geneid | 1998 |
---|---|
ensemblid | ENSG00000109381.21 |
hgncid | 3317 |
symbol | ELF2 |
name | E74 like ETS transcription factor 2 |
refseq_nuc | NM_001331036.3 |
refseq_prot | NP_001317965.1 |
ensembl_nuc | ENST00000686138.1 |
ensembl_prot | ENSP00000510098.1 |
mane_status | MANE Select |
chr | chr4 |
start | 139057265 |
end | 139177218 |
strand | - |
ver | v1.2 |
region | chr4:139057265-139177218 |
region5000 | chr4:139052265-139182218 |
regionname0 | ELF2_chr4_139057265_139177218 |
regionname5000 | ELF2_chr4_139052265_139182218 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 593 | 322 | 75 | 57 | 143 | 12 | 33 | 106 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0002 | 0/0 | 593 | 18 | 9 | 0 | 9 | 0 | 0 | 6 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0003 | 0/0 | 593 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1782 | 322 | 75 | 57 | 143 | 12 | 33 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
c0002 | 0/0 | 1782 | 18 | 9 | 0 | 9 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
c0003 | 0/0 | 1782 | 2 | 0 | 1 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2220 | 203 | 46 | 42 | 86 | 7 | 22 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
t0002 | 1/1 | 2222 | 117 | 31 | 11 | 58 | 5 | 10 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
t0003 | 0/0 | 2224 | 10 | 7 | 2 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
t0004 | 0/0 | 2222 | 3 | 0 | 0 | 3 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
t0005 | 0/0 | 2222 | 2 | 0 | 2 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
t0006 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
t0007 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
t0008 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
t0009 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
t0010 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
t0011 | 0/0 | 2222 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
t0012 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1782 | 322 | 75 | 57 | 143 | 12 | 33 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0002c0002 | 0/0 | 1782 | 18 | 9 | 0 | 9 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0003c0003 | 0/0 | 1782 | 2 | 0 | 1 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4001 | 202 | 45 | 42 | 86 | 7 | 22 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0001c0001t0002 | 1/1 | 4003 | 105 | 25 | 11 | 52 | 5 | 10 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0001c0001t0003 | 0/0 | 4005 | 6 | 5 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0001c0001t0005 | 0/0 | 4003 | 2 | 0 | 2 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0001c0001t0006 | 0/0 | 4001 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0001c0001t0007 | 0/0 | 4001 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0001c0001t0008 | 0/0 | 4001 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0001c0001t0009 | 0/0 | 4001 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0001c0001t0010 | 0/0 | 4001 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0001c0001t0011 | 0/0 | 4003 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0001c0001t0012 | 0/0 | 4001 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0002c0002t0001 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0002c0002t0002 | 0/0 | 4003 | 12 | 6 | 0 | 6 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0002c0002t0003 | 0/0 | 4005 | 2 | 2 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0002c0002t0004 | 0/0 | 4003 | 3 | 0 | 0 | 3 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
a0003c0003t0003 | 0/0 | 4005 | 2 | 0 | 1 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | copy fasta | chr4 | 139052265 | 139182218 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0007g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0009g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0010g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0002c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0003c0003t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
a0003c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | GBR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0133 | EUR | GBR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | GBR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0159 | EUR | GBR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0129 | EUR | FIN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0107 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0108 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01496 | hp1 | a0003 | c0003 | t0003 | g0147 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0127 | AMR | CLM | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0170 | EUR | IBS | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG01993 | hp2 | a0001 | c0001 | t0010 | g0253 | AMR | PEL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0334 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02074 | hp2 | a0001 | c0001 | t0011 | g0190 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CDX | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CDX | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CDX | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0205 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02280 | hp1 | a0002 | c0002 | t0003 | g0114 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0342 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0113 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0112 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03041 | hp1 | a0002 | c0002 | t0003 | g0115 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0340 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03491 | hp2 | a0001 | c0001 | t0009 | g0030 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ESN | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03540 | hp2 | a0002 | c0002 | t0002 | g0111 | AFR | GWD | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | STU | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03704 | hp1 | a0003 | c0003 | t0003 | g0148 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | STU | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | STU | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | YRI | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | YRI | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | YRI | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18941 | hp2 | a0002 | c0002 | t0004 | g0120 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18942 | hp2 | a0002 | c0002 | t0004 | g0110 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18950 | hp1 | a0002 | c0002 | t0004 | g0123 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18962 | hp2 | a0001 | c0001 | t0008 | g0243 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | LWK | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19057 | hp1 | a0001 | c0001 | t0007 | g0283 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19060 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19068 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0198 | AFR | YRI | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ASW | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ASW | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0168 | EUR | TSI | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | GIH | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0336 | SAS | GIH | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0337 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0121 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | MSL | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | USA | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | USA | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | LWK | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0164 | REF | REF | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0263 | REF | REF | ELF2_chr4_139052265_139182218 | ELF2 | chr4 | 139052265 | 139182218 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139072021
|
G | A | 1 | a0003 | 2 | HG01496.hp1 HG03704.hp1 |
missense_variant | MODERATE | c.371C>T | p.Pro124Leu | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/10 | 874/4003 | 371/1782 | 124/593 | chr4 | 139072021 | ||
chr4:139137695
|
A | T | 1 | a0002 | 18 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(15): Show |
missense_variant | MODERATE | c.7T>A | p.Ser3Thr | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/10 | 510/4003 | 7/1782 | 3/593 | chr4 | 139137695 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139057317
|
A | G | 1 | a0001c0001t0005 | 2 | HG01070.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1666T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 10/10 | 1666 | chr4 | 139057317 | |||||
chr4:139057910
|
A | G | 1 | a0001c0001t0011 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1073T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 10/10 | 1073 | chr4 | 139057910 | |||||
chr4:139058407
|
G | GTA | 3 | a0001c0001t0003a0002c0002t0003a0003c0003t0003 | 10 | HG01496.hp1 HG01496.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*574_*575dupTA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 10/10 | 575 | chr4 | 139058407 | |||||
chr4:139058407
|
GTA | G | 8 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(5): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*574_*575delTA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 10/10 | 574 | chr4 | 139058407 | |||||
chr4:139058409
|
A | G | 1 | a0002c0002t0004 | 3 | NA18941.hp2 NA18942.hp2 NA18950.hp1 |
3_prime_UTR_variant | MODIFIER | c.*574T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 10/10 | 574 | chr4 | 139058409 | |||||
chr4:139058411
|
A | G | 1 | a0001c0001t0010 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*572T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 10/10 | 572 | chr4 | 139058411 | |||||
chr4:139058413
|
A | G | 1 | a0001c0001t0009 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*570T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 10/10 | 570 | chr4 | 139058413 | |||||
chr4:139058428
|
T | C | 1 | a0001c0001t0012 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*555A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 10/10 | 555 | chr4 | 139058428 | |||||
chr4:139058459
|
C | T | 1 | a0001c0001t0008 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*524G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 10/10 | 524 | chr4 | 139058459 | |||||
chr4:139058731
|
C | T | 1 | a0001c0001t0007 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*252G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 10/10 | 252 | chr4 | 139058731 | |||||
chr4:139177116
|
C | T | 1 | a0001c0001t0006 | 1 | NA19068.hp2 | 5_prime_UTR_variant | MODIFIER | c.-401G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/10 | 39415 | chr4 | 139177116 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139059873
|
G | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(55): Show | 58 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1158-266C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 9/9 | chr4 | 139059873 | ||||||
chr4:139059921
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1158-314G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 9/9 | chr4 | 139059921 | ||||||
chr4:139060699
|
G | C | 1 | a0001c0001t0001g0079 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.807-25C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 8/9 | chr4 | 139060699 | ||||||
chr4:139060737
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.807-63C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 8/9 | chr4 | 139060737 | ||||||
chr4:139060764
|
T | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.807-90A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 8/9 | chr4 | 139060764 | ||||||
chr4:139060824
|
A | G | 1 | a0001c0001t0002g0166 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.807-150T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 8/9 | chr4 | 139060824 | ||||||
chr4:139061177
|
A | AT | 10 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(7): Show | 10 | HG01074.hp1 HG01099.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.807-504dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 8/9 | chr4 | 139061177 | ||||||
chr4:139061177
|
AT | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0088others(19): Show | 22 | HG00423.hp1 HG00423.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.807-504delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 8/9 | chr4 | 139061177 | ||||||
chr4:139061177
|
ATT | A | 88 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0090others(85): Show | 88 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.807-505_807-504del others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 8/9 | chr4 | 139061177 | ||||||
chr4:139061197
|
G | T | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-523C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 8/9 | chr4 | 139061197 | ||||||
chr4:139061198
|
A | T | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.807-524T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 8/9 | chr4 | 139061198 | ||||||
chr4:139061332
|
A | G | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.806+533T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 8/9 | chr4 | 139061332 | ||||||
chr4:139062174
|
C | CT | 70 | a0001c0001t0001g0043a0001c0001t0002g0003a0001c0001t0002g0062others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.614-118dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139062174 | ||||||
chr4:139062193
|
C | T | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.614-136G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139062193 | ||||||
chr4:139062503
|
T | C | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.614-446A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139062503 | ||||||
chr4:139062505
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.614-448A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139062505 | ||||||
chr4:139062544
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.614-487A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139062544 | ||||||
chr4:139062804
|
C | G | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.614-747G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139062804 | ||||||
chr4:139062821
|
G | T | 1 | a0001c0001t0001g0331 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.614-764C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139062821 | ||||||
chr4:139062848
|
C | T | 11 | a0001c0001t0002g0199a0001c0001t0002g0211a0001c0001t0002g0212others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.614-791G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139062848 | ||||||
chr4:139062859
|
T | C | 13 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 13 | HG01243.hp1 HG01361.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.614-802A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139062859 | ||||||
chr4:139063033
|
A | G | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.614-976T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063033 | ||||||
chr4:139063056
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.614-999C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063056 | ||||||
chr4:139063100
|
A | G | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.614-1043T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063100 | ||||||
chr4:139063204
|
G | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.614-1147C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063204 | ||||||
chr4:139063259
|
G | C | 11 | a0001c0001t0002g0199a0001c0001t0002g0211a0001c0001t0002g0212others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.614-1202C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063259 | ||||||
chr4:139063292
|
C | G | 70 | a0001c0001t0002g0003a0001c0001t0002g0062a0001c0001t0002g0073others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.614-1235G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063292 | ||||||
chr4:139063345
|
T | C | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.614-1288A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063345 | ||||||
chr4:139063610
|
A | G | 68 | a0001c0001t0002g0003a0001c0001t0002g0062a0001c0001t0002g0073others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.614-1553T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063610 | ||||||
chr4:139063651
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0106 | 2 | NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.614-1594T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063651 | ||||||
chr4:139063823
|
T | C | 1 | a0001c0001t0001g0325 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.614-1766A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063823 | ||||||
chr4:139063851
|
C | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0058 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.614-1794G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063851 | ||||||
chr4:139063866
|
A | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0282 | 3 | HG01257.hp1 HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.614-1809T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063866 | ||||||
chr4:139063868
|
C | T | 56 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(53): Show | 56 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.614-1811G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063868 | ||||||
chr4:139063972
|
T | G | 1 | a0001c0001t0002g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.614-1915A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139063972 | ||||||
chr4:139064022
|
C | A | 1 | a0001c0001t0001g0293 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.614-1965G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139064022 | ||||||
chr4:139064136
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.614-2079G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139064136 | ||||||
chr4:139064421
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0217 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.614-2364G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139064421 | ||||||
chr4:139064480
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.614-2423C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139064480 | ||||||
chr4:139064486
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.614-2429A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139064486 | ||||||
chr4:139064868
|
G | A | 1 | a0001c0001t0006g0001 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.614-2811C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139064868 | ||||||
chr4:139065239
|
A | C | 2 | a0001c0001t0001g0288a0001c0001t0001g0293 | 2 | HG01255.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.613+2445T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139065239 | ||||||
chr4:139065295
|
T | C | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.613+2389A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139065295 | ||||||
chr4:139065719
|
T | C | 1 | a0001c0001t0001g0326 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.613+1965A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139065719 | ||||||
chr4:139065750
|
G | A | 3 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0197 | 3 | HG02970.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.613+1934C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139065750 | ||||||
chr4:139065767
|
C | G | 1 | a0001c0001t0001g0273 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.613+1917G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139065767 | ||||||
chr4:139065889
|
A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0020others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+1795T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139065889 | ||||||
chr4:139066009
|
C | CT | 20 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0195others(17): Show | 20 | HG00544.hp1 HG02056.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.613+1674dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066009 | ||||||
chr4:139066009
|
C | CTT | 164 | a0001c0001t0001g0031a0001c0001t0001g0077a0001c0001t0001g0086others(161): Show | 164 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.613+1673_613+1674d others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066009 | ||||||
chr4:139066009
|
C | CTTT | 31 | a0001c0001t0001g0034a0001c0001t0001g0222a0001c0001t0001g0225others(28): Show | 31 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.613+1672_613+1674d others(5): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066009 | ||||||
chr4:139066009
|
CTTTTTT | C | 88 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 88 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.613+1669_613+1674d others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066009 | ||||||
chr4:139066009
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.613+1665_613+1674d others(12): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066009 | ||||||
chr4:139066009
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0089a0001c0001t0002g0096a0002c0002t0002g0122 | 3 | HG00438.hp2 NA18979.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.613+1663_613+1674d others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066009 | ||||||
chr4:139066206
|
A | C | 24 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.613+1478T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066206 | ||||||
chr4:139066395
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.613+1289C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066395 | ||||||
chr4:139066499
|
G | T | 70 | a0001c0001t0002g0003a0001c0001t0002g0062a0001c0001t0002g0073others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.613+1185C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066499 | ||||||
chr4:139066641
|
C | A | 1 | a0001c0001t0001g0054 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.613+1043G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066641 | ||||||
chr4:139066659
|
G | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.613+1025C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066659 | ||||||
chr4:139066763
|
T | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0195a0001c0001t0001g0219others(1): Show | 4 | HG01243.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.613+921A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139066763 | ||||||
chr4:139067116
|
T | TA | 11 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0061others(8): Show | 11 | HG01175.hp1 HG01358.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+567dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139067116 | ||||||
chr4:139067247
|
C | T | 2 | a0002c0002t0002g0111a0002c0002t0002g0121 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.613+437G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 7/9 | chr4 | 139067247 | ||||||
chr4:139068115
|
G | A | 87 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(84): Show | 87 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.527-345C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068115 | ||||||
chr4:139068149
|
T | C | 97 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0232others(94): Show | 97 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.527-379A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068149 | ||||||
chr4:139068332
|
A | G | 3 | a0001c0001t0001g0126a0001c0001t0001g0219a0001c0001t0002g0230 | 3 | HG01243.hp1 HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.527-562T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068332 | ||||||
chr4:139068618
|
G | C | 1 | a0001c0001t0001g0331 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.527-848C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068618 | ||||||
chr4:139068721
|
T | C | 9 | a0002c0002t0002g0116a0002c0002t0002g0117a0002c0002t0002g0118others(6): Show | 9 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-951A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068721 | ||||||
chr4:139068725
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.527-955G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068725 | ||||||
chr4:139068748
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.527-978A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068748 | ||||||
chr4:139068830
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.527-1060C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068830 | ||||||
chr4:139068892
|
T | C | 2 | a0001c0001t0002g0169a0001c0001t0002g0335 | 2 | NA18992.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.527-1122A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068892 | ||||||
chr4:139068920
|
C | A | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.527-1150G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068920 | ||||||
chr4:139068923
|
G | A | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.527-1153C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068923 | ||||||
chr4:139068992
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0020others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.527-1222G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139068992 | ||||||
chr4:139069408
|
G | A | 1 | a0002c0002t0002g0117 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.527-1638C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069408 | ||||||
chr4:139069437
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.527-1667A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069437 | ||||||
chr4:139069556
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.527-1786C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069556 | ||||||
chr4:139069558
|
C | T | 1 | a0001c0001t0002g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.527-1788G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069558 | ||||||
chr4:139069616
|
C | CAAT | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-1847_527-1846i others(5): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069616 | ||||||
chr4:139069786
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.527-2016G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069786 | ||||||
chr4:139069848
|
A | AT | 104 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0088others(101): Show | 104 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.526+2017dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069848 | ||||||
chr4:139069865
|
G | C | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+2001C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069865 | ||||||
chr4:139069899
|
T | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.526+1967A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069899 | ||||||
chr4:139069910
|
G | A | 2 | a0002c0002t0002g0111a0002c0002t0002g0121 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.526+1956C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069910 | ||||||
chr4:139069966
|
G | A | 9 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0196others(6): Show | 9 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.526+1900C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069966 | ||||||
chr4:139069972
|
C | G | 4 | a0001c0001t0001g0242a0001c0001t0001g0251a0001c0001t0001g0324others(1): Show | 4 | HG01167.hp2 HG01243.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.526+1894G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139069972 | ||||||
chr4:139070201
|
T | C | 1 | a0001c0001t0003g0127 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.526+1665A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139070201 | ||||||
chr4:139070362
|
C | T | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.526+1504G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139070362 | ||||||
chr4:139070393
|
C | A | 2 | a0001c0001t0001g0104a0001c0001t0002g0102 | 2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.526+1473G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139070393 | ||||||
chr4:139070395
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.526+1471T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139070395 | ||||||
chr4:139070493
|
G | A | 2 | a0001c0001t0002g0206a0001c0001t0002g0207 | 2 | HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.526+1373C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139070493 | ||||||
chr4:139070663
|
C | A | 2 | a0001c0001t0001g0306a0001c0001t0002g0296 | 2 | HG02080.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.526+1203G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139070663 | ||||||
chr4:139071004
|
G | T | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+862C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139071004 | ||||||
chr4:139071035
|
A | T | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.526+831T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139071035 | ||||||
chr4:139071092
|
G | C | 23 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0087others(20): Show | 23 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.526+774C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139071092 | ||||||
chr4:139071145
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.526+721G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139071145 | ||||||
chr4:139071278
|
AT | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0234others(1): Show | 4 | HG00140.hp1 HG02738.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+587delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139071278 | ||||||
chr4:139071476
|
G | T | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.526+390C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139071476 | ||||||
chr4:139071573
|
T | C | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+293A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139071573 | ||||||
chr4:139071590
|
C | G | 1 | a0001c0001t0002g0141 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.526+276G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139071590 | ||||||
chr4:139071596
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.526+270T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139071596 | ||||||
chr4:139071696
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.526+170G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139071696 | ||||||
chr4:139071704
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526+162A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 6/9 | chr4 | 139071704 | ||||||
chr4:139072207
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.353-168G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 5/9 | chr4 | 139072207 | ||||||
chr4:139072310
|
C | G | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.353-271G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 5/9 | chr4 | 139072310 | ||||||
chr4:139072320
|
A | G | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.353-281T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 5/9 | chr4 | 139072320 | ||||||
chr4:139072436
|
C | T | 9 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0196others(6): Show | 9 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.353-397G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 5/9 | chr4 | 139072436 | ||||||
chr4:139072569
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.353-530G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 5/9 | chr4 | 139072569 | ||||||
chr4:139072822
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.352+632A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 5/9 | chr4 | 139072822 | ||||||
chr4:139072856
|
G | A | 322 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(319): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.352+598C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 5/9 | chr4 | 139072856 | ||||||
chr4:139073079
|
C | A | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+375G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 5/9 | chr4 | 139073079 | ||||||
chr4:139073125
|
C | CAACT | 3 | a0001c0001t0002g0199a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01256.hp1 HG01258.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.352+325_352+328dup others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 5/9 | chr4 | 139073125 | ||||||
chr4:139073416
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.352+38A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 5/9 | chr4 | 139073416 | ||||||
chr4:139073429
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.352+25T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 5/9 | chr4 | 139073429 | ||||||
chr4:139073709
|
T | C | 97 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0232others(94): Show | 97 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.239-142A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139073709 | ||||||
chr4:139073712
|
A | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0078 | 3 | HG02145.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.239-145T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139073712 | ||||||
chr4:139073848
|
T | A | 2 | a0001c0001t0001g0219a0001c0001t0002g0230 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.239-281A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139073848 | ||||||
chr4:139073943
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.239-376T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139073943 | ||||||
chr4:139074011
|
C | G | 107 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.239-444G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139074011 | ||||||
chr4:139074089
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.239-522G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139074089 | ||||||
chr4:139074493
|
G | A | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.239-926C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139074493 | ||||||
chr4:139074535
|
G | C | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.239-968C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139074535 | ||||||
chr4:139074683
|
C | G | 23 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0087others(20): Show | 23 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.239-1116G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139074683 | ||||||
chr4:139074759
|
C | CA | 72 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0077others(69): Show | 72 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.239-1193dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139074759 | ||||||
chr4:139074759
|
C | CAA | 25 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0087others(22): Show | 25 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(22): Show |
intron_variant | MODIFIER | c.239-1194_239-1193d others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139074759 | ||||||
chr4:139074772
|
C | A | 1 | a0001c0001t0002g0096 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.239-1205G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139074772 | ||||||
chr4:139075070
|
A | C | 25 | a0001c0001t0001g0241a0001c0001t0001g0250a0001c0001t0001g0267others(22): Show | 25 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.239-1503T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139075070 | ||||||
chr4:139075163
|
C | T | 2 | a0002c0002t0002g0198a0002c0002t0002g0205 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.239-1596G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139075163 | ||||||
chr4:139075192
|
T | C | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239-1625A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139075192 | ||||||
chr4:139075372
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239-1805G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139075372 | ||||||
chr4:139075417
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.239-1850G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139075417 | ||||||
chr4:139075465
|
C | G | 97 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0232others(94): Show | 97 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.239-1898G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139075465 | ||||||
chr4:139075509
|
A | G | 1 | a0001c0001t0001g0325 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.239-1942T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139075509 | ||||||
chr4:139075895
|
G | A | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.239-2328C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139075895 | ||||||
chr4:139075904
|
T | C | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.239-2337A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139075904 | ||||||
chr4:139076399
|
T | C | 1 | a0002c0002t0002g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.239-2832A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139076399 | ||||||
chr4:139076421
|
C | T | 8 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0254others(5): Show | 8 | HG00544.hp2 HG00558.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-2854G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139076421 | ||||||
chr4:139076434
|
C | T | 1 | a0001c0001t0002g0172 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.239-2867G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139076434 | ||||||
chr4:139076452
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.239-2885T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139076452 | ||||||
chr4:139076515
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.239-2948A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139076515 | ||||||
chr4:139076573
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.239-3006G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139076573 | ||||||
chr4:139077016
|
T | C | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.239-3449A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139077016 | ||||||
chr4:139077270
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.239-3703G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139077270 | ||||||
chr4:139077655
|
A | C | 336 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(333): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.239-4088T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139077655 | ||||||
chr4:139077749
|
T | C | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.239-4182A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139077749 | ||||||
chr4:139077764
|
A | C | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.239-4197T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139077764 | ||||||
chr4:139077859
|
G | GA | 319 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.239-4293dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139077859 | ||||||
chr4:139077968
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.239-4401A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139077968 | ||||||
chr4:139078126
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.239-4559G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139078126 | ||||||
chr4:139078327
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.239-4760T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139078327 | ||||||
chr4:139078348
|
TAGTACAA | T | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-4788_239-4782d others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139078348 | ||||||
chr4:139078574
|
C | CT | 10 | a0001c0001t0001g0233a0001c0001t0001g0267a0001c0001t0001g0295others(7): Show | 10 | HG00597.hp1 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-5008dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139078574 | ||||||
chr4:139078574
|
CT | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(30): Show | 33 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.239-5008delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139078574 | ||||||
chr4:139078919
|
C | T | 330 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.239-5352G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139078919 | ||||||
chr4:139079074
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.239-5507G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139079074 | ||||||
chr4:139079100
|
A | AT | 10 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0196others(7): Show | 10 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-5534dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139079100 | ||||||
chr4:139079117
|
C | T | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.239-5550G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139079117 | ||||||
chr4:139079131
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.239-5564A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139079131 | ||||||
chr4:139079444
|
G | C | 1 | a0001c0001t0002g0131 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.239-5877C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139079444 | ||||||
chr4:139079489
|
G | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239-5922C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139079489 | ||||||
chr4:139079515
|
C | T | 11 | a0001c0001t0002g0199a0001c0001t0002g0211a0001c0001t0002g0212others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.239-5948G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139079515 | ||||||
chr4:139079659
|
C | T | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.239-6092G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139079659 | ||||||
chr4:139080360
|
T | G | 1 | a0001c0001t0002g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.239-6793A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139080360 | ||||||
chr4:139080520
|
A | T | 97 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0232others(94): Show | 97 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.239-6953T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139080520 | ||||||
chr4:139080698
|
C | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0202a0001c0001t0001g0204 | 3 | HG02896.hp1 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.239-7131G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139080698 | ||||||
chr4:139080746
|
G | A | 2 | a0001c0001t0002g0143a0001c0001t0002g0175 | 2 | NA18962.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.239-7179C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139080746 | ||||||
chr4:139080803
|
A | G | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-7236T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139080803 | ||||||
chr4:139080943
|
G | GA | 42 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0066others(39): Show | 42 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.239-7377dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139080943 | ||||||
chr4:139080943
|
G | GAA | 11 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0196others(8): Show | 11 | HG00438.hp1 HG01361.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.239-7378_239-7377d others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139080943 | ||||||
chr4:139081143
|
C | G | 1 | a0001c0001t0001g0018 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.239-7576G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081143 | ||||||
chr4:139081242
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0002g0226 | 2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.239-7675G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081242 | ||||||
chr4:139081306
|
C | T | 7 | a0001c0001t0002g0135a0001c0001t0002g0181a0001c0001t0002g0182others(4): Show | 7 | NA18946.hp2 NA18963.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-7739G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081306 | ||||||
chr4:139081471
|
T | C | 2 | a0001c0001t0002g0314a0001c0001t0002g0316 | 2 | NA18963.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.239-7904A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081471 | ||||||
chr4:139081560
|
G | T | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-7993C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081560 | ||||||
chr4:139081628
|
GATAAAAA others(8): Show |
G | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239-8076_239-8062d others(17): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081628 | ||||||
chr4:139081679
|
C | T | 4 | a0001c0001t0002g0007a0001c0001t0002g0193a0001c0001t0002g0194others(1): Show | 4 | HG01106.hp1 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-8112G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081679 | ||||||
chr4:139081737
|
T | C | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-8170A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081737 | ||||||
chr4:139081906
|
T | A | 107 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.239-8339A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081906 | ||||||
chr4:139081910
|
GAACATTA others(2): Show |
G | 107 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.239-8352_239-8344d others(11): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081910 | ||||||
chr4:139081984
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.239-8417T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081984 | ||||||
chr4:139081994
|
A | G | 1 | a0001c0001t0002g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.239-8427T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139081994 | ||||||
chr4:139082045
|
C | G | 68 | a0001c0001t0002g0003a0001c0001t0002g0062a0001c0001t0002g0073others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.239-8478G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139082045 | ||||||
chr4:139082066
|
G | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.239-8499C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139082066 | ||||||
chr4:139082884
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.239-9317C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139082884 | ||||||
chr4:139082920
|
C | G | 1 | a0002c0002t0004g0120 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.239-9353G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139082920 | ||||||
chr4:139082960
|
G | A | 3 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0002g0296 | 3 | HG02080.hp1 NA18977.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.239-9393C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139082960 | ||||||
chr4:139082961
|
C | A | 3 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0002g0296 | 3 | HG02080.hp1 NA18977.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.239-9394G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139082961 | ||||||
chr4:139083072
|
G | A | 3 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0002g0296 | 3 | HG02080.hp1 NA18977.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.239-9505C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139083072 | ||||||
chr4:139083181
|
TG | T | 94 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.239-9615delC | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139083181 | ||||||
chr4:139083187
|
G | C | 1 | a0001c0001t0001g0004 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.239-9620C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139083187 | ||||||
chr4:139083545
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.239-9978C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139083545 | ||||||
chr4:139083587
|
C | G | 1 | a0001c0001t0001g0273 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.239-10020G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139083587 | ||||||
chr4:139083610
|
CG | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0095 | 3 | NA18964.hp1 NA18983.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.239-10044delC | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139083610 | ||||||
chr4:139083681
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.239-10114C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139083681 | ||||||
chr4:139083816
|
G | A | 1 | a0001c0001t0002g0135 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.239-10249C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139083816 | ||||||
chr4:139083900
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.239-10333G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139083900 | ||||||
chr4:139083918
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.239-10351C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139083918 | ||||||
chr4:139084014
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.239-10447A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139084014 | ||||||
chr4:139084036
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.239-10469G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139084036 | ||||||
chr4:139084301
|
ACACT | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0040 | 3 | HG00280.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.239-10738_239-1073 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139084301 | ||||||
chr4:139084424
|
G | A | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0257 | 3 | HG00733.hp1 HG01175.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.239-10857C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139084424 | ||||||
chr4:139084438
|
G | GGGC | 23 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0242others(20): Show | 23 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.239-10874_239-1087 others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139084438 | ||||||
chr4:139084438
|
G | GGGCGGC | 67 | a0001c0001t0002g0003a0001c0001t0002g0062a0001c0001t0002g0073others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.239-10877_239-1087 others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139084438 | ||||||
chr4:139084457
|
G | GGCGGCT | 4 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0104others(1): Show | 4 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-10896_239-1089 others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139084457 | ||||||
chr4:139084460
|
G | GGCT | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0002g0070 | 3 | HG02486.hp2 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.239-10896_239-1089 others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139084460 | ||||||
chr4:139084753
|
G | A | 17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.239-11186C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139084753 | ||||||
chr4:139085188
|
A | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(2): Show | 5 | HG00280.hp2 HG00733.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-11621T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139085188 | ||||||
chr4:139085495
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.239-11928G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139085495 | ||||||
chr4:139085526
|
G | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(84): Show | 87 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.239-11959C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139085526 | ||||||
chr4:139085610
|
T | C | 1 | a0001c0001t0002g0336 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.239-12043A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139085610 | ||||||
chr4:139085617
|
C | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0055 | 2 | NA18970.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.239-12050G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139085617 | ||||||
chr4:139085723
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0002g0070 | 3 | HG02486.hp2 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.239-12156C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139085723 | ||||||
chr4:139085724
|
C | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0002g0070 | 3 | HG02486.hp2 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.239-12157G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139085724 | ||||||
chr4:139085739
|
G | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0002g0070 | 3 | HG02486.hp2 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.239-12172C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139085739 | ||||||
chr4:139085970
|
G | A | 3 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210 | 3 | HG02258.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.239-12403C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139085970 | ||||||
chr4:139086041
|
T | C | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-12474A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139086041 | ||||||
chr4:139086200
|
G | A | 1 | a0001c0001t0003g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.239-12633C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139086200 | ||||||
chr4:139086224
|
C | CTT | 322 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(319): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.239-12658_239-1265 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139086224 | ||||||
chr4:139086347
|
C | T | 1 | a0001c0001t0002g0297 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.239-12780G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139086347 | ||||||
chr4:139086579
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.239-13012G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139086579 | ||||||
chr4:139086616
|
C | T | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.239-13049G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139086616 | ||||||
chr4:139086787
|
T | TATACAGT others(22): Show |
1 | a0001c0001t0001g0326 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.239-13249_239-1322 others(33): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139086787 | ||||||
chr4:139087330
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.239-13763C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139087330 | ||||||
chr4:139087807
|
T | A | 1 | a0001c0001t0001g0071 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.239-14240A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139087807 | ||||||
chr4:139087861
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.239-14294G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139087861 | ||||||
chr4:139087937
|
G | C | 1 | a0002c0002t0002g0113 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.239-14370C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139087937 | ||||||
chr4:139087946
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.239-14379C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139087946 | ||||||
chr4:139088091
|
A | G | 23 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0087others(20): Show | 23 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.239-14524T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088091 | ||||||
chr4:139088172
|
AG | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0195a0001c0001t0001g0219others(1): Show | 4 | HG01243.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-14606delC | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088172 | ||||||
chr4:139088277
|
C | G | 107 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.239-14710G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088277 | ||||||
chr4:139088280
|
T | A | 24 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.239-14713A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088280 | ||||||
chr4:139088284
|
TA | T | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.239-14718delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088284 | ||||||
chr4:139088284
|
TAA | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0061others(10): Show | 13 | HG00323.hp1 HG00639.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-14719_239-1471 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088284 | ||||||
chr4:139088380
|
C | A | 1 | a0001c0001t0001g0339 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.239-14813G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088380 | ||||||
chr4:139088398
|
C | A | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.239-14831G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088398 | ||||||
chr4:139088611
|
A | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0285 | 2 | HG00408.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.239-15044T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088611 | ||||||
chr4:139088717
|
C | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0080 | 2 | NA18953.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.239-15150G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088717 | ||||||
chr4:139088720
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0238 | 2 | HG03688.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.239-15153A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088720 | ||||||
chr4:139088726
|
G | A | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-15159C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088726 | ||||||
chr4:139088817
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.239-15250C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088817 | ||||||
chr4:139088818
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.239-15251C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088818 | ||||||
chr4:139088967
|
A | G | 1 | a0001c0001t0001g0327 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.239-15400T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139088967 | ||||||
chr4:139089044
|
G | A | 2 | a0001c0001t0002g0145a0001c0001t0002g0161 | 2 | HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.239-15477C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139089044 | ||||||
chr4:139089107
|
T | C | 1 | a0001c0001t0002g0149 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.239-15540A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139089107 | ||||||
chr4:139089124
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.239-15557T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139089124 | ||||||
chr4:139089558
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.239-15991C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139089558 | ||||||
chr4:139089564
|
C | G | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.239-15997G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139089564 | ||||||
chr4:139089794
|
T | C | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-16227A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139089794 | ||||||
chr4:139089875
|
T | A | 1 | a0001c0001t0002g0171 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.239-16308A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139089875 | ||||||
chr4:139090141
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.239-16574C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090141 | ||||||
chr4:139090224
|
G | C | 2 | a0002c0002t0002g0112a0002c0002t0002g0113 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.239-16657C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090224 | ||||||
chr4:139090284
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.239-16717C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090284 | ||||||
chr4:139090291
|
C | T | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.239-16724G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090291 | ||||||
chr4:139090299
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.239-16732G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090299 | ||||||
chr4:139090347
|
A | C | 5 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0003g0208others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-16780T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090347 | ||||||
chr4:139090470
|
A | T | 1 | a0001c0001t0002g0096 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.239-16903T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090470 | ||||||
chr4:139090483
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(15): Show | 18 | HG00280.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.239-16916G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090483 | ||||||
chr4:139090646
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.239-17079C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090646 | ||||||
chr4:139090913
|
G | T | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.239-17346C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090913 | ||||||
chr4:139090913
|
GTTTGT | G | 313 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.239-17351_239-1734 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090913 | ||||||
chr4:139090913
|
GTTTGTTT others(3): Show |
G | 3 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0002g0102 | 3 | HG02615.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.239-17356_239-1734 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139090913 | ||||||
chr4:139091037
|
C | T | 2 | a0002c0002t0002g0112a0002c0002t0002g0113 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.239-17470G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091037 | ||||||
chr4:139091220
|
T | G | 322 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(319): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.239-17653A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091220 | ||||||
chr4:139091541
|
C | T | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-17974G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091541 | ||||||
chr4:139091542
|
G | A | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-17975C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091542 | ||||||
chr4:139091591
|
C | T | 5 | a0001c0001t0002g0199a0001c0001t0002g0215a0001c0001t0002g0216others(2): Show | 5 | HG01256.hp1 HG01258.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-18024G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091591 | ||||||
chr4:139091643
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.239-18076G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091643 | ||||||
chr4:139091700
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0240 | 2 | HG02559.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.239-18133C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091700 | ||||||
chr4:139091713
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0095 | 3 | NA18964.hp1 NA18983.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.239-18146G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091713 | ||||||
chr4:139091859
|
C | T | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-18292G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091859 | ||||||
chr4:139091870
|
G | T | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239-18303C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091870 | ||||||
chr4:139091907
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.239-18340A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091907 | ||||||
chr4:139091919
|
A | G | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-18352T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091919 | ||||||
chr4:139091975
|
C | T | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-18408G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139091975 | ||||||
chr4:139092062
|
T | A | 24 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.239-18495A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092062 | ||||||
chr4:139092166
|
A | G | 1 | a0001c0001t0001g0333 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239-18599T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092166 | ||||||
chr4:139092366
|
T | TCATAACA others(3): Show |
1 | a0002c0002t0004g0123 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.239-18800_239-1879 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092366 | ||||||
chr4:139092366
|
TCATAACG others(3): Show |
T | 1 | a0001c0001t0001g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.239-18809_239-1880 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092366 | ||||||
chr4:139092366
|
TCATAACG others(47): Show |
T | 2 | a0001c0001t0002g0062a0001c0001t0002g0336 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.239-18853_239-1880 others(58): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092366 | ||||||
chr4:139092366
|
TCATAACG others(57): Show |
T | 1 | a0001c0001t0001g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.239-18863_239-1880 others(68): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092366 | ||||||
chr4:139092368
|
ATAACG | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0072others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-18806_239-1880 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092368 | ||||||
chr4:139092373
|
G | A | 333 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.239-18806C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092373 | ||||||
chr4:139092384
|
T | TAACATAA others(17): Show |
1 | a0001c0001t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.239-18841_239-1881 others(28): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092384 | ||||||
chr4:139092389
|
T | TAACATAA others(12): Show |
1 | a0001c0001t0002g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.239-18841_239-1882 others(23): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092389 | ||||||
chr4:139092394
|
T | TAACATAA others(7): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0227a0001c0001t0005g0107others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-18841_239-1882 others(18): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092394 | ||||||
chr4:139092395
|
AACATAAC others(12): Show |
A | 1 | a0001c0001t0001g0043 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.239-18847_239-1882 others(23): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092395 | ||||||
chr4:139092399
|
T | TAACATAA others(2): Show |
10 | a0001c0001t0001g0026a0001c0001t0001g0223a0001c0001t0001g0224others(7): Show | 10 | HG01255.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-18841_239-1883 others(13): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092399 | ||||||
chr4:139092404
|
T | TAACA | 5 | a0001c0001t0001g0069a0001c0001t0001g0079a0001c0001t0001g0222others(2): Show | 5 | HG02630.hp1 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-18841_239-1883 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092404 | ||||||
chr4:139092408
|
AT | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0040others(1): Show | 4 | HG00280.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-18842delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092408 | ||||||
chr4:139092409
|
TAACATAC others(8): Show |
T | 1 | a0002c0002t0002g0117 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.239-18857_239-1884 others(19): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092409 | ||||||
chr4:139092413
|
A | AAACAT | 15 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0020others(12): Show | 15 | HG00423.hp1 HG00673.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.239-18847_239-1884 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092413 | ||||||
chr4:139092413
|
A | AAACATAA others(3): Show |
21 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0087others(18): Show | 21 | HG01168.hp2 HG01169.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.239-18847_239-1884 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092413 | ||||||
chr4:139092413
|
A | AAACATAA others(8): Show |
18 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(15): Show | 18 | HG00140.hp2 HG00639.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.239-18847_239-1884 others(19): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092413 | ||||||
chr4:139092413
|
A | AAACATAA others(13): Show |
2 | a0001c0001t0001g0100a0001c0001t0002g0211 | 2 | HG03195.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.239-18847_239-1884 others(24): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092413 | ||||||
chr4:139092413
|
A | AAACATAA others(18): Show |
1 | a0001c0001t0002g0186 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.239-18847_239-1884 others(29): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092413 | ||||||
chr4:139092413
|
A | AAACATAA others(28): Show |
1 | a0001c0001t0009g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.239-18847_239-1884 others(39): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092413 | ||||||
chr4:139092413
|
ATACAT | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0074others(3): Show | 6 | HG01071.hp2 HG02004.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-18851_239-1884 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092413 | ||||||
chr4:139092414
|
T | A | 78 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(75): Show | 78 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.239-18847A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TA | 33 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0026others(30): Show | 33 | HG00280.hp1 HG00558.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.239-18848dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACAA | 30 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0049others(27): Show | 30 | HG00140.hp1 HG00597.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.239-18848_239-1884 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACAAAC others(3): Show |
41 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0027others(38): Show | 41 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.239-18848_239-1884 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACAAAC others(8): Show |
32 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0035others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(29): Show |
intron_variant | MODIFIER | c.239-18848_239-1884 others(19): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACAAAC others(13): Show |
26 | a0001c0001t0001g0065a0001c0001t0001g0200a0001c0001t0001g0204others(23): Show | 26 | HG00639.hp1 HG01070.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.239-18848_239-1884 others(24): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACAAAC others(18): Show |
13 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0092others(10): Show | 13 | HG00544.hp2 HG00741.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-18848_239-1884 others(29): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACAAAC others(23): Show |
2 | a0001c0001t0002g0173a0001c0001t0007g0283 | 2 | NA19057.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.239-18848_239-1884 others(34): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(3): Show |
13 | a0001c0001t0001g0018a0001c0001t0001g0076a0001c0001t0001g0086others(10): Show | 13 | HG00733.hp1 HG01993.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.239-18848_239-1884 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(8): Show |
9 | a0001c0001t0001g0058a0001c0001t0001g0077a0001c0001t0001g0270others(6): Show | 9 | HG00621.hp1 HG01074.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.239-18848_239-1884 others(19): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(13): Show |
13 | a0001c0001t0001g0080a0001c0001t0001g0286a0001c0001t0001g0333others(10): Show | 13 | HG00558.hp1 HG01993.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-18848_239-1884 others(24): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(18): Show |
4 | a0001c0001t0002g0164a0001c0001t0002g0169a0001c0001t0002g0300others(1): Show | 4 | HG00597.hp1 NA18992.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-18848_239-1884 others(29): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(23): Show |
1 | a0001c0001t0001g0284 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.239-18848_239-1884 others(34): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(13): Show |
1 | a0001c0001t0001g0288 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.239-18848_239-1884 others(24): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(23): Show |
4 | a0001c0001t0001g0101a0001c0001t0002g0188a0001c0001t0002g0189others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-18848_239-1884 others(34): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(23): Show |
1 | a0001c0001t0012g0002 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.239-18848_239-1884 others(34): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(44): Show |
1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239-18848_239-1884 others(55): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(89): Show |
1 | a0001c0001t0001g0006 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.239-18848_239-1884 others(100): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(154): Show |
1 | a0001c0001t0001g0279 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.239-18848_239-1884 others(165): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TAACATAA others(164): Show |
1 | a0001c0001t0001g0041 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.239-18848_239-1884 others(175): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
T | TACATAAC others(3): Show |
1 | a0001c0001t0002g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.239-18857_239-1884 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
TACATA | T | 4 | a0001c0001t0002g0197a0001c0001t0002g0340a0002c0002t0002g0111others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-18852_239-1884 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092414
|
TACATAAC others(3): Show |
T | 4 | a0001c0001t0003g0127a0002c0002t0002g0116a0002c0002t0002g0119others(1): Show | 4 | HG01496.hp2 HG02040.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-18857_239-1884 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092414 | ||||||
chr4:139092416
|
C | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0240others(2): Show | 5 | HG00323.hp2 HG03471.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-18849G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092416 | ||||||
chr4:139092417
|
A | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0240others(2): Show | 5 | HG00323.hp2 HG03471.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-18850T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092417 | ||||||
chr4:139092418
|
T | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0240others(2): Show | 5 | HG00323.hp2 HG03471.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-18851A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092418 | ||||||
chr4:139092418
|
T | TAACA | 3 | a0001c0001t0001g0009a0001c0001t0001g0311a0001c0001t0001g0330 | 3 | HG00558.hp2 HG00673.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.239-18855_239-1885 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092418 | ||||||
chr4:139092445
|
A | C | 1 | a0001c0001t0001g0043 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.239-18878T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092445 | ||||||
chr4:139092472
|
A | AT | 4 | a0001c0001t0002g0073a0001c0001t0002g0228a0001c0001t0003g0229others(1): Show | 4 | HG03516.hp1 HG03704.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-18906dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092472 | ||||||
chr4:139092486
|
G | T | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-18919C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092486 | ||||||
chr4:139092509
|
C | G | 321 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.239-18942G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092509 | ||||||
chr4:139092528
|
C | A | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.239-18961G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092528 | ||||||
chr4:139092604
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.239-19037A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092604 | ||||||
chr4:139092733
|
G | A | 4 | a0002c0002t0002g0116a0002c0002t0002g0117a0002c0002t0002g0119others(1): Show | 4 | HG02040.hp1 HG02056.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-19166C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092733 | ||||||
chr4:139092758
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.239-19191C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092758 | ||||||
chr4:139092778
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.239-19211C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092778 | ||||||
chr4:139092833
|
A | T | 1 | a0001c0001t0001g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.239-19266T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092833 | ||||||
chr4:139092907
|
T | C | 1 | a0001c0001t0001g0325 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.239-19340A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092907 | ||||||
chr4:139092965
|
A | AT | 20 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0235others(17): Show | 20 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.239-19399dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092965 | ||||||
chr4:139092965
|
A | T | 4 | a0001c0001t0001g0284a0001c0001t0001g0286a0001c0001t0002g0109others(1): Show | 4 | HG00408.hp2 HG00558.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-19398T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092965 | ||||||
chr4:139092965
|
AT | A | 16 | a0001c0001t0001g0014a0001c0001t0001g0046a0001c0001t0001g0203others(13): Show | 16 | HG01070.hp1 HG01993.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-19399delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139092965 | ||||||
chr4:139093068
|
C | T | 70 | a0001c0001t0002g0003a0001c0001t0002g0062a0001c0001t0002g0073others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.239-19501G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093068 | ||||||
chr4:139093207
|
C | T | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.239-19640G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093207 | ||||||
chr4:139093214
|
C | T | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.239-19647G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093214 | ||||||
chr4:139093327
|
A | C | 1 | a0002c0002t0002g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.239-19760T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093327 | ||||||
chr4:139093477
|
C | T | 112 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.239-19910G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093477 | ||||||
chr4:139093628
|
C | T | 120 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0077others(117): Show | 120 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.239-20061G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093628 | ||||||
chr4:139093708
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239-20141A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093708 | ||||||
chr4:139093806
|
A | C | 5 | a0001c0001t0001g0196a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01361.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-20239T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093806 | ||||||
chr4:139093896
|
CT | C | 279 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.239-20330delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093896 | ||||||
chr4:139093896
|
CTT | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0137others(7): Show | 10 | HG02109.hp1 HG02698.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-20331_239-2033 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093896 | ||||||
chr4:139093896
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0059a0001c0001t0001g0217 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.239-20339_239-2033 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093896 | ||||||
chr4:139093998
|
G | A | 4 | a0001c0001t0001g0250a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG01257.hp1 HG01943.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-20431C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139093998 | ||||||
chr4:139094130
|
C | T | 5 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0003g0208others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-20563G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139094130 | ||||||
chr4:139094216
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.239-20649G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139094216 | ||||||
chr4:139094364
|
G | A | 330 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.239-20797C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139094364 | ||||||
chr4:139094396
|
T | C | 8 | a0001c0001t0001g0301a0001c0001t0001g0317a0001c0001t0001g0318others(5): Show | 8 | HG00423.hp2 HG00738.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-20829A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139094396 | ||||||
chr4:139094432
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.239-20865C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139094432 | ||||||
chr4:139094449
|
C | A | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.239-20882G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139094449 | ||||||
chr4:139094721
|
AAAGAT | A | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.239-21159_239-2115 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139094721 | ||||||
chr4:139094805
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.239-21238A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139094805 | ||||||
chr4:139094950
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.239-21383G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139094950 | ||||||
chr4:139094980
|
T | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0292 | 2 | HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.239-21413A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139094980 | ||||||
chr4:139095011
|
T | G | 3 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0340 | 3 | HG03130.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.239-21444A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139095011 | ||||||
chr4:139095050
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.239-21483A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139095050 | ||||||
chr4:139095185
|
A | AT | 62 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(59): Show | 62 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.239-21619dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139095185 | ||||||
chr4:139095185
|
AT | A | 25 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(22): Show | 25 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.239-21619delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139095185 | ||||||
chr4:139095367
|
T | A | 17 | a0001c0001t0001g0241a0001c0001t0001g0250a0001c0001t0001g0268others(14): Show | 17 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.239-21800A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139095367 | ||||||
chr4:139095728
|
G | A | 5 | a0001c0001t0002g0133a0001c0001t0002g0159a0001c0001t0002g0163others(2): Show | 5 | HG00099.hp2 HG00140.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-22161C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139095728 | ||||||
chr4:139095916
|
C | T | 68 | a0001c0001t0002g0003a0001c0001t0002g0062a0001c0001t0002g0073others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.239-22349G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139095916 | ||||||
chr4:139096023
|
A | C | 2 | a0001c0001t0002g0145a0001c0001t0002g0161 | 2 | HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.239-22456T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139096023 | ||||||
chr4:139096114
|
T | C | 1 | a0001c0001t0002g0183 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.239-22547A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139096114 | ||||||
chr4:139096183
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.239-22616T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139096183 | ||||||
chr4:139096229
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0265 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.239-22662C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139096229 | ||||||
chr4:139096250
|
T | G | 5 | a0001c0001t0001g0126a0001c0001t0001g0195a0001c0001t0001g0219others(2): Show | 5 | HG01243.hp1 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-22683A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139096250 | ||||||
chr4:139096474
|
T | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.239-22907A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139096474 | ||||||
chr4:139096531
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0332 | 3 | HG00423.hp1 HG02155.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.239-22964C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139096531 | ||||||
chr4:139096625
|
C | CT | 47 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(44): Show | 47 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.239-23059dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139096625 | ||||||
chr4:139096625
|
CT | C | 9 | a0001c0001t0001g0027a0001c0001t0001g0057a0001c0001t0001g0087others(6): Show | 9 | HG01168.hp1 HG01515.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.239-23059delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139096625 | ||||||
chr4:139096778
|
A | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.239-23211T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139096778 | ||||||
chr4:139097061
|
T | C | 108 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.239-23494A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139097061 | ||||||
chr4:139097120
|
A | C | 6 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-23553T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139097120 | ||||||
chr4:139097192
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0332 | 3 | HG00423.hp1 HG02155.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.239-23625C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139097192 | ||||||
chr4:139097292
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.239-23725A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139097292 | ||||||
chr4:139097476
|
G | T | 1 | a0001c0001t0002g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.239-23909C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139097476 | ||||||
chr4:139097479
|
T | G | 1 | a0001c0001t0001g0309 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.239-23912A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139097479 | ||||||
chr4:139097606
|
G | C | 2 | a0001c0001t0001g0249a0001c0001t0001g0310 | 2 | NA19063.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.239-24039C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139097606 | ||||||
chr4:139097616
|
C | CA | 9 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0035others(6): Show | 9 | HG01081.hp1 HG01256.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-24050dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139097616 | ||||||
chr4:139097796
|
T | C | 5 | a0001c0001t0001g0126a0001c0001t0001g0195a0001c0001t0001g0219others(2): Show | 5 | HG01243.hp1 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-24229A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139097796 | ||||||
chr4:139098068
|
A | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.239-24501T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139098068 | ||||||
chr4:139098445
|
A | T | 1 | a0001c0001t0002g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.239-24878T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139098445 | ||||||
chr4:139098469
|
C | CT | 7 | a0001c0001t0001g0094a0001c0001t0001g0233a0001c0001t0001g0323others(4): Show | 7 | HG01099.hp2 HG02080.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-24903dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139098469 | ||||||
chr4:139098469
|
CT | C | 8 | a0001c0001t0002g0098a0001c0001t0002g0165a0001c0001t0002g0183others(5): Show | 8 | HG01993.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-24903delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139098469 | ||||||
chr4:139098616
|
C | A | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.239-25049G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139098616 | ||||||
chr4:139098736
|
G | A | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.239-25169C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139098736 | ||||||
chr4:139098801
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.239-25234A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139098801 | ||||||
chr4:139098803
|
T | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-25236A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139098803 | ||||||
chr4:139098813
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.239-25246C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139098813 | ||||||
chr4:139098904
|
C | A | 70 | a0001c0001t0002g0003a0001c0001t0002g0062a0001c0001t0002g0073others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.239-25337G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139098904 | ||||||
chr4:139099027
|
T | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239-25460A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139099027 | ||||||
chr4:139099054
|
T | C | 97 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0232others(94): Show | 97 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.239-25487A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139099054 | ||||||
chr4:139099080
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0058 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.239-25513G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139099080 | ||||||
chr4:139099284
|
C | T | 6 | a0001c0001t0002g0158a0001c0001t0002g0166a0001c0001t0002g0168others(3): Show | 6 | HG00738.hp2 HG01070.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-25717G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139099284 | ||||||
chr4:139099366
|
G | C | 1 | a0001c0001t0001g0103 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.238+25798C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139099366 | ||||||
chr4:139099444
|
G | A | 11 | a0001c0001t0002g0133a0001c0001t0002g0158a0001c0001t0002g0159others(8): Show | 11 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.238+25720C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139099444 | ||||||
chr4:139099787
|
G | C | 1 | a0001c0001t0001g0303 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.238+25377C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139099787 | ||||||
chr4:139100274
|
C | CT | 109 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.238+24889dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139100274 | ||||||
chr4:139100393
|
C | T | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+24771G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139100393 | ||||||
chr4:139100400
|
G | A | 69 | a0001c0001t0002g0003a0001c0001t0002g0062a0001c0001t0002g0073others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.238+24764C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139100400 | ||||||
chr4:139100436
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.238+24728A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139100436 | ||||||
chr4:139100438
|
G | A | 21 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(18): Show | 21 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.238+24726C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139100438 | ||||||
chr4:139100534
|
G | A | 1 | a0001c0001t0002g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.238+24630C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139100534 | ||||||
chr4:139100614
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.238+24550T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139100614 | ||||||
chr4:139100796
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.238+24368A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139100796 | ||||||
chr4:139100866
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0002g0197 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.238+24298A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139100866 | ||||||
chr4:139101095
|
A | C | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.238+24069T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139101095 | ||||||
chr4:139101433
|
C | A | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+23731G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139101433 | ||||||
chr4:139101733
|
G | A | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+23431C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139101733 | ||||||
chr4:139101743
|
T | C | 5 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0003g0208others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+23421A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139101743 | ||||||
chr4:139101931
|
A | C | 2 | a0003c0003t0003g0147a0003c0003t0003g0148 | 2 | HG01496.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.238+23233T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139101931 | ||||||
chr4:139101975
|
G | A | 6 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(3): Show | 6 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+23189C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139101975 | ||||||
chr4:139102249
|
G | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+22915C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102249 | ||||||
chr4:139102262
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.238+22902G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102262 | ||||||
chr4:139102358
|
G | GA | 36 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(33): Show | 36 | HG00423.hp1 HG00673.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.238+22805dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102358 | ||||||
chr4:139102358
|
GA | G | 103 | a0001c0001t0001g0081a0001c0001t0001g0086a0001c0001t0001g0195others(100): Show | 103 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.238+22805delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102358 | ||||||
chr4:139102400
|
G | A | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.238+22764C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102400 | ||||||
chr4:139102405
|
T | G | 206 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.238+22759A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102405 | ||||||
chr4:139102488
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0219 | 2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.238+22676C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102488 | ||||||
chr4:139102541
|
A | G | 1 | a0001c0001t0002g0193 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.238+22623T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102541 | ||||||
chr4:139102640
|
A | C | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.238+22524T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102640 | ||||||
chr4:139102684
|
T | TA | 96 | a0001c0001t0001g0086a0001c0001t0001g0232a0001c0001t0001g0239others(93): Show | 96 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.238+22479dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102684 | ||||||
chr4:139102871
|
G | T | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22293C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102871 | ||||||
chr4:139102873
|
T | G | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22291A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102873 | ||||||
chr4:139102874
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22290G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102874 | ||||||
chr4:139102875
|
G | T | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22289C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102875 | ||||||
chr4:139102876
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22288C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102876 | ||||||
chr4:139102877
|
A | G | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22287T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102877 | ||||||
chr4:139102878
|
G | C | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22286C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102878 | ||||||
chr4:139102880
|
C | A | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22284G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102880 | ||||||
chr4:139102882
|
T | A | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22282A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102882 | ||||||
chr4:139102884
|
A | G | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22280T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102884 | ||||||
chr4:139102887
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22277C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102887 | ||||||
chr4:139102887
|
GT | G | 6 | a0001c0001t0002g0230a0001c0001t0003g0130a0002c0002t0002g0112others(3): Show | 6 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+22276delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102887 | ||||||
chr4:139102888
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22276A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102888 | ||||||
chr4:139102891
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22273A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102891 | ||||||
chr4:139102898
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.238+22266A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102898 | ||||||
chr4:139102899
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22265G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102899 | ||||||
chr4:139102904
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22260G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102904 | ||||||
chr4:139102905
|
T | G | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+22259A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139102905 | ||||||
chr4:139103357
|
G | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+21807C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139103357 | ||||||
chr4:139103500
|
C | G | 327 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(324): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.238+21664G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139103500 | ||||||
chr4:139103718
|
T | C | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+21446A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139103718 | ||||||
chr4:139103848
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.238+21316T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139103848 | ||||||
chr4:139104352
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.238+20812T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139104352 | ||||||
chr4:139104508
|
C | CA | 100 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0080others(97): Show | 100 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.238+20655dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139104508 | ||||||
chr4:139104508
|
C | CAA | 6 | a0001c0001t0001g0089a0001c0001t0001g0106a0001c0001t0001g0241others(3): Show | 6 | HG00423.hp1 HG01981.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+20654_238+2065 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139104508 | ||||||
chr4:139104508
|
CA | C | 7 | a0001c0001t0001g0027a0001c0001t0002g0341a0002c0002t0002g0112others(4): Show | 7 | HG01515.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+20655delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139104508 | ||||||
chr4:139104523
|
A | G | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.238+20641T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139104523 | ||||||
chr4:139104771
|
T | G | 1 | a0001c0001t0002g0340 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.238+20393A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139104771 | ||||||
chr4:139104959
|
C | G | 1 | a0001c0001t0002g0181 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.238+20205G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139104959 | ||||||
chr4:139104959
|
C | T | 73 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0062others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.238+20205G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139104959 | ||||||
chr4:139105045
|
T | C | 1 | a0001c0001t0002g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.238+20119A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139105045 | ||||||
chr4:139105108
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.238+20056G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139105108 | ||||||
chr4:139105122
|
G | C | 2 | a0001c0001t0002g0062a0001c0001t0002g0336 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.238+20042C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139105122 | ||||||
chr4:139105320
|
CTT | C | 17 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.238+19842_238+1984 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139105320 | ||||||
chr4:139105371
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0040others(4): Show | 7 | HG00280.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+19793G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139105371 | ||||||
chr4:139105410
|
T | G | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+19754A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139105410 | ||||||
chr4:139105524
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.238+19640A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139105524 | ||||||
chr4:139105588
|
T | C | 1 | a0001c0001t0001g0333 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.238+19576A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139105588 | ||||||
chr4:139105717
|
C | T | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+19447G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139105717 | ||||||
chr4:139105888
|
C | A | 1 | a0001c0001t0001g0055 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.238+19276G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139105888 | ||||||
chr4:139105975
|
T | G | 1 | a0002c0002t0002g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.238+19189A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139105975 | ||||||
chr4:139106008
|
A | G | 87 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.238+19156T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139106008 | ||||||
chr4:139106268
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.238+18896C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139106268 | ||||||
chr4:139106335
|
TAGAGA | T | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+18824_238+1882 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139106335 | ||||||
chr4:139106569
|
T | G | 9 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0196others(6): Show | 9 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+18595A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139106569 | ||||||
chr4:139106740
|
CT | C | 240 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(237): Show | 240 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.238+18423delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139106740 | ||||||
chr4:139106740
|
CTT | C | 9 | a0001c0001t0001g0029a0001c0001t0001g0137a0001c0001t0001g0265others(6): Show | 9 | HG01099.hp1 HG01168.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+18422_238+1842 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139106740 | ||||||
chr4:139106773
|
C | T | 4 | a0002c0002t0002g0116a0002c0002t0002g0117a0002c0002t0002g0119others(1): Show | 4 | HG02040.hp1 HG02056.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+18391G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139106773 | ||||||
chr4:139106822
|
C | A | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.238+18342G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139106822 | ||||||
chr4:139106893
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+18271C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139106893 | ||||||
chr4:139106920
|
G | T | 1 | a0001c0001t0001g0245 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.238+18244C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139106920 | ||||||
chr4:139107011
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.238+18153C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139107011 | ||||||
chr4:139107211
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.238+17953C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139107211 | ||||||
chr4:139107300
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.238+17864A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139107300 | ||||||
chr4:139107452
|
C | T | 328 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(325): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.238+17712G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139107452 | ||||||
chr4:139107485
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.238+17679C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139107485 | ||||||
chr4:139107493
|
A | C | 2 | a0002c0002t0002g0112a0002c0002t0002g0113 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.238+17671T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139107493 | ||||||
chr4:139107520
|
A | T | 74 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0062others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.238+17644T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139107520 | ||||||
chr4:139107751
|
A | G | 1 | a0001c0001t0002g0129 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.238+17413T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139107751 | ||||||
chr4:139107886
|
A | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.238+17278T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139107886 | ||||||
chr4:139108124
|
T | A | 1 | a0001c0001t0001g0279 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.238+17040A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108124 | ||||||
chr4:139108157
|
C | T | 1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+17007G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108157 | ||||||
chr4:139108229
|
A | G | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(1): Show | 4 | HG01071.hp2 HG01361.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+16935T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108229 | ||||||
chr4:139108257
|
G | A | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+16907C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108257 | ||||||
chr4:139108269
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.238+16895C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108269 | ||||||
chr4:139108430
|
G | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+16734C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108430 | ||||||
chr4:139108431
|
G | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+16733C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108431 | ||||||
chr4:139108796
|
G | A | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+16368C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108796 | ||||||
chr4:139108880
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.238+16284A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108880 | ||||||
chr4:139108881
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.238+16283A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108881 | ||||||
chr4:139108890
|
G | A | 21 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(18): Show | 21 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.238+16274C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108890 | ||||||
chr4:139108917
|
C | T | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+16247G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139108917 | ||||||
chr4:139109051
|
A | G | 59 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.238+16113T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139109051 | ||||||
chr4:139109196
|
G | T | 1 | a0001c0001t0002g0157 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.238+15968C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139109196 | ||||||
chr4:139109198
|
C | G | 24 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.238+15966G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139109198 | ||||||
chr4:139109639
|
G | C | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+15525C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139109639 | ||||||
chr4:139109900
|
G | A | 5 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0003g0208others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+15264C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139109900 | ||||||
chr4:139110058
|
C | T | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+15106G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139110058 | ||||||
chr4:139110208
|
A | T | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+14956T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139110208 | ||||||
chr4:139110210
|
A | G | 3 | a0001c0001t0001g0275a0001c0001t0001g0284a0001c0001t0001g0286 | 3 | HG00408.hp2 HG00558.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.238+14954T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139110210 | ||||||
chr4:139110501
|
T | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+14663A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139110501 | ||||||
chr4:139110501
|
T | C | 3 | a0001c0001t0002g0214a0001c0001t0005g0107a0001c0001t0005g0108 | 3 | HG01070.hp1 HG01071.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.238+14663A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139110501 | ||||||
chr4:139110574
|
G | A | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+14590C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139110574 | ||||||
chr4:139110637
|
T | A | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+14527A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139110637 | ||||||
chr4:139110706
|
A | AG | 35 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(32): Show | 35 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.238+14457dupC | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139110706 | ||||||
chr4:139110752
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.238+14412T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139110752 | ||||||
chr4:139110791
|
T | A | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.238+14373A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139110791 | ||||||
chr4:139110842
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0061a0001c0001t0001g0067others(4): Show | 7 | HG01175.hp1 HG01358.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+14322C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139110842 | ||||||
chr4:139111030
|
A | T | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+14134T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111030 | ||||||
chr4:139111164
|
A | G | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+14000T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111164 | ||||||
chr4:139111247
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.238+13917T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111247 | ||||||
chr4:139111262
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.238+13902T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111262 | ||||||
chr4:139111356
|
C | CT | 77 | a0001c0001t0001g0225a0001c0001t0001g0299a0001c0001t0002g0003others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.238+13807dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111356 | ||||||
chr4:139111409
|
C | A | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+13755G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111409 | ||||||
chr4:139111453
|
G | A | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+13711C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111453 | ||||||
chr4:139111491
|
C | CT | 11 | a0001c0001t0001g0008a0001c0001t0001g0067a0001c0001t0001g0087others(8): Show | 11 | HG01175.hp1 HG01358.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.238+13672dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111491 | ||||||
chr4:139111631
|
T | C | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+13533A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111631 | ||||||
chr4:139111686
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.238+13478C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111686 | ||||||
chr4:139111725
|
A | G | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+13439T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111725 | ||||||
chr4:139111740
|
T | C | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+13424A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111740 | ||||||
chr4:139111929
|
C | A | 23 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0087others(20): Show | 23 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.238+13235G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139111929 | ||||||
chr4:139112006
|
T | G | 1 | a0001c0001t0009g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.238+13158A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112006 | ||||||
chr4:139112078
|
T | C | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+13086A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112078 | ||||||
chr4:139112147
|
C | CTT | 23 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0087others(20): Show | 23 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(20): Show |
intron_variant | MODIFIER | c.238+13016_238+1301 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112147 | ||||||
chr4:139112601
|
G | C | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.238+12563C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112601 | ||||||
chr4:139112668
|
C | T | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.238+12496G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112668 | ||||||
chr4:139112703
|
T | A | 1 | a0001c0001t0002g0228 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.238+12461A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112703 | ||||||
chr4:139112732
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.238+12432T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112732 | ||||||
chr4:139112752
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+12412C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112752 | ||||||
chr4:139112813
|
T | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+12351A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112813 | ||||||
chr4:139112828
|
G | C | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+12336C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112828 | ||||||
chr4:139112889
|
C | T | 1 | a0002c0002t0002g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.238+12275G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112889 | ||||||
chr4:139112903
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.238+12261A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112903 | ||||||
chr4:139112915
|
A | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.238+12249T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139112915 | ||||||
chr4:139113136
|
T | C | 5 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0003g0208others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+12028A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139113136 | ||||||
chr4:139113387
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.238+11777C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139113387 | ||||||
chr4:139113516
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.238+11648C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139113516 | ||||||
chr4:139113640
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.238+11524T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139113640 | ||||||
chr4:139113808
|
C | G | 1 | a0001c0001t0002g0150 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.238+11356G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139113808 | ||||||
chr4:139113854
|
CA | C | 318 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.238+11309delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139113854 | ||||||
chr4:139113870
|
T | G | 1 | a0001c0001t0001g0269 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.238+11294A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139113870 | ||||||
chr4:139113914
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.238+11250A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139113914 | ||||||
chr4:139113960
|
T | C | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | NA18964.hp1 NA18979.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+11204A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139113960 | ||||||
chr4:139113978
|
A | C | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.238+11186T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139113978 | ||||||
chr4:139114366
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0021 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.238+10798G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114366 | ||||||
chr4:139114559
|
T | TCACACAC others(3): Show |
1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.238+10604_238+1060 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114559 | ||||||
chr4:139114559
|
T | TCACACAC others(5): Show |
3 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0218 | 3 | HG01361.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.238+10604_238+1060 others(16): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114559 | ||||||
chr4:139114559
|
T | TCACACAC others(7): Show |
1 | a0001c0001t0001g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.238+10604_238+1060 others(18): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114559 | ||||||
chr4:139114561
|
T | A | 5 | a0001c0001t0001g0196a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01361.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+10603A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCA | 26 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0140others(23): Show | 26 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.238+10601_238+1060 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCACA | 12 | a0001c0001t0001g0136a0001c0001t0002g0155a0001c0001t0003g0208others(9): Show | 12 | HG01884.hp2 HG02040.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.238+10599_238+1060 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCACACAC others(1): Show |
7 | a0001c0001t0002g0197a0001c0001t0002g0211a0001c0001t0002g0215others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+10595_238+1060 others(12): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCACACAC others(3): Show |
5 | a0001c0001t0002g0228a0001c0001t0002g0342a0001c0001t0005g0107others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+10593_238+1060 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCACACAC others(5): Show |
6 | a0001c0001t0001g0126a0001c0001t0002g0199a0001c0001t0002g0214others(3): Show | 6 | HG01981.hp2 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+10591_238+1060 others(16): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCACACAC others(7): Show |
3 | a0001c0001t0001g0195a0001c0001t0001g0202a0001c0001t0002g0213 | 3 | HG02818.hp1 HG02896.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.238+10589_238+1060 others(18): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCACACAC others(9): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0204 | 2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.238+10587_238+1060 others(20): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCACACAC others(15): Show |
1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+10581_238+1060 others(26): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCACACAC others(17): Show |
1 | a0001c0001t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.238+10579_238+1060 others(28): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCA others(10): Show |
1 | a0001c0001t0001g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.238+10602_238+1060 others(21): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCA others(20): Show |
1 | a0001c0001t0001g0333 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.238+10602_238+1060 others(31): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCA others(26): Show |
1 | a0001c0001t0001g0278 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.238+10602_238+1060 others(37): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCA others(42): Show |
1 | a0001c0001t0001g0331 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.238+10602_238+1060 others(53): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(4): Show |
17 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0014others(14): Show | 17 | HG00621.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.238+10602_238+1060 others(15): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(6): Show |
34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(31): Show | 34 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.238+10602_238+1060 others(17): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(8): Show |
18 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(15): Show | 18 | HG01515.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+10602_238+1060 others(19): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(10): Show |
13 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0058others(10): Show | 13 | HG00323.hp2 HG00741.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.238+10602_238+1060 others(21): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(12): Show |
38 | a0001c0001t0001g0038a0001c0001t0001g0047a0001c0001t0001g0054others(35): Show | 38 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+10602_238+1060 others(23): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(14): Show |
23 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0034others(20): Show | 23 | HG00558.hp2 HG01175.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.238+10602_238+1060 others(25): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(16): Show |
15 | a0001c0001t0001g0086a0001c0001t0001g0099a0001c0001t0001g0101others(12): Show | 15 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.238+10602_238+1060 others(27): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(18): Show |
7 | a0001c0001t0001g0247a0001c0001t0001g0262a0001c0001t0001g0288others(4): Show | 7 | HG00597.hp1 HG01169.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+10602_238+1060 others(29): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(20): Show |
4 | a0001c0001t0001g0232a0001c0001t0001g0270a0001c0001t0001g0320others(1): Show | 4 | HG01074.hp2 NA18955.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+10602_238+1060 others(31): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(22): Show |
5 | a0001c0001t0001g0284a0001c0001t0001g0286a0001c0001t0001g0301others(2): Show | 5 | HG00408.hp2 HG00558.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+10602_238+1060 others(33): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(24): Show |
4 | a0001c0001t0001g0274a0001c0001t0001g0325a0001c0001t0001g0328others(1): Show | 4 | NA18945.hp1 NA18988.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+10602_238+1060 others(35): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(26): Show |
3 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0290 | 3 | HG02083.hp2 NA18952.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.238+10602_238+1060 others(37): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(28): Show |
1 | a0001c0001t0001g0273 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.238+10602_238+1060 others(39): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(30): Show |
2 | a0001c0001t0001g0269a0001c0001t0001g0311 | 2 | HG00673.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.238+10602_238+1060 others(41): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(32): Show |
2 | a0001c0001t0001g0276a0001c0001t0001g0289 | 2 | NA18946.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.238+10602_238+1060 others(43): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(34): Show |
1 | a0001c0001t0001g0267 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.238+10602_238+1060 others(45): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(36): Show |
2 | a0001c0001t0001g0250a0001c0001t0001g0277 | 2 | HG02056.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.238+10602_238+1060 others(47): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(38): Show |
1 | a0001c0001t0001g0271 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.238+10602_238+1060 others(49): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(40): Show |
2 | a0001c0001t0001g0275a0001c0001t0001g0287 | 2 | NA18943.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.238+10602_238+1060 others(51): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(42): Show |
1 | a0001c0001t0007g0283 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.238+10602_238+1060 others(53): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(44): Show |
2 | a0001c0001t0001g0241a0001c0001t0001g0272 | 2 | HG00544.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.238+10602_238+1060 others(55): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(54): Show |
1 | a0001c0001t0002g0281 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.238+10602_238+1060 others(65): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(58): Show |
1 | a0001c0001t0001g0282 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.238+10602_238+1060 others(69): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114561
|
T | TCCAGTCT others(80): Show |
1 | a0001c0001t0001g0268 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.238+10602_238+1060 others(91): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114561 | ||||||
chr4:139114563
|
A | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0315 | 2 | HG01168.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.238+10601T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114563 | ||||||
chr4:139114565
|
A | T | 1 | a0001c0001t0001g0057 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.238+10599T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114565 | ||||||
chr4:139114642
|
C | CT | 7 | a0001c0001t0002g0096a0001c0001t0002g0230a0002c0002t0001g0337others(4): Show | 7 | HG02109.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+10521dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114642 | ||||||
chr4:139114642
|
C | CTT | 133 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0086others(130): Show | 133 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.238+10520_238+1052 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114642 | ||||||
chr4:139114642
|
C | CTTT | 57 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0200others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.238+10519_238+1052 others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114642 | ||||||
chr4:139114642
|
C | CTTTT | 28 | a0001c0001t0001g0196a0001c0001t0002g0131a0001c0001t0002g0134others(25): Show | 28 | HG00621.hp2 HG01070.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.238+10518_238+1052 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114642 | ||||||
chr4:139114642
|
CT | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0025others(10): Show | 13 | HG01175.hp1 HG01256.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.238+10521delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114642 | ||||||
chr4:139114642
|
CTTTTTTT others(1): Show |
C | 11 | a0001c0001t0002g0199a0001c0001t0002g0211a0001c0001t0002g0212others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.238+10514_238+1052 others(12): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114642 | ||||||
chr4:139114643
|
T | TTTC | 37 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.238+10520_238+1052 others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114643 | ||||||
chr4:139114646
|
T | C | 35 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 35 | HG00140.hp1 HG00621.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.238+10518A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114646 | ||||||
chr4:139114647
|
T | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0025others(10): Show | 13 | HG01175.hp1 HG01256.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.238+10517A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114647 | ||||||
chr4:139114649
|
T | C | 1 | a0001c0001t0001g0006 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.238+10515A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114649 | ||||||
chr4:139114702
|
A | T | 1 | a0001c0001t0001g0028 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.238+10462T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114702 | ||||||
chr4:139114724
|
A | C | 3 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210 | 3 | HG02258.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.238+10440T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114724 | ||||||
chr4:139114730
|
C | A | 1 | a0001c0001t0001g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.238+10434G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114730 | ||||||
chr4:139114820
|
T | C | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+10344A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114820 | ||||||
chr4:139114875
|
G | A | 111 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.238+10289C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114875 | ||||||
chr4:139114922
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.238+10242C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114922 | ||||||
chr4:139114968
|
G | A | 1 | a0001c0001t0003g0209 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.238+10196C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139114968 | ||||||
chr4:139115011
|
G | T | 2 | a0001c0001t0002g0062a0001c0001t0002g0336 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.238+10153C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115011 | ||||||
chr4:139115033
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238+10131A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115033 | ||||||
chr4:139115134
|
C | T | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.238+10030G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115134 | ||||||
chr4:139115266
|
G | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0067a0001c0001t0001g0191 | 3 | HG01175.hp1 HG01358.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.238+9898C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115266 | ||||||
chr4:139115268
|
T | C | 327 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(324): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.238+9896A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115268 | ||||||
chr4:139115273
|
G | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+9891C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115273 | ||||||
chr4:139115342
|
C | T | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+9822G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115342 | ||||||
chr4:139115474
|
A | G | 330 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.238+9690T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115474 | ||||||
chr4:139115532
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.238+9632G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115532 | ||||||
chr4:139115533
|
G | A | 6 | a0001c0001t0001g0242a0001c0001t0001g0245a0001c0001t0001g0251others(3): Show | 6 | HG00099.hp1 HG00639.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.238+9631C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115533 | ||||||
chr4:139115534
|
C | T | 1 | a0001c0001t0003g0127 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.238+9630G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115534 | ||||||
chr4:139115542
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.238+9622C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115542 | ||||||
chr4:139115725
|
A | G | 2 | a0001c0001t0005g0107a0001c0001t0005g0108 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.238+9439T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139115725 | ||||||
chr4:139116065
|
G | A | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.238+9099C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139116065 | ||||||
chr4:139116090
|
T | G | 1 | a0001c0001t0002g0340 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.238+9074A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139116090 | ||||||
chr4:139116101
|
C | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0285 | 2 | HG00408.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.238+9063G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139116101 | ||||||
chr4:139116114
|
C | T | 1 | a0001c0001t0002g0220 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.238+9050G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139116114 | ||||||
chr4:139116160
|
T | C | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+9004A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139116160 | ||||||
chr4:139116412
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0058 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.238+8752C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139116412 | ||||||
chr4:139116455
|
G | A | 1 | a0001c0001t0002g0167 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.238+8709C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139116455 | ||||||
chr4:139116457
|
A | T | 1 | a0001c0001t0002g0167 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.238+8707T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139116457 | ||||||
chr4:139116893
|
CCTTAT | C | 5 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+8266_238+8270d others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139116893 | ||||||
chr4:139116961
|
T | C | 2 | a0001c0001t0002g0160a0001c0001t0002g0162 | 2 | NA18945.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.238+8203A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139116961 | ||||||
chr4:139117040
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0058 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.238+8124C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139117040 | ||||||
chr4:139117269
|
A | C | 1 | a0001c0001t0003g0127 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.238+7895T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139117269 | ||||||
chr4:139117953
|
C | CA | 332 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(329): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.238+7210dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139117953 | ||||||
chr4:139117953
|
C | CAA | 8 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0126others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.238+7209_238+7210d others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139117953 | ||||||
chr4:139118008
|
CAACT | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.238+7152_238+7155d others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139118008 | ||||||
chr4:139118084
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.238+7080C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139118084 | ||||||
chr4:139118323
|
G | C | 1 | a0001c0001t0001g0045 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.238+6841C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139118323 | ||||||
chr4:139118328
|
C | G | 1 | a0001c0001t0002g0220 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.238+6836G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139118328 | ||||||
chr4:139118599
|
T | C | 9 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0196others(6): Show | 9 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+6565A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139118599 | ||||||
chr4:139118835
|
G | GCA | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0095 | 3 | NA18964.hp1 NA18983.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.238+6327_238+6328d others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139118835 | ||||||
chr4:139118878
|
T | C | 1 | a0001c0001t0001g0333 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.238+6286A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139118878 | ||||||
chr4:139118953
|
GA | G | 326 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(323): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.238+6210delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139118953 | ||||||
chr4:139119041
|
A | G | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.238+6123T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139119041 | ||||||
chr4:139119441
|
G | A | 1 | a0001c0001t0001g0279 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.238+5723C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139119441 | ||||||
chr4:139119444
|
C | A | 1 | a0001c0001t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.238+5720G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139119444 | ||||||
chr4:139119502
|
C | G | 9 | a0002c0002t0002g0116a0002c0002t0002g0117a0002c0002t0002g0118others(6): Show | 9 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+5662G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139119502 | ||||||
chr4:139119639
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0061others(9): Show | 12 | HG01175.hp1 HG01358.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.238+5525C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139119639 | ||||||
chr4:139119651
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.238+5513A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139119651 | ||||||
chr4:139119800
|
A | G | 1 | a0001c0001t0012g0002 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.238+5364T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139119800 | ||||||
chr4:139119962
|
TG | T | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+5201delC | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139119962 | ||||||
chr4:139120002
|
G | C | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+5162C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139120002 | ||||||
chr4:139120053
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.238+5111G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139120053 | ||||||
chr4:139120257
|
TTA | T | 23 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(20): Show | 23 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.238+4905_238+4906d others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139120257 | ||||||
chr4:139120281
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.238+4883A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139120281 | ||||||
chr4:139120313
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.238+4851G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139120313 | ||||||
chr4:139120587
|
C | T | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+4577G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139120587 | ||||||
chr4:139120613
|
A | AT | 104 | a0001c0001t0001g0103a0001c0001t0001g0136a0001c0001t0001g0137others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.238+4550dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139120613 | ||||||
chr4:139120734
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.238+4430T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139120734 | ||||||
chr4:139121012
|
C | A | 1 | a0001c0001t0002g0124 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.238+4152G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121012 | ||||||
chr4:139121095
|
A | AT | 26 | a0001c0001t0001g0050a0001c0001t0001g0067a0001c0001t0001g0082others(23): Show | 26 | HG00558.hp2 HG00741.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.238+4068dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121095 | ||||||
chr4:139121095
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.238+4054_238+4068d others(17): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121095 | ||||||
chr4:139121095
|
AT | A | 88 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.238+4068delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121095 | ||||||
chr4:139121095
|
ATT | A | 7 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0047others(4): Show | 7 | HG00733.hp2 HG01256.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+4067_238+4068d others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121095 | ||||||
chr4:139121095
|
ATTTTTT | A | 17 | a0001c0001t0002g0062a0001c0001t0002g0141a0001c0001t0002g0142others(14): Show | 17 | HG00621.hp2 HG00738.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.238+4063_238+4068d others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121095 | ||||||
chr4:139121095
|
ATTTTTTT | A | 71 | a0001c0001t0001g0299a0001c0001t0002g0003a0001c0001t0002g0007others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.238+4062_238+4068d others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121095 | ||||||
chr4:139121095
|
ATTTTTTT others(3): Show |
A | 4 | a0001c0001t0001g0034a0001c0001t0001g0092a0001c0001t0001g0332others(1): Show | 4 | HG00423.hp1 HG02155.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+4059_238+4068d others(12): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121095 | ||||||
chr4:139121095
|
ATTTTTTT others(4): Show |
A | 15 | a0001c0001t0001g0031a0001c0001t0001g0087a0001c0001t0001g0088others(12): Show | 15 | HG00673.hp2 HG02615.hp1 HG03139.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+4058_238+4068d others(13): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121095 | ||||||
chr4:139121095
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.238+4057_238+4068d others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121095 | ||||||
chr4:139121132
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0055 | 2 | NA18970.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.238+4032C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121132 | ||||||
chr4:139121139
|
T | C | 1 | a0001c0001t0009g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.238+4025A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121139 | ||||||
chr4:139121155
|
C | A | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.238+4009G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121155 | ||||||
chr4:139121162
|
G | A | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.238+4002C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121162 | ||||||
chr4:139121164
|
A | G | 1 | a0001c0001t0002g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.238+4000T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121164 | ||||||
chr4:139121171
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.238+3993G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121171 | ||||||
chr4:139121189
|
A | G | 2 | a0001c0001t0002g0197a0002c0002t0002g0122 | 2 | HG00438.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.238+3975T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121189 | ||||||
chr4:139121234
|
G | A | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.238+3930C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121234 | ||||||
chr4:139121310
|
G | T | 2 | a0003c0003t0003g0147a0003c0003t0003g0148 | 2 | HG01496.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.238+3854C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121310 | ||||||
chr4:139121316
|
G | C | 1 | a0001c0001t0002g0168 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.238+3848C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121316 | ||||||
chr4:139121316
|
G | T | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.238+3848C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121316 | ||||||
chr4:139121319
|
A | G | 2 | a0001c0001t0001g0267a0001c0001t0007g0283 | 2 | NA18949.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.238+3845T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121319 | ||||||
chr4:139121330
|
G | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0061others(11): Show | 14 | HG00544.hp1 HG01175.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.238+3834C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121330 | ||||||
chr4:139121330
|
G | C | 5 | a0001c0001t0002g0197a0001c0001t0002g0214a0001c0001t0002g0231others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+3834C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121330 | ||||||
chr4:139121349
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.238+3815A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121349 | ||||||
chr4:139121359
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.238+3805A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121359 | ||||||
chr4:139121367
|
G | C | 1 | a0001c0001t0002g0336 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.238+3797C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121367 | ||||||
chr4:139121387
|
T | C | 2 | a0001c0001t0002g0158a0001c0001t0002g0174 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.238+3777A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121387 | ||||||
chr4:139121390
|
G | A | 2 | a0002c0002t0002g0116a0002c0002t0002g0117 | 2 | NA19085.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.238+3774C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121390 | ||||||
chr4:139121392
|
A | G | 2 | a0001c0001t0002g0158a0001c0001t0002g0174 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.238+3772T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121392 | ||||||
chr4:139121458
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.238+3706A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121458 | ||||||
chr4:139121468
|
C | T | 12 | a0001c0001t0002g0168a0002c0002t0002g0111a0002c0002t0002g0116others(9): Show | 12 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.238+3696G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121468 | ||||||
chr4:139121825
|
A | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+3339T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121825 | ||||||
chr4:139121867
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0061others(9): Show | 12 | HG01175.hp1 HG01358.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.238+3297G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139121867 | ||||||
chr4:139122118
|
T | C | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+3046A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122118 | ||||||
chr4:139122176
|
A | G | 2 | a0002c0002t0002g0111a0002c0002t0002g0121 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.238+2988T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122176 | ||||||
chr4:139122244
|
A | C | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+2920T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122244 | ||||||
chr4:139122265
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.238+2899T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122265 | ||||||
chr4:139122305
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0068 | 2 | HG03492.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.238+2859A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122305 | ||||||
chr4:139122496
|
T | TTTTTGTT others(3): Show |
242 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(239): Show | 242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.238+2658_238+2667d others(12): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122496 | ||||||
chr4:139122496
|
T | TTTTTGTT others(8): Show |
69 | a0001c0001t0001g0086a0001c0001t0001g0104a0001c0001t0001g0232others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.238+2653_238+2667d others(17): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122496 | ||||||
chr4:139122496
|
T | TTTTTGTT others(13): Show |
4 | a0001c0001t0001g0275a0001c0001t0003g0208a0001c0001t0003g0209others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+2648_238+2667d others(22): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122496 | ||||||
chr4:139122547
|
C | G | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+2617G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122547 | ||||||
chr4:139122556
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.238+2608G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122556 | ||||||
chr4:139122566
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0074others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+2598T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122566 | ||||||
chr4:139122621
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.238+2543G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122621 | ||||||
chr4:139122716
|
T | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.238+2448A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122716 | ||||||
chr4:139122915
|
T | A | 1 | a0001c0001t0003g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.238+2249A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122915 | ||||||
chr4:139122934
|
C | T | 1 | a0002c0002t0002g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.238+2230G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139122934 | ||||||
chr4:139123016
|
C | G | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+2148G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139123016 | ||||||
chr4:139123091
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.238+2073C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139123091 | ||||||
chr4:139123137
|
T | C | 4 | a0001c0001t0002g0109a0001c0001t0002g0138a0001c0001t0002g0139others(1): Show | 4 | NA18952.hp1 NA18954.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+2027A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139123137 | ||||||
chr4:139123170
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.238+1994C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139123170 | ||||||
chr4:139123182
|
C | CA | 9 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0239others(6): Show | 9 | HG01175.hp2 HG02027.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+1981dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139123182 | ||||||
chr4:139123347
|
AC | A | 5 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0003g0208others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+1816delG | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139123347 | ||||||
chr4:139123543
|
T | C | 1 | a0001c0001t0002g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.238+1621A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139123543 | ||||||
chr4:139123940
|
A | G | 3 | a0001c0001t0002g0199a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01256.hp1 HG01258.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.238+1224T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139123940 | ||||||
chr4:139124049
|
GTTTA | G | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+1111_238+1114d others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139124049 | ||||||
chr4:139124141
|
T | C | 1 | a0001c0001t0001g0006 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.238+1023A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139124141 | ||||||
chr4:139124529
|
AAG | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(6): Show | 9 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+633_238+634del others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139124529 | ||||||
chr4:139124640
|
G | A | 38 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.238+524C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139124640 | ||||||
chr4:139124672
|
G | T | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.238+492C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139124672 | ||||||
chr4:139124684
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0021 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.238+480C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139124684 | ||||||
chr4:139124798
|
C | A | 2 | a0001c0001t0001g0288a0001c0001t0001g0293 | 2 | HG01255.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.238+366G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139124798 | ||||||
chr4:139125072
|
GT | G | 5 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0003g0208others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+91delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 4/9 | chr4 | 139125072 | ||||||
chr4:139125753
|
C | T | 57 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(54): Show | 57 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.73-424G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139125753 | ||||||
chr4:139125779
|
C | CA | 27 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0052others(24): Show | 27 | HG01169.hp2 HG01243.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.73-451dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139125779 | ||||||
chr4:139125779
|
CAAAA | C | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.73-454_73-451delTT others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139125779 | ||||||
chr4:139125779
|
CAAAAAA | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.73-456_73-451delTT others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139125779 | ||||||
chr4:139125885
|
C | G | 11 | a0002c0002t0002g0111a0002c0002t0002g0116a0002c0002t0002g0117others(8): Show | 11 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-556G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139125885 | ||||||
chr4:139125982
|
T | C | 3 | a0001c0001t0002g0313a0001c0001t0002g0314a0001c0001t0002g0316 | 3 | NA18963.hp1 NA19056.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.73-653A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139125982 | ||||||
chr4:139126372
|
G | A | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.73-1043C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139126372 | ||||||
chr4:139126377
|
GA | G | 115 | a0001c0001t0001g0010a0001c0001t0001g0126a0001c0001t0001g0136others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.73-1049delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139126377 | ||||||
chr4:139126377
|
GAA | G | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.73-1050_73-1049del others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139126377 | ||||||
chr4:139126392
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.73-1063A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139126392 | ||||||
chr4:139126895
|
T | C | 59 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.73-1566A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139126895 | ||||||
chr4:139127097
|
T | C | 1 | a0001c0001t0002g0158 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.73-1768A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139127097 | ||||||
chr4:139127120
|
T | C | 1 | a0001c0001t0002g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.73-1791A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139127120 | ||||||
chr4:139127312
|
C | T | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.73-1983G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139127312 | ||||||
chr4:139127430
|
A | G | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-2101T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139127430 | ||||||
chr4:139127595
|
T | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0265 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.73-2266A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139127595 | ||||||
chr4:139127909
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.73-2580C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139127909 | ||||||
chr4:139127964
|
C | CA | 18 | a0001c0001t0001g0045a0001c0001t0001g0077a0001c0001t0001g0089others(15): Show | 18 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.73-2636dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139127964 | ||||||
chr4:139127964
|
CA | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0090a0001c0001t0002g0168others(7): Show | 10 | HG01515.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-2636delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139127964 | ||||||
chr4:139127964
|
CAA | C | 13 | a0001c0001t0001g0066a0002c0002t0001g0337a0002c0002t0002g0111others(10): Show | 13 | HG00438.hp2 HG00597.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-2637_73-2636del others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139127964 | ||||||
chr4:139127984
|
T | A | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.73-2655A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139127984 | ||||||
chr4:139128009
|
C | A | 1 | a0001c0001t0001g0305 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.73-2680G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128009 | ||||||
chr4:139128106
|
G | C | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.73-2777C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128106 | ||||||
chr4:139128110
|
A | C | 1 | a0001c0001t0002g0281 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.73-2781T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128110 | ||||||
chr4:139128131
|
C | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.73-2802G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128131 | ||||||
chr4:139128188
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.73-2859A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128188 | ||||||
chr4:139128240
|
A | C | 1 | a0001c0001t0001g0339 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.73-2911T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128240 | ||||||
chr4:139128276
|
TA | T | 245 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.73-2948delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128276 | ||||||
chr4:139128524
|
C | CT | 7 | a0001c0001t0001g0059a0001c0001t0001g0089a0001c0001t0001g0234others(4): Show | 7 | HG01515.hp2 HG01884.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-3196dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128524 | ||||||
chr4:139128599
|
G | A | 21 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(18): Show | 21 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.73-3270C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128599 | ||||||
chr4:139128656
|
G | A | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.73-3327C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128656 | ||||||
chr4:139128690
|
T | C | 2 | a0002c0002t0004g0110a0002c0002t0004g0120 | 2 | NA18941.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.73-3361A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128690 | ||||||
chr4:139128756
|
G | A | 2 | a0001c0001t0002g0215a0001c0001t0002g0216 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.73-3427C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128756 | ||||||
chr4:139128774
|
A | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.73-3445T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128774 | ||||||
chr4:139128841
|
C | A | 1 | a0001c0001t0001g0298 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.73-3512G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128841 | ||||||
chr4:139128852
|
T | A | 3 | a0001c0001t0002g0313a0001c0001t0002g0314a0001c0001t0002g0316 | 3 | NA18963.hp1 NA19056.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.73-3523A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139128852 | ||||||
chr4:139129034
|
G | A | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.73-3705C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139129034 | ||||||
chr4:139129062
|
C | T | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73-3733G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139129062 | ||||||
chr4:139129063
|
T | C | 135 | a0001c0001t0001g0089a0001c0001t0001g0126a0001c0001t0001g0136others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.73-3734A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139129063 | ||||||
chr4:139129181
|
G | A | 69 | a0001c0001t0001g0086a0001c0001t0001g0232a0001c0001t0001g0241others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.73-3852C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139129181 | ||||||
chr4:139129224
|
G | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(16): Show | 19 | HG00280.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.73-3895C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139129224 | ||||||
chr4:139129321
|
C | T | 134 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(131): Show | 134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.73-3992G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139129321 | ||||||
chr4:139129807
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.73-4478C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139129807 | ||||||
chr4:139129917
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.73-4588T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139129917 | ||||||
chr4:139130230
|
AAAC | A | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-4904_73-4902del others(3): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139130230 | ||||||
chr4:139130277
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.73-4948A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139130277 | ||||||
chr4:139130332
|
A | G | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.73-5003T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139130332 | ||||||
chr4:139130510
|
C | T | 30 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.73-5181G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139130510 | ||||||
chr4:139130529
|
T | G | 1 | a0001c0001t0002g0297 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.73-5200A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139130529 | ||||||
chr4:139130693
|
A | C | 68 | a0001c0001t0002g0003a0001c0001t0002g0062a0001c0001t0002g0073others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.73-5364T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139130693 | ||||||
chr4:139130765
|
A | G | 1 | a0001c0001t0001g0015 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.73-5436T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139130765 | ||||||
chr4:139130893
|
T | A | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.73-5564A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139130893 | ||||||
chr4:139131642
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72+5988C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139131642 | ||||||
chr4:139131798
|
CA | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.72+5831delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139131798 | ||||||
chr4:139131897
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.72+5733T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139131897 | ||||||
chr4:139131999
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.72+5631A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139131999 | ||||||
chr4:139132685
|
A | C | 11 | a0002c0002t0002g0111a0002c0002t0002g0116a0002c0002t0002g0117others(8): Show | 11 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+4945T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132685 | ||||||
chr4:139132725
|
C | T | 135 | a0001c0001t0001g0089a0001c0001t0001g0126a0001c0001t0001g0136others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.72+4905G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132725 | ||||||
chr4:139132806
|
A | C | 88 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 88 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.72+4824T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132806 | ||||||
chr4:139132841
|
C | CAT | 31 | a0001c0001t0001g0099a0001c0001t0001g0241a0001c0001t0001g0242others(28): Show | 31 | HG00544.hp2 HG00558.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.72+4787_72+4788dup others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
C | CATAT | 12 | a0001c0001t0001g0247a0001c0001t0001g0258a0001c0001t0001g0265others(9): Show | 12 | HG01168.hp2 HG01169.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+4785_72+4788dup others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
C | CATATAT | 3 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0212 | 3 | HG01257.hp2 HG01258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.72+4783_72+4788dup others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
C | CATATATA others(3): Show |
3 | a0001c0001t0001g0196a0001c0001t0001g0201a0001c0001t0001g0292 | 3 | HG02258.hp2 HG02647.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.72+4779_72+4788dup others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
C | CATATATA others(5): Show |
2 | a0001c0001t0001g0200a0001c0001t0001g0218 | 2 | HG01361.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.72+4777_72+4788dup others(12): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
C | CATATATA others(7): Show |
1 | a0001c0001t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.72+4775_72+4788dup others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
C | CATATATA others(9): Show |
3 | a0001c0001t0001g0136a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG01884.hp2 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+4773_72+4788dup others(16): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
C | CATATATA others(13): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0204 | 2 | HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.72+4769_72+4788dup others(20): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
CAT | C | 92 | a0001c0001t0001g0081a0001c0001t0001g0086a0001c0001t0001g0101others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.72+4787_72+4788del others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
CATAT | C | 30 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0031others(27): Show | 30 | HG00323.hp2 HG00673.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.72+4785_72+4788del others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
CATATAT | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0024others(30): Show | 33 | HG00280.hp2 HG00597.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.72+4783_72+4788del others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
CATATATA others(1): Show |
C | 55 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(52): Show | 55 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.72+4781_72+4788del others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
CATATATA others(3): Show |
C | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+4779_72+4788del others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132841
|
CATATATA others(9): Show |
C | 17 | a0001c0001t0002g0341a0002c0002t0002g0111a0002c0002t0002g0112others(14): Show | 17 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.72+4773_72+4788del others(16): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132841 | ||||||
chr4:139132859
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0217 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.72+4771A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132859 | ||||||
chr4:139132873
|
T | A | 52 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.72+4757A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132873 | ||||||
chr4:139132903
|
G | A | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+4727C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132903 | ||||||
chr4:139132985
|
C | G | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+4645G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139132985 | ||||||
chr4:139133131
|
C | A | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+4499G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139133131 | ||||||
chr4:139133157
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.72+4473C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139133157 | ||||||
chr4:139133190
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.72+4440C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139133190 | ||||||
chr4:139133345
|
A | G | 6 | a0001c0001t0002g0158a0001c0001t0002g0166a0001c0001t0002g0168others(3): Show | 6 | HG00738.hp2 HG01070.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+4285T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139133345 | ||||||
chr4:139133363
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.72+4267C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139133363 | ||||||
chr4:139133636
|
C | CT | 6 | a0001c0001t0001g0242a0001c0001t0001g0251a0001c0001t0001g0324others(3): Show | 6 | HG00140.hp2 HG01167.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+3993dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139133636 | ||||||
chr4:139133636
|
CT | C | 59 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.72+3993delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139133636 | ||||||
chr4:139134069
|
A | G | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.72+3561T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134069 | ||||||
chr4:139134085
|
T | C | 9 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0196others(6): Show | 9 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.72+3545A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134085 | ||||||
chr4:139134249
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.72+3381A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134249 | ||||||
chr4:139134252
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.72+3378A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134252 | ||||||
chr4:139134348
|
T | G | 2 | a0001c0001t0002g0062a0001c0001t0002g0336 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.72+3282A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134348 | ||||||
chr4:139134489
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.72+3141A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134489 | ||||||
chr4:139134527
|
T | TTATTGTA others(8): Show |
4 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG01496.hp2 HG02486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+3088_72+3102dup others(15): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134527 | ||||||
chr4:139134527
|
T | TTATTGTA others(23): Show |
1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.72+3102_72+3103ins others(30): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134527 | ||||||
chr4:139134528
|
T | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+3102A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134528 | ||||||
chr4:139134564
|
GTTATTTT others(14): Show |
G | 2 | a0002c0002t0002g0111a0002c0002t0002g0121 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.72+3045_72+3065del others(21): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134564 | ||||||
chr4:139134584
|
A | ATTTAT | 6 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0328others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+3041_72+3045dup others(5): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134584 | ||||||
chr4:139134584
|
A | ATTTATTT others(8): Show |
1 | a0001c0001t0001g0101 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.72+3031_72+3045dup others(15): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134584 | ||||||
chr4:139134584
|
ATTTAT | A | 200 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.72+3041_72+3045del others(5): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134584 | ||||||
chr4:139134584
|
ATTTATTT others(3): Show |
A | 1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.72+3036_72+3045del others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134584 | ||||||
chr4:139134584
|
ATTTATTT others(8): Show |
A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+3031_72+3045del others(15): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134584 | ||||||
chr4:139134613
|
ATTTTATT others(3): Show |
A | 24 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.72+3007_72+3016del others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134613 | ||||||
chr4:139134613
|
ATTTTATT others(8): Show |
A | 4 | a0001c0001t0001g0061a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG01175.hp1 HG01358.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+3002_72+3016del others(15): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134613 | ||||||
chr4:139134617
|
T | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0074a0001c0001t0001g0221others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.72+3013A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134617 | ||||||
chr4:139134618
|
A | T | 9 | a0001c0001t0001g0017a0001c0001t0001g0074a0001c0001t0001g0221others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.72+3012T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134618 | ||||||
chr4:139134685
|
A | G | 1 | a0001c0001t0002g0179 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.72+2945T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139134685 | ||||||
chr4:139135152
|
C | CTGATTAC others(205): Show |
1 | a0001c0001t0009g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.72+2477_72+2478ins others(212): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135152 | ||||||
chr4:139135229
|
CTA | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(1): Show | 4 | HG00280.hp2 HG00733.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+2399_72+2400del others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135229 | ||||||
chr4:139135232
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0066 | 3 | HG00597.hp2 NA18955.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.72+2398A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135232 | ||||||
chr4:139135235
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.72+2395T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135235 | ||||||
chr4:139135235
|
ATATG | A | 7 | a0001c0001t0002g0132a0001c0001t0002g0134a0001c0001t0002g0140others(4): Show | 7 | HG02132.hp2 HG02258.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+2391_72+2394del others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135235 | ||||||
chr4:139135235
|
ATATGTG | A | 14 | a0001c0001t0002g0135a0001c0001t0002g0141a0001c0001t0002g0142others(11): Show | 14 | HG01515.hp2 HG02055.hp1 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.72+2389_72+2394del others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135235 | ||||||
chr4:139135235
|
ATATGTGT others(1): Show |
A | 52 | a0001c0001t0002g0003a0001c0001t0002g0062a0001c0001t0002g0073others(49): Show | 52 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.72+2387_72+2394del others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135235 | ||||||
chr4:139135235
|
ATATGTGT others(3): Show |
A | 10 | a0001c0001t0002g0007a0001c0001t0002g0150a0001c0001t0002g0153others(7): Show | 10 | HG01106.hp1 HG02109.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+2385_72+2394del others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135235 | ||||||
chr4:139135235
|
ATATGTGT others(5): Show |
A | 3 | a0001c0001t0002g0160a0001c0001t0002g0162a0002c0002t0002g0118 | 3 | NA18945.hp2 NA18971.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.72+2383_72+2394del others(12): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135235 | ||||||
chr4:139135235
|
ATATGTGT others(19): Show |
A | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.72+2369_72+2394del others(26): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135235 | ||||||
chr4:139135237
|
A | ATG | 7 | a0001c0001t0001g0126a0001c0001t0001g0219a0001c0001t0001g0240others(4): Show | 7 | HG00733.hp1 HG01243.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+2391_72+2392dup others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135237 | ||||||
chr4:139135237
|
A | ATGTG | 11 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0021others(8): Show | 11 | HG00280.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+2389_72+2392dup others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135237 | ||||||
chr4:139135237
|
A | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0038others(27): Show | 30 | HG00597.hp2 HG01071.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.72+2393T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135237 | ||||||
chr4:139135237
|
ATG | A | 20 | a0001c0001t0001g0097a0001c0001t0001g0244a0001c0001t0001g0247others(17): Show | 20 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.72+2391_72+2392del others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135237 | ||||||
chr4:139135237
|
ATGTG | A | 9 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0196others(6): Show | 9 | HG00099.hp1 HG01361.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.72+2389_72+2392del others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135237 | ||||||
chr4:139135237
|
ATGTGTGT others(1): Show |
A | 16 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0001g0072others(13): Show | 16 | HG01070.hp1 HG01071.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.72+2385_72+2392del others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135237 | ||||||
chr4:139135237
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72+2377_72+2392del others(16): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135237 | ||||||
chr4:139135259
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0001g0045 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.72+2370_72+2371ins others(12): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135259 | ||||||
chr4:139135277
|
G | A | 55 | a0001c0001t0001g0086a0001c0001t0001g0232a0001c0001t0001g0241others(52): Show | 55 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.72+2353C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135277 | ||||||
chr4:139135277
|
G | GTA | 12 | a0001c0001t0001g0277a0001c0001t0001g0284a0001c0001t0001g0285others(9): Show | 12 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+2352_72+2353ins others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135277 | ||||||
chr4:139135279
|
G | A | 92 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(89): Show | 92 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.72+2351C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135279 | ||||||
chr4:139135279
|
G | GTA | 27 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(24): Show | 27 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.72+2349_72+2350dup others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135279 | ||||||
chr4:139135279
|
G | GTGTA | 27 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(24): Show | 27 | HG00621.hp1 HG00639.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.72+2350_72+2351ins others(4): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135279 | ||||||
chr4:139135279
|
G | GTGTGTA | 13 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 13 | HG01346.hp2 HG02145.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.72+2350_72+2351ins others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135279 | ||||||
chr4:139135279
|
G | GTGTGTGT others(1): Show |
6 | a0001c0001t0001g0008a0001c0001t0001g0068a0001c0001t0001g0076others(3): Show | 6 | HG02559.hp1 HG02698.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+2350_72+2351ins others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135279 | ||||||
chr4:139135279
|
G | GTGTGTGT others(3): Show |
3 | a0001c0001t0001g0052a0001c0001t0001g0339a0001c0001t0002g0033 | 3 | HG02027.hp1 HG02630.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.72+2350_72+2351ins others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135279 | ||||||
chr4:139135279
|
G | GTGTGTGT others(5): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0074 | 2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.72+2350_72+2351ins others(12): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135279 | ||||||
chr4:139135279
|
GTA | G | 4 | a0001c0001t0002g0230a0001c0001t0003g0209a0002c0002t0002g0112others(1): Show | 4 | HG02965.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+2349_72+2350del others(2): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135279 | ||||||
chr4:139135281
|
A | G | 25 | a0001c0001t0002g0109a0001c0001t0002g0124a0001c0001t0002g0132others(22): Show | 25 | HG00438.hp2 HG01496.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.72+2349T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135281 | ||||||
chr4:139135283
|
A | G | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+2347T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135283 | ||||||
chr4:139135495
|
C | G | 15 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(12): Show | 15 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.72+2135G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139135495 | ||||||
chr4:139136028
|
G | C | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+1602C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136028 | ||||||
chr4:139136262
|
G | A | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+1368C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136262 | ||||||
chr4:139136486
|
ATTATACC others(1): Show |
A | 8 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0045others(5): Show | 8 | HG00323.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+1136_72+1143del others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136486 | ||||||
chr4:139136630
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.72+1000A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136630 | ||||||
chr4:139136664
|
C | CT | 80 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.72+965dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136664 | ||||||
chr4:139136664
|
CTT | C | 15 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(12): Show | 15 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.72+964_72+965delAA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136664 | ||||||
chr4:139136687
|
C | T | 11 | a0001c0001t0002g0199a0001c0001t0002g0211a0001c0001t0002g0212others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+943G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136687 | ||||||
chr4:139136751
|
G | A | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+879C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136751 | ||||||
chr4:139136786
|
T | C | 1 | a0001c0001t0003g0229 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.72+844A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136786 | ||||||
chr4:139136809
|
C | T | 11 | a0002c0002t0002g0111a0002c0002t0002g0116a0002c0002t0002g0117others(8): Show | 11 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+821G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136809 | ||||||
chr4:139136823
|
C | G | 2 | a0001c0001t0005g0107a0001c0001t0005g0108 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.72+807G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136823 | ||||||
chr4:139136831
|
AT | A | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+798delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136831 | ||||||
chr4:139136890
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.72+740A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136890 | ||||||
chr4:139136892
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.72+738G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136892 | ||||||
chr4:139136956
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.72+674G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139136956 | ||||||
chr4:139137019
|
C | T | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72+611G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139137019 | ||||||
chr4:139137037
|
T | TA | 23 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(20): Show | 23 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.72+592dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139137037 | ||||||
chr4:139137095
|
C | A | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.72+535G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139137095 | ||||||
chr4:139137117
|
G | A | 13 | a0001c0001t0001g0086a0001c0001t0001g0248a0001c0001t0001g0295others(10): Show | 13 | HG00597.hp1 NA18942.hp1 NA18944.hp1 others(10): Show |
intron_variant | MODIFIER | c.72+513C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139137117 | ||||||
chr4:139137171
|
G | C | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72+459C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139137171 | ||||||
chr4:139137466
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.72+164A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139137466 | ||||||
chr4:139137500
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.72+130G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 3/9 | chr4 | 139137500 | ||||||
chr4:139138020
|
T | C | 5 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(2): Show | 5 | HG01496.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-166-153A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138020 | ||||||
chr4:139138193
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-166-326G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138193 | ||||||
chr4:139138332
|
A | G | 18 | a0002c0002t0001g0337a0002c0002t0002g0111a0002c0002t0002g0112others(15): Show | 18 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.-166-465T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138332 | ||||||
chr4:139138415
|
C | CA | 18 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(15): Show | 18 | HG00438.hp2 HG01496.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.-166-549dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138415 | ||||||
chr4:139138420
|
A | AC | 23 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(20): Show | 23 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-166-554_-166-553i others(3): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138420 | ||||||
chr4:139138421
|
A | G | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-166-554T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138421 | ||||||
chr4:139138660
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-167+753A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138660 | ||||||
chr4:139138698
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-167+715C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138698 | ||||||
chr4:139138698
|
G | C | 110 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-167+715C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138698 | ||||||
chr4:139138743
|
A | C | 2 | a0001c0001t0002g0155a0001c0001t0002g0176 | 2 | HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-167+670T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138743 | ||||||
chr4:139138857
|
G | A | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-167+556C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138857 | ||||||
chr4:139138877
|
T | C | 59 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-167+536A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138877 | ||||||
chr4:139138897
|
A | G | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-167+516T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138897 | ||||||
chr4:139138972
|
T | A | 340 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(337): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.-167+441A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 2/9 | chr4 | 139138972 | ||||||
chr4:139139620
|
C | T | 12 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(9): Show | 12 | HG01243.hp1 HG01361.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-251-123G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139139620 | ||||||
chr4:139139805
|
T | C | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-251-308A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139139805 | ||||||
chr4:139139820
|
T | C | 1 | a0001c0001t0002g0150 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-251-323A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139139820 | ||||||
chr4:139139881
|
G | A | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-251-384C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139139881 | ||||||
chr4:139140161
|
G | T | 340 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(337): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.-251-664C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139140161 | ||||||
chr4:139140162
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-251-665C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139140162 | ||||||
chr4:139140261
|
C | G | 1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-251-764G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139140261 | ||||||
chr4:139140519
|
G | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-1022C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139140519 | ||||||
chr4:139140667
|
C | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-1170G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139140667 | ||||||
chr4:139140708
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-251-1211G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139140708 | ||||||
chr4:139141011
|
C | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-1514G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139141011 | ||||||
chr4:139141173
|
G | A | 11 | a0002c0002t0002g0111a0002c0002t0002g0116a0002c0002t0002g0117others(8): Show | 11 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-251-1676C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139141173 | ||||||
chr4:139141291
|
T | C | 5 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0003g0208others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-251-1794A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139141291 | ||||||
chr4:139141482
|
G | T | 1 | a0001c0001t0001g0255 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-251-1985C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139141482 | ||||||
chr4:139141631
|
A | C | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-2134T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139141631 | ||||||
chr4:139141632
|
C | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-2135G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139141632 | ||||||
chr4:139141752
|
A | T | 1 | a0001c0001t0001g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-251-2255T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139141752 | ||||||
chr4:139142321
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0080 | 2 | NA18953.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-251-2824G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139142321 | ||||||
chr4:139142413
|
TGAA | T | 109 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-251-2919_-251-291 others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139142413 | ||||||
chr4:139142436
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-251-2939C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139142436 | ||||||
chr4:139142783
|
G | A | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-251-3286C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139142783 | ||||||
chr4:139142788
|
G | A | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-3291C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139142788 | ||||||
chr4:139142829
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-251-3332A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139142829 | ||||||
chr4:139142850
|
G | C | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-251-3353C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139142850 | ||||||
chr4:139142858
|
C | A | 1 | a0001c0001t0003g0127 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-251-3361G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139142858 | ||||||
chr4:139142866
|
CA | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-251-3370delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139142866 | ||||||
chr4:139143002
|
C | CAGA | 18 | a0002c0002t0001g0337a0002c0002t0002g0111a0002c0002t0002g0112others(15): Show | 18 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.-251-3508_-251-350 others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139143002 | ||||||
chr4:139143201
|
G | A | 1 | a0001c0001t0009g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-251-3704C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139143201 | ||||||
chr4:139143242
|
T | C | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-3745A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139143242 | ||||||
chr4:139143481
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-251-3984G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139143481 | ||||||
chr4:139143614
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-251-4117C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139143614 | ||||||
chr4:139143616
|
C | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-4119G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139143616 | ||||||
chr4:139143646
|
G | A | 1 | a0001c0001t0009g0030 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-251-4149C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139143646 | ||||||
chr4:139143652
|
G | A | 1 | a0001c0001t0001g0333 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-251-4155C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139143652 | ||||||
chr4:139143678
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0002g0096 | 2 | NA18979.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-251-4181C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139143678 | ||||||
chr4:139143699
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-251-4202C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139143699 | ||||||
chr4:139143816
|
T | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(37): Show | 40 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-251-4319A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139143816 | ||||||
chr4:139144317
|
G | C | 1 | a0001c0001t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-251-4820C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144317 | ||||||
chr4:139144332
|
T | C | 2 | a0001c0001t0002g0145a0001c0001t0002g0161 | 2 | HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-251-4835A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144332 | ||||||
chr4:139144335
|
G | A | 9 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0196others(6): Show | 9 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-251-4838C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144335 | ||||||
chr4:139144336
|
C | T | 1 | a0001c0001t0003g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-251-4839G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144336 | ||||||
chr4:139144353
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-251-4856T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144353 | ||||||
chr4:139144384
|
G | A | 1 | a0001c0001t0002g0173 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-251-4887C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144384 | ||||||
chr4:139144404
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0002g0197 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-251-4907T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144404 | ||||||
chr4:139144443
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-251-4946T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144443 | ||||||
chr4:139144537
|
CACAG | C | 9 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0196others(6): Show | 9 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-251-5044_-251-504 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144537 | ||||||
chr4:139144551
|
T | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0234others(1): Show | 4 | HG00140.hp1 HG02738.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-251-5054A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144551 | ||||||
chr4:139144556
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-251-5059A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144556 | ||||||
chr4:139144569
|
C | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0078 | 3 | HG02145.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-251-5072G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144569 | ||||||
chr4:139144587
|
C | T | 1 | a0001c0001t0002g0281 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-251-5090G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144587 | ||||||
chr4:139144614
|
T | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(31): Show | 34 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.-251-5117A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144614 | ||||||
chr4:139144707
|
C | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-251-5210G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144707 | ||||||
chr4:139144998
|
T | C | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-251-5501A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139144998 | ||||||
chr4:139145128
|
G | A | 74 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0062others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-251-5631C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139145128 | ||||||
chr4:139145130
|
G | A | 74 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0062others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-251-5633C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139145130 | ||||||
chr4:139145409
|
T | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0105others(1): Show | 4 | HG02523.hp2 NA18960.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.-251-5912A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139145409 | ||||||
chr4:139145618
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-251-6121C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139145618 | ||||||
chr4:139145680
|
A | C | 5 | a0001c0001t0002g0134a0001c0001t0002g0177a0001c0001t0002g0178others(2): Show | 5 | HG00621.hp2 HG02083.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-251-6183T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139145680 | ||||||
chr4:139145994
|
C | A | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-251-6497G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139145994 | ||||||
chr4:139146080
|
C | A | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-6583G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139146080 | ||||||
chr4:139146089
|
G | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0061a0001c0001t0001g0067others(8): Show | 11 | HG01175.hp1 HG01358.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-251-6592C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139146089 | ||||||
chr4:139146116
|
C | A | 1 | a0001c0001t0002g0140 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-251-6619G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139146116 | ||||||
chr4:139146150
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-251-6653A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139146150 | ||||||
chr4:139146183
|
G | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0251a0001c0001t0001g0324others(1): Show | 4 | HG01167.hp2 HG01243.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-251-6686C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139146183 | ||||||
chr4:139146324
|
G | A | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0282 | 3 | HG01257.hp1 HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-251-6827C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139146324 | ||||||
chr4:139146348
|
T | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0093 | 2 | HG00673.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.-251-6851A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139146348 | ||||||
chr4:139146372
|
T | C | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-251-6875A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139146372 | ||||||
chr4:139146724
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-251-7227A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139146724 | ||||||
chr4:139146727
|
A | C | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0257 | 3 | HG00733.hp1 HG01175.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-251-7230T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139146727 | ||||||
chr4:139146826
|
T | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-251-7329A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139146826 | ||||||
chr4:139147076
|
G | C | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-251-7579C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139147076 | ||||||
chr4:139147439
|
T | G | 1 | a0001c0001t0001g0285 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-251-7942A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139147439 | ||||||
chr4:139147548
|
G | A | 2 | a0002c0002t0002g0112a0002c0002t0002g0113 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-251-8051C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139147548 | ||||||
chr4:139147699
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-251-8202G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139147699 | ||||||
chr4:139147778
|
A | AT | 56 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0058others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.-251-8282dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139147778 | ||||||
chr4:139147778
|
AT | A | 8 | a0001c0001t0001g0012a0001c0001t0002g0036a0001c0001t0002g0037others(5): Show | 8 | HG00099.hp2 HG00140.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-251-8282delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139147778 | ||||||
chr4:139147798
|
T | C | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-251-8301A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139147798 | ||||||
chr4:139147799
|
T | C | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-251-8302A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139147799 | ||||||
chr4:139147911
|
C | T | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-251-8414G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139147911 | ||||||
chr4:139147950
|
C | T | 1 | a0002c0002t0002g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-251-8453G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139147950 | ||||||
chr4:139148100
|
T | TA | 168 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0019others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-251-8604dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148100 | ||||||
chr4:139148100
|
T | TAA | 61 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0011others(58): Show | 61 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.-251-8605_-251-860 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148100 | ||||||
chr4:139148100
|
T | TAAA | 10 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0018others(7): Show | 10 | HG02027.hp1 NA18949.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.-251-8606_-251-860 others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148100 | ||||||
chr4:139148116
|
T | A | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-251-8619A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148116 | ||||||
chr4:139148159
|
T | C | 15 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(12): Show | 15 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.-251-8662A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148159 | ||||||
chr4:139148220
|
C | T | 332 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(329): Show | 332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.-251-8723G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148220 | ||||||
chr4:139148316
|
A | AT | 141 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 141 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-251-8820dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148316 | ||||||
chr4:139148316
|
A | ATT | 52 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0018others(49): Show | 52 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.-251-8821_-251-882 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148316 | ||||||
chr4:139148316
|
A | ATTT | 8 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0065others(5): Show | 8 | HG01255.hp1 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-251-8822_-251-882 others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148316 | ||||||
chr4:139148316
|
AT | A | 53 | a0001c0001t0001g0195a0001c0001t0001g0221a0001c0001t0001g0225others(50): Show | 53 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.-251-8820delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148316 | ||||||
chr4:139148316
|
ATTTTT | A | 6 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(3): Show | 6 | HG02056.hp1 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-251-8824_-251-882 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148316 | ||||||
chr4:139148316
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0002g0308 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-251-8831_-251-882 others(16): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148316 | ||||||
chr4:139148316
|
ATTTTTTT others(6): Show |
A | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-251-8832_-251-882 others(17): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148316 | ||||||
chr4:139148427
|
T | G | 2 | a0001c0001t0005g0107a0001c0001t0005g0108 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-251-8930A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148427 | ||||||
chr4:139148482
|
T | C | 3 | a0001c0001t0002g0133a0001c0001t0002g0164a0001c0001t0002g0171 | 3 | HG00099.hp2 HG02257.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-251-8985A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148482 | ||||||
chr4:139148565
|
T | C | 3 | a0001c0001t0001g0225a0002c0002t0001g0337a0002c0002t0003g0115 | 3 | HG02109.hp1 HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-251-9068A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148565 | ||||||
chr4:139148799
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-251-9302C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148799 | ||||||
chr4:139148922
|
G | A | 18 | a0002c0002t0001g0337a0002c0002t0002g0111a0002c0002t0002g0112others(15): Show | 18 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.-251-9425C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139148922 | ||||||
chr4:139149097
|
T | TACTG | 8 | a0001c0001t0001g0301a0001c0001t0001g0317a0001c0001t0001g0318others(5): Show | 8 | HG00423.hp2 HG00738.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-251-9604_-251-960 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139149097 | ||||||
chr4:139149261
|
T | C | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-251-9764A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139149261 | ||||||
chr4:139149364
|
C | A | 3 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210 | 3 | HG02258.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-251-9867G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139149364 | ||||||
chr4:139149727
|
A | T | 1 | a0001c0001t0001g0267 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-251-10230T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139149727 | ||||||
chr4:139149759
|
G | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-251-10262C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139149759 | ||||||
chr4:139149844
|
G | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0045others(5): Show | 8 | HG00323.hp2 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-251-10347C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139149844 | ||||||
chr4:139150229
|
T | C | 1 | a0001c0001t0002g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-251-10732A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150229 | ||||||
chr4:139150440
|
G | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-251-10943C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150440 | ||||||
chr4:139150450
|
T | C | 1 | a0001c0001t0002g0168 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-251-10953A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150450 | ||||||
chr4:139150456
|
C | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-10959G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150456 | ||||||
chr4:139150488
|
C | T | 7 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(4): Show | 7 | HG01496.hp2 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-251-10991G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150488 | ||||||
chr4:139150518
|
C | CA | 63 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(60): Show | 63 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-251-11022dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150518 | ||||||
chr4:139150518
|
C | CAA | 18 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(15): Show | 18 | HG00280.hp1 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-251-11023_-251-11 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150518 | ||||||
chr4:139150518
|
CA | C | 7 | a0001c0001t0001g0022a0001c0001t0002g0037a0001c0001t0002g0172others(4): Show | 7 | HG01258.hp2 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-251-11022delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150518 | ||||||
chr4:139150592
|
G | A | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-251-11095C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150592 | ||||||
chr4:139150830
|
C | G | 1 | a0001c0001t0001g0039 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-251-11333G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150830 | ||||||
chr4:139150949
|
C | T | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-251-11452G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150949 | ||||||
chr4:139150957
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-251-11460C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150957 | ||||||
chr4:139150967
|
T | TGAGCCGA others(2): Show |
108 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-251-11479_-251-11 others(15): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139150967 | ||||||
chr4:139151006
|
G | A | 11 | a0002c0002t0002g0111a0002c0002t0002g0116a0002c0002t0002g0117others(8): Show | 11 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-251-11509C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151006 | ||||||
chr4:139151016
|
T | A | 2 | a0001c0001t0001g0195a0001c0001t0002g0197 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-251-11519A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151016 | ||||||
chr4:139151017
|
C | G | 2 | a0001c0001t0001g0195a0001c0001t0002g0197 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-251-11520G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151017 | ||||||
chr4:139151018
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0002g0197 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-251-11521G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151018 | ||||||
chr4:139151019
|
A | AAAGAAAG others(16): Show |
1 | a0001c0001t0001g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-251-11523_-251-11 others(29): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151019 | ||||||
chr4:139151020
|
T | A | 2 | a0001c0001t0001g0195a0001c0001t0002g0197 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-251-11523A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151020 | ||||||
chr4:139151021
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0002g0197 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-251-11524G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151021 | ||||||
chr4:139151022
|
T | A | 1 | a0001c0001t0001g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-251-11525A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151022 | ||||||
chr4:139151022
|
T | G | 1 | a0001c0001t0002g0197 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-251-11525A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151022 | ||||||
chr4:139151023
|
C | A | 1 | a0001c0001t0002g0197 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-251-11526G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151023 | ||||||
chr4:139151023
|
C | CA | 9 | a0001c0001t0001g0086a0001c0001t0001g0272a0001c0001t0001g0279others(6): Show | 9 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.-251-11527dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151023 | ||||||
chr4:139151023
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-251-11526G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151023 | ||||||
chr4:139151024
|
A | AAAACAAG others(96): Show |
1 | a0001c0001t0001g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-251-11528_-251-11 others(109): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151024 | ||||||
chr4:139151024
|
A | AAAACAAG others(82): Show |
1 | a0001c0001t0001g0218 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-251-11528_-251-11 others(95): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151024 | ||||||
chr4:139151024
|
A | AAAACAAG others(148): Show |
1 | a0001c0001t0001g0202 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-251-11528_-251-11 others(161): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151024 | ||||||
chr4:139151024
|
A | AAAACAAG others(112): Show |
1 | a0001c0001t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-251-11528_-251-11 others(125): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151024 | ||||||
chr4:139151024
|
A | AAAACAAG others(96): Show |
1 | a0001c0001t0001g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-251-11528_-251-11 others(109): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151024 | ||||||
chr4:139151024
|
A | AAGAAAGA others(28): Show |
1 | a0001c0001t0002g0197 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-251-11528_-251-11 others(41): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151024 | ||||||
chr4:139151026
|
A | AACAAGAA others(84): Show |
1 | a0001c0001t0001g0200 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-251-11530_-251-11 others(97): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151026 | ||||||
chr4:139151026
|
A | AACAAGAA others(88): Show |
1 | a0001c0001t0001g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-251-11530_-251-11 others(101): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151026 | ||||||
chr4:139151026
|
A | AACAAGAA others(104): Show |
1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-251-11530_-251-11 others(117): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151026 | ||||||
chr4:139151027
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-251-11530T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151027 | ||||||
chr4:139151028
|
A | AAAAGAAA others(13): Show |
1 | a0001c0001t0001g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-251-11532_-251-11 others(26): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151028 | ||||||
chr4:139151028
|
A | AAAAGAAA others(32): Show |
1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-251-11532_-251-11 others(45): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151028 | ||||||
chr4:139151028
|
A | AAAGAAAG others(341): Show |
1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-251-11532_-251-11 others(354): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151028 | ||||||
chr4:139151028
|
A | G | 7 | a0001c0001t0001g0136a0001c0001t0001g0196a0001c0001t0001g0201others(4): Show | 7 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-251-11531T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151028 | ||||||
chr4:139151029
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-251-11532T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151029 | ||||||
chr4:139151029
|
AAAAAAAG others(4): Show |
A | 1 | a0001c0001t0002g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-251-11543_-251-11 others(17): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151029 | ||||||
chr4:139151029
|
AAAAAAAG others(12): Show |
A | 1 | a0001c0001t0002g0036 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-251-11551_-251-11 others(25): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151029 | ||||||
chr4:139151030
|
A | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0203 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-251-11533T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151030 | ||||||
chr4:139151031
|
A | AAGAAAAG others(15): Show |
2 | a0001c0001t0003g0208a0001c0001t0003g0209 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-251-11535_-251-11 others(28): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151031 | ||||||
chr4:139151031
|
A | AAGAAAAG others(25): Show |
2 | a0001c0001t0002g0207a0001c0001t0003g0210 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-251-11535_-251-11 others(38): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151031 | ||||||
chr4:139151031
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-251-11534T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151031 | ||||||
chr4:139151032
|
A | AAAAAAAA others(183): Show |
1 | a0001c0001t0002g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(196): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAAAAA others(194): Show |
1 | a0001c0001t0002g0214 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(207): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAAAAA others(102): Show |
1 | a0001c0001t0005g0107 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(115): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAAAAA others(106): Show |
1 | a0001c0001t0005g0108 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(119): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAAAAA others(122): Show |
1 | a0001c0001t0002g0213 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(135): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAAAAA others(142): Show |
1 | a0001c0001t0002g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(155): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAAAAA others(28): Show |
2 | a0001c0001t0002g0228a0001c0001t0003g0229 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-251-11536_-251-11 others(41): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAAAAG others(41): Show |
1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(54): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAAG | 10 | a0001c0001t0001g0065a0001c0001t0001g0268a0001c0001t0001g0275others(7): Show | 10 | HG00408.hp2 HG00558.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.-251-11536_-251-11 others(11): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAAGAA others(18): Show |
1 | a0001c0001t0001g0290 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(31): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAG | 21 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0022others(18): Show | 21 | HG00639.hp2 HG01099.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-251-11539_-251-11 others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAGAAA others(1): Show |
12 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0026others(9): Show | 12 | HG00280.hp2 HG00639.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.-251-11543_-251-11 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAGAAA others(5): Show |
4 | a0001c0001t0001g0092a0001c0001t0001g0222a0001c0001t0001g0224others(1): Show | 4 | HG02145.hp2 HG02155.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-251-11547_-251-11 others(18): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAGAAA others(9): Show |
2 | a0001c0001t0001g0278a0001c0001t0001g0324 | 2 | HG01243.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.-251-11551_-251-11 others(22): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAAGAAA others(13): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0223 | 2 | HG00323.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-251-11555_-251-11 others(26): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAGAAAG others(4): Show |
1 | a0001c0001t0001g0270 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(17): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAAGAAAG others(16): Show |
1 | a0001c0001t0003g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(29): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AAGAAAGA others(3): Show |
1 | a0001c0001t0001g0257 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(16): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AGAAAAGA others(29): Show |
1 | a0001c0001t0001g0217 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(42): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | AGAAAAGA others(33): Show |
1 | a0001c0001t0002g0206 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-251-11536_-251-11 others(46): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
A | G | 19 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(16): Show | 19 | HG00597.hp1 HG00741.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-251-11535T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
AAAAG | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(26): Show | 29 | HG00621.hp1 HG01071.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-251-11539_-251-11 others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
AAAAGAAA others(1): Show |
A | 21 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0031others(18): Show | 21 | HG00280.hp1 HG01081.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.-251-11543_-251-11 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
AAAAGAAA others(5): Show |
A | 11 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0023others(8): Show | 11 | HG01175.hp1 HG01358.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-251-11547_-251-11 others(18): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
AAAAGAAA others(9): Show |
A | 4 | a0001c0001t0001g0055a0001c0001t0002g0160a0001c0001t0002g0169others(1): Show | 4 | HG02698.hp1 NA18992.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-251-11551_-251-11 others(22): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
AAAAGAAA others(13): Show |
A | 13 | a0001c0001t0002g0128a0001c0001t0002g0133a0001c0001t0002g0141others(10): Show | 13 | HG00099.hp2 HG01433.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.-251-11555_-251-11 others(26): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
AAAAGAAA others(17): Show |
A | 50 | a0001c0001t0001g0251a0001c0001t0002g0062a0001c0001t0002g0109others(47): Show | 50 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.-251-11559_-251-11 others(30): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
AAAAGAAA others(21): Show |
A | 15 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(12): Show | 15 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.-251-11563_-251-11 others(34): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151032
|
AAAAGAAA others(25): Show |
A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-251-11567_-251-11 others(38): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151032 | ||||||
chr4:139151033
|
AAAG | A | 16 | a0001c0001t0001g0241a0001c0001t0001g0248a0001c0001t0001g0249others(13): Show | 16 | NA18612.hp2 NA18942.hp1 NA18945.hp1 others(13): Show |
intron_variant | MODIFIER | c.-251-11539_-251-11 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151033 | ||||||
chr4:139151033
|
AAAGAAAG | A | 10 | a0001c0001t0001g0074a0001c0001t0001g0269a0001c0001t0001g0277others(7): Show | 10 | HG01257.hp1 HG01943.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-251-11543_-251-11 others(13): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151033 | ||||||
chr4:139151033
|
AAAGAAAG others(4): Show |
A | 3 | a0001c0001t0001g0294a0001c0001t0002g0314a0001c0001t0002g0316 | 3 | HG02165.hp2 NA18963.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-251-11547_-251-11 others(17): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151033 | ||||||
chr4:139151033
|
AAAGAAAG others(12): Show |
A | 1 | a0001c0001t0001g0232 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-251-11555_-251-11 others(25): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151033 | ||||||
chr4:139151033
|
AAAGAAAG others(16): Show |
A | 3 | a0001c0001t0001g0233a0001c0001t0001g0285a0001c0001t0001g0317 | 3 | HG00408.hp1 HG00423.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.-251-11559_-251-11 others(29): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151033 | ||||||
chr4:139151033
|
AAAGAAAG others(20): Show |
A | 7 | a0001c0001t0001g0301a0001c0001t0001g0318a0001c0001t0001g0320others(4): Show | 7 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-251-11563_-251-11 others(33): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151033 | ||||||
chr4:139151034
|
A | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0203 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-251-11537T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151034 | ||||||
chr4:139151036
|
G | A | 3 | a0001c0001t0002g0199a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01256.hp1 HG01258.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.-251-11539C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151036 | ||||||
chr4:139151037
|
A | G | 1 | a0001c0001t0003g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-251-11540T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151037 | ||||||
chr4:139151039
|
A | AGAAAGGA others(16): Show |
3 | a0001c0001t0002g0199a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01256.hp1 HG01258.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.-251-11543_-251-11 others(29): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151039 | ||||||
chr4:139151040
|
G | A | 2 | a0001c0001t0003g0208a0001c0001t0003g0209 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-251-11543C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151040 | ||||||
chr4:139151078
|
A | G | 3 | a0001c0001t0002g0213a0001c0001t0005g0107a0001c0001t0005g0108 | 3 | HG01070.hp1 HG01071.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-251-11581T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151078 | ||||||
chr4:139151081
|
A | AAGAAAGA others(3): Show |
8 | a0001c0001t0001g0136a0001c0001t0001g0196a0001c0001t0001g0200others(5): Show | 8 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-251-11585_-251-11 others(16): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151081 | ||||||
chr4:139151081
|
A | AAGAAAGA others(785): Show |
1 | a0001c0001t0001g0137 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-251-11585_-251-11 others(798): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151081 | ||||||
chr4:139151082
|
A | G | 10 | a0001c0001t0002g0199a0001c0001t0002g0211a0001c0001t0002g0212others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-251-11585T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151082 | ||||||
chr4:139151096
|
A | G | 14 | a0001c0001t0001g0195a0001c0001t0001g0225a0001c0001t0002g0197others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.-251-11599T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151096 | ||||||
chr4:139151097
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-251-11600T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151097 | ||||||
chr4:139151203
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-251-11706T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151203 | ||||||
chr4:139151269
|
C | G | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-251-11772G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151269 | ||||||
chr4:139151458
|
C | G | 1 | a0001c0001t0002g0183 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-251-11961G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151458 | ||||||
chr4:139151572
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0035 | 2 | HG01081.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-251-12075T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151572 | ||||||
chr4:139151653
|
A | C | 1 | a0001c0001t0001g0289 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-251-12156T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151653 | ||||||
chr4:139151762
|
C | A | 2 | a0002c0002t0002g0111a0002c0002t0002g0121 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-251-12265G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151762 | ||||||
chr4:139151930
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0046 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-251-12433G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139151930 | ||||||
chr4:139152155
|
T | C | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-251-12658A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139152155 | ||||||
chr4:139152331
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-251-12834A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139152331 | ||||||
chr4:139152371
|
G | A | 5 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(2): Show | 5 | HG01496.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-251-12874C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139152371 | ||||||
chr4:139152828
|
T | TTA | 3 | a0001c0001t0001g0250a0001c0001t0002g0158a0001c0001t0002g0174 | 3 | HG00738.hp2 HG01106.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-251-13333_-251-13 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139152828 | ||||||
chr4:139152828
|
TTA | T | 11 | a0002c0002t0002g0111a0002c0002t0002g0116a0002c0002t0002g0117others(8): Show | 11 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-251-13333_-251-13 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139152828 | ||||||
chr4:139152885
|
G | C | 244 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.-251-13388C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139152885 | ||||||
chr4:139152891
|
C | CT | 124 | a0001c0001t0001g0006a0001c0001t0001g0032a0001c0001t0001g0044others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-251-13395dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139152891 | ||||||
chr4:139152891
|
C | CTT | 8 | a0001c0001t0001g0137a0001c0001t0001g0217a0001c0001t0002g0109others(5): Show | 8 | HG02083.hp1 HG02109.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-251-13396_-251-13 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139152891 | ||||||
chr4:139152891
|
CT | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0055others(4): Show | 7 | HG01943.hp1 HG02976.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-251-13395delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139152891 | ||||||
chr4:139152935
|
G | T | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-251-13438C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139152935 | ||||||
chr4:139153154
|
G | C | 3 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0340 | 3 | HG03130.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-251-13657C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153154 | ||||||
chr4:139153443
|
A | AAAAT | 8 | a0001c0001t0001g0136a0001c0001t0001g0196a0001c0001t0001g0200others(5): Show | 8 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-251-13950_-251-13 others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153443 | ||||||
chr4:139153443
|
AAAATAAA others(5): Show |
A | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-251-13958_-251-13 others(18): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153443 | ||||||
chr4:139153471
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-251-13974C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153471 | ||||||
chr4:139153474
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-251-13977T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153474 | ||||||
chr4:139153643
|
C | G | 1 | a0001c0001t0001g0310 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-251-14146G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153643 | ||||||
chr4:139153654
|
C | T | 5 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(2): Show | 5 | HG01496.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-251-14157G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153654 | ||||||
chr4:139153731
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-251-14234G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153731 | ||||||
chr4:139153813
|
C | T | 2 | a0002c0002t0002g0111a0002c0002t0002g0121 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-251-14316G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153813 | ||||||
chr4:139153898
|
G | A | 108 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(105): Show | 108 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-251-14401C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153898 | ||||||
chr4:139153959
|
T | C | 4 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG01496.hp2 HG02486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-251-14462A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153959 | ||||||
chr4:139153991
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-251-14494C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139153991 | ||||||
chr4:139154027
|
T | C | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-251-14530A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139154027 | ||||||
chr4:139154327
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0074others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-251-14830C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139154327 | ||||||
chr4:139154335
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-251-14838C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139154335 | ||||||
chr4:139154423
|
TTAA | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(56): Show | 59 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-251-14929_-251-14 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139154423 | ||||||
chr4:139154703
|
T | C | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-251-15206A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139154703 | ||||||
chr4:139154704
|
C | T | 70 | a0001c0001t0001g0086a0001c0001t0001g0232a0001c0001t0001g0233others(67): Show | 70 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-251-15207G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139154704 | ||||||
chr4:139154741
|
CTCTGCTA others(1): Show |
C | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-251-15252_-251-15 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139154741 | ||||||
chr4:139154745
|
G | C | 1 | a0001c0001t0002g0098 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-251-15248C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139154745 | ||||||
chr4:139154825
|
G | C | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-251-15328C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139154825 | ||||||
chr4:139154952
|
C | G | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-251-15455G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139154952 | ||||||
chr4:139155282
|
T | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-251-15785A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139155282 | ||||||
chr4:139155331
|
C | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0161 | 2 | HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-251-15834G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139155331 | ||||||
chr4:139155458
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-251-15961T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139155458 | ||||||
chr4:139155665
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-251-16168G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139155665 | ||||||
chr4:139155703
|
A | G | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-251-16206T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139155703 | ||||||
chr4:139155910
|
TA | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-16414delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139155910 | ||||||
chr4:139156001
|
A | AATTG | 134 | a0001c0001t0001g0089a0001c0001t0001g0126a0001c0001t0001g0136others(131): Show | 134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-251-16508_-251-16 others(10): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156001 | ||||||
chr4:139156009
|
A | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0246 | 2 | HG02040.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-251-16512T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156009 | ||||||
chr4:139156104
|
T | C | 23 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(20): Show | 23 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-251-16607A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156104 | ||||||
chr4:139156119
|
GACACTGA others(12): Show |
G | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-251-16641_-251-16 others(25): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156119 | ||||||
chr4:139156139
|
A | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0026others(3): Show | 6 | HG01074.hp1 HG01099.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-251-16642T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156139 | ||||||
chr4:139156198
|
C | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-251-16701G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156198 | ||||||
chr4:139156268
|
C | T | 4 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0104others(1): Show | 4 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-251-16771G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156268 | ||||||
chr4:139156300
|
C | G | 5 | a0001c0001t0001g0196a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | HG01361.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-251-16803G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156300 | ||||||
chr4:139156621
|
T | TTTG | 3 | a0001c0001t0002g0150a0001c0001t0002g0188a0001c0001t0002g0189 | 3 | HG01257.hp2 HG01258.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-251-17127_-251-17 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156621 | ||||||
chr4:139156621
|
TTTG | T | 3 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0340 | 3 | HG03130.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-251-17127_-251-17 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156621 | ||||||
chr4:139156646
|
C | CTGT | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-251-17152_-251-17 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156646 | ||||||
chr4:139156657
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-251-17160T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156657 | ||||||
chr4:139156913
|
C | T | 1 | a0001c0001t0002g0335 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-251-17416G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139156913 | ||||||
chr4:139157057
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-251-17560G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139157057 | ||||||
chr4:139157059
|
T | C | 4 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG01496.hp2 HG02486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-251-17562A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139157059 | ||||||
chr4:139157542
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-251-18045A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139157542 | ||||||
chr4:139157627
|
C | T | 3 | a0001c0001t0001g0248a0001c0001t0001g0304a0001c0001t0002g0308 | 3 | NA18942.hp1 NA18953.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-251-18130G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139157627 | ||||||
chr4:139157732
|
T | G | 2 | a0002c0002t0002g0112a0002c0002t0002g0113 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-251-18235A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139157732 | ||||||
chr4:139157794
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-251-18297C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139157794 | ||||||
chr4:139158003
|
A | C | 1 | a0002c0002t0002g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-251-18506T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139158003 | ||||||
chr4:139158316
|
G | A | 1 | a0001c0001t0001g0009 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-252+18651C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139158316 | ||||||
chr4:139158457
|
G | A | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0257 | 3 | HG00733.hp1 HG01175.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-252+18510C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139158457 | ||||||
chr4:139158469
|
A | G | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-252+18498T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139158469 | ||||||
chr4:139158501
|
G | A | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-252+18466C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139158501 | ||||||
chr4:139158546
|
G | T | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-252+18421C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139158546 | ||||||
chr4:139158553
|
G | C | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-252+18414C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139158553 | ||||||
chr4:139158628
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-252+18339G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139158628 | ||||||
chr4:139159119
|
A | G | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-252+17848T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159119 | ||||||
chr4:139159139
|
T | A | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-252+17828A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159139 | ||||||
chr4:139159171
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-252+17796C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159171 | ||||||
chr4:139159198
|
G | C | 1 | a0001c0001t0007g0283 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-252+17769C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159198 | ||||||
chr4:139159230
|
A | G | 1 | a0001c0001t0002g0153 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-252+17737T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159230 | ||||||
chr4:139159243
|
G | T | 21 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(18): Show | 21 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.-252+17724C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159243 | ||||||
chr4:139159286
|
G | A | 2 | a0001c0001t0002g0144a0001c0001t0002g0152 | 2 | HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-252+17681C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159286 | ||||||
chr4:139159430
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0002g0161 | 2 | HG02129.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-252+17537T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159430 | ||||||
chr4:139159622
|
G | C | 1 | a0002c0002t0002g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-252+17345C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159622 | ||||||
chr4:139159623
|
C | T | 1 | a0002c0002t0002g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-252+17344G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159623 | ||||||
chr4:139159726
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-252+17241C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159726 | ||||||
chr4:139159758
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-252+17209C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159758 | ||||||
chr4:139159799
|
A | G | 2 | a0002c0002t0002g0198a0002c0002t0002g0205 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-252+17168T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159799 | ||||||
chr4:139159810
|
T | C | 4 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG01496.hp2 HG02486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-252+17157A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159810 | ||||||
chr4:139159922
|
T | C | 1 | a0001c0001t0001g0004 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-252+17045A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139159922 | ||||||
chr4:139160066
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-252+16901T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139160066 | ||||||
chr4:139160070
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-252+16897C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139160070 | ||||||
chr4:139160137
|
A | G | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-252+16830T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139160137 | ||||||
chr4:139160210
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-252+16757C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139160210 | ||||||
chr4:139160236
|
G | A | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-252+16731C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139160236 | ||||||
chr4:139160252
|
C | T | 23 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(20): Show | 23 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-252+16715G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139160252 | ||||||
chr4:139160285
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-252+16682T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139160285 | ||||||
chr4:139160734
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-252+16233C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139160734 | ||||||
chr4:139160772
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-252+16195C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139160772 | ||||||
chr4:139160918
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-252+16049C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139160918 | ||||||
chr4:139160931
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0246 | 2 | HG02040.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-252+16036G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139160931 | ||||||
chr4:139161033
|
T | C | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-252+15934A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161033 | ||||||
chr4:139161043
|
C | T | 21 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(18): Show | 21 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.-252+15924G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161043 | ||||||
chr4:139161105
|
G | A | 1 | a0002c0002t0002g0334 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-252+15862C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161105 | ||||||
chr4:139161200
|
C | T | 1 | a0001c0001t0002g0146 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-252+15767G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161200 | ||||||
chr4:139161271
|
G | T | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-252+15696C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161271 | ||||||
chr4:139161366
|
G | A | 30 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.-252+15601C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161366 | ||||||
chr4:139161399
|
C | A | 30 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(27): Show | 30 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.-252+15568G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161399 | ||||||
chr4:139161599
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-252+15368C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161599 | ||||||
chr4:139161652
|
T | TA | 138 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(135): Show | 138 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-252+15314dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161652 | ||||||
chr4:139161652
|
T | TAA | 30 | a0001c0001t0001g0058a0001c0001t0001g0106a0001c0001t0001g0136others(27): Show | 30 | HG00558.hp1 HG00621.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.-252+15313_-252+15 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161652 | ||||||
chr4:139161652
|
T | TAAA | 9 | a0001c0001t0001g0196a0001c0001t0001g0203a0001c0001t0001g0204others(6): Show | 9 | HG02257.hp2 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-252+15312_-252+15 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161652 | ||||||
chr4:139161652
|
TA | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0294others(4): Show | 7 | HG01074.hp1 HG02165.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.-252+15314delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161652 | ||||||
chr4:139161652
|
TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0001g0064a0002c0002t0002g0117 | 2 | NA18988.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-252+15305_-252+15 others(16): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161652 | ||||||
chr4:139161652
|
TAAAAAAA others(4): Show |
T | 4 | a0001c0001t0001g0080a0001c0001t0001g0195a0001c0001t0001g0219others(1): Show | 4 | HG01243.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-252+15304_-252+15 others(17): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161652 | ||||||
chr4:139161681
|
T | A | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-252+15286A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161681 | ||||||
chr4:139161799
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0332 | 3 | HG00423.hp1 HG02155.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.-252+15168G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161799 | ||||||
chr4:139161867
|
G | T | 1 | a0001c0001t0002g0160 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-252+15100C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161867 | ||||||
chr4:139161957
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-252+15010C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161957 | ||||||
chr4:139161971
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-252+14996C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139161971 | ||||||
chr4:139162021
|
G | A | 1 | a0002c0002t0003g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-252+14946C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139162021 | ||||||
chr4:139162102
|
A | C | 4 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG01496.hp2 HG02486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-252+14865T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139162102 | ||||||
chr4:139162295
|
G | T | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-252+14672C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139162295 | ||||||
chr4:139162343
|
C | T | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-252+14624G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139162343 | ||||||
chr4:139162422
|
T | G | 1 | a0001c0001t0002g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-252+14545A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139162422 | ||||||
chr4:139162618
|
T | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0219a0001c0001t0002g0197 | 3 | HG01243.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-252+14349A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139162618 | ||||||
chr4:139162864
|
A | T | 1 | a0001c0001t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-252+14103T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139162864 | ||||||
chr4:139163218
|
T | G | 1 | a0001c0001t0001g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-252+13749A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139163218 | ||||||
chr4:139163293
|
T | C | 1 | a0001c0001t0001g0232 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-252+13674A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139163293 | ||||||
chr4:139163362
|
G | T | 1 | a0001c0001t0002g0145 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-252+13605C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139163362 | ||||||
chr4:139163558
|
G | C | 1 | a0001c0001t0001g0267 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-252+13409C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139163558 | ||||||
chr4:139163714
|
G | C | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-252+13253C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139163714 | ||||||
chr4:139163733
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-252+13234T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139163733 | ||||||
chr4:139163764
|
A | C | 2 | a0002c0002t0002g0198a0002c0002t0002g0205 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-252+13203T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139163764 | ||||||
chr4:139163802
|
T | C | 1 | a0001c0001t0002g0175 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-252+13165A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139163802 | ||||||
chr4:139163839
|
G | A | 1 | a0002c0002t0002g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-252+13128C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139163839 | ||||||
chr4:139164018
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-252+12949C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139164018 | ||||||
chr4:139164082
|
G | A | 1 | a0001c0001t0003g0127 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-252+12885C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139164082 | ||||||
chr4:139164139
|
AAG | A | 3 | a0001c0001t0002g0199a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01256.hp1 HG01258.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.-252+12826_-252+12 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139164139 | ||||||
chr4:139164190
|
T | C | 71 | a0001c0001t0002g0062a0001c0001t0002g0109a0001c0001t0002g0128others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-252+12777A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139164190 | ||||||
chr4:139165120
|
G | GT | 85 | a0001c0001t0001g0217a0001c0001t0001g0221a0001c0001t0001g0222others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-252+11846dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139165120 | ||||||
chr4:139165170
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-252+11797G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139165170 | ||||||
chr4:139165244
|
A | C | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-252+11723T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139165244 | ||||||
chr4:139165261
|
T | C | 11 | a0002c0002t0002g0111a0002c0002t0002g0116a0002c0002t0002g0117others(8): Show | 11 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-252+11706A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139165261 | ||||||
chr4:139165321
|
T | A | 4 | a0002c0002t0002g0112a0002c0002t0002g0113a0002c0002t0002g0198others(1): Show | 4 | HG02257.hp2 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-252+11646A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139165321 | ||||||
chr4:139165394
|
T | G | 1 | a0001c0001t0001g0008 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-252+11573A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139165394 | ||||||
chr4:139165667
|
A | T | 23 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(20): Show | 23 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-252+11300T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139165667 | ||||||
chr4:139165809
|
C | A | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-252+11158G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139165809 | ||||||
chr4:139165893
|
AG | A | 3 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0340 | 3 | HG03130.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-252+11073delC | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139165893 | ||||||
chr4:139166076
|
G | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0219a0001c0001t0002g0197 | 3 | HG01243.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-252+10891C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139166076 | ||||||
chr4:139166461
|
C | T | 7 | a0001c0001t0002g0135a0001c0001t0002g0181a0001c0001t0002g0182others(4): Show | 7 | NA18946.hp2 NA18963.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-252+10506G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139166461 | ||||||
chr4:139166517
|
A | T | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-252+10450T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139166517 | ||||||
chr4:139166597
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-252+10370C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139166597 | ||||||
chr4:139166607
|
G | A | 4 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG01496.hp2 HG02486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-252+10360C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139166607 | ||||||
chr4:139166609
|
C | T | 4 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG01496.hp2 HG02486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-252+10358G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139166609 | ||||||
chr4:139166635
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-252+10332C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139166635 | ||||||
chr4:139166644
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-252+10323C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139166644 | ||||||
chr4:139166964
|
C | T | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-252+10003G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139166964 | ||||||
chr4:139167577
|
G | T | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-252+9390C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139167577 | ||||||
chr4:139167757
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-252+9210G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139167757 | ||||||
chr4:139167822
|
T | C | 3 | a0002c0002t0004g0110a0002c0002t0004g0120a0002c0002t0004g0123 | 3 | NA18941.hp2 NA18942.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-252+9145A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139167822 | ||||||
chr4:139167846
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-252+9121C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139167846 | ||||||
chr4:139167901
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-252+9066G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139167901 | ||||||
chr4:139167913
|
C | G | 53 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(50): Show | 53 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.-252+9054G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139167913 | ||||||
chr4:139167914
|
G | A | 22 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(19): Show | 22 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(19): Show |
intron_variant | MODIFIER | c.-252+9053C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139167914 | ||||||
chr4:139167922
|
T | C | 21 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(18): Show | 21 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.-252+9045A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139167922 | ||||||
chr4:139168015
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-252+8952G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139168015 | ||||||
chr4:139168153
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-252+8814G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139168153 | ||||||
chr4:139168477
|
T | C | 2 | a0002c0002t0002g0198a0002c0002t0002g0205 | 2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-252+8490A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139168477 | ||||||
chr4:139168503
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-252+8464A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139168503 | ||||||
chr4:139168580
|
A | AGGGTCCT others(10): Show |
1 | a0001c0001t0001g0008 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-252+8370_-252+838 others(21): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139168580 | ||||||
chr4:139168699
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0058 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-252+8268A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139168699 | ||||||
chr4:139168710
|
T | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0219a0001c0001t0002g0197 | 3 | HG01243.hp1 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-252+8257A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139168710 | ||||||
chr4:139168743
|
G | GT | 4 | a0001c0001t0001g0195a0001c0001t0001g0219a0001c0001t0001g0234others(1): Show | 4 | HG01243.hp1 HG02738.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-252+8223dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139168743 | ||||||
chr4:139168810
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-252+8157G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139168810 | ||||||
chr4:139168944
|
C | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-252+8023G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139168944 | ||||||
chr4:139169070
|
G | A | 1 | a0001c0001t0002g0335 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-252+7897C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169070 | ||||||
chr4:139169075
|
AGGCAGAT others(40): Show |
A | 1 | a0001c0001t0001g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-252+7845_-252+789 others(51): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169075 | ||||||
chr4:139169235
|
G | C | 18 | a0002c0002t0001g0337a0002c0002t0002g0111a0002c0002t0002g0112others(15): Show | 18 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.-252+7732C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169235 | ||||||
chr4:139169284
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-252+7683C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169284 | ||||||
chr4:139169289
|
G | A | 132 | a0001c0001t0001g0126a0001c0001t0001g0136a0001c0001t0001g0137others(129): Show | 132 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-252+7678C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169289 | ||||||
chr4:139169303
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-252+7664C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169303 | ||||||
chr4:139169304
|
C | T | 2 | a0001c0001t0002g0154a0001c0001t0002g0187 | 2 | HG02738.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-252+7663G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169304 | ||||||
chr4:139169328
|
A | C | 1 | a0001c0001t0001g0299 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-252+7639T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169328 | ||||||
chr4:139169344
|
T | TC | 15 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0065others(12): Show | 15 | HG00558.hp1 HG00733.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.-252+7622_-252+762 others(5): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169344 | ||||||
chr4:139169345
|
T | C | 300 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(297): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.-252+7622A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169345 | ||||||
chr4:139169346
|
T | C | 15 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0065others(12): Show | 15 | HG00558.hp1 HG00733.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.-252+7621A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169346 | ||||||
chr4:139169346
|
TA | T | 49 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0025others(46): Show | 49 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-252+7620delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169346 | ||||||
chr4:139169347
|
A | C | 252 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(249): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.-252+7620T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169347 | ||||||
chr4:139169348
|
A | C | 48 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0025others(45): Show | 48 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.-252+7619T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169348 | ||||||
chr4:139169356
|
A | G | 1 | a0001c0001t0001g0325 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-252+7611T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169356 | ||||||
chr4:139169684
|
T | C | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-252+7283A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169684 | ||||||
chr4:139169750
|
G | A | 1 | a0002c0002t0002g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-252+7217C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169750 | ||||||
chr4:139169833
|
C | T | 223 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-252+7134G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169833 | ||||||
chr4:139169844
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-252+7123C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169844 | ||||||
chr4:139169857
|
T | TA | 32 | a0001c0001t0001g0054a0001c0001t0001g0136a0001c0001t0001g0137others(29): Show | 32 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.-252+7109dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169857 | ||||||
chr4:139169857
|
T | TAA | 68 | a0001c0001t0002g0062a0001c0001t0002g0109a0001c0001t0002g0128others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-252+7108_-252+710 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169857 | ||||||
chr4:139169857
|
T | TAAA | 6 | a0001c0001t0002g0153a0001c0001t0002g0176a0001c0001t0002g0220others(3): Show | 6 | HG02055.hp1 HG02074.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-252+7107_-252+710 others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169857 | ||||||
chr4:139169857
|
TA | T | 66 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(63): Show | 66 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.-252+7109delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169857 | ||||||
chr4:139169880
|
A | G | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-252+7087T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169880 | ||||||
chr4:139169922
|
G | A | 5 | a0001c0001t0002g0199a0001c0001t0002g0215a0001c0001t0002g0216others(2): Show | 5 | HG01256.hp1 HG01258.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-252+7045C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169922 | ||||||
chr4:139169965
|
T | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0080 | 2 | NA18953.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-252+7002A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139169965 | ||||||
chr4:139170259
|
C | CT | 28 | a0001c0001t0001g0233a0001c0001t0001g0239a0001c0001t0001g0242others(25): Show | 28 | HG00099.hp1 HG00544.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.-252+6707dupA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170259 | ||||||
chr4:139170259
|
CT | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0060a0001c0001t0001g0065others(29): Show | 32 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.-252+6707delA | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170259 | ||||||
chr4:139170259
|
CTT | C | 148 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0016others(145): Show | 148 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-252+6706_-252+670 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170259 | ||||||
chr4:139170259
|
CTTT | C | 39 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-252+6705_-252+670 others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170259 | ||||||
chr4:139170259
|
CTTTT | C | 15 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(12): Show | 15 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.-252+6704_-252+670 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170259 | ||||||
chr4:139170262
|
T | C | 1 | a0001c0001t0002g0336 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-252+6705A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170262 | ||||||
chr4:139170425
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-252+6542C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170425 | ||||||
chr4:139170630
|
C | T | 18 | a0002c0002t0001g0337a0002c0002t0002g0111a0002c0002t0002g0112others(15): Show | 18 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.-252+6337G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170630 | ||||||
chr4:139170636
|
A | G | 1 | a0002c0002t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-252+6331T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170636 | ||||||
chr4:139170659
|
T | TA | 133 | a0001c0001t0001g0075a0001c0001t0001g0126a0001c0001t0001g0136others(130): Show | 133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-252+6307dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170659 | ||||||
chr4:139170716
|
C | CATTAT | 270 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(267): Show | 270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.-252+6246_-252+625 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170716 | ||||||
chr4:139170716
|
C | CATTATAT others(3): Show |
5 | a0001c0001t0001g0008a0001c0001t0002g0140a0001c0001t0002g0231others(2): Show | 5 | HG02055.hp1 HG02132.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-252+6241_-252+625 others(14): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170716 | ||||||
chr4:139170716
|
C | CATTATAT others(8): Show |
1 | a0002c0002t0002g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-252+6236_-252+625 others(19): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170716 | ||||||
chr4:139170729
|
T | TATATG | 23 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0195others(20): Show | 23 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-252+6237_-252+623 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170729 | ||||||
chr4:139170961
|
G | T | 1 | a0001c0001t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-252+6006C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139170961 | ||||||
chr4:139171245
|
T | A | 1 | a0001c0001t0010g0253 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-252+5722A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171245 | ||||||
chr4:139171252
|
G | T | 1 | a0001c0001t0010g0253 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-252+5715C>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171252 | ||||||
chr4:139171436
|
C | T | 16 | a0002c0002t0002g0111a0002c0002t0002g0112a0002c0002t0002g0113others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-252+5531G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171436 | ||||||
chr4:139171439
|
C | T | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-252+5528G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171439 | ||||||
chr4:139171609
|
C | A | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-252+5358G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171609 | ||||||
chr4:139171609
|
CA | C | 131 | a0001c0001t0001g0008a0001c0001t0001g0126a0001c0001t0001g0136others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.-252+5357delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171609 | ||||||
chr4:139171610
|
A | C | 1 | a0001c0001t0002g0154 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-252+5357T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171610 | ||||||
chr4:139171616
|
A | G | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-252+5351T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171616 | ||||||
chr4:139171620
|
A | C | 5 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(2): Show | 5 | HG01496.hp2 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-252+5347T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171620 | ||||||
chr4:139171627
|
A | G | 2 | a0002c0002t0001g0337a0002c0002t0003g0115 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-252+5340T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171627 | ||||||
chr4:139171665
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-252+5302A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171665 | ||||||
chr4:139171752
|
G | A | 66 | a0001c0001t0002g0062a0001c0001t0002g0109a0001c0001t0002g0128others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-252+5215C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171752 | ||||||
chr4:139171759
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-252+5208G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171759 | ||||||
chr4:139171843
|
G | C | 1 | a0001c0001t0001g0217 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-252+5124C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171843 | ||||||
chr4:139171990
|
T | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG02145.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-252+4977A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139171990 | ||||||
chr4:139172011
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-252+4956G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172011 | ||||||
chr4:139172373
|
A | C | 1 | a0001c0001t0002g0155 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-252+4594T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172373 | ||||||
chr4:139172411
|
C | T | 73 | a0001c0001t0001g0191a0001c0001t0002g0003a0001c0001t0002g0062others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-252+4556G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172411 | ||||||
chr4:139172412
|
G | A | 69 | a0001c0001t0001g0086a0001c0001t0001g0232a0001c0001t0001g0233others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-252+4555C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172412 | ||||||
chr4:139172459
|
C | G | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-252+4508G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172459 | ||||||
chr4:139172748
|
C | A | 1 | a0001c0001t0002g0192 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-252+4219G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172748 | ||||||
chr4:139172816
|
T | G | 16 | a0002c0002t0001g0337a0002c0002t0002g0111a0002c0002t0002g0112others(13): Show | 16 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.-252+4151A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172816 | ||||||
chr4:139172882
|
CG | C | 27 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(24): Show | 27 | HG00280.hp1 HG00639.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-252+4084delC | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172882 | ||||||
chr4:139172882
|
CGG | C | 38 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(35): Show | 38 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.-252+4083_-252+408 others(6): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172882 | ||||||
chr4:139172882
|
CGGG | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0024others(65): Show | 68 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-252+4082_-252+408 others(7): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172882 | ||||||
chr4:139172882
|
CGGGG | C | 105 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0063others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-252+4081_-252+408 others(8): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172882 | ||||||
chr4:139172882
|
CGGGGG | C | 23 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0081others(20): Show | 23 | HG00597.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-252+4080_-252+408 others(9): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172882 | ||||||
chr4:139172882
|
CGGGGGGG others(5): Show |
C | 1 | a0001c0001t0001g0061 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-252+4073_-252+408 others(16): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172882 | ||||||
chr4:139172882
|
CGGGGGGG others(8): Show |
C | 1 | a0001c0001t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-252+4070_-252+408 others(19): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172882 | ||||||
chr4:139172887
|
G | GGGGGGGG others(40): Show |
1 | a0001c0001t0001g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-252+4079_-252+408 others(51): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172887 | ||||||
chr4:139172890
|
G | GA | 6 | a0001c0001t0001g0250a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 6 | HG00544.hp1 NA18943.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.-252+4076_-252+407 others(5): Show |
ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172890 | ||||||
chr4:139172891
|
G | A | 9 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(6): Show | 9 | HG01943.hp1 HG02056.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.-252+4076C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172891 | ||||||
chr4:139172892
|
G | A | 14 | a0001c0001t0001g0241a0001c0001t0001g0284a0001c0001t0001g0285others(11): Show | 14 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.-252+4075C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172892 | ||||||
chr4:139172893
|
G | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0086others(48): Show | 51 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.-252+4074C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172893 | ||||||
chr4:139172894
|
G | A | 98 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-252+4073C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172894 | ||||||
chr4:139172895
|
G | A | 48 | a0001c0001t0001g0066a0001c0001t0001g0091a0001c0001t0001g0092others(45): Show | 48 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-252+4072C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172895 | ||||||
chr4:139172896
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0217a0002c0002t0004g0123 | 3 | HG02559.hp2 HG02647.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-252+4071C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172896 | ||||||
chr4:139172898
|
G | A | 4 | a0001c0001t0001g0126a0001c0001t0002g0124a0001c0001t0002g0125others(1): Show | 4 | HG01496.hp2 HG02486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-252+4069C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139172898 | ||||||
chr4:139173019
|
G | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0251a0001c0001t0001g0324others(1): Show | 4 | HG01167.hp2 HG01243.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-252+3948C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173019 | ||||||
chr4:139173160
|
T | C | 7 | a0001c0001t0002g0135a0001c0001t0002g0181a0001c0001t0002g0182others(4): Show | 7 | NA18946.hp2 NA18963.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-252+3807A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173160 | ||||||
chr4:139173170
|
T | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0251a0001c0001t0001g0324others(1): Show | 4 | HG01167.hp2 HG01243.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-252+3797A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173170 | ||||||
chr4:139173179
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-252+3788A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173179 | ||||||
chr4:139173197
|
T | G | 12 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0002g0177others(9): Show | 12 | HG00621.hp2 HG02083.hp1 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.-252+3770A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173197 | ||||||
chr4:139173525
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0067others(8): Show | 11 | HG01175.hp1 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-252+3442C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173525 | ||||||
chr4:139173533
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-252+3434G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173533 | ||||||
chr4:139173534
|
G | A | 3 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189 | 3 | HG01257.hp2 HG01258.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-252+3433C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173534 | ||||||
chr4:139173626
|
C | T | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-252+3341G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173626 | ||||||
chr4:139173726
|
C | A | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-252+3241G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173726 | ||||||
chr4:139173744
|
C | A | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-252+3223G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173744 | ||||||
chr4:139173753
|
G | A | 22 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(19): Show | 22 | HG00423.hp1 HG00673.hp2 HG02155.hp1 others(19): Show |
intron_variant | MODIFIER | c.-252+3214C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173753 | ||||||
chr4:139173757
|
C | CA | 19 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(16): Show | 19 | HG00438.hp1 HG00621.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-252+3209dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173757 | ||||||
chr4:139173757
|
CA | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0087others(11): Show | 14 | HG01167.hp1 HG01256.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-252+3209delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173757 | ||||||
chr4:139173850
|
G | C | 110 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0191others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-252+3117C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173850 | ||||||
chr4:139173861
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-252+3106C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173861 | ||||||
chr4:139173863
|
G | C | 1 | a0001c0001t0001g0330 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-252+3104C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173863 | ||||||
chr4:139173866
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-252+3101A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173866 | ||||||
chr4:139173896
|
T | A | 1 | a0001c0001t0001g0331 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-252+3071A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173896 | ||||||
chr4:139173936
|
T | C | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.-252+3031A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139173936 | ||||||
chr4:139174067
|
CA | C | 73 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0024others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-252+2899delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174067 | ||||||
chr4:139174105
|
C | T | 2 | a0002c0002t0002g0112a0002c0002t0002g0113 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-252+2862G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174105 | ||||||
chr4:139174182
|
A | G | 1 | a0002c0002t0002g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-252+2785T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174182 | ||||||
chr4:139174194
|
G | A | 89 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 89 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.-252+2773C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174194 | ||||||
chr4:139174206
|
T | TA | 16 | a0001c0001t0001g0080a0001c0001t0001g0099a0001c0001t0001g0100others(13): Show | 16 | HG01496.hp2 HG02055.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-252+2760dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174206 | ||||||
chr4:139174206
|
TA | T | 7 | a0001c0001t0001g0241a0001c0001t0001g0244a0001c0001t0001g0245others(4): Show | 7 | HG00099.hp1 HG01169.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.-252+2760delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174206 | ||||||
chr4:139174207
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-252+2760T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174207 | ||||||
chr4:139174222
|
AG | A | 22 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(19): Show | 22 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.-252+2744delC | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174222 | ||||||
chr4:139174223
|
G | A | 220 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(217): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-252+2744C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174223 | ||||||
chr4:139174243
|
T | A | 10 | a0001c0001t0001g0081a0001c0001t0001g0221a0001c0001t0001g0222others(7): Show | 10 | HG02145.hp2 HG02559.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.-252+2724A>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174243 | ||||||
chr4:139174243
|
TA | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0241others(2): Show | 5 | HG00323.hp1 HG01358.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.-252+2723delT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174243 | ||||||
chr4:139174244
|
A | T | 1 | a0001c0001t0002g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-252+2723T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174244 | ||||||
chr4:139174287
|
T | C | 110 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0191others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-252+2680A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174287 | ||||||
chr4:139174336
|
C | T | 1 | a0001c0001t0002g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-252+2631G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174336 | ||||||
chr4:139174473
|
G | A | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-252+2494C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174473 | ||||||
chr4:139174599
|
C | CA | 110 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0191others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-252+2367dupT | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174599 | ||||||
chr4:139174800
|
T | G | 2 | a0001c0001t0002g0228a0001c0001t0003g0229 | 2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-252+2167A>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174800 | ||||||
chr4:139174922
|
A | G | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG01175.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-252+2045T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174922 | ||||||
chr4:139174997
|
A | G | 1 | a0001c0001t0001g0006 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-252+1970T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174997 | ||||||
chr4:139174998
|
G | A | 1 | a0001c0001t0001g0006 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-252+1969C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174998 | ||||||
chr4:139174999
|
A | T | 1 | a0001c0001t0001g0006 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-252+1968T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139174999 | ||||||
chr4:139175005
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-252+1962T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139175005 | ||||||
chr4:139175033
|
T | C | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(1): Show | 4 | HG01071.hp2 HG01361.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-252+1934A>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139175033 | ||||||
chr4:139175056
|
A | T | 1 | a0001c0001t0002g0109 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-252+1911T>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139175056 | ||||||
chr4:139175066
|
A | G | 2 | a0001c0001t0005g0107a0001c0001t0005g0108 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-252+1901T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139175066 | ||||||
chr4:139175130
|
C | A | 223 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-252+1837G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139175130 | ||||||
chr4:139175151
|
A | G | 1 | a0001c0001t0001g0004 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-252+1816T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139175151 | ||||||
chr4:139175345
|
C | G | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-252+1622G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139175345 | ||||||
chr4:139175594
|
C | G | 1 | a0001c0001t0002g0003 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-252+1373G>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139175594 | ||||||
chr4:139175956
|
A | C | 1 | a0001c0001t0001g0233 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-252+1011T>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139175956 | ||||||
chr4:139176052
|
G | C | 1 | a0001c0001t0001g0232 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-252+915C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176052 | ||||||
chr4:139176054
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-252+913T>C | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176054 | ||||||
chr4:139176081
|
C | T | 1 | a0001c0001t0012g0002 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-252+886G>A | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176081 | ||||||
chr4:139176117
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-252+850C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176117 | ||||||
chr4:139176361
|
G | C | 1 | a0001c0001t0002g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-252+606C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176361 | ||||||
chr4:139176397
|
GC | G | 237 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(234): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.-252+569delG | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176397 | ||||||
chr4:139176405
|
C | A | 1 | a0001c0001t0002g0336 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-252+562G>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176405 | ||||||
chr4:139176621
|
G | A | 1 | a0002c0002t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-252+346C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176621 | ||||||
chr4:139176664
|
G | C | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-252+303C>G | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176664 | ||||||
chr4:139176802
|
G | A | 1 | a0001c0001t0002g0340 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-252+165C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176802 | ||||||
chr4:139176844
|
G | A | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-252+123C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176844 | ||||||
chr4:139176907
|
G | A | 1 | a0001c0001t0002g0342 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-252+60C>T | ELF2 | ENSG00000109381.21 | transcript | ENST00000686138.1 | protein_coding | 1/9 | chr4 | 139176907 |