0002t0001g0139 | 3 | HG02735.hp2 HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.135+3456C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518465 | ||||||
chr19:18518467
|
A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+3454T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518467 | ||||||
chr19:18518483
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+3438G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518483 | ||||||
chr19:18518489
|
C | CA | 50 | a0001c0001t0001g0144a0001c0001t0001g0234a0001c0001t0002g0105others(47): Show | 50 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.135+3431dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518489 | ||||||
chr19:18518489
|
CA | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 7 | HG01169.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+3431delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518489 | ||||||
chr19:18518603
|
C | T | 7 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(4): Show | 7 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+3318G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518603 | ||||||
chr19:18518716
|
G | A | 1 | a0001c0004t0006g0158 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.135+3205C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518716 | ||||||
chr19:18518787
|
T | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+3134A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518787 | ||||||
chr19:18519020
|
T | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+2901A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519020 | ||||||
chr19:18519093
|
T | G | 5 | a0001c0001t0004g0150a0001c0001t0004g0151a0001c0001t0004g0152others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+2828A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519093 | ||||||
chr19:18519100
|
C | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.135+2821G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519100 | ||||||
chr19:18519197
|
A | C | 1 | a0001c0001t0002g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.135+2724T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519197 | ||||||
chr19:18519229
|
C | A | 1 | a0001c0001t0002g0106 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.135+2692G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519229 | ||||||
chr19:18519449
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+2472C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519449 | ||||||
chr19:18519457
|
C | T | 2 | a0002c0002t0001g0240a0002c0002t0001g0241 | 2 | HG00323.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.135+2464G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519457 | ||||||
chr19:18519664
|
G | A | 1 | a0001c0001t0003g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.135+2257C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519664 | ||||||
chr19:18519755
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG01891.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.135+2166G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519755 | ||||||
chr19:18519770
|
T | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+2151A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519770 | ||||||
chr19:18519806
|
C | CA | 5 | a0001c0001t0002g0108a0002c0002t0001g0140a0002c0002t0001g0141others(2): Show | 5 | HG02257.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+2114dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519806 | ||||||
chr19:18519820
|
AAAAAG | A | 8 | a0001c0001t0001g0155a0001c0001t0001g0177a0001c0001t0001g0178others(5): Show | 8 | HG01975.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+2096_135+2100d others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519820 | ||||||
chr19:18519821
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.135+2100T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519821 | ||||||
chr19:18519821
|
AAAAG | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 89 | HG00280.hp2 HG00642.hp2 HG01069.hp1 others(86): Show |
intron_variant | MODIFIER | c.135+2096_135+2099d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519821 | ||||||
chr19:18519822
|
AAAG | A | 5 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(2): Show | 5 | HG00408.hp2 HG00735.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+2096_135+2098d others(5): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519822 | ||||||
chr19:18519892
|
A | T | 5 | a0001c0001t0004g0150a0001c0001t0004g0151a0001c0001t0004g0152others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+2029T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519892 | ||||||
chr19:18520446
|
G | C | 4 | a0001c0001t0001g0144a0001c0005t0007g0174a0001c0005t0007g0175others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+1475C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520446 | ||||||
chr19:18520522
|
C | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+1399G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520522 | ||||||
chr19:18520663
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+1258C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520663 | ||||||
chr19:18520821
|
G | A | 63 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(60): Show | 63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.135+1100C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520821 | ||||||
chr19:18520910
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.135+1011G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520910 | ||||||
chr19:18520984
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+937G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520984 | ||||||
chr19:18521007
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+914T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521007 | ||||||
chr19:18521035
|
C | G | 4 | a0002c0002t0001g0240a0002c0002t0001g0241a0002c0002t0001g0242others(1): Show | 4 | HG00323.hp2 HG03017.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+886G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521035 | ||||||
chr19:18521414
|
C | T | 5 | a0002c0002t0001g0012a0002c0002t0001g0013a0002c0002t0001g0014others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+507G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521414 | ||||||
chr19:18521415
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+506A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521415 | ||||||
chr19:18521650
|
G | A | 4 | a0002c0002t0001g0240a0002c0002t0001g0241a0002c0002t0001g0242others(1): Show | 4 | HG00323.hp2 HG03017.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+271C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521650 | ||||||
chr19:18521678
|
CGA | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(7): Show | 10 | HG01891.hp1 HG02280.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.135+241_135+242del others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521678 |