geneid | 1871 |
---|---|
ensemblid | ENSG00000112242.16 |
hgncid | 3115 |
symbol | E2F3 |
name | E2F transcription factor 3 |
refseq_nuc | NM_001949.5 |
refseq_prot | NP_001940.1 |
ensembl_nuc | ENST00000346618.8 |
ensembl_prot | ENSP00000262904.4 |
mane_status | MANE Select |
chr | chr6 |
start | 20401879 |
end | 20493714 |
strand | + |
ver | v1.2 |
region | chr6:20401879-20493714 |
region5000 | chr6:20396879-20498714 |
regionname0 | E2F3_chr6_20401879_20493714 |
regionname5000 | E2F3_chr6_20396879_20498714 |
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 | 465 | 323 | 89 | 55 | 127 | 11 | 39 | 100 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0002 | 0/0 | 462 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0003 | 0/0 | 465 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0004 | 0/0 | 465 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0005 | 0/0 | 465 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0006 | 0/0 | 465 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
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 | 1398 | 321 | 89 | 54 | 126 | 11 | 39 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
c0002 | 0/0 | 1389 | 4 | 3 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
c0003 | 0/0 | 1398 | 3 | 3 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
c0004 | 0/0 | 1398 | 3 | 3 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
c0005 | 0/0 | 1398 | 2 | 0 | 0 | 1 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
c0006 | 0/0 | 1398 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
c0007 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
c0008 | 0/0 | 1398 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
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 | 3639 | 128 | 48 | 22 | 34 | 6 | 18 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0002 | 1/0 | 3639 | 58 | 2 | 10 | 31 | 5 | 9 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0003 | 0/0 | 3638 | 48 | 5 | 9 | 27 | 1 | 6 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0004 | 0/0 | 3639 | 22 | 21 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0005 | 0/0 | 3639 | 13 | 0 | 3 | 9 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0006 | 0/0 | 3639 | 12 | 0 | 0 | 9 | 0 | 3 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0007 | 0/0 | 3639 | 8 | 2 | 6 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0008 | 0/0 | 3639 | 8 | 1 | 0 | 7 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0009 | 0/0 | 3639 | 7 | 6 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0010 | 0/0 | 3639 | 6 | 4 | 2 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0011 | 0/0 | 3638 | 3 | 0 | 0 | 3 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0012 | 0/0 | 3640 | 2 | 1 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0013 | 0/0 | 3638 | 2 | 0 | 0 | 2 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0014 | 0/0 | 3640 | 2 | 0 | 1 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0015 | 0/0 | 3639 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0016 | 0/0 | 3639 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0017 | 0/0 | 3638 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0018 | 0/0 | 3639 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0019 | 0/0 | 3639 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0020 | 0/0 | 3640 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0021 | 0/0 | 3639 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0022 | 0/0 | 3640 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0023 | 0/0 | 3639 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0024 | 0/0 | 3639 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0025 | 0/1 | 3639 | 1 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0026 | 0/0 | 3639 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0027 | 0/0 | 3639 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0028 | 0/0 | 3640 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0029 | 0/0 | 3639 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0030 | 0/0 | 3639 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
t0031 | 0/0 | 3638 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
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 | 3 | 3 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
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 | 1398 | 321 | 89 | 54 | 126 | 11 | 39 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0007 | 0/0 | 1398 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0008 | 0/0 | 1398 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0002c0002 | 0/0 | 1389 | 4 | 3 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0003c0004 | 0/0 | 1398 | 3 | 3 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0004c0003 | 0/0 | 1398 | 3 | 3 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0005c0005 | 0/0 | 1398 | 2 | 0 | 0 | 1 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0006c0006 | 0/0 | 1398 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5036 | 122 | 44 | 20 | 34 | 6 | 18 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0002 | 1/0 | 5036 | 56 | 2 | 10 | 30 | 4 | 9 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0003 | 0/0 | 5035 | 44 | 2 | 9 | 27 | 1 | 5 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0004 | 0/0 | 5036 | 21 | 20 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0005 | 0/0 | 5036 | 13 | 0 | 3 | 9 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0006 | 0/0 | 5036 | 11 | 0 | 0 | 8 | 0 | 3 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0007 | 0/0 | 5036 | 8 | 2 | 6 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0008 | 0/0 | 5036 | 8 | 1 | 0 | 7 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0009 | 0/0 | 5036 | 6 | 5 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0010 | 0/0 | 5036 | 6 | 4 | 2 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0011 | 0/0 | 5035 | 3 | 0 | 0 | 3 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0012 | 0/0 | 5037 | 2 | 1 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0013 | 0/0 | 5035 | 2 | 0 | 0 | 2 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0014 | 0/0 | 5037 | 2 | 0 | 1 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0015 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0016 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0017 | 0/0 | 5035 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0018 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0019 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0020 | 0/0 | 5037 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0021 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0022 | 0/0 | 5037 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0023 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0024 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0025 | 0/1 | 5036 | 1 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0026 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0027 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0028 | 0/0 | 5037 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0029 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0030 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0001t0031 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0007t0002 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0001c0008t0001 | 0/0 | 5036 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0002c0002t0001 | 0/0 | 5027 | 3 | 2 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0002c0002t0004 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0003c0004t0001 | 0/0 | 5036 | 2 | 2 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0003c0004t0009 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0004c0003t0003 | 0/0 | 5035 | 3 | 3 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0005c0005t0003 | 0/0 | 5035 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0005c0005t0006 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
a0006c0006t0002 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | copy fasta | chr6 | 20396879 | 20498714 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0006g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0007g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0007g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0007g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0007g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0008g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0008g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0008g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0009g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0009g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0009g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0010g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0010g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0010g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0010g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0011g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0011g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0011g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0012g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0012g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0013g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0013g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0014g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0014g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0015g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0016g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0017g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0018g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0019g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0020g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0021g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0022g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0023g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0024g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0025g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0026g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0027g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0028g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0029g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0030g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0001t0031g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0007t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0001c0008t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0002c0002t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0003c0004t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0003c0004t0009g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0004c0003t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0004c0003t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0004c0003t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0005c0005t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0005c0005t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
a0006c0006t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0224 | EUR | GBR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0318 | EUR | GBR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | GBR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00140 | hp2 | a0006 | c0006 | t0002 | g0017 | EUR | GBR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0234 | EUR | FIN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0131 | EUR | FIN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | FIN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0319 | EUR | FIN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00438 | hp2 | a0001 | c0001 | t0017 | g0219 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00544 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00642 | hp2 | a0001 | c0001 | t0010 | g0002 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0304 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01081 | hp1 | a0001 | c0008 | t0001 | g0161 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01081 | hp2 | a0001 | c0001 | t0010 | g0002 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01109 | hp1 | a0001 | c0001 | t0009 | g0104 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01175 | hp1 | a0001 | c0001 | t0007 | g0289 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0294 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0295 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01192 | hp2 | a0001 | c0001 | t0012 | g0291 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01256 | hp2 | a0001 | c0001 | t0007 | g0003 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01258 | hp2 | a0001 | c0001 | t0007 | g0003 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01358 | hp2 | a0001 | c0001 | t0007 | g0137 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | IBS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0300 | EUR | IBS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | IBS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01884 | hp1 | a0001 | c0001 | t0027 | g0309 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01884 | hp2 | a0001 | c0001 | t0009 | g0103 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01975 | hp1 | a0001 | c0001 | t0014 | g0248 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0171 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0045 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02015 | hp1 | a0001 | c0001 | t0008 | g0038 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02040 | hp1 | a0001 | c0001 | t0006 | g0259 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02040 | hp2 | a0001 | c0001 | t0008 | g0153 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02056 | hp1 | a0001 | c0001 | t0008 | g0260 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0186 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02083 | hp1 | a0001 | c0001 | t0008 | g0261 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02129 | hp2 | a0005 | c0005 | t0006 | g0180 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02145 | hp2 | a0001 | c0001 | t0009 | g0110 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0150 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02155 | hp1 | a0001 | c0001 | t0008 | g0182 | EAS | CDX | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CDX | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0321 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0310 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0213 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02451 | hp2 | a0001 | c0001 | t0029 | g0330 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02523 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02572 | hp1 | a0001 | c0001 | t0031 | g0111 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0142 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02615 | hp2 | a0001 | c0001 | t0024 | g0105 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02622 | hp1 | a0004 | c0003 | t0003 | g0147 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0087 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02630 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02647 | hp1 | a0004 | c0003 | t0003 | g0122 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02647 | hp2 | a0001 | c0001 | t0023 | g0145 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02717 | hp2 | a0003 | c0004 | t0009 | g0322 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0076 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0075 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0099 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0082 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0164 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0329 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03209 | hp1 | a0001 | c0001 | t0020 | g0307 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03225 | hp2 | a0001 | c0001 | t0009 | g0323 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0151 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03453 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0217 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03540 | hp1 | a0001 | c0001 | t0026 | g0138 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03579 | hp1 | a0001 | c0001 | t0028 | g0072 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03654 | hp1 | a0001 | c0001 | t0019 | g0220 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0057 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03688 | hp2 | a0001 | c0001 | t0006 | g0269 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0270 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03834 | hp2 | a0001 | c0001 | t0016 | g0237 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03942 | hp1 | a0001 | c0001 | t0015 | g0064 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03942 | hp2 | a0005 | c0005 | t0003 | g0148 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0065 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0268 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18522 | hp1 | a0004 | c0003 | t0003 | g0071 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18940 | hp1 | a0001 | c0001 | t0006 | g0174 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0189 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18962 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0188 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18970 | hp2 | a0001 | c0001 | t0013 | g0223 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18981 | hp2 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18982 | hp1 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18984 | hp2 | a0001 | c0001 | t0021 | g0214 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18992 | hp1 | a0001 | c0001 | t0022 | g0205 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18995 | hp2 | a0001 | c0001 | t0011 | g0287 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18997 | hp1 | a0001 | c0001 | t0030 | g0035 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18999 | hp1 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19002 | hp2 | a0001 | c0001 | t0018 | g0193 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19007 | hp1 | a0001 | c0007 | t0002 | g0233 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19011 | hp2 | a0001 | c0001 | t0011 | g0275 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19030 | hp1 | a0002 | c0002 | t0004 | g0092 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0324 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19054 | hp1 | a0001 | c0001 | t0006 | g0239 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19058 | hp1 | a0001 | c0001 | t0014 | g0024 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19068 | hp2 | a0001 | c0001 | t0011 | g0262 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19070 | hp1 | a0001 | c0001 | t0006 | g0303 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19070 | hp2 | a0001 | c0001 | t0013 | g0226 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19074 | hp1 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0290 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0320 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0314 | AFR | ASW | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ASW | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | GIH | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | GIH | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02109 | hp1 | a0001 | c0001 | t0010 | g0112 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0070 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02559 | hp1 | a0001 | c0001 | t0008 | g0263 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | USA | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0079 | AFR | USA | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | USA | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | USA | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0025 | g0265 | REF | REF | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0160 | REF | REF | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:20402363
|
TCGCCGCC others(2): Show |
T | 1 | a0002 | 4 | HG01255.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.141_149delCGCCGCCG others(1): Show |
p.Ala48_Ala50del | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/7 | 495/5036 | 141/1398 | 47/465 | INFO_REALIGN_3_PRIME | chr6 | 20402363 | |
chr6:20402458
|
A | G | 1 | a0005 | 2 | HG02129.hp2 HG03942.hp2 |
missense_variant | MODERATE | c.226A>G | p.Ser76Gly | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/7 | 580/5036 | 226/1398 | 76/465 | chr6 | 20402458 | ||
chr6:20402579
|
C | T | 1 | a0003 | 3 | HG02630.hp1 HG02717.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.347C>T | p.Pro116Leu | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/7 | 701/5036 | 347/1398 | 116/465 | chr6 | 20402579 | ||
chr6:20490197
|
G | A | 1 | a0006 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1165G>A | p.Asp389Asn | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1519/5036 | 1165/1398 | 389/465 | chr6 | 20490197 | ||
chr6:20490212
|
A | T | 1 | a0004 | 3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1180A>T | p.Met394Leu | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1534/5036 | 1180/1398 | 394/465 | chr6 | 20490212 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:20402505
|
G | T | 1 | a0001c0008 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.273G>T | p.Ala91Ala | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/7 | 627/5036 | 273/1398 | 91/465 | chr6 | 20402505 | ||
chr6:20479911
|
C | T | 1 | a0001c0007 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.459C>T | p.Pro153Pro | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/7 | 813/5036 | 459/1398 | 153/465 | chr6 | 20479911 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:20401946
|
C | T | 1 | a0001c0001t0031 | 1 | HG02572.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-287C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/7 | chr6 | 20401946 | ||||||
chr6:20490562
|
G | T | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 132 | chr6 | 20490562 | |||||
chr6:20490563
|
A | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*133A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 133 | chr6 | 20490563 | |||||
chr6:20490565
|
G | T | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*135G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 135 | chr6 | 20490565 | |||||
chr6:20490575
|
A | T | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 145 | chr6 | 20490575 | |||||
chr6:20490576
|
T | C | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 146 | chr6 | 20490576 | |||||
chr6:20490579
|
T | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*149T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 149 | chr6 | 20490579 | |||||
chr6:20490580
|
A | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*150A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 150 | chr6 | 20490580 | |||||
chr6:20490582
|
T | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*152T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 152 | chr6 | 20490582 | |||||
chr6:20490586
|
T | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*156T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 156 | chr6 | 20490586 | |||||
chr6:20490587
|
T | A | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*157T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 157 | chr6 | 20490587 | |||||
chr6:20490588
|
T | A | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*158T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 158 | chr6 | 20490588 | |||||
chr6:20490589
|
T | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*159T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 159 | chr6 | 20490589 | |||||
chr6:20490590
|
T | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*160T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 160 | chr6 | 20490590 | |||||
chr6:20490592
|
A | T | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 162 | chr6 | 20490592 | |||||
chr6:20490594
|
A | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*164A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 164 | chr6 | 20490594 | |||||
chr6:20490598
|
T | C | 2 | a0001c0001t0015a0001c0001t0016 | 2 | HG03834.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*168T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 168 | chr6 | 20490598 | |||||
chr6:20490598
|
T | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*168T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 168 | chr6 | 20490598 | |||||
chr6:20490599
|
T | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*169T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 169 | chr6 | 20490599 | |||||
chr6:20490600
|
A | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*170A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 170 | chr6 | 20490600 | |||||
chr6:20490602
|
T | C | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*172T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 172 | chr6 | 20490602 | |||||
chr6:20490610
|
T | C | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*180T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 180 | chr6 | 20490610 | |||||
chr6:20490618
|
A | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 188 | chr6 | 20490618 | |||||
chr6:20490619
|
C | A | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*189C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 189 | chr6 | 20490619 | |||||
chr6:20490620
|
G | C | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 190 | chr6 | 20490620 | |||||
chr6:20490623
|
C | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*193C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 193 | chr6 | 20490623 | |||||
chr6:20490628
|
G | C | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*198G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 198 | chr6 | 20490628 | |||||
chr6:20490628
|
G | T | 1 | a0001c0001t0029 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*198G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 198 | chr6 | 20490628 | |||||
chr6:20490629
|
C | T | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*199C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 199 | chr6 | 20490629 | |||||
chr6:20490630
|
A | G | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 200 | chr6 | 20490630 | |||||
chr6:20490632
|
G | T | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*202G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 202 | chr6 | 20490632 | |||||
chr6:20491162
|
C | T | 1 | a0001c0001t0011 | 3 | NA18995.hp2 NA19011.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*732C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 732 | chr6 | 20491162 | |||||
chr6:20491356
|
C | T | 1 | a0001c0001t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*926C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 926 | chr6 | 20491356 | |||||
chr6:20491446
|
G | A | 1 | a0001c0001t0030 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1016G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1016 | chr6 | 20491446 | |||||
chr6:20491552
|
G | A | 1 | a0001c0001t0017 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1122G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1122 | chr6 | 20491552 | |||||
chr6:20491642
|
G | T | 1 | a0001c0001t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1212G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1212 | chr6 | 20491642 | |||||
chr6:20491679
|
A | G | 1 | a0001c0001t0008 | 8 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1249A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1249 | chr6 | 20491679 | |||||
chr6:20491976
|
G | A | 2 | a0001c0001t0009a0003c0004t0009 | 7 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1546G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1546 | chr6 | 20491976 | |||||
chr6:20492029
|
C | G | 1 | a0001c0001t0026 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1599C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1599 | chr6 | 20492029 | |||||
chr6:20492149
|
G | GA | 2 | a0001c0001t0007a0001c0001t0012 | 10 | HG01175.hp1 HG01175.hp2 HG01192.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1731dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1732 | INFO_REALIGN_3_PRIME | chr6 | 20492149 | ||||
chr6:20492176
|
C | G | 2 | a0001c0001t0006a0005c0005t0006 | 12 | HG02040.hp1 HG02129.hp2 HG03654.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1746C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1746 | chr6 | 20492176 | |||||
chr6:20492352
|
C | G | 1 | a0001c0001t0025 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1922C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1922 | chr6 | 20492352 | |||||
chr6:20492764
|
T | C | 36 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(33): Show | 275 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*2334T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2334 | chr6 | 20492764 | |||||
chr6:20492774
|
G | A | 1 | a0001c0001t0010 | 6 | HG00642.hp2 HG01081.hp2 HG02109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2344G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2344 | chr6 | 20492774 | |||||
chr6:20492920
|
T | C | 1 | a0001c0001t0018 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2490T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2490 | chr6 | 20492920 | |||||
chr6:20492982
|
C | T | 1 | a0001c0001t0026 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2552C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2552 | chr6 | 20492982 | |||||
chr6:20493004
|
G | A | 1 | a0001c0001t0019 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2574G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2574 | chr6 | 20493004 | |||||
chr6:20493078
|
C | T | 1 | a0001c0001t0024 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2648C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2648 | chr6 | 20493078 | |||||
chr6:20493230
|
T | C | 7 | a0001c0001t0004a0001c0001t0009a0001c0001t0015others(4): Show | 32 | HG00738.hp1 HG01109.hp1 HG01884.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2800T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2800 | chr6 | 20493230 | |||||
chr6:20493233
|
G | T | 1 | a0001c0001t0023 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2803G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2803 | chr6 | 20493233 | |||||
chr6:20493447
|
G | A | 1 | a0001c0001t0021 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3017G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 3017 | chr6 | 20493447 | |||||
chr6:20493555
|
A | G | 1 | a0001c0001t0013 | 2 | NA18970.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3125A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 3125 | chr6 | 20493555 | |||||
chr6:20493558
|
T | TA | 4 | a0001c0001t0014a0001c0001t0020a0001c0001t0022others(1): Show | 5 | HG01975.hp1 HG03209.hp1 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3137dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 3138 | INFO_REALIGN_3_PRIME | chr6 | 20493558 | ||||
chr6:20493567
|
AC | A | 8 | a0001c0001t0003a0001c0001t0007a0001c0001t0011others(5): Show | 63 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3138delC | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 3138 | chr6 | 20493567 | |||||
chr6:20493568
|
C | A | 3 | a0001c0001t0005a0001c0001t0008a0001c0001t0018 | 22 | HG00544.hp2 HG01975.hp2 HG01978.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3138C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 3138 | chr6 | 20493568 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:20402751
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.393+126T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20402751 | ||||||
chr6:20402843
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0004g0007a0001c0001t0004g0008 | 3 | HG02723.hp2 HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.393+218G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20402843 | ||||||
chr6:20403046
|
G | T | 2 | a0001c0001t0009g0329a0001c0001t0029g0330 | 2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.393+421G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403046 | ||||||
chr6:20403220
|
C | T | 3 | a0001c0001t0001g0326a0001c0001t0003g0327a0001c0001t0003g0328 | 3 | NA18955.hp1 NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.393+595C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403220 | ||||||
chr6:20403253
|
G | A | 1 | a0001c0001t0002g0010 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.393+628G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403253 | ||||||
chr6:20403301
|
C | T | 1 | a0001c0001t0003g0325 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.393+676C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403301 | ||||||
chr6:20403356
|
G | T | 6 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0324others(3): Show | 7 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+731G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403356 | ||||||
chr6:20403547
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.393+922G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403547 | ||||||
chr6:20403582
|
A | C | 1 | a0001c0001t0001g0319 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.393+957A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403582 | ||||||
chr6:20403711
|
C | G | 1 | a0001c0001t0001g0318 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.393+1086C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403711 | ||||||
chr6:20403715
|
C | T | 9 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+1090C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403715 | ||||||
chr6:20403915
|
G | T | 2 | a0001c0001t0001g0308a0001c0001t0020g0307 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.393+1290G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403915 | ||||||
chr6:20404012
|
T | C | 3 | a0001c0001t0001g0012a0001c0001t0004g0001a0001c0001t0004g0013 | 5 | HG01361.hp2 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+1387T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404012 | ||||||
chr6:20404048
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.393+1423G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404048 | ||||||
chr6:20404114
|
A | AG | 86 | a0001c0001t0001g0011a0001c0001t0001g0228a0001c0001t0001g0235others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.393+1494dupG | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20404114 | |||||
chr6:20404189
|
T | C | 248 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(245): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.393+1564T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404189 | ||||||
chr6:20404251
|
C | T | 1 | a0004c0003t0003g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.393+1626C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404251 | ||||||
chr6:20404651
|
G | C | 1 | a0005c0005t0003g0148 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.393+2026G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404651 | ||||||
chr6:20404714
|
AG | A | 54 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(51): Show | 54 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.393+2090delG | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404714 | ||||||
chr6:20404762
|
C | A | 1 | a0001c0001t0001g0015 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.393+2137C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404762 | ||||||
chr6:20404788
|
G | A | 225 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(222): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.393+2163G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404788 | ||||||
chr6:20405035
|
A | C | 11 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(8): Show | 11 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.393+2410A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405035 | ||||||
chr6:20405308
|
A | G | 186 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(183): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.393+2683A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405308 | ||||||
chr6:20405344
|
A | AT | 11 | a0001c0001t0001g0093a0001c0001t0001g0146a0001c0001t0001g0218others(8): Show | 11 | HG00099.hp1 HG00438.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.393+2739dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20405344 | |||||
chr6:20405344
|
AT | A | 30 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(27): Show | 30 | HG00738.hp1 HG01167.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.393+2739delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20405344 | |||||
chr6:20405344
|
ATT | A | 176 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(173): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.393+2738_393+2739d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20405344 | |||||
chr6:20405415
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.393+2790C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405415 | ||||||
chr6:20405563
|
G | A | 3 | a0001c0001t0009g0329a0001c0001t0010g0112a0001c0001t0029g0330 | 3 | HG02109.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.393+2938G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405563 | ||||||
chr6:20405574
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.393+2949C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405574 | ||||||
chr6:20405606
|
C | T | 1 | a0001c0001t0031g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.393+2981C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405606 | ||||||
chr6:20405640
|
T | A | 7 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(4): Show | 7 | HG00741.hp1 HG02486.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+3015T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405640 | ||||||
chr6:20405916
|
T | C | 2 | a0001c0001t0004g0123a0001c0001t0004g0124 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393+3291T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405916 | ||||||
chr6:20406043
|
TA | T | 4 | a0001c0001t0001g0073a0001c0001t0010g0070a0001c0001t0028g0072others(1): Show | 4 | HG00741.hp1 HG02486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+3421delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20406043 | |||||
chr6:20406066
|
G | C | 1 | a0001c0001t0001g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.393+3441G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406066 | ||||||
chr6:20406196
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.393+3571G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406196 | ||||||
chr6:20406470
|
T | C | 2 | a0001c0001t0002g0225a0001c0001t0013g0226 | 2 | NA19068.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.393+3845T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406470 | ||||||
chr6:20406502
|
G | A | 3 | a0001c0001t0009g0329a0001c0001t0010g0112a0001c0001t0029g0330 | 3 | HG02109.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.393+3877G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406502 | ||||||
chr6:20406708
|
T | A | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+4083T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406708 | ||||||
chr6:20406796
|
T | C | 1 | a0001c0001t0031g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.393+4171T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406796 | ||||||
chr6:20406831
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.393+4206T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406831 | ||||||
chr6:20406834
|
T | C | 1 | a0001c0001t0009g0323 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.393+4209T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406834 | ||||||
chr6:20406910
|
G | C | 2 | a0001c0001t0004g0123a0001c0001t0004g0124 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393+4285G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406910 | ||||||
chr6:20407051
|
G | A | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+4426G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407051 | ||||||
chr6:20407264
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.393+4639C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407264 | ||||||
chr6:20407278
|
G | C | 1 | a0001c0001t0003g0152 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.393+4653G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407278 | ||||||
chr6:20407310
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.393+4685C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407310 | ||||||
chr6:20407393
|
A | G | 17 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0080others(14): Show | 18 | HG00642.hp2 HG01081.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.393+4768A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407393 | ||||||
chr6:20407435
|
A | G | 2 | a0001c0001t0004g0123a0001c0001t0004g0124 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393+4810A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407435 | ||||||
chr6:20407589
|
T | C | 1 | a0001c0001t0004g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.393+4964T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407589 | ||||||
chr6:20407680
|
T | C | 3 | a0001c0001t0001g0218a0001c0001t0002g0154a0001c0001t0008g0153 | 3 | HG00438.hp1 HG02040.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.393+5055T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407680 | ||||||
chr6:20407691
|
G | A | 6 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0324others(3): Show | 7 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+5066G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407691 | ||||||
chr6:20408254
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.393+5629A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408254 | ||||||
chr6:20408330
|
AGT | A | 54 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(51): Show | 54 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.393+5707_393+5708d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20408330 | |||||
chr6:20408360
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0004g0001a0001c0001t0004g0013 | 5 | HG01361.hp2 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+5735C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408360 | ||||||
chr6:20408498
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.393+5873T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408498 | ||||||
chr6:20408570
|
A | G | 1 | a0003c0004t0009g0322 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.393+5945A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408570 | ||||||
chr6:20408656
|
A | G | 2 | a0001c0001t0001g0308a0001c0001t0020g0307 | 2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.393+6031A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408656 | ||||||
chr6:20408688
|
T | C | 60 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(57): Show | 60 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.393+6063T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408688 | ||||||
chr6:20408899
|
T | C | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+6274T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408899 | ||||||
chr6:20408912
|
G | T | 1 | a0001c0001t0009g0110 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.393+6287G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408912 | ||||||
chr6:20409003
|
A | C | 1 | a0001c0001t0003g0217 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.393+6378A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409003 | ||||||
chr6:20409201
|
C | T | 1 | a0001c0001t0010g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.393+6576C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409201 | ||||||
chr6:20409275
|
G | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0067a0001c0001t0001g0068others(7): Show | 12 | HG00741.hp1 HG01361.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+6650G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409275 | ||||||
chr6:20409531
|
G | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0308a0001c0001t0020g0307 | 3 | HG02965.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.393+6906G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409531 | ||||||
chr6:20409544
|
A | C | 210 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(207): Show | 213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.393+6919A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409544 | ||||||
chr6:20409551
|
T | G | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0007t0002g0233 | 3 | NA18950.hp2 NA18995.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.393+6926T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409551 | ||||||
chr6:20409703
|
C | G | 6 | a0001c0001t0004g0320a0001c0001t0004g0321a0001c0001t0004g0324others(3): Show | 7 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+7078C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409703 | ||||||
chr6:20409806
|
G | C | 1 | a0001c0001t0004g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.393+7181G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409806 | ||||||
chr6:20409920
|
C | T | 1 | a0001c0001t0009g0110 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.393+7295C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409920 | ||||||
chr6:20410046
|
G | C | 1 | a0006c0006t0002g0017 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.393+7421G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410046 | ||||||
chr6:20410094
|
T | C | 3 | a0001c0001t0001g0012a0001c0001t0004g0001a0001c0001t0004g0013 | 5 | HG01361.hp2 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+7469T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410094 | ||||||
chr6:20410371
|
C | T | 3 | a0001c0001t0001g0218a0001c0001t0002g0154a0001c0001t0008g0153 | 3 | HG00438.hp1 HG02040.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.393+7746C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410371 | ||||||
chr6:20410537
|
A | T | 2 | a0001c0001t0001g0062a0006c0006t0002g0017 | 2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.393+7912A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410537 | ||||||
chr6:20410578
|
C | G | 1 | a0001c0001t0021g0214 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.393+7953C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410578 | ||||||
chr6:20410584
|
G | A | 1 | a0001c0001t0004g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.393+7959G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410584 | ||||||
chr6:20410736
|
A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 6 | HG00140.hp2 HG02683.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+8111A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410736 | ||||||
chr6:20410776
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0004g0001a0001c0001t0004g0013 | 5 | HG01361.hp2 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+8151G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410776 | ||||||
chr6:20410939
|
T | G | 2 | a0001c0001t0001g0078a0001c0001t0007g0079 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.393+8314T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410939 | ||||||
chr6:20411079
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.393+8454T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411079 | ||||||
chr6:20411274
|
T | C | 1 | a0001c0001t0001g0326 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.393+8649T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411274 | ||||||
chr6:20411333
|
C | T | 4 | a0002c0002t0001g0075a0002c0002t0001g0076a0002c0002t0001g0077others(1): Show | 4 | HG01255.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+8708C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411333 | ||||||
chr6:20411444
|
C | T | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+8819C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411444 | ||||||
chr6:20411455
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.393+8830G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411455 | ||||||
chr6:20411482
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.393+8857G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411482 | ||||||
chr6:20411524
|
C | T | 4 | a0002c0002t0001g0075a0002c0002t0001g0076a0002c0002t0001g0077others(1): Show | 4 | HG01255.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+8899C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411524 | ||||||
chr6:20411579
|
C | T | 1 | a0001c0001t0004g0321 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.393+8954C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411579 | ||||||
chr6:20411676
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0059a0001c0001t0002g0058 | 3 | HG03017.hp2 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.393+9051C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411676 | ||||||
chr6:20411708
|
C | T | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+9083C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411708 | ||||||
chr6:20411905
|
G | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0319others(2): Show | 5 | HG00323.hp2 HG01106.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+9280G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411905 | ||||||
chr6:20412019
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.393+9394A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412019 | ||||||
chr6:20412109
|
T | G | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+9484T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412109 | ||||||
chr6:20412321
|
C | T | 3 | a0001c0001t0009g0329a0001c0001t0010g0112a0001c0001t0029g0330 | 3 | HG02109.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.393+9696C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412321 | ||||||
chr6:20412541
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.393+9916C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412541 | ||||||
chr6:20412616
|
T | G | 3 | a0001c0001t0001g0127a0001c0001t0004g0125a0001c0001t0004g0128 | 3 | HG02896.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.393+9991T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412616 | ||||||
chr6:20412908
|
G | A | 4 | a0001c0001t0004g0324a0001c0001t0009g0323a0003c0004t0001g0005others(1): Show | 5 | HG02630.hp1 HG02717.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+10283G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412908 | ||||||
chr6:20413139
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0007g0079a0001c0001t0012g0213 | 3 | HG01109.hp2 HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.393+10514A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413139 | ||||||
chr6:20413286
|
C | CAG | 31 | a0001c0001t0001g0009a0001c0001t0001g0095a0001c0001t0001g0096others(28): Show | 31 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.393+10663_393+1066 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20413286 | |||||
chr6:20413354
|
T | G | 1 | a0001c0001t0009g0323 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.393+10729T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413354 | ||||||
chr6:20413369
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.393+10744C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413369 | ||||||
chr6:20413490
|
A | G | 227 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(224): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.393+10865A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413490 | ||||||
chr6:20413586
|
G | A | 1 | a0001c0001t0002g0157 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.393+10961G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413586 | ||||||
chr6:20413586
|
G | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(70): Show | 74 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.393+10961G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413586 | ||||||
chr6:20413645
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.393+11020G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413645 | ||||||
chr6:20413655
|
G | A | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 8 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.393+11030G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413655 | ||||||
chr6:20413855
|
C | T | 4 | a0002c0002t0001g0075a0002c0002t0001g0076a0002c0002t0001g0077others(1): Show | 4 | HG01255.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+11230C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413855 | ||||||
chr6:20413870
|
G | T | 4 | a0001c0001t0001g0293a0001c0001t0001g0306a0001c0001t0007g0294others(1): Show | 4 | HG01175.hp2 HG01192.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+11245G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413870 | ||||||
chr6:20414008
|
A | G | 3 | a0001c0001t0009g0329a0001c0001t0010g0112a0001c0001t0029g0330 | 3 | HG02109.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.393+11383A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414008 | ||||||
chr6:20414058
|
A | G | 2 | a0001c0001t0004g0320a0001c0001t0004g0321 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.393+11433A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414058 | ||||||
chr6:20414071
|
G | C | 1 | a0001c0001t0002g0302 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.393+11446G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414071 | ||||||
chr6:20414109
|
T | C | 60 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.393+11484T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414109 | ||||||
chr6:20414223
|
A | G | 2 | a0001c0001t0001g0292a0001c0001t0012g0291 | 2 | HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.393+11598A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414223 | ||||||
chr6:20414455
|
A | G | 127 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(124): Show | 129 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.393+11830A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414455 | ||||||
chr6:20414479
|
A | G | 1 | a0001c0001t0005g0290 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.393+11854A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414479 | ||||||
chr6:20414497
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.393+11872A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414497 | ||||||
chr6:20414567
|
C | T | 79 | a0001c0001t0001g0011a0001c0001t0001g0215a0001c0001t0001g0218others(76): Show | 79 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.393+11942C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414567 | ||||||
chr6:20414589
|
A | G | 124 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(121): Show | 126 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.393+11964A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414589 | ||||||
chr6:20414663
|
T | C | 2 | a0001c0001t0004g0123a0001c0001t0004g0124 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393+12038T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414663 | ||||||
chr6:20414774
|
C | T | 70 | a0001c0001t0001g0016a0001c0001t0001g0155a0001c0001t0001g0175others(67): Show | 71 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.393+12149C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414774 | ||||||
chr6:20414822
|
A | G | 212 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(209): Show | 215 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.393+12197A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414822 | ||||||
chr6:20414939
|
A | G | 1 | a0001c0001t0006g0168 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.393+12314A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414939 | ||||||
chr6:20414973
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.393+12348G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414973 | ||||||
chr6:20414992
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0007g0289 | 2 | HG01175.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.393+12367A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414992 | ||||||
chr6:20415019
|
C | T | 1 | a0001c0001t0004g0001 | 3 | HG03471.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.393+12394C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415019 | ||||||
chr6:20415053
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.393+12428A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415053 | ||||||
chr6:20415074
|
G | A | 2 | a0001c0001t0002g0172a0001c0001t0002g0173 | 2 | HG00408.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.393+12449G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415074 | ||||||
chr6:20415395
|
C | T | 32 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(29): Show | 34 | HG00741.hp1 HG01255.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.393+12770C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415395 | ||||||
chr6:20415405
|
A | G | 7 | a0001c0001t0004g0087a0001c0001t0004g0088a0001c0001t0004g0109others(4): Show | 7 | HG01255.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.393+12780A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415405 | ||||||
chr6:20415463
|
A | C | 21 | a0001c0001t0001g0012a0001c0001t0001g0073a0001c0001t0001g0081others(18): Show | 21 | HG00741.hp1 HG01361.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.393+12838A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415463 | ||||||
chr6:20415637
|
T | C | 1 | a0001c0001t0004g0123 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.393+13012T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415637 | ||||||
chr6:20415665
|
G | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+13040G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415665 | ||||||
chr6:20415695
|
A | G | 4 | a0001c0001t0001g0299a0001c0001t0003g0297a0001c0001t0003g0298others(1): Show | 4 | HG00140.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+13070A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415695 | ||||||
chr6:20415883
|
A | G | 5 | a0001c0001t0001g0108a0001c0001t0004g0087a0001c0001t0004g0088others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+13258A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415883 | ||||||
chr6:20416084
|
G | T | 1 | a0001c0001t0009g0323 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.393+13459G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416084 | ||||||
chr6:20416119
|
C | T | 111 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0053others(108): Show | 115 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.393+13494C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416119 | ||||||
chr6:20416182
|
G | C | 1 | a0001c0001t0010g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.393+13557G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416182 | ||||||
chr6:20416264
|
A | G | 1 | a0001c0001t0010g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.393+13639A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416264 | ||||||
chr6:20416289
|
G | C | 1 | a0003c0004t0001g0005 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.393+13664G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416289 | ||||||
chr6:20416341
|
G | T | 127 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0016others(124): Show | 131 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.393+13716G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416341 | ||||||
chr6:20416638
|
C | T | 1 | a0001c0001t0004g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.393+14013C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416638 | ||||||
chr6:20416670
|
C | T | 8 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(5): Show | 8 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+14045C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416670 | ||||||
chr6:20416913
|
G | A | 2 | a0001c0001t0026g0138a0003c0004t0009g0322 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+14288G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416913 | ||||||
chr6:20416961
|
C | T | 68 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0040others(65): Show | 69 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.393+14336C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416961 | ||||||
chr6:20417067
|
C | A | 8 | a0001c0001t0002g0191a0001c0001t0003g0327a0001c0001t0005g0187others(5): Show | 8 | NA18943.hp1 NA18950.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+14442C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20417067 | ||||||
chr6:20417368
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.393+14743C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20417368 | ||||||
chr6:20417588
|
TA | T | 10 | a0001c0001t0001g0037a0001c0001t0001g0288a0001c0001t0002g0231others(7): Show | 10 | HG01069.hp2 HG02280.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.393+14978delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20417588 | |||||
chr6:20417588
|
TAA | T | 27 | a0001c0001t0001g0016a0001c0001t0001g0060a0001c0001t0001g0061others(24): Show | 30 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.393+14977_393+1497 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20417588 | |||||
chr6:20417588
|
TAAAA | T | 8 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(5): Show | 8 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+14975_393+1497 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20417588 | |||||
chr6:20417745
|
G | T | 81 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0028others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.393+15120G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20417745 | ||||||
chr6:20417755
|
C | T | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.393+15130C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20417755 | ||||||
chr6:20417930
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.393+15305C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20417930 | ||||||
chr6:20418098
|
C | T | 52 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0040others(49): Show | 53 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.393+15473C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20418098 | ||||||
chr6:20418172
|
C | G | 52 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0040others(49): Show | 53 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.393+15547C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20418172 | ||||||
chr6:20418177
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0073a0001c0001t0001g0080others(10): Show | 13 | HG00741.hp1 HG01496.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.393+15552C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20418177 | ||||||
chr6:20418487
|
G | A | 7 | a0001c0001t0002g0023a0001c0001t0002g0025a0001c0001t0002g0026others(4): Show | 7 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+15862G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20418487 | ||||||
chr6:20418678
|
AATGATCC others(1): Show |
A | 12 | a0001c0001t0001g0009a0001c0001t0001g0073a0001c0001t0001g0126others(9): Show | 12 | HG00741.hp1 HG01496.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.393+16056_393+1606 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20418678 | |||||
chr6:20418749
|
A | G | 2 | a0001c0001t0026g0138a0003c0004t0009g0322 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+16124A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20418749 | ||||||
chr6:20418840
|
C | CT | 90 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0053others(87): Show | 91 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.393+16226dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20418840 | |||||
chr6:20419078
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.393+16453C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419078 | ||||||
chr6:20419104
|
T | C | 6 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+16479T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419104 | ||||||
chr6:20419270
|
A | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0053others(88): Show | 92 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+16645A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419270 | ||||||
chr6:20419334
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.393+16709G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419334 | ||||||
chr6:20419428
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.393+16803C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419428 | ||||||
chr6:20419529
|
T | TTTTA | 4 | a0001c0001t0001g0318a0001c0001t0006g0268a0001c0001t0006g0269others(1): Show | 4 | HG00099.hp2 HG02615.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+16929_393+1693 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20419529 | |||||
chr6:20419529
|
TTTTA | T | 60 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0061others(57): Show | 63 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(60): Show |
intron_variant | MODIFIER | c.393+16929_393+1693 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20419529 | |||||
chr6:20419554
|
T | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0028others(15): Show | 18 | HG00741.hp1 HG01496.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.393+16929T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419554 | ||||||
chr6:20419554
|
TTTAC | T | 83 | a0001c0001t0001g0016a0001c0001t0001g0053a0001c0001t0001g0054others(80): Show | 84 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.393+16949_393+1695 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20419554 | |||||
chr6:20419558
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0002g0173a0001c0001t0003g0207others(3): Show | 6 | HG02074.hp1 HG03017.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+16933C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419558 | ||||||
chr6:20419695
|
AGCTGGAC others(11): Show |
A | 8 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+17073_393+1709 others(22): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20419695 | |||||
chr6:20419720
|
A | G | 151 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0016others(148): Show | 155 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.393+17095A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419720 | ||||||
chr6:20419831
|
G | C | 2 | a0001c0001t0001g0293a0001c0001t0001g0306 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.393+17206G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419831 | ||||||
chr6:20419892
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+17267G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419892 | ||||||
chr6:20420011
|
G | A | 147 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0053others(144): Show | 151 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.393+17386G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420011 | ||||||
chr6:20420197
|
T | C | 5 | a0001c0001t0001g0108a0001c0001t0004g0087a0001c0001t0004g0088others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+17572T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420197 | ||||||
chr6:20420438
|
G | GGT | 6 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0184others(3): Show | 6 | HG01109.hp1 HG01261.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+17838_393+1783 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20420438 | |||||
chr6:20420438
|
GGT | G | 133 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0053others(130): Show | 134 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.393+17838_393+1783 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20420438 | |||||
chr6:20420438
|
GGTGT | G | 2 | a0001c0001t0001g0073a0003c0004t0001g0005 | 3 | HG00741.hp1 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.393+17836_393+1783 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20420438 | |||||
chr6:20420559
|
C | T | 52 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0040others(49): Show | 53 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.393+17934C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420559 | ||||||
chr6:20420775
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0078 | 3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+18150T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420775 | ||||||
chr6:20420803
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393+18178C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420803 | ||||||
chr6:20420843
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.393+18218T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420843 | ||||||
chr6:20420975
|
A | C | 16 | a0001c0001t0001g0054a0001c0001t0001g0204a0001c0001t0001g0206others(13): Show | 16 | NA18612.hp1 NA18950.hp2 NA18955.hp1 others(13): Show |
intron_variant | MODIFIER | c.393+18350A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420975 | ||||||
chr6:20421039
|
G | A | 1 | a0004c0003t0003g0122 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.393+18414G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421039 | ||||||
chr6:20421122
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+18497C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421122 | ||||||
chr6:20421322
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.393+18697A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421322 | ||||||
chr6:20421724
|
C | T | 1 | a0001c0001t0004g0128 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.393+19099C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421724 | ||||||
chr6:20421776
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.393+19151G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421776 | ||||||
chr6:20421787
|
C | T | 5 | a0001c0001t0001g0108a0001c0001t0004g0087a0001c0001t0004g0088others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+19162C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421787 | ||||||
chr6:20421879
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0007g0295 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.393+19254G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421879 | ||||||
chr6:20421880
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393+19255C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421880 | ||||||
chr6:20421881
|
G | A | 2 | a0001c0001t0001g0311a0001c0001t0004g0310 | 2 | HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.393+19256G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421881 | ||||||
chr6:20421918
|
T | C | 2 | a0001c0001t0026g0138a0003c0004t0009g0322 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+19293T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421918 | ||||||
chr6:20422348
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393+19723T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422348 | ||||||
chr6:20422448
|
C | G | 2 | a0001c0001t0026g0138a0003c0004t0009g0322 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+19823C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422448 | ||||||
chr6:20422544
|
G | C | 2 | a0001c0001t0026g0138a0003c0004t0009g0322 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+19919G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422544 | ||||||
chr6:20422546
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.393+19921C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422546 | ||||||
chr6:20422580
|
C | G | 2 | a0001c0001t0026g0138a0003c0004t0009g0322 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+19955C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422580 | ||||||
chr6:20422595
|
G | A | 148 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0053others(145): Show | 152 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.393+19970G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422595 | ||||||
chr6:20422608
|
T | G | 150 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0053others(147): Show | 154 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.393+19983T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422608 | ||||||
chr6:20422638
|
C | T | 8 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0001t0001g0250others(5): Show | 8 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(5): Show |
intron_variant | MODIFIER | c.393+20013C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422638 | ||||||
chr6:20422645
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.393+20020G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422645 | ||||||
chr6:20422716
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(1): Show | 4 | HG02965.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+20091G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422716 | ||||||
chr6:20422768
|
A | G | 6 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(3): Show | 6 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+20143A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422768 | ||||||
chr6:20422900
|
C | T | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0002g0170 | 3 | HG01978.hp2 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.393+20275C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422900 | ||||||
chr6:20422996
|
G | A | 148 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0053others(145): Show | 152 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.393+20371G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422996 | ||||||
chr6:20423027
|
C | T | 2 | a0001c0001t0026g0138a0003c0004t0009g0322 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+20402C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423027 | ||||||
chr6:20423029
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.393+20404A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423029 | ||||||
chr6:20423108
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.393+20483C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423108 | ||||||
chr6:20423385
|
CT | C | 50 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0040others(47): Show | 51 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.393+20762delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20423385 | |||||
chr6:20423463
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.393+20838T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423463 | ||||||
chr6:20423545
|
A | T | 3 | a0001c0001t0002g0036a0001c0001t0002g0229a0001c0001t0002g0230 | 3 | NA18953.hp1 NA18957.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.393+20920A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423545 | ||||||
chr6:20423574
|
G | A | 1 | a0003c0004t0001g0005 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.393+20949G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423574 | ||||||
chr6:20423690
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.393+21065C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423690 | ||||||
chr6:20423691
|
G | A | 2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+21066G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423691 | ||||||
chr6:20423713
|
C | T | 50 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0040others(47): Show | 51 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.393+21088C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423713 | ||||||
chr6:20423764
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.393+21139C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423764 | ||||||
chr6:20423765
|
G | A | 6 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+21140G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423765 | ||||||
chr6:20424064
|
A | G | 2 | a0001c0001t0004g0007a0001c0001t0004g0008 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.393+21439A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424064 | ||||||
chr6:20424210
|
G | GGT | 67 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0028others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.393+21624_393+2162 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
G | GGTATGT | 11 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0090others(8): Show | 11 | HG01168.hp1 HG01496.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
G | GGTATGTG others(1): Show |
12 | a0001c0001t0001g0108a0001c0001t0001g0308a0001c0001t0003g0151others(9): Show | 12 | HG01255.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
G | GGTATGTG others(3): Show |
22 | a0001c0001t0001g0009a0001c0001t0001g0062a0001c0001t0001g0119others(19): Show | 22 | HG00438.hp1 HG00597.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
G | GGTATGTG others(5): Show |
43 | a0001c0001t0001g0054a0001c0001t0001g0081a0001c0001t0001g0117others(40): Show | 45 | HG00140.hp1 HG00544.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(16): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
G | GGTATGTG others(7): Show |
34 | a0001c0001t0001g0016a0001c0001t0001g0121a0001c0001t0001g0204others(31): Show | 35 | HG00408.hp2 HG01109.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(18): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
G | GGTATGTG others(9): Show |
12 | a0001c0001t0001g0282a0001c0001t0001g0284a0001c0001t0001g0285others(9): Show | 12 | HG02129.hp1 HG02145.hp2 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
G | GGTATGTG others(11): Show |
2 | a0001c0001t0002g0194a0001c0001t0003g0207 | 2 | HG00597.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.393+21587_393+2158 others(22): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
G | GGTGT | 18 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0039others(15): Show | 18 | HG00738.hp1 HG01167.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.393+21622_393+2162 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
G | GGTGTGT | 38 | a0001c0001t0001g0037a0001c0001t0001g0114a0001c0001t0001g0134others(35): Show | 39 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.393+21620_393+2162 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
G | GGTGTGTG others(1): Show |
5 | a0001c0001t0001g0018a0001c0001t0001g0221a0001c0001t0001g0267others(2): Show | 5 | HG00741.hp2 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+21618_393+2162 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0053 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.393+21616_393+2162 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
GGT | G | 5 | a0001c0001t0001g0080a0001c0001t0001g0102a0001c0001t0002g0056others(2): Show | 6 | HG02572.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+21624_393+2162 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
GGTGT | G | 12 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(9): Show | 12 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+21622_393+2162 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424210
|
GGTGTGT | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+21620_393+2162 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | |||||
chr6:20424212
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.393+21587T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424212 | ||||||
chr6:20424213
|
G | A | 7 | a0001c0001t0001g0073a0001c0001t0001g0118a0001c0001t0001g0120others(4): Show | 7 | HG00741.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+21588G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424213 | ||||||
chr6:20424215
|
G | A | 2 | a0001c0001t0001g0080a0003c0004t0001g0005 | 3 | HG02630.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.393+21590G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424215 | ||||||
chr6:20424217
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0078 | 3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+21592G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424217 | ||||||
chr6:20424219
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+21594G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424219 | ||||||
chr6:20424250
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.393+21625_393+2162 others(15): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424250 | ||||||
chr6:20424250
|
T | TGTGTGTG others(8): Show |
3 | a0001c0001t0001g0120a0001c0001t0001g0272a0001c0001t0002g0195 | 3 | HG02055.hp1 HG03927.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.393+21625_393+2162 others(19): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424250 | ||||||
chr6:20424331
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.393+21706C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424331 | ||||||
chr6:20424383
|
ATG | A | 162 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(159): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.393+21784_393+2178 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424383 | |||||
chr6:20424383
|
ATGTG | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(9): Show | 12 | HG00280.hp1 HG01516.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+21782_393+2178 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424383 | |||||
chr6:20424383
|
ATGTGTG | A | 143 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0053others(140): Show | 147 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.393+21780_393+2178 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424383 | |||||
chr6:20424383
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0002g0157 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.393+21776_393+2178 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424383 | |||||
chr6:20424508
|
T | A | 3 | a0001c0001t0001g0282a0001c0001t0001g0284a0001c0001t0002g0283 | 3 | NA18990.hp1 NA19009.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.393+21883T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424508 | ||||||
chr6:20424588
|
C | T | 50 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0040others(47): Show | 51 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.393+21963C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424588 | ||||||
chr6:20424590
|
T | C | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+21965T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424590 | ||||||
chr6:20424592
|
CT | C | 148 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0053others(145): Show | 152 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.393+21977delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424592 | |||||
chr6:20424613
|
A | G | 4 | a0001c0001t0001g0141a0001c0001t0001g0319a0001c0001t0002g0234others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+21988A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424613 | ||||||
chr6:20424657
|
T | C | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+22032T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424657 | ||||||
chr6:20424694
|
G | GA | 21 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(18): Show | 21 | HG01255.hp1 HG02055.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.393+22077dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424694 | |||||
chr6:20424833
|
G | C | 153 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0053others(150): Show | 157 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.393+22208G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424833 | ||||||
chr6:20424887
|
A | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0009g0099 | 3 | HG02559.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.393+22262A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424887 | ||||||
chr6:20424889
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.393+22264G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424889 | ||||||
chr6:20424906
|
A | G | 1 | a0001c0001t0002g0247 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.393+22281A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424906 | ||||||
chr6:20424917
|
A | G | 8 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(5): Show | 8 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+22292A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424917 | ||||||
chr6:20424986
|
C | T | 1 | a0001c0001t0025g0265 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.393+22361C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424986 | ||||||
chr6:20425227
|
G | A | 204 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0018others(201): Show | 209 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.393+22602G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425227 | ||||||
chr6:20425365
|
G | A | 147 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0053others(144): Show | 151 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.393+22740G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425365 | ||||||
chr6:20425387
|
C | CT | 29 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0061others(26): Show | 29 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.393+22781dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20425387 | |||||
chr6:20425447
|
G | A | 1 | a0001c0001t0016g0237 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.393+22822G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425447 | ||||||
chr6:20425510
|
G | T | 314 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(311): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.393+22885G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425510 | ||||||
chr6:20425593
|
C | T | 2 | a0001c0001t0009g0110a0003c0004t0009g0322 | 2 | HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.393+22968C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425593 | ||||||
chr6:20425725
|
C | G | 5 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0306others(2): Show | 5 | HG01071.hp2 HG01192.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+23100C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425725 | ||||||
chr6:20425836
|
A | G | 2 | a0001c0001t0003g0253a0001c0001t0007g0294 | 2 | HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.393+23211A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425836 | ||||||
chr6:20425940
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.393+23315T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425940 | ||||||
chr6:20426093
|
A | C | 2 | a0001c0001t0002g0191a0001c0001t0018g0193 | 2 | NA18990.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.393+23468A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426093 | ||||||
chr6:20426504
|
G | A | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+23879G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426504 | ||||||
chr6:20426524
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.393+23899G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426524 | ||||||
chr6:20426547
|
CT | C | 261 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(258): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.393+23924delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20426547 | |||||
chr6:20426647
|
G | A | 268 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(265): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.393+24022G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426647 | ||||||
chr6:20426757
|
T | A | 1 | a0001c0001t0001g0053 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.393+24132T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426757 | ||||||
chr6:20426898
|
T | A | 1 | a0001c0001t0001g0285 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.393+24273T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426898 | ||||||
chr6:20426969
|
A | G | 2 | a0001c0001t0003g0066a0001c0001t0003g0255 | 2 | NA18948.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.393+24344A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426969 | ||||||
chr6:20426998
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.393+24373C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426998 | ||||||
chr6:20427148
|
C | A | 1 | a0003c0004t0001g0005 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.393+24523C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427148 | ||||||
chr6:20427158
|
T | G | 1 | a0001c0001t0002g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.393+24533T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427158 | ||||||
chr6:20427238
|
A | G | 273 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(270): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.393+24613A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427238 | ||||||
chr6:20427260
|
C | G | 267 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(264): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.393+24635C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427260 | ||||||
chr6:20427308
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.393+24683A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427308 | ||||||
chr6:20427477
|
G | A | 2 | a0001c0001t0010g0112a0001c0001t0028g0072 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.393+24852G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427477 | ||||||
chr6:20427604
|
T | G | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+24979T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427604 | ||||||
chr6:20427669
|
C | T | 88 | a0001c0001t0001g0016a0001c0001t0001g0053a0001c0001t0001g0054others(85): Show | 89 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.393+25044C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427669 | ||||||
chr6:20427763
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.393+25138A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427763 | ||||||
chr6:20427851
|
G | A | 1 | a0001c0001t0010g0002 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.393+25226G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427851 | ||||||
chr6:20427953
|
C | T | 236 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(233): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.393+25328C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427953 | ||||||
chr6:20427965
|
A | G | 1 | a0001c0001t0007g0079 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.393+25340A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427965 | ||||||
chr6:20428201
|
C | A | 86 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0027others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.393+25576C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428201 | ||||||
chr6:20428228
|
T | A | 5 | a0001c0001t0004g0109a0002c0002t0001g0075a0002c0002t0001g0076others(2): Show | 5 | HG01255.hp1 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+25603T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428228 | ||||||
chr6:20428290
|
C | A | 1 | a0001c0001t0004g0128 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.393+25665C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428290 | ||||||
chr6:20428354
|
G | C | 52 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0039others(49): Show | 53 | HG00544.hp2 HG00741.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.393+25729G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428354 | ||||||
chr6:20428411
|
C | T | 22 | a0001c0001t0001g0020a0001c0001t0001g0080a0001c0001t0001g0095others(19): Show | 22 | HG01255.hp2 HG02896.hp2 HG02965.hp1 others(19): Show |
intron_variant | MODIFIER | c.393+25786C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428411 | ||||||
chr6:20428471
|
C | T | 1 | a0001c0001t0014g0248 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.393+25846C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428471 | ||||||
chr6:20428550
|
G | A | 269 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(266): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.393+25925G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428550 | ||||||
chr6:20428686
|
G | A | 6 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+26061G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428686 | ||||||
chr6:20429171
|
G | A | 1 | a0001c0001t0004g0320 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.393+26546G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429171 | ||||||
chr6:20429288
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.393+26663G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429288 | ||||||
chr6:20429369
|
G | T | 36 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0067others(33): Show | 39 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.393+26744G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429369 | ||||||
chr6:20429452
|
C | G | 11 | a0001c0001t0001g0117a0001c0001t0004g0001a0001c0001t0004g0128others(8): Show | 13 | HG02109.hp1 HG02451.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.393+26827C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429452 | ||||||
chr6:20429573
|
C | G | 1 | a0001c0001t0001g0097 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.393+26948C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429573 | ||||||
chr6:20429573
|
C | T | 2 | a0001c0001t0003g0253a0001c0001t0007g0294 | 2 | HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.393+26948C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429573 | ||||||
chr6:20429623
|
A | G | 1 | a0001c0001t0006g0239 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.393+26998A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429623 | ||||||
chr6:20429654
|
A | G | 6 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+27029A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429654 | ||||||
chr6:20429813
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.393+27188T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429813 | ||||||
chr6:20430084
|
CT | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+27460delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430084 | ||||||
chr6:20430373
|
C | T | 23 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(20): Show | 23 | HG01255.hp1 HG02109.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.393+27748C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430373 | ||||||
chr6:20430374
|
G | A | 1 | a0001c0001t0019g0220 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.393+27749G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430374 | ||||||
chr6:20430558
|
T | G | 2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+27933T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430558 | ||||||
chr6:20430842
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.393+28217T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430842 | ||||||
chr6:20430964
|
G | T | 1 | a0001c0001t0002g0247 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.393+28339G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430964 | ||||||
chr6:20431192
|
G | A | 2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+28567G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431192 | ||||||
chr6:20431208
|
C | T | 1 | a0004c0003t0003g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.393+28583C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431208 | ||||||
chr6:20431397
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0078 | 3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+28772G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431397 | ||||||
chr6:20431423
|
C | T | 18 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(15): Show | 18 | HG01255.hp1 HG02258.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.393+28798C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431423 | ||||||
chr6:20431424
|
G | A | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+28799G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431424 | ||||||
chr6:20431465
|
T | G | 1 | a0001c0001t0001g0256 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.393+28840T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431465 | ||||||
chr6:20431510
|
G | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0056 | 2 | HG00642.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.393+28885G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431510 | ||||||
chr6:20431543
|
C | A | 1 | a0001c0001t0005g0019 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.393+28918C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431543 | ||||||
chr6:20431558
|
G | A | 8 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+28933G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431558 | ||||||
chr6:20431565
|
G | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.393+28940G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431565 | ||||||
chr6:20431834
|
C | T | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+29209C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431834 | ||||||
chr6:20431876
|
A | T | 8 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0098others(5): Show | 8 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+29251A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431876 | ||||||
chr6:20432005
|
T | C | 232 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.393+29380T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432005 | ||||||
chr6:20432081
|
A | T | 1 | a0001c0001t0009g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.393+29456A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432081 | ||||||
chr6:20432253
|
A | C | 25 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(22): Show | 27 | HG01255.hp1 HG02109.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+29628A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432253 | ||||||
chr6:20432253
|
A | G | 241 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.393+29628A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432253 | ||||||
chr6:20432273
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.393+29648G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432273 | ||||||
chr6:20432313
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0005g0019 | 2 | NA19010.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.393+29688G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432313 | ||||||
chr6:20432317
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.393+29692G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432317 | ||||||
chr6:20432349
|
C | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.393+29724C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432349 | ||||||
chr6:20432375
|
A | G | 4 | a0001c0001t0001g0047a0001c0001t0001g0215a0001c0001t0001g0222others(1): Show | 4 | HG02083.hp2 NA18954.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+29750A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432375 | ||||||
chr6:20432496
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.393+29871G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432496 | ||||||
chr6:20432498
|
G | A | 23 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(20): Show | 23 | HG01255.hp1 HG02109.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.393+29873G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432498 | ||||||
chr6:20432621
|
T | A | 1 | a0001c0001t0004g0013 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.393+29996T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432621 | ||||||
chr6:20432683
|
G | A | 1 | a0001c0001t0003g0051 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.393+30058G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432683 | ||||||
chr6:20432745
|
C | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(6): Show | 9 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+30120C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432745 | ||||||
chr6:20432759
|
G | A | 6 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+30134G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432759 | ||||||
chr6:20432762
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.393+30137G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432762 | ||||||
chr6:20432846
|
A | G | 290 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(287): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.393+30221A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432846 | ||||||
chr6:20433066
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.393+30441A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433066 | ||||||
chr6:20433153
|
T | A | 15 | a0001c0001t0001g0117a0001c0001t0004g0013a0001c0001t0004g0109others(12): Show | 15 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.393+30528T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433153 | ||||||
chr6:20433406
|
C | G | 1 | a0001c0001t0007g0289 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.393+30781C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433406 | ||||||
chr6:20433617
|
G | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+30992G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433617 | ||||||
chr6:20433646
|
CAGA | C | 8 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+31026_393+3102 others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20433646 | |||||
chr6:20433736
|
A | C | 15 | a0001c0001t0001g0054a0001c0001t0001g0204a0001c0001t0001g0206others(12): Show | 15 | NA18612.hp1 NA18950.hp2 NA18955.hp1 others(12): Show |
intron_variant | MODIFIER | c.393+31111A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433736 | ||||||
chr6:20433835
|
C | T | 8 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(5): Show | 8 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+31210C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433835 | ||||||
chr6:20433935
|
T | C | 1 | a0004c0003t0003g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.393+31310T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433935 | ||||||
chr6:20434162
|
T | G | 1 | a0001c0001t0003g0328 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.393+31537T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434162 | ||||||
chr6:20434344
|
G | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0078 | 3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+31719G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434344 | ||||||
chr6:20434636
|
T | C | 16 | a0001c0001t0001g0098a0001c0001t0001g0117a0001c0001t0004g0013others(13): Show | 16 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.393+32011T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434636 | ||||||
chr6:20434727
|
C | A | 6 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+32102C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434727 | ||||||
chr6:20434732
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+32107C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434732 | ||||||
chr6:20434888
|
C | T | 1 | a0001c0001t0012g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.393+32263C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434888 | ||||||
chr6:20435025
|
T | G | 1 | a0001c0001t0001g0037 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.393+32400T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435025 | ||||||
chr6:20435073
|
AGAATATT others(4): Show |
A | 2 | a0001c0001t0004g0007a0001c0001t0004g0008 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.393+32450_393+3246 others(15): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20435073 | |||||
chr6:20435083
|
A | T | 1 | a0004c0003t0003g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.393+32458A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435083 | ||||||
chr6:20435090
|
G | C | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+32465G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435090 | ||||||
chr6:20435189
|
C | G | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.393+32564C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435189 | ||||||
chr6:20435322
|
A | G | 1 | a0001c0001t0003g0280 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.393+32697A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435322 | ||||||
chr6:20435371
|
C | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.393+32746C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435371 | ||||||
chr6:20435441
|
A | G | 1 | a0002c0002t0001g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.393+32816A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435441 | ||||||
chr6:20435623
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.393+32998C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435623 | ||||||
chr6:20435974
|
C | CT | 7 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0159others(4): Show | 7 | HG02145.hp2 HG02717.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.393+33371dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20435974 | |||||
chr6:20435974
|
CT | C | 27 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0098others(24): Show | 30 | HG00642.hp2 HG01081.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.393+33371delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20435974 | |||||
chr6:20435974
|
CTTTTTTT others(4): Show |
C | 227 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.393+33361_393+3337 others(15): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20435974 | |||||
chr6:20436006
|
A | G | 1 | a0001c0001t0028g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.393+33381A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436006 | ||||||
chr6:20436022
|
C | G | 9 | a0001c0001t0001g0098a0001c0001t0001g0117a0001c0001t0004g0128others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+33397C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436022 | ||||||
chr6:20436043
|
T | C | 252 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(249): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.393+33418T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436043 | ||||||
chr6:20436137
|
C | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(6): Show | 9 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+33512C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436137 | ||||||
chr6:20436208
|
T | C | 2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+33583T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436208 | ||||||
chr6:20436260
|
C | T | 7 | a0001c0001t0004g0013a0001c0001t0004g0109a0002c0002t0001g0075others(4): Show | 7 | HG01255.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.393+33635C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436260 | ||||||
chr6:20436304
|
G | C | 8 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(5): Show | 8 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+33679G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436304 | ||||||
chr6:20436307
|
A | G | 4 | a0001c0001t0001g0288a0001c0001t0002g0231a0001c0001t0002g0232others(1): Show | 4 | NA18950.hp2 NA18995.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+33682A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436307 | ||||||
chr6:20436421
|
A | C | 227 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.393+33796A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436421 | ||||||
chr6:20436452
|
A | AAC | 10 | a0001c0001t0001g0093a0001c0001t0001g0129a0001c0001t0001g0238others(7): Show | 10 | HG01175.hp1 HG02055.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.393+33853_393+3385 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | |||||
chr6:20436452
|
A | AACAC | 3 | a0001c0001t0001g0020a0001c0001t0005g0019a0001c0001t0007g0294 | 3 | HG01175.hp2 NA19010.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.393+33851_393+3385 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | |||||
chr6:20436452
|
A | AACACACA others(5): Show |
1 | a0002c0002t0001g0076 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.393+33843_393+3385 others(16): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | |||||
chr6:20436452
|
A | AACACACA others(7): Show |
5 | a0001c0001t0004g0013a0001c0001t0004g0109a0002c0002t0001g0077others(2): Show | 5 | HG01255.hp1 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+33841_393+3385 others(18): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | |||||
chr6:20436452
|
A | AACACACA others(9): Show |
1 | a0002c0002t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.393+33839_393+3385 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | |||||
chr6:20436452
|
AAC | A | 22 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0061others(19): Show | 23 | HG01243.hp2 HG01358.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.393+33853_393+3385 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | |||||
chr6:20436452
|
AACAC | A | 14 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0001g0086others(11): Show | 14 | HG00741.hp1 HG02109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.393+33851_393+3385 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | |||||
chr6:20436464
|
CACACACA others(9): Show |
C | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.393+33841_393+3385 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436464 | |||||
chr6:20436476
|
C | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0078 | 3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+33851C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436476 | ||||||
chr6:20436476
|
CACAG | C | 2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+33853_393+3385 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436476 | |||||
chr6:20436476
|
CACAGAGA others(3): Show |
C | 1 | a0001c0001t0010g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.393+33853_393+3386 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436476 | |||||
chr6:20436478
|
C | G | 35 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0061others(32): Show | 37 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.393+33853C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436478 | ||||||
chr6:20436478
|
CAG | C | 5 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0118others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+33869_393+3387 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436478 | |||||
chr6:20436478
|
CAGAGAG | C | 5 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(2): Show | 5 | HG02965.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+33865_393+3387 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436478 | |||||
chr6:20436478
|
CAGAGAGA others(3): Show |
C | 1 | a0001c0001t0028g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.393+33861_393+3387 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436478 | |||||
chr6:20436480
|
G | C | 112 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.393+33855G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436480 | ||||||
chr6:20436482
|
G | C | 11 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(8): Show | 11 | HG01167.hp2 HG01255.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.393+33857G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436482 | ||||||
chr6:20436484
|
G | C | 1 | a0001c0001t0029g0330 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.393+33859G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436484 | ||||||
chr6:20436486
|
G | C | 6 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(3): Show | 6 | HG02451.hp2 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+33861G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436486 | ||||||
chr6:20436488
|
G | C | 6 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(3): Show | 6 | HG02451.hp2 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+33863G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436488 | ||||||
chr6:20436494
|
G | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0126a0001c0001t0001g0136others(9): Show | 13 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.393+33869G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436494 | ||||||
chr6:20436494
|
GAA | G | 127 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0037others(124): Show | 129 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.393+33873_393+3387 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436494 | |||||
chr6:20436496
|
A | G | 100 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.393+33871A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436496 | ||||||
chr6:20436508
|
C | T | 15 | a0001c0001t0001g0117a0001c0001t0004g0013a0001c0001t0004g0109others(12): Show | 15 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.393+33883C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436508 | ||||||
chr6:20436615
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.393+33990C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436615 | ||||||
chr6:20436623
|
C | T | 8 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+33998C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436623 | ||||||
chr6:20436718
|
C | T | 15 | a0001c0001t0001g0117a0001c0001t0004g0013a0001c0001t0004g0109others(12): Show | 15 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.393+34093C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436718 | ||||||
chr6:20436823
|
C | T | 9 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(6): Show | 9 | HG01069.hp2 HG01261.hp2 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+34198C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436823 | ||||||
chr6:20436956
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0004g0001a0001c0001t0024g0105 | 5 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+34331C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436956 | ||||||
chr6:20437182
|
T | A | 2 | a0001c0001t0003g0055a0001c0001t0003g0198 | 2 | HG01943.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.393+34557T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20437182 | ||||||
chr6:20437383
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.393+34758G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20437383 | ||||||
chr6:20437480
|
CT | C | 14 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(11): Show | 14 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.393+34865delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20437480 | |||||
chr6:20437534
|
T | C | 85 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0062others(82): Show | 86 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.393+34909T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20437534 | ||||||
chr6:20437726
|
G | A | 7 | a0001c0001t0004g0013a0001c0001t0004g0109a0002c0002t0001g0075others(4): Show | 7 | HG01255.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.393+35101G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20437726 | ||||||
chr6:20437898
|
T | A | 15 | a0001c0001t0001g0117a0001c0001t0004g0013a0001c0001t0004g0109others(12): Show | 15 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.393+35273T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20437898 | ||||||
chr6:20438110
|
A | AC | 15 | a0001c0001t0001g0117a0001c0001t0004g0013a0001c0001t0004g0109others(12): Show | 15 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.393+35485_393+3548 others(5): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438110 | ||||||
chr6:20438190
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0004g0001a0001c0001t0024g0105 | 5 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+35565C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438190 | ||||||
chr6:20438201
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0267 | 2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.393+35576G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438201 | ||||||
chr6:20438412
|
C | G | 1 | a0001c0001t0003g0270 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.393+35787C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438412 | ||||||
chr6:20438430
|
C | T | 283 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(280): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.393+35805C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438430 | ||||||
chr6:20438549
|
G | A | 1 | a0001c0001t0007g0289 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.393+35924G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438549 | ||||||
chr6:20438615
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.393+35990C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438615 | ||||||
chr6:20438635
|
C | G | 5 | a0001c0001t0001g0108a0001c0001t0004g0087a0001c0001t0004g0088others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+36010C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438635 | ||||||
chr6:20438731
|
A | G | 5 | a0001c0001t0004g0123a0001c0001t0004g0124a0001c0001t0009g0110others(2): Show | 5 | HG02145.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+36106A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438731 | ||||||
chr6:20439049
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393+36424A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439049 | ||||||
chr6:20439097
|
A | G | 14 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0068others(11): Show | 14 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.393+36472A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439097 | ||||||
chr6:20439201
|
AT | A | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG01167.hp2 HG02145.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+36582delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20439201 | |||||
chr6:20439226
|
T | C | 8 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+36601T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439226 | ||||||
chr6:20439229
|
A | G | 4 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(1): Show | 4 | HG02965.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+36604A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439229 | ||||||
chr6:20439266
|
A | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0126a0001c0001t0001g0136others(3): Show | 6 | HG01496.hp1 HG02258.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+36641A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439266 | ||||||
chr6:20439278
|
T | G | 3 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0003g0254 | 3 | HG02074.hp2 HG02080.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.393+36653T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439278 | ||||||
chr6:20439334
|
C | T | 9 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(6): Show | 9 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+36709C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439334 | ||||||
chr6:20439397
|
G | A | 57 | a0001c0001t0001g0018a0001c0001t0001g0037a0001c0001t0001g0039others(54): Show | 58 | HG00544.hp2 HG00741.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.393+36772G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439397 | ||||||
chr6:20439592
|
C | G | 1 | a0001c0001t0001g0053 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.393+36967C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439592 | ||||||
chr6:20439711
|
T | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+37086T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439711 | ||||||
chr6:20439907
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.393+37282A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439907 | ||||||
chr6:20439922
|
A | G | 1 | a0001c0001t0004g0324 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.393+37297A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439922 | ||||||
chr6:20439951
|
C | T | 1 | a0001c0001t0003g0305 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.393+37326C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439951 | ||||||
chr6:20439981
|
G | A | 2 | a0001c0001t0003g0199a0001c0001t0003g0200 | 2 | NA18953.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.393+37356G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439981 | ||||||
chr6:20439998
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.393+37373C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439998 | ||||||
chr6:20440071
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0158a0001c0001t0002g0159 | 3 | NA18968.hp2 NA19062.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.393+37446C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20440071 | ||||||
chr6:20440303
|
T | C | 2 | a0001c0001t0004g0123a0001c0001t0004g0124 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393+37678T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20440303 | ||||||
chr6:20440352
|
A | G | 8 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+37727A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20440352 | ||||||
chr6:20440404
|
G | A | 1 | a0004c0003t0003g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.393+37779G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20440404 | ||||||
chr6:20440602
|
G | T | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+37977G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20440602 | ||||||
chr6:20441112
|
A | G | 1 | a0001c0001t0004g0013 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.393+38487A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441112 | ||||||
chr6:20441315
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.394-38531T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441315 | ||||||
chr6:20441441
|
T | G | 3 | a0001c0001t0002g0139a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG02602.hp1 NA18980.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.394-38405T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441441 | ||||||
chr6:20441541
|
C | T | 1 | a0001c0001t0003g0328 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.394-38305C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441541 | ||||||
chr6:20441570
|
T | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0326 | 2 | NA18955.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.394-38276T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441570 | ||||||
chr6:20441571
|
G | GTGTTTT | 7 | a0001c0001t0003g0217a0001c0001t0007g0003a0001c0001t0007g0079others(4): Show | 8 | HG01175.hp1 HG01192.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-38261_394-3825 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20441571 | |||||
chr6:20441725
|
A | AT | 9 | a0001c0001t0001g0084a0001c0001t0001g0326a0001c0001t0002g0010others(6): Show | 9 | HG01175.hp1 HG02074.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-38099dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20441725 | |||||
chr6:20441725
|
AT | A | 146 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(143): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.394-38099delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20441725 | |||||
chr6:20441730
|
T | A | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-38116T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441730 | ||||||
chr6:20441735
|
T | A | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-38111T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441735 | ||||||
chr6:20441759
|
C | G | 284 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.394-38087C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441759 | ||||||
chr6:20441830
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0068others(11): Show | 14 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-38016C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441830 | ||||||
chr6:20441857
|
C | T | 227 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(224): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.394-37989C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441857 | ||||||
chr6:20441997
|
C | CT | 25 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0068others(22): Show | 26 | HG01496.hp1 HG02258.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-37836dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20441997 | |||||
chr6:20441997
|
C | CTT | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(6): Show | 9 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-37837_394-3783 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20441997 | |||||
chr6:20442077
|
C | A | 231 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(228): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.394-37769C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442077 | ||||||
chr6:20442078
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-37768G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442078 | ||||||
chr6:20442083
|
T | G | 2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-37763T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442083 | ||||||
chr6:20442123
|
C | T | 177 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.394-37723C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442123 | ||||||
chr6:20442259
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.394-37587C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442259 | ||||||
chr6:20442599
|
T | C | 3 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0279 | 3 | NA18953.hp2 NA18971.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.394-37247T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442599 | ||||||
chr6:20442623
|
A | G | 237 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.394-37223A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442623 | ||||||
chr6:20442693
|
G | A | 1 | a0001c0001t0006g0052 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.394-37153G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442693 | ||||||
chr6:20442798
|
C | T | 1 | a0001c0001t0031g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.394-37048C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442798 | ||||||
chr6:20442867
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.394-36979G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442867 | ||||||
chr6:20442920
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-36926A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442920 | ||||||
chr6:20442967
|
C | CA | 282 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(279): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.394-36866dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20442967 | |||||
chr6:20442980
|
A | T | 2 | a0004c0003t0003g0071a0004c0003t0003g0122 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-36866A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442980 | ||||||
chr6:20442993
|
T | G | 1 | a0001c0001t0004g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.394-36853T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442993 | ||||||
chr6:20443295
|
A | C | 2 | a0001c0001t0004g0013a0001c0001t0026g0138 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.394-36551A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443295 | ||||||
chr6:20443319
|
CAA | C | 53 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0037others(50): Show | 54 | HG00544.hp2 HG00741.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.394-36524_394-3652 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20443319 | |||||
chr6:20443347
|
C | T | 6 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-36499C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443347 | ||||||
chr6:20443451
|
T | C | 34 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0061others(31): Show | 35 | HG00741.hp1 HG01243.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.394-36395T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443451 | ||||||
chr6:20443602
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.394-36244G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443602 | ||||||
chr6:20443693
|
T | C | 1 | a0004c0003t0003g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-36153T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443693 | ||||||
chr6:20443798
|
A | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0068others(11): Show | 14 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-36048A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443798 | ||||||
chr6:20443951
|
C | G | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(6): Show | 9 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-35895C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443951 | ||||||
chr6:20444176
|
G | A | 237 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.394-35670G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444176 | ||||||
chr6:20444193
|
A | T | 2 | a0001c0001t0010g0112a0001c0001t0028g0072 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.394-35653A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444193 | ||||||
chr6:20444211
|
G | A | 3 | a0001c0001t0001g0238a0005c0005t0003g0148a0005c0005t0006g0180 | 3 | HG02129.hp2 HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.394-35635G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444211 | ||||||
chr6:20444273
|
A | T | 273 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.394-35573A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444273 | ||||||
chr6:20444287
|
A | G | 239 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(236): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.394-35559A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444287 | ||||||
chr6:20444513
|
C | T | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(2): Show | 5 | HG02486.hp1 HG03516.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-35333C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444513 | ||||||
chr6:20444694
|
C | A | 14 | a0001c0001t0001g0117a0001c0001t0004g0109a0001c0001t0004g0128others(11): Show | 14 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-35152C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444694 | ||||||
chr6:20444756
|
AT | A | 41 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(38): Show | 44 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.394-35084delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20444756 | |||||
chr6:20445172
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-34674T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445172 | ||||||
chr6:20445247
|
C | CT | 12 | a0001c0001t0001g0117a0001c0001t0004g0001a0001c0001t0004g0128others(9): Show | 14 | HG02109.hp1 HG02451.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-34587dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20445247 | |||||
chr6:20445247
|
C | CTTT | 14 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(11): Show | 15 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.394-34589_394-3458 others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20445247 | |||||
chr6:20445455
|
G | T | 1 | a0001c0001t0002g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.394-34391G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445455 | ||||||
chr6:20445479
|
C | T | 1 | a0004c0003t0003g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.394-34367C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445479 | ||||||
chr6:20445622
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.394-34224G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445622 | ||||||
chr6:20445641
|
G | A | 16 | a0001c0001t0001g0117a0001c0001t0004g0001a0001c0001t0004g0109others(13): Show | 18 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.394-34205G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445641 | ||||||
chr6:20445741
|
A | G | 14 | a0001c0001t0001g0117a0001c0001t0004g0109a0001c0001t0004g0128others(11): Show | 14 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-34105A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445741 | ||||||
chr6:20445918
|
G | C | 12 | a0001c0001t0001g0054a0001c0001t0001g0271a0001c0001t0001g0282others(9): Show | 12 | NA18950.hp2 NA18955.hp1 NA18957.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-33928G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445918 | ||||||
chr6:20446215
|
T | C | 4 | a0001c0001t0004g0123a0001c0001t0004g0124a0001c0001t0009g0110others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-33631T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446215 | ||||||
chr6:20446405
|
A | G | 2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-33441A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446405 | ||||||
chr6:20446470
|
T | C | 1 | a0001c0001t0001g0215 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.394-33376T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446470 | ||||||
chr6:20446503
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0001g0264 | 2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.394-33343A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446503 | ||||||
chr6:20446795
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.394-33051G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446795 | ||||||
chr6:20446802
|
A | T | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-33044A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446802 | ||||||
chr6:20446803
|
G | T | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-33043G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446803 | ||||||
chr6:20446827
|
A | G | 2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-33019A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446827 | ||||||
chr6:20447017
|
C | A | 1 | a0001c0001t0001g0006 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.394-32829C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447017 | ||||||
chr6:20447062
|
A | G | 325 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(322): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.394-32784A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447062 | ||||||
chr6:20447069
|
G | A | 10 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(7): Show | 11 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.394-32777G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447069 | ||||||
chr6:20447119
|
G | C | 2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-32727G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447119 | ||||||
chr6:20447158
|
G | A | 6 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-32688G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447158 | ||||||
chr6:20447268
|
T | G | 1 | a0001c0001t0004g0013 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.394-32578T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447268 | ||||||
chr6:20447304
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.394-32542G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447304 | ||||||
chr6:20447322
|
A | ATG | 3 | a0001c0001t0003g0152a0001c0001t0003g0270a0001c0001t0030g0035 | 3 | HG03704.hp1 NA18997.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.394-32510_394-3250 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20447322 | |||||
chr6:20447373
|
G | C | 2 | a0004c0003t0003g0071a0004c0003t0003g0122 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-32473G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447373 | ||||||
chr6:20447541
|
C | CT | 16 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(13): Show | 17 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.394-32293dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20447541 | |||||
chr6:20447541
|
C | CTT | 6 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0118others(3): Show | 6 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-32294_394-3229 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20447541 | |||||
chr6:20447554
|
A | T | 1 | a0001c0001t0030g0035 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.394-32292A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447554 | ||||||
chr6:20447632
|
G | A | 289 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(286): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.394-32214G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447632 | ||||||
chr6:20447996
|
G | A | 1 | a0003c0004t0001g0005 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.394-31850G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447996 | ||||||
chr6:20448053
|
C | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-31793C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20448053 | ||||||
chr6:20448386
|
T | C | 2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-31460T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20448386 | ||||||
chr6:20448464
|
T | TAC | 6 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0176others(3): Show | 6 | HG02055.hp1 HG02486.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-31364_394-3136 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20448464 | |||||
chr6:20448678
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.394-31168C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20448678 | ||||||
chr6:20448927
|
A | T | 1 | a0001c0001t0003g0144 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.394-30919A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20448927 | ||||||
chr6:20449012
|
T | C | 1 | a0001c0001t0001g0267 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.394-30834T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449012 | ||||||
chr6:20449084
|
C | T | 2 | a0001c0001t0010g0112a0001c0001t0028g0072 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.394-30762C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449084 | ||||||
chr6:20449375
|
C | T | 1 | a0001c0001t0005g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.394-30471C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449375 | ||||||
chr6:20449438
|
C | T | 8 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(5): Show | 8 | HG00741.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-30408C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449438 | ||||||
chr6:20449673
|
G | A | 87 | a0001c0001t0001g0016a0001c0001t0001g0053a0001c0001t0001g0054others(84): Show | 88 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.394-30173G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449673 | ||||||
chr6:20449731
|
T | C | 12 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(9): Show | 13 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-30115T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449731 | ||||||
chr6:20449800
|
C | G | 3 | a0001c0001t0004g0001a0001c0001t0024g0105a0001c0001t0028g0072 | 5 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-30046C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449800 | ||||||
chr6:20449883
|
G | A | 1 | a0001c0008t0001g0161 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.394-29963G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449883 | ||||||
chr6:20449891
|
G | A | 1 | a0001c0001t0006g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.394-29955G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449891 | ||||||
chr6:20449959
|
T | C | 2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-29887T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449959 | ||||||
chr6:20449960
|
T | TATGAGAT others(2): Show |
2 | a0001c0001t0004g0001a0001c0001t0024g0105 | 4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-29886_394-2988 others(13): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449960 | ||||||
chr6:20449985
|
A | G | 296 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(293): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.394-29861A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449985 | ||||||
chr6:20450090
|
A | C | 1 | a0001c0001t0010g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.394-29756A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450090 | ||||||
chr6:20450120
|
C | T | 1 | a0001c0001t0004g0013 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.394-29726C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450120 | ||||||
chr6:20450350
|
G | C | 3 | a0001c0001t0002g0036a0001c0001t0002g0229a0001c0001t0002g0230 | 3 | NA18953.hp1 NA18957.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.394-29496G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450350 | ||||||
chr6:20450438
|
T | A | 4 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(1): Show | 4 | HG02965.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-29408T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450438 | ||||||
chr6:20450461
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(1): Show | 4 | HG02965.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-29385T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450461 | ||||||
chr6:20450640
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.394-29206T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450640 | ||||||
chr6:20450751
|
A | G | 2 | a0001c0001t0005g0189a0001c0001t0005g0190 | 2 | NA18943.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.394-29095A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450751 | ||||||
chr6:20451231
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.394-28615G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20451231 | ||||||
chr6:20451290
|
T | A | 283 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(280): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.394-28556T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20451290 | ||||||
chr6:20451335
|
A | G | 1 | a0001c0001t0003g0152 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.394-28511A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20451335 | ||||||
chr6:20451559
|
C | T | 8 | a0001c0001t0008g0004a0001c0001t0008g0038a0001c0001t0008g0153others(5): Show | 9 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-28287C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20451559 | ||||||
chr6:20452041
|
G | A | 1 | a0001c0001t0019g0220 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.394-27805G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452041 | ||||||
chr6:20452260
|
G | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0319a0001c0001t0014g0248 | 3 | HG00323.hp2 HG01106.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.394-27586G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452260 | ||||||
chr6:20452309
|
C | A | 2 | a0004c0003t0003g0071a0004c0003t0003g0122 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-27537C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452309 | ||||||
chr6:20452467
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0129 | 2 | HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.394-27379C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452467 | ||||||
chr6:20452504
|
T | C | 290 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(287): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.394-27342T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452504 | ||||||
chr6:20452878
|
C | T | 1 | a0003c0004t0001g0005 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.394-26968C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452878 | ||||||
chr6:20452991
|
TTTTG | T | 273 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(270): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.394-26827_394-2682 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20452991 | |||||
chr6:20452991
|
TTTTGTTT others(1): Show |
T | 17 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(14): Show | 20 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.394-26831_394-2682 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20452991 | |||||
chr6:20452997
|
T | C | 11 | a0001c0001t0003g0066a0001c0001t0003g0246a0001c0001t0003g0255others(8): Show | 12 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-26849T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452997 | ||||||
chr6:20452999
|
G | T | 11 | a0001c0001t0003g0066a0001c0001t0003g0246a0001c0001t0003g0255others(8): Show | 12 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-26847G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452999 | ||||||
chr6:20453432
|
GGA | G | 12 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(9): Show | 14 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-26413_394-2641 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453432 | ||||||
chr6:20453435
|
A | T | 12 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(9): Show | 14 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-26411A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453435 | ||||||
chr6:20453436
|
A | T | 12 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0073others(9): Show | 14 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-26410A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453436 | ||||||
chr6:20453492
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0004g0128a0001c0001t0004g0320others(1): Show | 4 | HG02965.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-26354G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453492 | ||||||
chr6:20453601
|
G | A | 1 | a0001c0001t0010g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.394-26245G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453601 | ||||||
chr6:20453602
|
A | G | 1 | a0001c0001t0002g0033 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.394-26244A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453602 | ||||||
chr6:20453608
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.394-26238C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453608 | ||||||
chr6:20453649
|
C | T | 1 | a0003c0004t0001g0005 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.394-26197C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453649 | ||||||
chr6:20453854
|
T | C | 3 | a0001c0001t0003g0094a0001c0001t0010g0002a0001c0001t0010g0082 | 4 | HG00642.hp2 HG01081.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-25992T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453854 | ||||||
chr6:20454143
|
AACAGGAG others(21): Show |
A | 1 | a0001c0001t0001g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.394-25702_394-2567 others(32): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454143 | ||||||
chr6:20454233
|
T | C | 5 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0156others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-25613T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454233 | ||||||
chr6:20454369
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.394-25477C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454369 | ||||||
chr6:20454543
|
G | C | 5 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-25303G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454543 | ||||||
chr6:20454637
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.394-25209A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454637 | ||||||
chr6:20454653
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.394-25193T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454653 | ||||||
chr6:20454779
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.394-25067C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454779 | ||||||
chr6:20454861
|
G | A | 3 | a0001c0001t0001g0313a0001c0001t0004g0314a0001c0001t0027g0309 | 3 | HG01884.hp1 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.394-24985G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454861 | ||||||
chr6:20454921
|
A | G | 1 | a0001c0001t0003g0286 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.394-24925A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454921 | ||||||
chr6:20454981
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.394-24865A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454981 | ||||||
chr6:20454993
|
T | C | 1 | a0004c0003t0003g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-24853T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454993 | ||||||
chr6:20455049
|
G | A | 291 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(288): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.394-24797G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455049 | ||||||
chr6:20455052
|
C | T | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24794C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455052 | ||||||
chr6:20455333
|
C | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0054others(86): Show | 90 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.394-24513C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455333 | ||||||
chr6:20455574
|
A | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24272A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455574 | ||||||
chr6:20455675
|
G | T | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24171G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455675 | ||||||
chr6:20455676
|
G | T | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24170G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455676 | ||||||
chr6:20455677
|
C | T | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24169C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455677 | ||||||
chr6:20455679
|
C | T | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24167C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455679 | ||||||
chr6:20455680
|
T | TC | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24166_394-2416 others(5): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455680 | ||||||
chr6:20455681
|
G | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24165G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455681 | ||||||
chr6:20455682
|
T | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24164T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455682 | ||||||
chr6:20455685
|
T | A | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24161T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455685 | ||||||
chr6:20455686
|
T | G | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24160T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455686 | ||||||
chr6:20455852
|
C | G | 2 | a0001c0001t0003g0253a0001c0001t0007g0294 | 2 | HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.394-23994C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455852 | ||||||
chr6:20456179
|
G | A | 3 | a0001c0001t0003g0094a0001c0001t0010g0002a0001c0001t0010g0082 | 4 | HG00642.hp2 HG01081.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-23667G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456179 | ||||||
chr6:20456278
|
A | G | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-23568A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456278 | ||||||
chr6:20456313
|
TA | T | 11 | a0001c0001t0001g0235a0001c0001t0002g0026a0001c0001t0002g0132others(8): Show | 11 | HG00323.hp1 HG01169.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.394-23517delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20456313 | |||||
chr6:20456460
|
G | A | 87 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0062others(84): Show | 88 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.394-23386G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456460 | ||||||
chr6:20456547
|
G | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.394-23299G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456547 | ||||||
chr6:20456641
|
C | A | 1 | a0001c0001t0030g0035 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.394-23205C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456641 | ||||||
chr6:20456671
|
T | C | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-23175T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456671 | ||||||
chr6:20456696
|
T | G | 2 | a0001c0001t0003g0253a0001c0001t0007g0294 | 2 | HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.394-23150T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456696 | ||||||
chr6:20456869
|
A | C | 2 | a0001c0001t0003g0253a0001c0001t0007g0294 | 2 | HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.394-22977A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456869 | ||||||
chr6:20457241
|
C | A | 1 | a0001c0001t0003g0325 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.394-22605C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457241 | ||||||
chr6:20457261
|
G | A | 1 | a0001c0001t0003g0246 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.394-22585G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457261 | ||||||
chr6:20457268
|
AG | A | 3 | a0001c0001t0012g0213a0001c0001t0015g0064a0001c0001t0016g0237 | 3 | HG02451.hp1 HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-22576delG | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20457268 | |||||
chr6:20457292
|
G | A | 2 | a0001c0001t0002g0185a0001c0001t0002g0302 | 2 | HG02523.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.394-22554G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457292 | ||||||
chr6:20457295
|
C | G | 3 | a0001c0001t0001g0293a0001c0001t0001g0306a0001c0001t0025g0265 | 3 | HG01516.hp1 HG01517.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.394-22551C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457295 | ||||||
chr6:20457348
|
C | CT | 125 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0027others(122): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.394-22478dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20457348 | |||||
chr6:20457348
|
C | CTT | 131 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0037others(128): Show | 133 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.394-22479_394-2247 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20457348 | |||||
chr6:20457348
|
C | CTTT | 16 | a0001c0001t0001g0299a0001c0001t0002g0234a0001c0001t0003g0029others(13): Show | 16 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.394-22480_394-2247 others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20457348 | |||||
chr6:20457514
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-22332G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457514 | ||||||
chr6:20457596
|
G | A | 74 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0062others(71): Show | 75 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.394-22250G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457596 | ||||||
chr6:20457612
|
A | C | 2 | a0001c0001t0001g0098a0001c0001t0004g0128 | 2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.394-22234A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457612 | ||||||
chr6:20457689
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.394-22157C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457689 | ||||||
chr6:20457948
|
C | T | 16 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0127others(13): Show | 16 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.394-21898C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457948 | ||||||
chr6:20458074
|
G | C | 1 | a0004c0003t0003g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.394-21772G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458074 | ||||||
chr6:20458294
|
A | G | 20 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(17): Show | 20 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.394-21552A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458294 | ||||||
chr6:20458475
|
A | G | 16 | a0001c0001t0001g0108a0001c0001t0001g0117a0001c0001t0001g0127others(13): Show | 16 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.394-21371A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458475 | ||||||
chr6:20458830
|
C | T | 1 | a0001c0001t0003g0277 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.394-21016C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458830 | ||||||
chr6:20458845
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0004g0320a0001c0001t0004g0324 | 3 | HG03098.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.394-21001G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458845 | ||||||
chr6:20458951
|
GT | G | 280 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(277): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.394-20887delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20458951 | |||||
chr6:20458990
|
G | A | 1 | a0001c0001t0009g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.394-20856G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458990 | ||||||
chr6:20459137
|
T | C | 3 | a0001c0001t0012g0213a0001c0001t0015g0064a0001c0001t0016g0237 | 3 | HG02451.hp1 HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-20709T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20459137 | ||||||
chr6:20459141
|
C | T | 1 | a0001c0001t0003g0255 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.394-20705C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20459141 | ||||||
chr6:20459230
|
C | T | 1 | a0003c0004t0001g0005 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.394-20616C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20459230 | ||||||
chr6:20459442
|
C | T | 281 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(278): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.394-20404C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20459442 | ||||||
chr6:20460039
|
T | C | 285 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(282): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.394-19807T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460039 | ||||||
chr6:20460054
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0004g0128 | 2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.394-19792C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460054 | ||||||
chr6:20460072
|
C | G | 4 | a0001c0001t0004g0109a0001c0001t0004g0314a0002c0002t0004g0092others(1): Show | 4 | HG02622.hp1 NA19030.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-19774C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460072 | ||||||
chr6:20460075
|
A | G | 1 | a0001c0001t0002g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.394-19771A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460075 | ||||||
chr6:20460241
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394-19605A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460241 | ||||||
chr6:20460465
|
T | G | 286 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.394-19381T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460465 | ||||||
chr6:20460552
|
T | G | 1 | a0001c0001t0012g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-19294T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460552 | ||||||
chr6:20460563
|
A | C | 1 | a0001c0001t0001g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394-19283A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460563 | ||||||
chr6:20460656
|
C | G | 1 | a0001c0001t0001g0272 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.394-19190C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460656 | ||||||
chr6:20460678
|
A | G | 8 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0040others(5): Show | 8 | HG01069.hp2 HG01261.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-19168A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460678 | ||||||
chr6:20460794
|
G | A | 1 | a0001c0001t0017g0219 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.394-19052G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460794 | ||||||
chr6:20460996
|
C | CA | 28 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0020others(25): Show | 28 | HG00639.hp2 HG01081.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-18822dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20460996 | |||||
chr6:20460996
|
CAAA | C | 61 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0040others(58): Show | 63 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.394-18824_394-1882 others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20460996 | |||||
chr6:20460996
|
CAAAA | C | 208 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0015others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.394-18825_394-1882 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20460996 | |||||
chr6:20460996
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394-18831_394-1882 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20460996 | |||||
chr6:20460996
|
CAAAAAAA others(9): Show |
C | 4 | a0001c0001t0001g0084a0001c0001t0003g0246a0001c0001t0009g0329others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-18837_394-1882 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20460996 | |||||
chr6:20461071
|
T | C | 177 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0015others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.394-18775T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461071 | ||||||
chr6:20461079
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.394-18767C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461079 | ||||||
chr6:20461174
|
A | G | 76 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0059others(73): Show | 77 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.394-18672A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461174 | ||||||
chr6:20461201
|
A | G | 102 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0059others(99): Show | 104 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.394-18645A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461201 | ||||||
chr6:20461215
|
C | T | 1 | a0001c0001t0019g0220 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.394-18631C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461215 | ||||||
chr6:20461382
|
C | T | 278 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(275): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.394-18464C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461382 | ||||||
chr6:20461462
|
C | G | 1 | a0001c0001t0005g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.394-18384C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461462 | ||||||
chr6:20461737
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-18109C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461737 | ||||||
chr6:20461816
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.394-18030A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461816 | ||||||
chr6:20461889
|
G | A | 280 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(277): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.394-17957G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461889 | ||||||
chr6:20461907
|
G | A | 281 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(278): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.394-17939G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461907 | ||||||
chr6:20462135
|
A | G | 1 | a0001c0001t0002g0021 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.394-17711A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462135 | ||||||
chr6:20462299
|
G | A | 1 | a0001c0001t0003g0270 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.394-17547G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462299 | ||||||
chr6:20462428
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.394-17418A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462428 | ||||||
chr6:20462458
|
CT | C | 19 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0001g0117others(16): Show | 19 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.394-17373delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462458 | |||||
chr6:20462519
|
G | A | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0009g0099 | 3 | HG02559.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.394-17327G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462519 | ||||||
chr6:20462672
|
G | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0184 | 3 | HG01069.hp2 HG01261.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.394-17174G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462672 | ||||||
chr6:20462738
|
G | A | 1 | a0001c0001t0010g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.394-17108G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462738 | ||||||
chr6:20462797
|
G | A | 1 | a0001c0001t0003g0246 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.394-17049G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462797 | ||||||
chr6:20462859
|
CT | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0097a0001c0001t0001g0120others(4): Show | 7 | HG02055.hp1 HG03654.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-16950delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTT | C | 10 | a0001c0001t0001g0078a0001c0001t0001g0121a0001c0001t0001g0127others(7): Show | 10 | HG01243.hp2 HG01255.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.394-16951_394-1695 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTT | C | 12 | a0001c0001t0001g0061a0001c0001t0001g0136a0001c0001t0001g0311others(9): Show | 13 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-16952_394-1695 others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTTT | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(8): Show | 11 | HG00741.hp1 HG01496.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.394-16953_394-1695 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTTTT | C | 23 | a0001c0001t0001g0032a0001c0001t0001g0080a0001c0001t0001g0089others(20): Show | 25 | HG01109.hp1 HG01255.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.394-16954_394-1695 others(9): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTTTTT | C | 60 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0015others(57): Show | 60 | HG00639.hp1 HG00642.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.394-16955_394-1695 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTTTTTT | C | 85 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0040others(82): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.394-16956_394-1695 others(11): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0037a0001c0001t0001g0116a0001c0001t0001g0215others(6): Show | 9 | HG01069.hp2 HG01167.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-16957_394-1695 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTTTTTT others(2): Show |
C | 65 | a0001c0001t0001g0053a0001c0001t0001g0059a0001c0001t0001g0062others(62): Show | 66 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.394-16958_394-1695 others(13): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0003g0183a0001c0001t0003g0202a0001c0001t0003g0277others(2): Show | 5 | HG01069.hp1 HG01167.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-16959_394-1695 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0118a0001c0001t0012g0213 | 2 | HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.394-16961_394-1695 others(16): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0081a0001c0001t0001g0119a0001c0001t0001g0308others(1): Show | 4 | HG02257.hp2 HG02809.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-16962_394-1695 others(17): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTTTTTT others(10): Show |
C | 4 | a0001c0001t0001g0117a0001c0001t0001g0133a0001c0001t0004g0320others(1): Show | 4 | HG03098.hp2 HG03579.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-16966_394-1695 others(21): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462859
|
CTTTTTTT others(12): Show |
C | 3 | a0001c0001t0001g0238a0005c0005t0003g0148a0005c0005t0006g0180 | 3 | HG02129.hp2 HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.394-16968_394-1695 others(23): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | |||||
chr6:20462860
|
T | TC | 6 | a0001c0001t0001g0069a0001c0001t0003g0094a0001c0001t0010g0002others(3): Show | 7 | HG00642.hp2 HG01081.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-16986_394-1698 others(5): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462860 | ||||||
chr6:20462861
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-16985T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462861 | ||||||
chr6:20462862
|
T | C | 7 | a0001c0001t0001g0069a0001c0001t0002g0273a0001c0001t0003g0094others(4): Show | 8 | HG00642.hp2 HG01081.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-16984T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462862 | ||||||
chr6:20462863
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-16983T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462863 | ||||||
chr6:20462864
|
T | C | 4 | a0001c0001t0002g0273a0001c0001t0003g0094a0001c0001t0010g0002others(1): Show | 5 | HG00642.hp2 HG01081.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-16982T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462864 | ||||||
chr6:20462866
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0113 | 3 | HG02965.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.394-16980T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462866 | ||||||
chr6:20462889
|
T | A | 2 | a0001c0001t0002g0242a0001c0001t0003g0243 | 2 | HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.394-16957T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462889 | ||||||
chr6:20462904
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.394-16942G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462904 | ||||||
chr6:20462910
|
A | T | 6 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-16936A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462910 | ||||||
chr6:20462949
|
G | T | 23 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0060others(20): Show | 25 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.394-16897G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462949 | ||||||
chr6:20462963
|
T | A | 2 | a0001c0001t0001g0098a0001c0001t0004g0128 | 2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.394-16883T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462963 | ||||||
chr6:20462980
|
T | TTTAGTGC others(9): Show |
9 | a0001c0001t0001g0009a0001c0001t0001g0126a0001c0001t0001g0311others(6): Show | 9 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-16864_394-1684 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462980 | |||||
chr6:20463020
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.394-16826G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463020 | ||||||
chr6:20463068
|
G | A | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394-16778G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463068 | ||||||
chr6:20463102
|
G | C | 5 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-16744G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463102 | ||||||
chr6:20463118
|
T | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(4): Show | 7 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-16728T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463118 | ||||||
chr6:20463205
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.394-16641G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463205 | ||||||
chr6:20463349
|
G | A | 5 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-16497G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463349 | ||||||
chr6:20463443
|
C | G | 288 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(285): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.394-16403C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463443 | ||||||
chr6:20463598
|
A | G | 1 | a0001c0001t0008g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.394-16248A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463598 | ||||||
chr6:20463733
|
A | G | 8 | a0001c0001t0001g0062a0001c0001t0003g0217a0001c0001t0007g0003others(5): Show | 9 | HG01175.hp1 HG01192.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-16113A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463733 | ||||||
chr6:20463864
|
C | A | 1 | a0001c0001t0002g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.394-15982C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463864 | ||||||
chr6:20463993
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.394-15853C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463993 | ||||||
chr6:20464155
|
G | A | 1 | a0001c0001t0010g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.394-15691G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464155 | ||||||
chr6:20464221
|
A | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0059others(89): Show | 93 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.394-15625A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464221 | ||||||
chr6:20464278
|
C | T | 153 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0018others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.394-15568C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464278 | ||||||
chr6:20464404
|
G | C | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-15442G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464404 | ||||||
chr6:20464405
|
ATCTCTTA others(9): Show |
A | 1 | a0001c0001t0001g0175 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.394-15438_394-1542 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20464405 | |||||
chr6:20464407
|
C | G | 7 | a0001c0001t0001g0081a0001c0001t0001g0098a0001c0001t0001g0118others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-15439C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464407 | ||||||
chr6:20464644
|
G | A | 2 | a0001c0001t0003g0048a0001c0001t0005g0236 | 2 | NA18948.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.394-15202G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464644 | ||||||
chr6:20464658
|
G | A | 7 | a0001c0001t0001g0081a0001c0001t0001g0098a0001c0001t0001g0118others(4): Show | 7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-15188G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464658 | ||||||
chr6:20464773
|
T | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | NA18951.hp1 NA19000.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.394-15073T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464773 | ||||||
chr6:20464840
|
G | A | 1 | a0004c0003t0003g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-15006G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464840 | ||||||
chr6:20464957
|
C | T | 1 | a0001c0001t0004g0087 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.394-14889C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464957 | ||||||
chr6:20464975
|
A | G | 1 | a0001c0001t0012g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-14871A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464975 | ||||||
chr6:20464976
|
G | A | 1 | a0001c0001t0005g0290 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.394-14870G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464976 | ||||||
chr6:20465339
|
T | A | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394-14507T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465339 | ||||||
chr6:20465394
|
C | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0133a0001c0008t0001g0161 | 3 | HG01081.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.394-14452C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465394 | ||||||
chr6:20465633
|
T | C | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.394-14213T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465633 | ||||||
chr6:20465679
|
T | A | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.394-14167T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465679 | ||||||
chr6:20465738
|
T | C | 11 | a0001c0001t0003g0066a0001c0001t0003g0246a0001c0001t0003g0255others(8): Show | 12 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-14108T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465738 | ||||||
chr6:20465808
|
C | CAT | 39 | a0001c0001t0001g0020a0001c0001t0001g0095a0001c0001t0001g0096others(36): Show | 40 | HG01255.hp2 HG02109.hp2 HG02129.hp2 others(37): Show |
intron_variant | MODIFIER | c.394-14026_394-1402 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20465808 | |||||
chr6:20465808
|
C | CATAT | 3 | a0001c0001t0004g0109a0001c0001t0004g0314a0002c0002t0004g0092 | 3 | NA19030.hp1 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.394-14028_394-1402 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20465808 | |||||
chr6:20465884
|
T | G | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-13962T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465884 | ||||||
chr6:20465929
|
G | T | 1 | a0004c0003t0003g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-13917G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465929 | ||||||
chr6:20466105
|
G | C | 311 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(308): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.394-13741G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466105 | ||||||
chr6:20466107
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.394-13739T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466107 | ||||||
chr6:20466122
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | NA18951.hp1 NA19000.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.394-13724C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466122 | ||||||
chr6:20466129
|
T | G | 311 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(308): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.394-13717T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466129 | ||||||
chr6:20466270
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0235 | 2 | HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.394-13576G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466270 | ||||||
chr6:20466305
|
G | A | 1 | a0001c0001t0003g0199 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.394-13541G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466305 | ||||||
chr6:20466685
|
CT | C | 226 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(223): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.394-13146delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20466685 | |||||
chr6:20466751
|
C | T | 3 | a0001c0001t0009g0329a0001c0001t0028g0072a0001c0001t0029g0330 | 3 | HG02451.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.394-13095C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466751 | ||||||
chr6:20466764
|
T | C | 236 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(233): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.394-13082T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466764 | ||||||
chr6:20466772
|
T | C | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394-13074T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466772 | ||||||
chr6:20466773
|
G | C | 311 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(308): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.394-13073G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466773 | ||||||
chr6:20466780
|
T | C | 3 | a0001c0001t0002g0162a0001c0001t0006g0163a0001c0001t0006g0168 | 3 | NA18946.hp1 NA18981.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.394-13066T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466780 | ||||||
chr6:20466838
|
C | T | 13 | a0001c0001t0002g0173a0001c0001t0002g0191a0001c0001t0003g0328others(10): Show | 13 | HG01975.hp2 HG01978.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-13008C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466838 | ||||||
chr6:20466908
|
C | CTGACCTC others(1): Show |
3 | a0001c0001t0001g0059a0001c0001t0003g0152a0001c0001t0003g0270 | 3 | HG03704.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.394-12932_394-1292 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20466908 | |||||
chr6:20466931
|
T | C | 236 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(233): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.394-12915T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466931 | ||||||
chr6:20466997
|
C | T | 74 | a0001c0001t0001g0053a0001c0001t0001g0059a0001c0001t0001g0062others(71): Show | 75 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.394-12849C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466997 | ||||||
chr6:20467132
|
A | G | 236 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(233): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.394-12714A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467132 | ||||||
chr6:20467150
|
A | T | 1 | a0001c0001t0004g0013 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.394-12696A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467150 | ||||||
chr6:20467347
|
G | A | 232 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(229): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.394-12499G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467347 | ||||||
chr6:20467372
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-12474C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467372 | ||||||
chr6:20467415
|
A | G | 1 | a0001c0001t0012g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-12431A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467415 | ||||||
chr6:20467448
|
G | C | 4 | a0001c0001t0004g0123a0001c0001t0004g0124a0001c0001t0009g0110others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-12398G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467448 | ||||||
chr6:20467540
|
A | G | 3 | a0001c0001t0001g0117a0001c0001t0004g0320a0001c0001t0004g0324 | 3 | HG03098.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.394-12306A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467540 | ||||||
chr6:20467613
|
G | A | 1 | a0001c0001t0012g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-12233G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467613 | ||||||
chr6:20467616
|
G | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02257.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.394-12230G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467616 | ||||||
chr6:20467642
|
T | A | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-12204T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467642 | ||||||
chr6:20467837
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0136 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.394-12009T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467837 | ||||||
chr6:20467863
|
A | ATGCCACT others(20): Show |
6 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-11962_394-1193 others(31): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20467863 | |||||
chr6:20467876
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.394-11970C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467876 | ||||||
chr6:20468157
|
G | A | 7 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(4): Show | 8 | HG00642.hp2 HG01081.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-11689G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468157 | ||||||
chr6:20468239
|
C | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0078 | 3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.394-11607C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468239 | ||||||
chr6:20468243
|
A | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0078 | 3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.394-11603A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468243 | ||||||
chr6:20468331
|
C | T | 7 | a0001c0001t0001g0062a0001c0001t0003g0217a0001c0001t0007g0003others(4): Show | 8 | HG01192.hp1 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-11515C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468331 | ||||||
chr6:20468403
|
G | A | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394-11443G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468403 | ||||||
chr6:20468404
|
A | G | 227 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0015others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.394-11442A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468404 | ||||||
chr6:20468558
|
T | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0059others(72): Show | 76 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.394-11288T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468558 | ||||||
chr6:20468674
|
C | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-11172C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468674 | ||||||
chr6:20468737
|
C | T | 38 | a0001c0001t0001g0020a0001c0001t0001g0095a0001c0001t0001g0096others(35): Show | 39 | HG01255.hp2 HG02109.hp2 HG02129.hp2 others(36): Show |
intron_variant | MODIFIER | c.394-11109C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468737 | ||||||
chr6:20469014
|
G | A | 2 | a0001c0001t0002g0179a0001c0001t0014g0024 | 2 | HG00639.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.394-10832G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469014 | ||||||
chr6:20469052
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394-10794T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469052 | ||||||
chr6:20469101
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.394-10745C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469101 | ||||||
chr6:20469270
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.394-10576A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469270 | ||||||
chr6:20469475
|
A | G | 2 | a0001c0001t0001g0292a0001c0001t0012g0291 | 2 | HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.394-10371A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469475 | ||||||
chr6:20469531
|
G | A | 326 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(323): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.394-10315G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469531 | ||||||
chr6:20469670
|
A | C | 8 | a0001c0001t0001g0299a0001c0001t0002g0234a0001c0001t0003g0201others(5): Show | 8 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-10176A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469670 | ||||||
chr6:20470094
|
A | G | 1 | a0001c0001t0012g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-9752A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470094 | ||||||
chr6:20470115
|
C | T | 4 | a0001c0001t0001g0311a0001c0001t0001g0313a0001c0001t0004g0310others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-9731C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470115 | ||||||
chr6:20470288
|
T | C | 1 | a0001c0001t0001g0018 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.394-9558T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470288 | ||||||
chr6:20470426
|
A | G | 9 | a0001c0001t0001g0108a0001c0001t0004g0087a0001c0001t0004g0088others(6): Show | 9 | HG02109.hp2 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-9420A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470426 | ||||||
chr6:20470562
|
GAT | G | 5 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-9283_394-9282d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470562 | ||||||
chr6:20470676
|
C | G | 1 | a0001c0001t0016g0237 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.394-9170C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470676 | ||||||
chr6:20470677
|
A | C | 180 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.394-9169A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470677 | ||||||
chr6:20470699
|
T | G | 180 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.394-9147T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470699 | ||||||
chr6:20470724
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.394-9122T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470724 | ||||||
chr6:20470918
|
A | G | 1 | a0004c0003t0003g0071 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.394-8928A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470918 | ||||||
chr6:20471130
|
T | G | 1 | a0001c0001t0003g0246 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.394-8716T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471130 | ||||||
chr6:20471304
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0264a0001c0001t0002g0131others(1): Show | 4 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-8542C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471304 | ||||||
chr6:20471311
|
G | T | 15 | a0001c0001t0001g0054a0001c0001t0001g0204a0001c0001t0001g0206others(12): Show | 15 | NA18612.hp1 NA18950.hp2 NA18955.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-8535G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471311 | ||||||
chr6:20471348
|
C | A | 7 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(4): Show | 8 | HG00642.hp2 HG01081.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-8498C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471348 | ||||||
chr6:20471359
|
C | T | 5 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-8487C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471359 | ||||||
chr6:20471459
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394-8387G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471459 | ||||||
chr6:20471516
|
G | A | 22 | a0001c0001t0001g0020a0001c0001t0001g0095a0001c0001t0001g0096others(19): Show | 22 | HG01255.hp2 HG02129.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.394-8330G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471516 | ||||||
chr6:20471569
|
G | A | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-8277G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471569 | ||||||
chr6:20471768
|
T | C | 311 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(308): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.394-8078T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471768 | ||||||
chr6:20472024
|
C | A | 1 | a0001c0001t0002g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.394-7822C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472024 | ||||||
chr6:20472025
|
A | AAC | 51 | a0001c0001t0001g0034a0001c0001t0001g0060a0001c0001t0001g0061others(48): Show | 52 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.394-7778_394-7777d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472025
|
A | AACAC | 38 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0028others(35): Show | 38 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.394-7780_394-7777d others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472025
|
A | AACACAC | 31 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0039others(28): Show | 33 | HG00408.hp1 HG00741.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.394-7782_394-7777d others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472025
|
A | AACACACA others(1): Show |
39 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0037others(36): Show | 39 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.394-7784_394-7777d others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472025
|
A | AACACACA others(3): Show |
7 | a0001c0001t0001g0097a0001c0001t0001g0293a0001c0001t0001g0316others(4): Show | 7 | HG01496.hp1 HG01516.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-7786_394-7777d others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472025
|
A | AACACACA others(5): Show |
1 | a0001c0001t0001g0040 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.394-7788_394-7777d others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472025
|
A | AACACACA others(7): Show |
1 | a0001c0001t0001g0020 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.394-7790_394-7777d others(16): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472025
|
AAC | A | 49 | a0001c0001t0001g0044a0001c0001t0001g0067a0001c0001t0001g0068others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.394-7778_394-7777d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472025
|
AACAC | A | 67 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(64): Show | 68 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.394-7780_394-7777d others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472025
|
AACACAC | A | 9 | a0001c0001t0001g0146a0001c0001t0001g0284a0001c0001t0002g0230others(6): Show | 9 | HG00438.hp2 HG02451.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-7782_394-7777d others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472025
|
AACACACA others(1): Show |
A | 8 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0090others(5): Show | 8 | HG02486.hp1 HG03516.hp1 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-7784_394-7777d others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472025
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0002g0195 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.394-7790_394-7777d others(16): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | |||||
chr6:20472070
|
T | A | 3 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0013 | 3 | HG02572.hp2 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.394-7776T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472070 | ||||||
chr6:20472126
|
A | T | 2 | a0001c0001t0004g0123a0001c0001t0004g0124 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.394-7720A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472126 | ||||||
chr6:20472159
|
AAAAT | A | 177 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0015others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.394-7680_394-7677d others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472159 | |||||
chr6:20472471
|
G | A | 1 | a0004c0003t0003g0122 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.394-7375G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472471 | ||||||
chr6:20472504
|
T | C | 2 | a0001c0001t0004g0125a0001c0001t0004g0321 | 2 | HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.394-7342T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472504 | ||||||
chr6:20472511
|
A | G | 23 | a0001c0001t0001g0020a0001c0001t0001g0095a0001c0001t0001g0096others(20): Show | 23 | HG01255.hp2 HG02129.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.394-7335A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472511 | ||||||
chr6:20472606
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0126a0001c0001t0001g0136others(7): Show | 10 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-7240C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472606 | ||||||
chr6:20472842
|
T | G | 320 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(317): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.394-7004T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472842 | ||||||
chr6:20473006
|
G | C | 1 | a0001c0001t0001g0326 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.394-6840G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473006 | ||||||
chr6:20473218
|
A | G | 1 | a0001c0001t0014g0024 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.394-6628A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473218 | ||||||
chr6:20473312
|
A | G | 2 | a0001c0001t0002g0131a0001c0001t0002g0132 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.394-6534A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473312 | ||||||
chr6:20473441
|
A | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0113 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.394-6405A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473441 | ||||||
chr6:20473533
|
G | GT | 3 | a0001c0001t0012g0213a0001c0001t0015g0064a0001c0001t0016g0237 | 3 | HG02451.hp1 HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-6312dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20473533 | |||||
chr6:20473626
|
G | A | 177 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0015others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.394-6220G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473626 | ||||||
chr6:20473654
|
C | T | 1 | a0001c0001t0002g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.394-6192C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473654 | ||||||
chr6:20474095
|
T | TG | 5 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 5 | HG02970.hp2 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-5749dupG | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20474095 | |||||
chr6:20474097
|
G | GT | 301 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(298): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.394-5741dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20474097 | |||||
chr6:20474243
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394-5603T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474243 | ||||||
chr6:20474387
|
C | T | 23 | a0001c0001t0001g0020a0001c0001t0001g0095a0001c0001t0001g0096others(20): Show | 24 | HG01255.hp2 HG02129.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.394-5459C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474387 | ||||||
chr6:20474536
|
A | G | 23 | a0001c0001t0001g0020a0001c0001t0001g0095a0001c0001t0001g0096others(20): Show | 24 | HG01255.hp2 HG02129.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.394-5310A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474536 | ||||||
chr6:20474541
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0022g0205 | 2 | NA18956.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.394-5305G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474541 | ||||||
chr6:20474570
|
C | T | 5 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-5276C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474570 | ||||||
chr6:20474666
|
C | T | 25 | a0001c0001t0001g0020a0001c0001t0001g0095a0001c0001t0001g0096others(22): Show | 26 | HG01255.hp2 HG02129.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-5180C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474666 | ||||||
chr6:20474799
|
T | A | 7 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(4): Show | 8 | HG00642.hp2 HG01081.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-5047T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474799 | ||||||
chr6:20474914
|
G | A | 1 | a0001c0001t0028g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.394-4932G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474914 | ||||||
chr6:20475144
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.394-4702T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20475144 | ||||||
chr6:20475272
|
G | T | 1 | a0001c0001t0003g0140 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.394-4574G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20475272 | ||||||
chr6:20475772
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.394-4074C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20475772 | ||||||
chr6:20475970
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.394-3876C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20475970 | ||||||
chr6:20476052
|
A | G | 2 | a0001c0001t0006g0174a0001c0001t0006g0239 | 2 | NA18940.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.394-3794A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476052 | ||||||
chr6:20476137
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.394-3709C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476137 | ||||||
chr6:20476147
|
G | A | 1 | a0001c0001t0007g0164 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.394-3699G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476147 | ||||||
chr6:20476243
|
C | T | 20 | a0001c0001t0001g0020a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 21 | HG01255.hp2 HG02129.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.394-3603C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476243 | ||||||
chr6:20476274
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.394-3572G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476274 | ||||||
chr6:20476296
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.394-3550G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476296 | ||||||
chr6:20476303
|
G | A | 5 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-3543G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476303 | ||||||
chr6:20476357
|
C | T | 8 | a0001c0001t0001g0117a0001c0001t0001g0127a0001c0001t0004g0109others(5): Show | 8 | HG02622.hp1 HG02970.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-3489C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476357 | ||||||
chr6:20476365
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.394-3481C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476365 | ||||||
chr6:20476372
|
CA | C | 15 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(12): Show | 16 | HG00642.hp2 HG01081.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.394-3462delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20476372 | |||||
chr6:20476385
|
T | C | 1 | a0001c0001t0003g0286 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.394-3461T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476385 | ||||||
chr6:20476663
|
A | T | 24 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0060others(21): Show | 26 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-3183A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476663 | ||||||
chr6:20477179
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394-2667G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477179 | ||||||
chr6:20477423
|
T | C | 2 | a0001c0001t0003g0199a0001c0001t0003g0200 | 2 | NA18953.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.394-2423T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477423 | ||||||
chr6:20477448
|
G | A | 2 | a0004c0003t0003g0071a0004c0003t0003g0122 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-2398G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477448 | ||||||
chr6:20477734
|
C | T | 1 | a0003c0004t0009g0322 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.394-2112C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477734 | ||||||
chr6:20477752
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394-2094G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477752 | ||||||
chr6:20477934
|
G | A | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-1912G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477934 | ||||||
chr6:20478030
|
CA | C | 51 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0020others(48): Show | 55 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.394-1803delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20478030 | |||||
chr6:20478030
|
CAA | C | 14 | a0001c0001t0001g0081a0001c0001t0001g0117a0001c0001t0001g0118others(11): Show | 14 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-1804_394-1803d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20478030 | |||||
chr6:20478223
|
G | A | 8 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(5): Show | 9 | HG00642.hp2 HG01081.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-1623G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478223 | ||||||
chr6:20478414
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.394-1432G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478414 | ||||||
chr6:20478499
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.394-1347G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478499 | ||||||
chr6:20478547
|
G | A | 1 | a0001c0001t0025g0265 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.394-1299G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478547 | ||||||
chr6:20478678
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394-1168G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478678 | ||||||
chr6:20478936
|
A | G | 7 | a0001c0001t0001g0098a0001c0001t0001g0108a0001c0001t0004g0087others(4): Show | 7 | HG02109.hp2 HG02622.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-910A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478936 | ||||||
chr6:20478983
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.394-863G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478983 | ||||||
chr6:20479036
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.394-810C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479036 | ||||||
chr6:20479062
|
T | C | 1 | a0001c0001t0017g0219 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.394-784T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479062 | ||||||
chr6:20479072
|
A | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0126a0001c0001t0001g0136others(7): Show | 10 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-774A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479072 | ||||||
chr6:20479096
|
T | G | 2 | a0004c0003t0003g0071a0004c0003t0003g0122 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-750T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479096 | ||||||
chr6:20479153
|
T | G | 1 | a0002c0002t0001g0077 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.394-693T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479153 | ||||||
chr6:20479204
|
A | G | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-642A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479204 | ||||||
chr6:20479251
|
G | A | 1 | a0001c0001t0012g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-595G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479251 | ||||||
chr6:20479352
|
T | G | 6 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-494T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479352 | ||||||
chr6:20479415
|
G | A | 1 | a0001c0001t0012g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-431G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479415 | ||||||
chr6:20479486
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.394-360G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479486 | ||||||
chr6:20479510
|
C | T | 1 | a0001c0001t0002g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.394-336C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479510 | ||||||
chr6:20479682
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.394-164C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479682 | ||||||
chr6:20480355
|
A | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0039others(85): Show | 89 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.505+398A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480355 | ||||||
chr6:20480360
|
G | A | 22 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0060others(19): Show | 24 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.505+403G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480360 | ||||||
chr6:20480404
|
C | T | 1 | a0001c0001t0007g0295 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.505+447C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480404 | ||||||
chr6:20480776
|
CTGTT | C | 13 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(10): Show | 13 | HG02258.hp2 HG02486.hp1 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.506-428_506-425del others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 20480776 | |||||
chr6:20480808
|
G | A | 1 | a0001c0001t0007g0295 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.506-398G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480808 | ||||||
chr6:20480909
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.506-297A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480909 | ||||||
chr6:20480974
|
A | C | 1 | a0001c0001t0005g0189 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.506-232A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480974 | ||||||
chr6:20480990
|
A | G | 2 | a0001c0001t0015g0064a0001c0001t0016g0237 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.506-216A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480990 | ||||||
chr6:20481041
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.506-165A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20481041 | ||||||
chr6:20481055
|
C | T | 3 | a0001c0001t0003g0094a0001c0001t0010g0002a0001c0001t0010g0082 | 4 | HG00642.hp2 HG01081.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.506-151C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20481055 | ||||||
chr6:20481447
|
G | C | 19 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0028others(16): Show | 19 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.725+22G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481447 | ||||||
chr6:20481518
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.725+93C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481518 | ||||||
chr6:20481594
|
T | C | 267 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(264): Show | 273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.725+169T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481594 | ||||||
chr6:20481671
|
C | T | 2 | a0001c0001t0010g0070a0001c0001t0010g0112 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.725+246C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481671 | ||||||
chr6:20481708
|
A | C | 2 | a0001c0001t0002g0173a0001c0001t0002g0177 | 2 | NA19011.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.725+283A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481708 | ||||||
chr6:20481962
|
G | A | 9 | a0001c0001t0005g0045a0001c0001t0005g0150a0001c0001t0005g0187others(6): Show | 9 | HG01978.hp1 HG02148.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.725+537G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481962 | ||||||
chr6:20481981
|
G | A | 3 | a0001c0001t0001g0293a0001c0001t0001g0306a0001c0001t0025g0265 | 3 | HG01516.hp1 HG01517.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.725+556G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481981 | ||||||
chr6:20482098
|
T | C | 1 | a0001c0001t0004g0314 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.726-664T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482098 | ||||||
chr6:20482104
|
G | A | 257 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(254): Show | 261 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.726-658G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482104 | ||||||
chr6:20482180
|
G | A | 143 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(140): Show | 145 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.726-582G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482180 | ||||||
chr6:20482222
|
C | T | 1 | a0001c0001t0012g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.726-540C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482222 | ||||||
chr6:20482342
|
G | GT | 64 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0053others(61): Show | 64 | HG00639.hp2 HG00741.hp2 HG01071.hp2 others(61): Show |
intron_variant | MODIFIER | c.726-405dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482342 | |||||
chr6:20482342
|
G | GTT | 8 | a0001c0001t0001g0095a0001c0001t0001g0165a0001c0001t0001g0288others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.726-406_726-405dup others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482342 | |||||
chr6:20482342
|
GT | G | 41 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(38): Show | 42 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.726-405delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482342 | |||||
chr6:20482350
|
T | G | 2 | a0002c0002t0001g0075a0002c0002t0001g0076 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.726-412T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482350 | ||||||
chr6:20482590
|
G | GA | 14 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0044others(11): Show | 14 | HG01192.hp1 HG01361.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.726-162dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482590 | |||||
chr6:20482590
|
G | GAA | 36 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0027others(33): Show | 36 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.726-163_726-162dup others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482590 | |||||
chr6:20482590
|
GAA | G | 22 | a0001c0001t0002g0021a0001c0001t0002g0036a0001c0001t0002g0058others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.726-163_726-162del others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482590 | |||||
chr6:20482597
|
A | AAT | 8 | a0001c0001t0002g0234a0001c0001t0003g0140a0001c0001t0003g0201others(5): Show | 8 | HG00280.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.726-164_726-163ins others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482597 | |||||
chr6:20482597
|
A | T | 12 | a0001c0001t0001g0047a0001c0001t0003g0055a0001c0001t0003g0286others(9): Show | 12 | HG01943.hp1 HG02083.hp2 NA18970.hp2 others(9): Show |
intron_variant | MODIFIER | c.726-165A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482597 | ||||||
chr6:20482599
|
A | AAT | 5 | a0001c0001t0001g0292a0001c0001t0003g0144a0001c0001t0003g0152others(2): Show | 5 | HG01071.hp2 HG01192.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.726-142_726-141dup others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482599 | |||||
chr6:20482599
|
A | AATAT | 5 | a0001c0001t0001g0134a0001c0001t0001g0176a0001c0001t0001g0296others(2): Show | 5 | HG00639.hp2 HG01891.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-144_726-141dup others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482599 | |||||
chr6:20482599
|
A | T | 62 | a0001c0001t0001g0039a0001c0001t0001g0047a0001c0001t0001g0238others(59): Show | 64 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.726-163A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482599 | ||||||
chr6:20482599
|
AAT | A | 67 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0040others(64): Show | 69 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.726-142_726-141del others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482599 | |||||
chr6:20482599
|
AATAT | A | 5 | a0001c0001t0004g0310a0001c0001t0004g0324a0001c0001t0010g0070others(2): Show | 5 | HG02109.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-144_726-141del others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482599 | |||||
chr6:20482600
|
AT | A | 24 | a0001c0001t0001g0009a0001c0001t0001g0068a0001c0001t0001g0069others(21): Show | 25 | HG00642.hp2 HG01081.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.726-161delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482600 | ||||||
chr6:20482600
|
ATAT | A | 6 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02257.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.726-161_726-159del others(3): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482600 | ||||||
chr6:20482601
|
T | A | 39 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0020others(36): Show | 39 | HG01109.hp2 HG01978.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.726-161T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482601 | ||||||
chr6:20482603
|
T | A | 26 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0080others(23): Show | 27 | HG00642.hp2 HG01081.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.726-159T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482603 | ||||||
chr6:20482605
|
T | A | 8 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0090others(5): Show | 8 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.726-157T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482605 | ||||||
chr6:20482620
|
A | ATG | 24 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(21): Show | 24 | HG00323.hp2 HG00738.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.726-138_726-137dup others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482620 | |||||
chr6:20482620
|
A | G | 25 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0022others(22): Show | 26 | HG00140.hp1 HG01081.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.726-142A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482620 | ||||||
chr6:20482959
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0004g0013 | 2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.884+39T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20482959 | ||||||
chr6:20482999
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.884+79A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20482999 | ||||||
chr6:20483045
|
C | G | 1 | a0001c0001t0005g0019 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.884+125C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483045 | ||||||
chr6:20483055
|
ATG | A | 5 | a0001c0001t0004g0109a0001c0001t0004g0310a0001c0001t0004g0314others(2): Show | 5 | HG02280.hp1 HG02451.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.884+148_884+149del others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 20483055 | |||||
chr6:20483072
|
C | T | 27 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0041others(24): Show | 27 | HG01069.hp2 HG01261.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.884+152C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483072 | ||||||
chr6:20483119
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG01167.hp2 HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.884+199T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483119 | ||||||
chr6:20483129
|
G | A | 1 | a0001c0001t0007g0079 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.884+209G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483129 | ||||||
chr6:20483176
|
C | T | 30 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.884+256C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483176 | ||||||
chr6:20483277
|
A | G | 1 | a0001c0001t0002g0234 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.884+357A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483277 | ||||||
chr6:20483339
|
C | T | 11 | a0001c0001t0001g0054a0001c0001t0001g0204a0001c0001t0001g0206others(8): Show | 11 | NA18612.hp1 NA18955.hp1 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.884+419C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483339 | ||||||
chr6:20483372
|
C | T | 10 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0001g0165others(7): Show | 10 | HG01071.hp2 HG01192.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.884+452C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483372 | ||||||
chr6:20483483
|
A | G | 2 | a0001c0001t0010g0070a0001c0001t0010g0112 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.884+563A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483483 | ||||||
chr6:20483490
|
A | G | 1 | a0001c0001t0020g0307 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.884+570A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483490 | ||||||
chr6:20483539
|
A | G | 27 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0041others(24): Show | 27 | HG01069.hp2 HG01261.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.884+619A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483539 | ||||||
chr6:20483664
|
C | T | 1 | a0001c0001t0026g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.884+744C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483664 | ||||||
chr6:20483777
|
C | G | 1 | a0001c0001t0013g0223 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.884+857C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483777 | ||||||
chr6:20483973
|
C | T | 1 | a0001c0001t0019g0220 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.884+1053C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483973 | ||||||
chr6:20484024
|
T | G | 11 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(8): Show | 11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.884+1104T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484024 | ||||||
chr6:20484041
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.884+1121A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484041 | ||||||
chr6:20484079
|
T | G | 4 | a0001c0001t0001g0034a0001c0001t0003g0066a0001c0001t0003g0246others(1): Show | 4 | NA18948.hp2 NA18956.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.884+1159T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484079 | ||||||
chr6:20484182
|
G | C | 1 | a0001c0001t0024g0105 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.884+1262G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484182 | ||||||
chr6:20484378
|
T | C | 2 | a0001c0001t0010g0070a0001c0001t0010g0112 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.884+1458T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484378 | ||||||
chr6:20484482
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.884+1562G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484482 | ||||||
chr6:20484498
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.884+1578C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484498 | ||||||
chr6:20484735
|
C | T | 1 | a0001c0001t0019g0220 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.884+1815C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484735 | ||||||
chr6:20484846
|
G | C | 80 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0281others(77): Show | 82 | HG00438.hp2 HG00544.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.885-1843G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484846 | ||||||
chr6:20484858
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0029g0330 | 2 | HG00741.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.885-1831C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484858 | ||||||
chr6:20484952
|
C | CA | 27 | a0001c0001t0001g0009a0001c0001t0001g0121a0001c0001t0001g0126others(24): Show | 27 | HG00280.hp2 HG01255.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.885-1720dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 20484952 | |||||
chr6:20484952
|
CA | C | 25 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0250others(22): Show | 26 | HG00642.hp2 HG00738.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.885-1720delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 20484952 | |||||
chr6:20485124
|
T | A | 3 | a0004c0003t0003g0071a0004c0003t0003g0122a0004c0003t0003g0147 | 3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-1565T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485124 | ||||||
chr6:20485146
|
C | T | 1 | a0001c0001t0004g0314 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.885-1543C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485146 | ||||||
chr6:20485230
|
T | C | 3 | a0004c0003t0003g0071a0004c0003t0003g0122a0004c0003t0003g0147 | 3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-1459T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485230 | ||||||
chr6:20485235
|
T | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0126a0001c0001t0001g0127others(6): Show | 9 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1454T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485235 | ||||||
chr6:20485313
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.885-1376C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485313 | ||||||
chr6:20485389
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.885-1300G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485389 | ||||||
chr6:20485400
|
A | G | 255 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(252): Show | 261 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.885-1289A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485400 | ||||||
chr6:20485440
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.885-1249T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485440 | ||||||
chr6:20485441
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.885-1248G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485441 | ||||||
chr6:20485534
|
G | C | 2 | a0001c0001t0004g0088a0001c0001t0004g0128 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.885-1155G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485534 | ||||||
chr6:20485633
|
T | C | 80 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0014others(77): Show | 83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.885-1056T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485633 | ||||||
chr6:20485667
|
C | T | 32 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0014others(29): Show | 33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.885-1022C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485667 | ||||||
chr6:20485712
|
A | T | 3 | a0004c0003t0003g0071a0004c0003t0003g0122a0004c0003t0003g0147 | 3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-977A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485712 | ||||||
chr6:20485736
|
C | T | 1 | a0001c0001t0003g0144 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.885-953C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485736 | ||||||
chr6:20485800
|
A | G | 3 | a0001c0001t0001g0098a0001c0001t0003g0094a0001c0001t0031g0111 | 3 | HG02572.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.885-889A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485800 | ||||||
chr6:20486083
|
C | T | 1 | a0001c0001t0011g0275 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.885-606C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486083 | ||||||
chr6:20486178
|
G | A | 1 | a0001c0001t0006g0239 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.885-511G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486178 | ||||||
chr6:20486260
|
T | G | 6 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0125others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.885-429T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486260 | ||||||
chr6:20486275
|
A | G | 197 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0014others(194): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.885-414A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486275 | ||||||
chr6:20486334
|
G | A | 126 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0034others(123): Show | 128 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.885-355G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486334 | ||||||
chr6:20486335
|
C | T | 1 | a0001c0001t0010g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.885-354C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486335 | ||||||
chr6:20486343
|
T | G | 50 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(47): Show | 51 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.885-346T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486343 | ||||||
chr6:20486383
|
C | T | 12 | a0001c0001t0001g0081a0001c0001t0001g0093a0001c0001t0001g0114others(9): Show | 12 | HG01167.hp2 HG01256.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.885-306C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486383 | ||||||
chr6:20486384
|
G | A | 3 | a0004c0003t0003g0071a0004c0003t0003g0122a0004c0003t0003g0147 | 3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-305G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486384 | ||||||
chr6:20486387
|
C | T | 3 | a0004c0003t0003g0071a0004c0003t0003g0122a0004c0003t0003g0147 | 3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-302C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486387 | ||||||
chr6:20486398
|
G | A | 3 | a0004c0003t0003g0071a0004c0003t0003g0122a0004c0003t0003g0147 | 3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-291G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486398 | ||||||
chr6:20486473
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.885-216C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486473 | ||||||
chr6:20486521
|
C | T | 1 | a0001c0001t0029g0330 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.885-168C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486521 | ||||||
chr6:20486523
|
C | T | 125 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0020others(122): Show | 127 | HG00438.hp2 HG00544.hp2 HG00738.hp2 others(124): Show |
intron_variant | MODIFIER | c.885-166C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486523 | ||||||
chr6:20486563
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0074others(9): Show | 12 | HG01081.hp1 HG01361.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.885-126C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486563 | ||||||
chr6:20486567
|
C | T | 23 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.885-122C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486567 | ||||||
chr6:20486604
|
T | G | 1 | a0001c0001t0024g0105 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.885-85T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486604 | ||||||
chr6:20486647
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG01167.hp2 HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.885-42T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486647 | ||||||
chr6:20487019
|
T | G | 199 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(196): Show | 204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.999+216T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487019 | ||||||
chr6:20487038
|
C | T | 2 | a0001c0001t0004g0007a0001c0001t0004g0008 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.999+235C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487038 | ||||||
chr6:20487138
|
G | C | 3 | a0001c0001t0001g0098a0001c0001t0003g0094a0001c0001t0031g0111 | 3 | HG02572.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.999+335G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487138 | ||||||
chr6:20487343
|
T | G | 12 | a0001c0001t0006g0052a0001c0001t0006g0057a0001c0001t0006g0163others(9): Show | 12 | HG02040.hp1 HG02129.hp2 HG03654.hp2 others(9): Show |
intron_variant | MODIFIER | c.999+540T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487343 | ||||||
chr6:20487346
|
A | C | 199 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0014others(196): Show | 205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.999+543A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487346 | ||||||
chr6:20487366
|
G | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0074others(9): Show | 12 | HG01081.hp1 HG01361.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.999+563G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487366 | ||||||
chr6:20487388
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.999+585G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487388 | ||||||
chr6:20487410
|
G | A | 7 | a0001c0001t0009g0099a0001c0001t0009g0103a0001c0001t0009g0104others(4): Show | 7 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+607G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487410 | ||||||
chr6:20487922
|
A | G | 33 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0086others(30): Show | 33 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.1000-191A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487922 | ||||||
chr6:20487960
|
A | G | 2 | a0001c0001t0003g0254a0001c0001t0005g0186 | 2 | HG02074.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1000-153A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487960 | ||||||
chr6:20488003
|
G | A | 127 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0034others(124): Show | 129 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.1000-110G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20488003 | ||||||
chr6:20488009
|
G | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0129others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-104G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20488009 | ||||||
chr6:20488424
|
G | A | 2 | a0001c0001t0003g0051a0001c0001t0003g0063 | 2 | NA19001.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1135+176G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488424 | ||||||
chr6:20488542
|
G | A | 1 | a0001c0001t0004g0013 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1135+294G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488542 | ||||||
chr6:20488656
|
T | C | 40 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0037others(37): Show | 41 | HG01069.hp2 HG01081.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.1135+408T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488656 | ||||||
chr6:20488663
|
C | G | 28 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(25): Show | 30 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.1135+415C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488663 | ||||||
chr6:20488666
|
A | G | 198 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(195): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1135+418A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488666 | ||||||
chr6:20488678
|
G | A | 6 | a0001c0001t0001g0080a0001c0001t0001g0121a0001c0001t0026g0138others(3): Show | 6 | HG02622.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135+430G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488678 | ||||||
chr6:20488886
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1135+638C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488886 | ||||||
chr6:20488956
|
G | T | 4 | a0001c0001t0004g0001a0001c0001t0004g0013a0001c0001t0004g0324others(1): Show | 6 | HG01255.hp1 HG02572.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135+708G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488956 | ||||||
chr6:20488990
|
T | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0218 | 2 | HG02155.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1135+742T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488990 | ||||||
chr6:20488994
|
A | AAAAAG | 9 | a0001c0001t0001g0009a0001c0001t0001g0126a0001c0001t0001g0127others(6): Show | 9 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1135+765_1135+769d others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 20488994 | |||||
chr6:20489142
|
A | C | 1 | a0001c0001t0004g0001 | 3 | HG03471.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1135+894A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489142 | ||||||
chr6:20489144
|
G | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0121a0001c0001t0026g0138 | 3 | HG02630.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1135+896G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489144 | ||||||
chr6:20489272
|
A | G | 3 | a0001c0001t0006g0057a0001c0001t0006g0268a0001c0001t0006g0269 | 3 | HG03654.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1136-896A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489272 | ||||||
chr6:20489386
|
C | T | 1 | a0001c0001t0002g0249 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1136-782C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489386 | ||||||
chr6:20489391
|
A | T | 1 | a0001c0001t0003g0051 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1136-777A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489391 | ||||||
chr6:20489432
|
A | C | 128 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0020others(125): Show | 130 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.1136-736A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489432 | ||||||
chr6:20489463
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1136-705C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489463 | ||||||
chr6:20489539
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1136-629T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489539 | ||||||
chr6:20489950
|
A | T | 1 | a0001c0001t0003g0051 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1136-218A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489950 | ||||||
chr6:20489983
|
G | A | 1 | a0001c0001t0003g0066 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1136-185G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489983 | ||||||
chr6:20490035
|
C | T | 4 | a0001c0001t0001g0081a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136-133C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20490035 | ||||||
chr6:20490159
|
T | G | 27 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0086others(24): Show | 27 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1136-9T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20490159 |