geneid | 51176 |
---|---|
ensemblid | ENSG00000138795.10 |
hgncid | 6551 |
symbol | LEF1 |
name | lymphoid enhancer binding factor 1 |
refseq_nuc | NM_016269.5 |
refseq_prot | NP_057353.1 |
ensembl_nuc | ENST00000265165.6 |
ensembl_prot | ENSP00000265165.1 |
mane_status | MANE Select |
chr | chr4 |
start | 108047548 |
end | 108168932 |
strand | - |
ver | v1.2 |
region | chr4:108047548-108168932 |
region5000 | chr4:108042548-108173932 |
regionname0 | LEF1_chr4_108047548_108168932 |
regionname5000 | LEF1_chr4_108042548_108173932 |
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 | 399 | 257 | 90 | 45 | 75 | 16 | 29 | 57 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0002 | 0/0 | 399 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0003 | 0/0 | 399 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0004 | 0/0 | 399 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0005 | 0/0 | 399 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
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 | 1200 | 251 | 86 | 44 | 74 | 16 | 29 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
c0002 | 0/0 | 1200 | 3 | 2 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
c0003 | 0/0 | 1200 | 3 | 0 | 0 | 3 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
c0004 | 0/0 | 1200 | 2 | 0 | 0 | 1 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
c0005 | 0/0 | 1200 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
c0006 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
c0007 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
c0008 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
c0009 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
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 | 2376 | 80 | 17 | 13 | 36 | 5 | 9 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0002 | 0/0 | 2376 | 71 | 6 | 16 | 33 | 6 | 10 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0003 | 1/1 | 2376 | 54 | 35 | 8 | 5 | 0 | 4 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0004 | 0/0 | 2376 | 9 | 4 | 0 | 2 | 0 | 3 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0005 | 0/0 | 2376 | 7 | 0 | 4 | 3 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0006 | 0/0 | 2376 | 6 | 6 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0007 | 0/0 | 2376 | 5 | 5 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0008 | 0/0 | 2376 | 4 | 0 | 1 | 0 | 3 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0009 | 0/0 | 2376 | 4 | 0 | 2 | 0 | 1 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0010 | 0/0 | 2376 | 3 | 3 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0011 | 0/0 | 2377 | 3 | 3 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0012 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0013 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0014 | 0/0 | 2376 | 2 | 0 | 0 | 0 | 0 | 2 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0015 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0016 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0017 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0018 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0019 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0020 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0021 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0022 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0023 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0024 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0025 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
t0026 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0204 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
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 | 1200 | 251 | 86 | 44 | 74 | 16 | 29 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0002 | 0/0 | 1200 | 3 | 2 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0006 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0007 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0008 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0002c0003 | 0/0 | 1200 | 3 | 0 | 0 | 3 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0003c0004 | 0/0 | 1200 | 2 | 0 | 0 | 1 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0004c0009 | 0/0 | 1200 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0005c0005 | 0/0 | 1200 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3575 | 75 | 15 | 12 | 35 | 5 | 8 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0002 | 0/0 | 3575 | 66 | 6 | 16 | 28 | 6 | 10 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0003 | 1/1 | 3575 | 53 | 35 | 7 | 5 | 0 | 4 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0004 | 0/0 | 3575 | 9 | 4 | 0 | 2 | 0 | 3 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0005 | 0/0 | 3575 | 7 | 0 | 4 | 3 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0006 | 0/0 | 3575 | 5 | 5 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0007 | 0/0 | 3575 | 4 | 4 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0008 | 0/0 | 3575 | 4 | 0 | 1 | 0 | 3 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0009 | 0/0 | 3575 | 4 | 0 | 2 | 0 | 1 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0010 | 0/0 | 3575 | 3 | 3 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0011 | 0/0 | 3576 | 3 | 3 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0012 | 0/0 | 3575 | 2 | 2 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0013 | 0/0 | 3575 | 2 | 2 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0014 | 0/0 | 3575 | 2 | 0 | 0 | 0 | 0 | 2 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0015 | 0/0 | 3575 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0016 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0017 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0018 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0019 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0020 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0021 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0022 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0023 | 0/0 | 3575 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0024 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0025 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0001t0026 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0002t0001 | 0/0 | 3575 | 3 | 2 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0006t0006 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0007t0002 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0001c0008t0007 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0002c0003t0002 | 0/0 | 3575 | 3 | 0 | 0 | 3 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0003c0004t0001 | 0/0 | 3575 | 2 | 0 | 0 | 1 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0004c0009t0002 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
a0005c0005t0003 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | copy fasta | chr4 | 108042548 | 108173932 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0204 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0008g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0008g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0008g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0009g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0009g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0009g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0009g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0010g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0011g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0011g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0012g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0013g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0013g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0014g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0014g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0017g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0018g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0019g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0020g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0021g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0022g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0023g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0024g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0025g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0001t0026g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0006t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0007t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0001c0008t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0002c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0003c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0003c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0004c0009t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
a0005c0005t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | GBR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | GBR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00140 | hp2 | a0001 | c0001 | t0008 | g0009 | EUR | GBR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00280 | hp1 | a0001 | c0001 | t0009 | g0015 | EUR | FIN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | FIN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | FIN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | CHS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00558 | hp2 | a0001 | c0001 | t0005 | g0151 | EAS | CHS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00642 | hp2 | a0005 | c0005 | t0003 | g0113 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01070 | hp1 | a0001 | c0001 | t0009 | g0012 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0013 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01099 | hp2 | a0001 | c0001 | t0008 | g0008 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01243 | hp2 | a0001 | c0001 | t0026 | g0264 | AMR | PUR | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | IBS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01515 | hp2 | a0001 | c0001 | t0015 | g0001 | EUR | IBS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01516 | hp1 | a0001 | c0001 | t0008 | g0007 | EUR | IBS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01884 | hp1 | a0001 | c0008 | t0007 | g0105 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0131 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0164 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0162 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02004 | hp2 | a0001 | c0001 | t0021 | g0098 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02135 | hp1 | a0001 | c0007 | t0002 | g0025 | EAS | KHV | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02257 | hp1 | a0001 | c0001 | t0016 | g0005 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0163 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0106 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02602 | hp1 | a0003 | c0004 | t0001 | g0114 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0222 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0254 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0109 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0102 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02723 | hp2 | a0001 | c0001 | t0011 | g0099 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02809 | hp2 | a0001 | c0006 | t0006 | g0253 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0104 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02886 | hp2 | a0001 | c0001 | t0025 | g0262 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02895 | hp1 | a0001 | c0001 | t0019 | g0095 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02896 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0003 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02976 | hp1 | a0001 | c0001 | t0024 | g0263 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03017 | hp2 | a0001 | c0001 | t0023 | g0166 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0255 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03130 | hp1 | a0001 | c0001 | t0012 | g0108 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0258 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03453 | hp2 | a0001 | c0001 | t0013 | g0110 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03486 | hp2 | a0001 | c0001 | t0013 | g0107 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0055 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0192 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03491 | hp2 | a0001 | c0001 | t0014 | g0112 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03492 | hp1 | a0001 | c0001 | t0014 | g0111 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0056 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0103 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | ESN | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0028 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | BEB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | STU | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | STU | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | STU | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | YRI | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0261 | AFR | YRI | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18983 | hp2 | a0001 | c0001 | t0017 | g0035 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18984 | hp2 | a0002 | c0003 | t0002 | g0074 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0259 | AFR | LWK | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | LWK | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | LWK | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19070 | hp2 | a0004 | c0009 | t0002 | g0096 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19076 | hp1 | a0003 | c0004 | t0001 | g0115 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19076 | hp2 | a0002 | c0003 | t0002 | g0072 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19082 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19085 | hp1 | a0002 | c0003 | t0002 | g0073 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | YRI | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA20129 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | ASW | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA20129 | hp2 | a0001 | c0001 | t0020 | g0097 | AFR | ASW | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | TSI | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA20752 | hp2 | a0001 | c0001 | t0008 | g0006 | EUR | TSI | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | GIH | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA20905 | hp2 | a0001 | c0001 | t0009 | g0040 | SAS | GIH | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0094 | AFR | ACB | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03471 | hp1 | a0001 | c0001 | t0022 | g0248 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | USA | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0101 | AFR | USA | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA20300 | hp1 | a0001 | c0001 | t0018 | g0019 | AFR | USA | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | USA | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | LWK | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
NA21309 | hp2 | a0001 | c0001 | t0012 | g0100 | AFR | LWK | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0204 | REF | REF | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0207 | REF | REF | LEF1_chr4_108042548_108173932 | LEF1 | chr4 | 108042548 | 108173932 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:108089160
|
G | A | 1 | a0005 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.512C>T | p.Pro171Leu | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/12 | 1677/3575 | 512/1200 | 171/399 | chr4 | 108089160 | ||
chr4:108163665
|
G | A | 1 | a0002 | 3 | NA18984.hp2 NA19076.hp2 NA19085.hp1 |
missense_variant | MODERATE | c.317C>T | p.Pro106Leu | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/12 | 1482/3575 | 317/1200 | 106/399 | chr4 | 108163665 | ||
chr4:108165124
|
C | T | 2 | a0003a0005 | 3 | HG00642.hp2 HG02602.hp1 NA19076.hp1 |
missense_variant | MODERATE | c.253G>A | p.Asp85Asn | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/12 | 1418/3575 | 253/1200 | 85/399 | chr4 | 108165124 | ||
chr4:108167638
|
G | C | 1 | a0004 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.130C>G | p.Pro44Ala | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 1295/3575 | 130/1200 | 44/399 | chr4 | 108167638 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:108089222
|
C | T | 1 | a0001c0007 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.450G>A | p.Ala150Ala | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/12 | 1615/3575 | 450/1200 | 150/399 | chr4 | 108089222 | ||
chr4:108163574
|
C | T | 1 | a0001c0006 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.408G>A | p.Pro136Pro | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/12 | 1573/3575 | 408/1200 | 136/399 | chr4 | 108163574 | ||
chr4:108163655
|
C | T | 1 | a0001c0002 | 3 | HG00735.hp2 HG02559.hp1 HG02572.hp1 |
synonymous_variant | LOW | c.327G>A | p.Ser109Ser | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/12 | 1492/3575 | 327/1200 | 109/399 | chr4 | 108163655 | ||
chr4:108165098
|
G | A | 1 | a0001c0008 | 1 | HG01884.hp1 | splice_region_variant&synonymous_variant | LOW | c.279C>T | p.Asp93Asp | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/12 | 1444/3575 | 279/1200 | 93/399 | chr4 | 108165098 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:108047712
|
A | G | 3 | a0001c0001t0007a0001c0001t0022a0001c0008t0007 | 6 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1046T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 12/12 | 15917 | chr4 | 108047712 | |||||
chr4:108047974
|
C | T | 1 | a0001c0001t0011 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*784G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 12/12 | 15655 | chr4 | 108047974 | |||||
chr4:108048205
|
A | C | 1 | a0001c0001t0017 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 12/12 | 15424 | chr4 | 108048205 | |||||
chr4:108048205
|
A | T | 3 | a0001c0001t0006a0001c0001t0019a0001c0006t0006 | 7 | HG02630.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*553T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 12/12 | 15424 | chr4 | 108048205 | |||||
chr4:108048265
|
G | GA | 1 | a0001c0001t0011 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*492_*493insT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 12/12 | 15363 | chr4 | 108048265 | |||||
chr4:108048344
|
G | A | 1 | a0001c0001t0018 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 12/12 | 15285 | chr4 | 108048344 | |||||
chr4:108048379
|
G | C | 2 | a0001c0001t0009a0001c0001t0023 | 5 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*379C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 12/12 | 15250 | chr4 | 108048379 | |||||
chr4:108048434
|
A | G | 18 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(15): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*324T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 12/12 | 15195 | chr4 | 108048434 | |||||
chr4:108048727
|
G | A | 1 | a0001c0001t0005 | 7 | HG00558.hp2 HG01934.hp1 HG01952.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*31C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 12/12 | 14902 | chr4 | 108048727 | |||||
chr4:108168015
|
C | T | 1 | a0001c0001t0014 | 2 | HG03491.hp2 HG03492.hp1 |
5_prime_UTR_variant | MODIFIER | c.-248G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 248 | chr4 | 108168015 | |||||
chr4:108168017
|
G | A | 2 | a0001c0001t0024a0001c0001t0025 | 2 | HG02886.hp2 HG02976.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-250C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | chr4 | 108168017 | ||||||
chr4:108168060
|
A | C | 7 | a0001c0001t0007a0001c0001t0011a0001c0001t0012others(4): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-293T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 293 | chr4 | 108168060 | |||||
chr4:108168064
|
C | T | 1 | a0001c0001t0021 | 1 | HG02004.hp2 | 5_prime_UTR_variant | MODIFIER | c.-297G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 297 | chr4 | 108168064 | |||||
chr4:108168082
|
G | A | 1 | a0001c0001t0020 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-315C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 315 | chr4 | 108168082 | |||||
chr4:108168144
|
C | T | 2 | a0001c0001t0024a0001c0001t0025 | 2 | HG02886.hp2 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-377G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 377 | chr4 | 108168144 | |||||
chr4:108168154
|
C | G | 1 | a0001c0001t0008 | 4 | HG00140.hp2 HG01099.hp2 HG01516.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-387G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 387 | chr4 | 108168154 | |||||
chr4:108168215
|
G | A | 1 | a0001c0001t0016 | 1 | HG02257.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-448C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | chr4 | 108168215 | ||||||
chr4:108168241
|
C | T | 1 | a0001c0001t0016 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-474G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 474 | chr4 | 108168241 | |||||
chr4:108168337
|
T | C | 2 | a0001c0001t0024a0001c0001t0025 | 2 | HG02886.hp2 HG02976.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-570A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | chr4 | 108168337 | ||||||
chr4:108168517
|
G | A | 1 | a0001c0001t0026 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-750C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 750 | chr4 | 108168517 | |||||
chr4:108168668
|
C | G | 12 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(9): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
5_prime_UTR_variant | MODIFIER | c.-901G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 901 | chr4 | 108168668 | |||||
chr4:108168788
|
C | T | 1 | a0001c0001t0010 | 3 | HG02896.hp1 HG02897.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-1021G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 1021 | chr4 | 108168788 | |||||
chr4:108168871
|
C | T | 1 | a0001c0001t0015 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1104G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/12 | 1104 | chr4 | 108168871 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:108049042
|
T | C | 1 | a0001c0001t0015g0001 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.*7-291A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108049042 | ||||||
chr4:108049043
|
T | C | 1 | a0001c0001t0004g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*7-292A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108049043 | ||||||
chr4:108049066
|
G | C | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.*7-315C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108049066 | ||||||
chr4:108049072
|
A | G | 3 | a0001c0002t0001g0121a0001c0002t0001g0129a0001c0002t0001g0130 | 3 | HG00735.hp2 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.*7-321T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108049072 | ||||||
chr4:108049188
|
A | T | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.*7-437T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108049188 | ||||||
chr4:108049315
|
C | A | 3 | a0001c0001t0003g0249a0001c0001t0003g0250a0001c0001t0003g0251 | 3 | HG03139.hp1 HG03195.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*7-564G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108049315 | ||||||
chr4:108049329
|
A | G | 54 | a0001c0001t0003g0117a0001c0001t0003g0122a0001c0001t0003g0123others(51): Show | 54 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.*7-578T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108049329 | ||||||
chr4:108049382
|
T | C | 1 | a0001c0001t0002g0050 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.*7-631A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108049382 | ||||||
chr4:108049504
|
G | C | 1 | a0001c0001t0009g0015 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.*7-753C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108049504 | ||||||
chr4:108050169
|
G | A | 4 | a0001c0001t0003g0192a0001c0001t0003g0245a0001c0001t0025g0262others(1): Show | 4 | HG00642.hp2 HG02886.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.*7-1418C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108050169 | ||||||
chr4:108050352
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.*7-1601C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108050352 | ||||||
chr4:108050524
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.*7-1773C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108050524 | ||||||
chr4:108050617
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.*7-1866G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108050617 | ||||||
chr4:108050722
|
G | A | 4 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.*7-1971C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108050722 | ||||||
chr4:108050804
|
G | T | 2 | a0001c0001t0003g0245a0001c0001t0025g0262 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.*7-2053C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108050804 | ||||||
chr4:108050931
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.*7-2180G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108050931 | ||||||
chr4:108050939
|
C | T | 1 | a0001c0001t0020g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*7-2188G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108050939 | ||||||
chr4:108051036
|
G | A | 2 | a0001c0001t0003g0245a0001c0001t0025g0262 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.*7-2285C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051036 | ||||||
chr4:108051091
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.*7-2340C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051091 | ||||||
chr4:108051215
|
A | C | 8 | a0001c0001t0003g0244a0001c0001t0006g0254a0001c0001t0006g0255others(5): Show | 8 | HG01255.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.*7-2464T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051215 | ||||||
chr4:108051250
|
G | T | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0003g0245others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.*7-2499C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051250 | ||||||
chr4:108051526
|
C | G | 1 | a0001c0001t0002g0034 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.*7-2775G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051526 | ||||||
chr4:108051551
|
C | A | 89 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0001g0128others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.*7-2800G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051551 | ||||||
chr4:108051568
|
G | A | 3 | a0002c0003t0002g0072a0002c0003t0002g0073a0002c0003t0002g0074 | 3 | NA18984.hp2 NA19076.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.*7-2817C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051568 | ||||||
chr4:108051597
|
G | A | 2 | a0001c0001t0014g0111a0001c0001t0014g0112 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.*7-2846C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051597 | ||||||
chr4:108051631
|
G | T | 7 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0003g0246others(4): Show | 7 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.*7-2880C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051631 | ||||||
chr4:108051752
|
C | T | 5 | a0001c0001t0003g0123a0001c0001t0003g0249a0001c0001t0003g0250others(2): Show | 5 | HG02257.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.*7-3001G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051752 | ||||||
chr4:108051758
|
T | C | 9 | a0001c0001t0002g0088a0001c0001t0003g0124a0001c0001t0003g0192others(6): Show | 9 | HG00642.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.*7-3007A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051758 | ||||||
chr4:108051759
|
G | A | 2 | a0001c0001t0003g0245a0001c0001t0025g0262 | 2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.*7-3008C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051759 | ||||||
chr4:108051816
|
A | G | 1 | a0001c0001t0004g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.*7-3065T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108051816 | ||||||
chr4:108052156
|
G | T | 7 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0046others(4): Show | 7 | HG00099.hp1 HG00735.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.*7-3405C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108052156 | ||||||
chr4:108052214
|
G | A | 3 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0224 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.*7-3463C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108052214 | ||||||
chr4:108052330
|
G | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0016g0005 | 3 | HG02257.hp1 NA18971.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.*7-3579C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108052330 | ||||||
chr4:108052967
|
C | T | 8 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(5): Show | 8 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.*7-4216G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108052967 | ||||||
chr4:108052989
|
G | T | 1 | a0001c0001t0002g0047 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.*7-4238C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108052989 | ||||||
chr4:108053061
|
T | G | 3 | a0001c0001t0001g0132a0001c0001t0001g0142a0004c0009t0002g0096 | 3 | NA18968.hp1 NA18982.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.*7-4310A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108053061 | ||||||
chr4:108053415
|
T | A | 1 | a0001c0001t0020g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*7-4664A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108053415 | ||||||
chr4:108053475
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.*7-4724C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108053475 | ||||||
chr4:108053601
|
G | A | 3 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0224 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.*7-4850C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108053601 | ||||||
chr4:108053735
|
G | A | 1 | a0001c0001t0002g0061 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.*7-4984C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108053735 | ||||||
chr4:108053856
|
T | C | 2 | a0001c0001t0002g0064a0001c0001t0002g0092 | 2 | NA18952.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.*7-5105A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108053856 | ||||||
chr4:108053884
|
T | A | 1 | a0001c0001t0003g0124 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.*7-5133A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108053884 | ||||||
chr4:108054095
|
T | G | 174 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.*7-5344A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054095 | ||||||
chr4:108054185
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.*7-5434A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054185 | ||||||
chr4:108054267
|
G | A | 7 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0214others(4): Show | 7 | HG01884.hp2 HG01975.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.*7-5516C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054267 | ||||||
chr4:108054271
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.*7-5520G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054271 | ||||||
chr4:108054406
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0227a0001c0001t0002g0079 | 3 | NA18994.hp2 NA19005.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.*7-5655G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054406 | ||||||
chr4:108054407
|
G | A | 8 | a0001c0001t0001g0236a0001c0001t0003g0218a0001c0001t0003g0219others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.*7-5656C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054407 | ||||||
chr4:108054494
|
A | G | 10 | a0001c0001t0002g0088a0001c0001t0003g0124a0001c0001t0003g0192others(7): Show | 10 | HG00642.hp2 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.*7-5743T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054494 | ||||||
chr4:108054553
|
T | C | 263 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.*7-5802A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054553 | ||||||
chr4:108054579
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.*7-5828C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054579 | ||||||
chr4:108054756
|
C | G | 223 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.*7-6005G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054756 | ||||||
chr4:108054935
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.*7-6184C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054935 | ||||||
chr4:108054940
|
G | A | 3 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0224 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.*7-6189C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108054940 | ||||||
chr4:108055281
|
C | T | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.*7-6530G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108055281 | ||||||
chr4:108055335
|
T | C | 223 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.*7-6584A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108055335 | ||||||
chr4:108055452
|
C | T | 223 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.*7-6701G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108055452 | ||||||
chr4:108055766
|
G | T | 1 | a0001c0001t0020g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*7-7015C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108055766 | ||||||
chr4:108056259
|
G | C | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.*6+7364C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108056259 | ||||||
chr4:108056336
|
T | C | 3 | a0001c0001t0003g0223a0001c0001t0003g0225a0001c0001t0003g0226 | 3 | HG01884.hp2 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.*6+7287A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108056336 | ||||||
chr4:108056474
|
C | A | 173 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.*6+7149G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108056474 | ||||||
chr4:108056510
|
A | C | 250 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.*6+7113T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108056510 | ||||||
chr4:108056528
|
C | T | 13 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(10): Show | 13 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.*6+7095G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108056528 | ||||||
chr4:108056762
|
C | T | 249 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.*6+6861G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108056762 | ||||||
chr4:108056906
|
C | CA | 22 | a0001c0001t0001g0116a0001c0001t0001g0140a0001c0001t0001g0145others(19): Show | 22 | HG00735.hp1 HG01109.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.*6+6716dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108056906 | ||||||
chr4:108056921
|
A | C | 2 | a0001c0001t0010g0002a0001c0001t0010g0003 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.*6+6702T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108056921 | ||||||
chr4:108056925
|
C | A | 1 | a0001c0002t0001g0129 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.*6+6698G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108056925 | ||||||
chr4:108056960
|
G | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0003g0117 | 3 | HG01109.hp1 HG01257.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.*6+6663C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108056960 | ||||||
chr4:108056986
|
C | T | 13 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(10): Show | 13 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.*6+6637G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108056986 | ||||||
chr4:108057038
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.*6+6585G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108057038 | ||||||
chr4:108057091
|
C | A | 1 | a0003c0004t0001g0115 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*6+6532G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108057091 | ||||||
chr4:108057116
|
C | T | 1 | a0001c0001t0012g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*6+6507G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108057116 | ||||||
chr4:108057159
|
C | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0184 | 3 | NA18950.hp2 NA18962.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.*6+6464G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108057159 | ||||||
chr4:108057294
|
T | C | 174 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.*6+6329A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108057294 | ||||||
chr4:108057356
|
C | T | 263 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.*6+6267G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108057356 | ||||||
chr4:108057560
|
C | A | 6 | a0001c0001t0001g0236a0001c0001t0003g0249a0001c0001t0003g0250others(3): Show | 6 | HG01515.hp2 HG02257.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6+6063G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108057560 | ||||||
chr4:108057574
|
T | G | 1 | a0001c0001t0005g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.*6+6049A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108057574 | ||||||
chr4:108057857
|
G | C | 1 | a0001c0001t0005g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.*6+5766C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108057857 | ||||||
chr4:108057860
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.*6+5763C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108057860 | ||||||
chr4:108057872
|
C | CT | 23 | a0001c0001t0002g0051a0001c0001t0003g0235a0001c0001t0003g0244others(20): Show | 23 | HG01255.hp1 HG01884.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.*6+5750dupA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108057872 | ||||||
chr4:108058019
|
G | A | 1 | a0001c0001t0004g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*6+5604C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108058019 | ||||||
chr4:108058027
|
C | T | 6 | a0001c0001t0001g0236a0001c0001t0003g0249a0001c0001t0003g0250others(3): Show | 6 | HG01515.hp2 HG02257.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6+5596G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108058027 | ||||||
chr4:108058231
|
C | T | 21 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(18): Show | 21 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.*6+5392G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108058231 | ||||||
chr4:108058254
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.*6+5369T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108058254 | ||||||
chr4:108058568
|
CA | C | 9 | a0001c0001t0003g0249a0001c0001t0003g0250a0001c0001t0004g0030others(6): Show | 9 | HG02451.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.*6+5054delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108058568 | ||||||
chr4:108058577
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.*6+5046G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108058577 | ||||||
chr4:108058849
|
G | A | 5 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(2): Show | 5 | HG01109.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.*6+4774C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108058849 | ||||||
chr4:108058884
|
C | T | 27 | a0001c0001t0001g0243a0001c0001t0003g0192a0001c0001t0003g0238others(24): Show | 27 | HG00642.hp2 HG01192.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.*6+4739G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108058884 | ||||||
chr4:108059047
|
G | A | 2 | a0001c0001t0006g0254a0001c0001t0006g0259 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.*6+4576C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059047 | ||||||
chr4:108059143
|
A | G | 13 | a0001c0001t0001g0236a0001c0001t0001g0256a0001c0001t0001g0257others(10): Show | 13 | HG01109.hp2 HG01255.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.*6+4480T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059143 | ||||||
chr4:108059154
|
T | C | 1 | a0001c0001t0003g0250 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.*6+4469A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059154 | ||||||
chr4:108059202
|
C | T | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.*6+4421G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059202 | ||||||
chr4:108059253
|
C | T | 23 | a0001c0001t0001g0243a0001c0001t0003g0238a0001c0001t0003g0239others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.*6+4370G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059253 | ||||||
chr4:108059263
|
G | A | 25 | a0001c0001t0003g0122a0001c0001t0003g0169a0001c0001t0003g0170others(22): Show | 25 | HG00558.hp1 HG01099.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.*6+4360C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059263 | ||||||
chr4:108059269
|
G | A | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.*6+4354C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059269 | ||||||
chr4:108059276
|
A | G | 4 | a0001c0001t0003g0247a0001c0001t0003g0249a0001c0001t0003g0250others(1): Show | 4 | HG03139.hp1 HG03195.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.*6+4347T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059276 | ||||||
chr4:108059439
|
C | A | 10 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(7): Show | 10 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.*6+4184G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059439 | ||||||
chr4:108059569
|
C | G | 1 | a0001c0001t0022g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.*6+4054G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059569 | ||||||
chr4:108059616
|
A | G | 225 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.*6+4007T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059616 | ||||||
chr4:108059757
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.*6+3866G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059757 | ||||||
chr4:108059809
|
C | T | 23 | a0001c0001t0001g0243a0001c0001t0003g0238a0001c0001t0003g0239others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.*6+3814G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059809 | ||||||
chr4:108059810
|
C | G | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.*6+3813G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059810 | ||||||
chr4:108059990
|
G | A | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.*6+3633C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108059990 | ||||||
chr4:108060334
|
G | T | 5 | a0001c0001t0001g0140a0001c0001t0002g0022a0001c0001t0002g0029others(2): Show | 5 | NA18951.hp1 NA18959.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.*6+3289C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108060334 | ||||||
chr4:108060698
|
C | T | 10 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(7): Show | 10 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.*6+2925G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108060698 | ||||||
chr4:108060842
|
C | T | 222 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.*6+2781G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108060842 | ||||||
chr4:108060926
|
G | T | 1 | a0001c0001t0002g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.*6+2697C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108060926 | ||||||
chr4:108060958
|
G | A | 1 | a0001c0001t0004g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.*6+2665C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108060958 | ||||||
chr4:108060982
|
T | G | 7 | a0001c0001t0003g0244a0001c0001t0006g0254a0001c0001t0006g0255others(4): Show | 7 | HG01255.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+2641A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108060982 | ||||||
chr4:108061215
|
TA | T | 10 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(7): Show | 10 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.*6+2407delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061215 | ||||||
chr4:108061219
|
G | C | 202 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.*6+2404C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061219 | ||||||
chr4:108061223
|
T | C | 2 | a0001c0001t0013g0110a0001c0001t0022g0248 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.*6+2400A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061223 | ||||||
chr4:108061224
|
A | G | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.*6+2399T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061224 | ||||||
chr4:108061317
|
C | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0002g0023 | 3 | NA18954.hp1 NA18957.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.*6+2306G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061317 | ||||||
chr4:108061335
|
G | A | 33 | a0001c0001t0001g0243a0001c0001t0003g0238a0001c0001t0003g0239others(30): Show | 33 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.*6+2288C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061335 | ||||||
chr4:108061642
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.*6+1981G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061642 | ||||||
chr4:108061642
|
CA | C | 178 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0127others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.*6+1980delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061642 | ||||||
chr4:108061642
|
CAA | C | 15 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0003g0238others(12): Show | 15 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.*6+1979_*6+1980del others(2): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061642 | ||||||
chr4:108061643
|
A | C | 4 | a0001c0001t0001g0188a0001c0001t0001g0243a0001c0001t0003g0241others(1): Show | 4 | HG02602.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.*6+1980T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061643 | ||||||
chr4:108061644
|
A | C | 1 | a0003c0004t0001g0115 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.*6+1979T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061644 | ||||||
chr4:108061692
|
T | C | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.*6+1931A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061692 | ||||||
chr4:108061808
|
G | A | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.*6+1815C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061808 | ||||||
chr4:108061876
|
G | T | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.*6+1747C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108061876 | ||||||
chr4:108062341
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.*6+1282C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108062341 | ||||||
chr4:108062368
|
G | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0009g0012others(3): Show | 6 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.*6+1255C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108062368 | ||||||
chr4:108062398
|
G | A | 1 | a0001c0001t0022g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.*6+1225C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108062398 | ||||||
chr4:108062470
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.*6+1153C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108062470 | ||||||
chr4:108062548
|
C | A | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.*6+1075G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108062548 | ||||||
chr4:108062577
|
C | T | 211 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.*6+1046G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108062577 | ||||||
chr4:108062626
|
G | A | 3 | a0001c0001t0009g0012a0001c0001t0009g0013a0001c0001t0009g0015 | 3 | HG00280.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.*6+997C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108062626 | ||||||
chr4:108062880
|
A | G | 15 | a0001c0001t0001g0243a0001c0001t0003g0238a0001c0001t0003g0239others(12): Show | 15 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.*6+743T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108062880 | ||||||
chr4:108063227
|
T | C | 2 | a0001c0001t0003g0212a0001c0001t0003g0213 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.*6+396A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108063227 | ||||||
chr4:108063249
|
C | T | 7 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0214others(4): Show | 7 | HG01884.hp2 HG01975.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.*6+374G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108063249 | ||||||
chr4:108063457
|
C | A | 1 | a0001c0001t0002g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.*6+166G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 11/11 | chr4 | 108063457 | ||||||
chr4:108063724
|
C | T | 3 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0002g0023 | 3 | NA18954.hp1 NA18957.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1166-61G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 10/11 | chr4 | 108063724 | ||||||
chr4:108064232
|
A | G | 227 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1165+104T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 10/11 | chr4 | 108064232 | ||||||
chr4:108064277
|
G | T | 16 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(13): Show | 16 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.1165+59C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 10/11 | chr4 | 108064277 | ||||||
chr4:108064619
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1117-235C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064619 | ||||||
chr4:108064645
|
TCTCTCTC others(1): Show |
T | 4 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1117-269_1117-262d others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064645 | ||||||
chr4:108064655
|
T | TCA | 5 | a0001c0001t0001g0116a0001c0001t0003g0223a0001c0001t0003g0225others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117-273_1117-272d others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064655 | ||||||
chr4:108064655
|
T | TCACA | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1117-275_1117-272d others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064655 | ||||||
chr4:108064655
|
TCACA | T | 13 | a0001c0001t0003g0171a0001c0001t0003g0200a0001c0001t0003g0218others(10): Show | 13 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1117-275_1117-272d others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064655 | ||||||
chr4:108064655
|
TCACACA | T | 41 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(38): Show | 41 | HG00642.hp2 HG01099.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1117-277_1117-272d others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064655 | ||||||
chr4:108064655
|
TCACACAC others(1): Show |
T | 19 | a0001c0001t0001g0236a0001c0001t0003g0124a0001c0001t0003g0192others(16): Show | 19 | HG01255.hp1 HG01515.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1117-279_1117-272d others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064655 | ||||||
chr4:108064655
|
TCACACAC others(3): Show |
T | 1 | a0001c0001t0003g0170 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1117-281_1117-272d others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064655 | ||||||
chr4:108064659
|
A | T | 4 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1117-275T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064659 | ||||||
chr4:108064672
|
CACACACA others(16): Show |
C | 1 | a0001c0001t0001g0140 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1117-311_1117-289d others(25): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064672 | ||||||
chr4:108064680
|
CACACACA others(8): Show |
C | 7 | a0001c0001t0002g0036a0001c0001t0002g0043a0001c0001t0005g0131others(4): Show | 7 | HG01934.hp1 HG01952.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117-311_1117-297d others(17): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064680 | ||||||
chr4:108064682
|
CACACACA others(6): Show |
C | 78 | a0001c0001t0001g0127a0001c0001t0001g0152a0001c0001t0001g0161others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.1117-311_1117-299d others(15): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064682 | ||||||
chr4:108064684
|
CACACACA others(4): Show |
C | 83 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1117-311_1117-301d others(13): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064684 | ||||||
chr4:108064741
|
T | A | 6 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0045others(3): Show | 6 | HG01256.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1117-357A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064741 | ||||||
chr4:108064777
|
G | T | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1117-393C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064777 | ||||||
chr4:108064803
|
G | A | 1 | a0003c0004t0001g0114 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1117-419C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064803 | ||||||
chr4:108064920
|
G | C | 1 | a0001c0001t0013g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1117-536C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108064920 | ||||||
chr4:108065147
|
A | C | 1 | a0001c0001t0001g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1117-763T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065147 | ||||||
chr4:108065156
|
T | C | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1117-772A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065156 | ||||||
chr4:108065237
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1117-853C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065237 | ||||||
chr4:108065252
|
C | T | 1 | a0001c0001t0003g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1117-868G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065252 | ||||||
chr4:108065259
|
A | G | 50 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0252others(47): Show | 50 | HG00642.hp2 HG01109.hp2 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.1117-875T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065259 | ||||||
chr4:108065346
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1117-962C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065346 | ||||||
chr4:108065409
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1117-1025G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065409 | ||||||
chr4:108065458
|
T | C | 25 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(22): Show | 25 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.1117-1074A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065458 | ||||||
chr4:108065560
|
C | G | 3 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0224 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1117-1176G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065560 | ||||||
chr4:108065767
|
T | C | 1 | a0001c0001t0012g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1117-1383A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065767 | ||||||
chr4:108065846
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1117-1462G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065846 | ||||||
chr4:108065851
|
C | T | 5 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(2): Show | 5 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1117-1467G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065851 | ||||||
chr4:108065909
|
ATTATTGT others(2): Show |
A | 11 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1117-1534_1117-152 others(13): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108065909 | ||||||
chr4:108066091
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1117-1707G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108066091 | ||||||
chr4:108066274
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1117-1890C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108066274 | ||||||
chr4:108066401
|
T | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0145a0001c0001t0001g0149 | 3 | NA18970.hp2 NA18982.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1117-2017A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108066401 | ||||||
chr4:108066412
|
G | C | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1117-2028C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108066412 | ||||||
chr4:108066603
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1117-2219G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108066603 | ||||||
chr4:108066665
|
T | G | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1117-2281A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108066665 | ||||||
chr4:108066714
|
T | C | 168 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1117-2330A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108066714 | ||||||
chr4:108066798
|
T | C | 1 | a0001c0001t0012g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1117-2414A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108066798 | ||||||
chr4:108066804
|
A | C | 1 | a0001c0001t0001g0177 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1117-2420T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108066804 | ||||||
chr4:108066806
|
T | C | 4 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0008others(1): Show | 4 | HG00140.hp2 HG01099.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1117-2422A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108066806 | ||||||
chr4:108067240
|
T | C | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1117-2856A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108067240 | ||||||
chr4:108067500
|
C | T | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1117-3116G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108067500 | ||||||
chr4:108067605
|
T | C | 25 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(22): Show | 25 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.1116+3058A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108067605 | ||||||
chr4:108067657
|
G | C | 1 | a0001c0001t0003g0247 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1116+3006C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108067657 | ||||||
chr4:108067985
|
G | A | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1116+2678C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108067985 | ||||||
chr4:108067989
|
C | T | 1 | a0001c0001t0002g0077 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1116+2674G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108067989 | ||||||
chr4:108068052
|
C | G | 11 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1116+2611G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108068052 | ||||||
chr4:108068066
|
G | A | 200 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1116+2597C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108068066 | ||||||
chr4:108068113
|
C | CAAAATTA others(317): Show |
1 | a0001c0001t0010g0003 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1116+2549_1116+255 others(328): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108068113 | ||||||
chr4:108068113
|
C | CAAAATTA others(318): Show |
5 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(2): Show | 5 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116+2549_1116+255 others(329): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108068113 | ||||||
chr4:108068113
|
C | CAAAATTA others(319): Show |
2 | a0001c0001t0010g0004a0003c0004t0001g0115 | 2 | NA19076.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1116+2549_1116+255 others(330): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108068113 | ||||||
chr4:108068237
|
A | G | 11 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1116+2426T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108068237 | ||||||
chr4:108068266
|
T | TCAAAA | 8 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(5): Show | 8 | HG01109.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1116+2392_1116+239 others(9): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108068266 | ||||||
chr4:108068281
|
A | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0081 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1116+2382T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108068281 | ||||||
chr4:108068379
|
T | A | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116+2284A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108068379 | ||||||
chr4:108068380
|
G | A | 25 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(22): Show | 25 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.1116+2283C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108068380 | ||||||
chr4:108068932
|
T | C | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1116+1731A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108068932 | ||||||
chr4:108069020
|
G | A | 3 | a0001c0001t0004g0016a0001c0001t0004g0030a0001c0001t0004g0031 | 3 | HG02451.hp2 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1116+1643C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069020 | ||||||
chr4:108069365
|
TATAAA | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG00280.hp2 HG02976.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116+1293_1116+129 others(9): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069365 | ||||||
chr4:108069415
|
A | G | 1 | a0001c0001t0003g0235 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1116+1248T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069415 | ||||||
chr4:108069492
|
T | C | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1116+1171A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069492 | ||||||
chr4:108069514
|
T | C | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1116+1149A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069514 | ||||||
chr4:108069549
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1116+1114C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069549 | ||||||
chr4:108069608
|
A | G | 2 | a0001c0001t0001g0134a0001c0001t0001g0216 | 2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1116+1055T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069608 | ||||||
chr4:108069857
|
C | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0195 | 2 | HG02109.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1116+806G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069857 | ||||||
chr4:108069952
|
T | C | 211 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1116+711A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069952 | ||||||
chr4:108069957
|
CA | C | 30 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0243others(27): Show | 30 | HG00323.hp2 HG01192.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1116+705delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069957 | ||||||
chr4:108069957
|
CAA | C | 189 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1116+704_1116+705d others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069957 | ||||||
chr4:108069986
|
T | C | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0184 | 3 | NA18950.hp2 NA18962.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1116+677A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108069986 | ||||||
chr4:108070022
|
A | G | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1116+641T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108070022 | ||||||
chr4:108070101
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1116+562C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108070101 | ||||||
chr4:108070219
|
T | G | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1116+444A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 9/11 | chr4 | 108070219 | ||||||
chr4:108070806
|
A | G | 2 | a0001c0001t0002g0064a0001c0001t0002g0092 | 2 | NA18952.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1009-36T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108070806 | ||||||
chr4:108070823
|
C | T | 219 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1009-53G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108070823 | ||||||
chr4:108071014
|
A | C | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009-244T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071014 | ||||||
chr4:108071212
|
A | T | 3 | a0001c0002t0001g0121a0001c0002t0001g0129a0001c0002t0001g0130 | 3 | HG00735.hp2 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1009-442T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071212 | ||||||
chr4:108071228
|
A | G | 11 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1009-458T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071228 | ||||||
chr4:108071353
|
C | T | 11 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1009-583G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071353 | ||||||
chr4:108071441
|
C | T | 169 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1009-671G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071441 | ||||||
chr4:108071450
|
ATTTAAG | A | 4 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0008others(1): Show | 4 | HG00140.hp2 HG01099.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009-686_1009-681d others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071450 | ||||||
chr4:108071470
|
C | G | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1009-700G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071470 | ||||||
chr4:108071611
|
G | A | 3 | a0001c0001t0003g0228a0001c0001t0014g0111a0001c0001t0014g0112 | 3 | HG03491.hp2 HG03492.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1009-841C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071611 | ||||||
chr4:108071734
|
G | T | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1009-964C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071734 | ||||||
chr4:108071843
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1009-1073G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071843 | ||||||
chr4:108071863
|
T | C | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1009-1093A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071863 | ||||||
chr4:108071938
|
C | T | 4 | a0001c0001t0003g0192a0003c0004t0001g0114a0003c0004t0001g0115others(1): Show | 4 | HG00642.hp2 HG02602.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-1168G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071938 | ||||||
chr4:108071961
|
T | C | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1009-1191A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071961 | ||||||
chr4:108071991
|
G | A | 11 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1009-1221C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108071991 | ||||||
chr4:108072195
|
A | T | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1009-1425T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108072195 | ||||||
chr4:108072202
|
G | A | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1009-1432C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108072202 | ||||||
chr4:108072217
|
T | TAGAGTGA others(1): Show |
213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1009-1455_1009-144 others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108072217 | ||||||
chr4:108072290
|
G | A | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1009-1520C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108072290 | ||||||
chr4:108072293
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1009-1523G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108072293 | ||||||
chr4:108072423
|
G | A | 8 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0190others(5): Show | 8 | HG01081.hp1 HG01106.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.1009-1653C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108072423 | ||||||
chr4:108072461
|
G | A | 6 | a0001c0001t0001g0236a0001c0001t0001g0256a0001c0001t0001g0257others(3): Show | 6 | HG01109.hp2 HG01515.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1009-1691C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108072461 | ||||||
chr4:108072706
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1009-1936T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108072706 | ||||||
chr4:108072730
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1009-1960C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108072730 | ||||||
chr4:108072856
|
C | T | 7 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0046others(4): Show | 7 | HG00099.hp1 HG00735.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009-2086G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108072856 | ||||||
chr4:108072901
|
T | TTTG | 25 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0124others(22): Show | 25 | HG00642.hp2 HG01192.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1009-2134_1009-213 others(7): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108072901 | ||||||
chr4:108073032
|
G | A | 4 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0214others(1): Show | 4 | HG01975.hp2 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-2262C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073032 | ||||||
chr4:108073123
|
T | C | 169 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1009-2353A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073123 | ||||||
chr4:108073344
|
C | T | 11 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1009-2574G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073344 | ||||||
chr4:108073606
|
T | C | 211 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1009-2836A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073606 | ||||||
chr4:108073642
|
C | G | 4 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009-2872G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073642 | ||||||
chr4:108073680
|
A | G | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1009-2910T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073680 | ||||||
chr4:108073748
|
T | A | 200 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1009-2978A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073748 | ||||||
chr4:108073823
|
AC | A | 188 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1009-3054delG | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073823 | ||||||
chr4:108073832
|
C | T | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0002g0026others(25): Show | 28 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1009-3062G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073832 | ||||||
chr4:108073833
|
C | T | 205 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1009-3063G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073833 | ||||||
chr4:108073857
|
G | A | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1009-3087C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073857 | ||||||
chr4:108073886
|
C | T | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1009-3116G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073886 | ||||||
chr4:108073888
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1009-3118G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108073888 | ||||||
chr4:108074080
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1009-3310A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108074080 | ||||||
chr4:108074317
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00323.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1009-3547A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108074317 | ||||||
chr4:108074415
|
A | G | 1 | a0001c0007t0002g0025 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1009-3645T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108074415 | ||||||
chr4:108074573
|
T | A | 11 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1008+3647A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108074573 | ||||||
chr4:108074788
|
G | A | 3 | a0001c0001t0001g0252a0001c0001t0003g0247a0001c0001t0003g0251 | 3 | HG02922.hp1 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1008+3432C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108074788 | ||||||
chr4:108074930
|
TAACTCAA others(16): Show |
T | 1 | a0001c0001t0002g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1008+3267_1008+328 others(27): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108074930 | ||||||
chr4:108074957
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1008+3263A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108074957 | ||||||
chr4:108075002
|
CCT | C | 25 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(22): Show | 25 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.1008+3216_1008+321 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108075002 | ||||||
chr4:108075532
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0156 | 2 | NA18983.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1008+2688C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108075532 | ||||||
chr4:108075997
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1008+2223C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108075997 | ||||||
chr4:108076026
|
T | TA | 211 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1008+2193dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076026 | ||||||
chr4:108076237
|
C | T | 211 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1008+1983G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076237 | ||||||
chr4:108076242
|
T | A | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+1978A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076242 | ||||||
chr4:108076243
|
T | C | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1008+1977A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076243 | ||||||
chr4:108076311
|
C | T | 219 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1008+1909G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076311 | ||||||
chr4:108076317
|
T | C | 7 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0214others(4): Show | 7 | HG01884.hp2 HG01975.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008+1903A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076317 | ||||||
chr4:108076321
|
C | T | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008+1899G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076321 | ||||||
chr4:108076438
|
G | A | 25 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(22): Show | 25 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.1008+1782C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076438 | ||||||
chr4:108076528
|
A | G | 2 | a0001c0001t0002g0018a0001c0001t0018g0019 | 2 | HG01358.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1008+1692T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076528 | ||||||
chr4:108076614
|
G | A | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+1606C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076614 | ||||||
chr4:108076854
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1008+1366G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076854 | ||||||
chr4:108076879
|
T | A | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008+1341A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108076879 | ||||||
chr4:108077016
|
G | A | 4 | a0001c0001t0009g0012a0001c0001t0009g0013a0001c0001t0009g0015others(1): Show | 4 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008+1204C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077016 | ||||||
chr4:108077025
|
C | CA | 113 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0001g0132others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.1008+1194dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077025 | ||||||
chr4:108077025
|
C | CAA | 101 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0128others(98): Show | 101 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.1008+1193_1008+119 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077025 | ||||||
chr4:108077141
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1008+1079G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077141 | ||||||
chr4:108077175
|
CA | C | 13 | a0001c0001t0002g0078a0001c0001t0003g0244a0001c0001t0006g0254others(10): Show | 13 | HG01255.hp1 HG02630.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008+1044delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077175 | ||||||
chr4:108077179
|
A | T | 192 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1008+1041T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077179 | ||||||
chr4:108077219
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1008+1001C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077219 | ||||||
chr4:108077364
|
G | A | 1 | a0001c0001t0003g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1008+856C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077364 | ||||||
chr4:108077375
|
T | C | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008+845A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077375 | ||||||
chr4:108077434
|
A | G | 168 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1008+786T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077434 | ||||||
chr4:108077434
|
ACCTCTGC others(33): Show |
A | 4 | a0001c0001t0003g0192a0003c0004t0001g0114a0003c0004t0001g0115others(1): Show | 4 | HG00642.hp2 HG02602.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008+746_1008+785d others(42): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077434 | ||||||
chr4:108077455
|
A | AGTCTGGG others(33): Show |
161 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0127others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1008+725_1008+764d others(42): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077455 | ||||||
chr4:108077455
|
A | C | 4 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+765T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077455 | ||||||
chr4:108077455
|
AGTCTGGG others(33): Show |
A | 23 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(20): Show | 23 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1008+725_1008+764d others(42): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077455 | ||||||
chr4:108077455
|
AGTCTGGG others(73): Show |
A | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1008+685_1008+764d others(82): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077455 | ||||||
chr4:108077491
|
G | GCCCCGTC others(33): Show |
1 | a0001c0001t0001g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1008+728_1008+729i others(42): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077491 | ||||||
chr4:108077495
|
C | CGTCTGGG others(33): Show |
1 | a0001c0001t0002g0027 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1008+724_1008+725i others(42): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077495 | ||||||
chr4:108077523
|
C | T | 1 | a0001c0001t0013g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1008+697G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077523 | ||||||
chr4:108077634
|
G | A | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1008+586C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077634 | ||||||
chr4:108077643
|
C | CGGCTGCC others(33): Show |
1 | a0001c0001t0003g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1008+576_1008+577i others(42): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077643 | ||||||
chr4:108077653
|
C | A | 4 | a0001c0001t0003g0192a0003c0004t0001g0114a0003c0004t0001g0115others(1): Show | 4 | HG00642.hp2 HG02602.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008+567G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077653 | ||||||
chr4:108077653
|
C | CCCGTCTG others(33): Show |
4 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+566_1008+567i others(42): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077653 | ||||||
chr4:108077676
|
T | C | 13 | a0001c0001t0001g0125a0001c0001t0001g0197a0001c0001t0001g0256others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1008+544A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077676 | ||||||
chr4:108077682
|
G | C | 11 | a0001c0001t0001g0125a0001c0001t0001g0256a0001c0001t0001g0257others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1008+538C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077682 | ||||||
chr4:108077684
|
A | G | 11 | a0001c0001t0001g0125a0001c0001t0001g0256a0001c0001t0001g0257others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1008+536T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077684 | ||||||
chr4:108077686
|
C | G | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008+534G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077686 | ||||||
chr4:108077696
|
A | G | 13 | a0001c0001t0001g0125a0001c0001t0001g0236a0001c0001t0001g0256others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1008+524T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077696 | ||||||
chr4:108077724
|
G | GGCTGCCG others(113): Show |
1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1008+495_1008+496i others(122): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077724 | ||||||
chr4:108077724
|
G | GGCTGCCG others(73): Show |
3 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260 | 3 | HG01109.hp2 HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1008+495_1008+496i others(82): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077724 | ||||||
chr4:108077730
|
T | C | 1 | a0001c0001t0020g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1008+490A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077730 | ||||||
chr4:108077736
|
A | G | 1 | a0001c0001t0009g0015 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1008+484T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077736 | ||||||
chr4:108077812
|
C | A | 169 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1008+408G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077812 | ||||||
chr4:108077900
|
C | G | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008+320G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077900 | ||||||
chr4:108077925
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1008+295G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077925 | ||||||
chr4:108077977
|
G | A | 169 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1008+243C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108077977 | ||||||
chr4:108078037
|
C | A | 1 | a0001c0006t0006g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1008+183G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108078037 | ||||||
chr4:108078037
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1008+183G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108078037 | ||||||
chr4:108078045
|
CA | C | 168 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1008+174delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108078045 | ||||||
chr4:108078144
|
G | T | 219 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1008+76C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108078144 | ||||||
chr4:108078210
|
G | A | 169 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1008+10C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 8/11 | chr4 | 108078210 | ||||||
chr4:108078620
|
T | C | 1 | a0001c0001t0003g0203 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.846-238A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 7/11 | chr4 | 108078620 | ||||||
chr4:108078682
|
G | A | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.846-300C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 7/11 | chr4 | 108078682 | ||||||
chr4:108079155
|
G | T | 11 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.845+337C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 7/11 | chr4 | 108079155 | ||||||
chr4:108079225
|
T | TC | 202 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.845+266dupG | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 7/11 | chr4 | 108079225 | ||||||
chr4:108079262
|
G | A | 171 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.845+230C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 7/11 | chr4 | 108079262 | ||||||
chr4:108079293
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0002g0021 | 3 | HG00280.hp2 HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.845+199G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 7/11 | chr4 | 108079293 | ||||||
chr4:108079380
|
T | C | 205 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.845+112A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 7/11 | chr4 | 108079380 | ||||||
chr4:108079398
|
C | T | 1 | a0001c0001t0004g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.845+94G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 7/11 | chr4 | 108079398 | ||||||
chr4:108079641
|
A | G | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.723-27T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108079641 | ||||||
chr4:108079642
|
T | G | 1 | a0001c0001t0002g0087 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.723-28A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108079642 | ||||||
chr4:108079773
|
T | C | 25 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(22): Show | 25 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.723-159A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108079773 | ||||||
chr4:108079791
|
C | T | 4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.723-177G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108079791 | ||||||
chr4:108079852
|
C | T | 2 | a0001c0001t0002g0083a0001c0001t0002g0087 | 2 | HG02622.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.723-238G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108079852 | ||||||
chr4:108080248
|
C | T | 193 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.723-634G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108080248 | ||||||
chr4:108080397
|
A | G | 10 | a0001c0001t0003g0244a0001c0001t0006g0254a0001c0001t0006g0255others(7): Show | 10 | HG01255.hp1 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.723-783T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108080397 | ||||||
chr4:108080539
|
A | G | 3 | a0001c0001t0002g0017a0001c0001t0002g0020a0001c0001t0002g0038 | 3 | NA19004.hp2 NA19056.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.723-925T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108080539 | ||||||
chr4:108080624
|
G | T | 1 | a0001c0001t0025g0262 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.722+962C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108080624 | ||||||
chr4:108080989
|
G | A | 3 | a0001c0001t0002g0065a0001c0001t0002g0068a0001c0001t0002g0070 | 3 | HG01081.hp2 HG01106.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.722+597C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108080989 | ||||||
chr4:108081003
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.722+583C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108081003 | ||||||
chr4:108081017
|
T | C | 227 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.722+569A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108081017 | ||||||
chr4:108081403
|
C | A | 3 | a0001c0001t0003g0223a0001c0001t0003g0225a0001c0001t0003g0226 | 3 | HG01884.hp2 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.722+183G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108081403 | ||||||
chr4:108081403
|
C | T | 86 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.722+183G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108081403 | ||||||
chr4:108081503
|
C | A | 1 | a0001c0001t0003g0250 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.722+83G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 6/11 | chr4 | 108081503 | ||||||
chr4:108081830
|
T | C | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.639-161A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108081830 | ||||||
chr4:108082107
|
A | G | 6 | a0001c0001t0001g0120a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG02280.hp2 HG02615.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.639-438T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108082107 | ||||||
chr4:108082156
|
T | C | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.639-487A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108082156 | ||||||
chr4:108082596
|
T | C | 90 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.638+760A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108082596 | ||||||
chr4:108082613
|
T | C | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.638+743A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108082613 | ||||||
chr4:108082638
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.638+718T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108082638 | ||||||
chr4:108082831
|
A | G | 1 | a0001c0001t0013g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.638+525T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108082831 | ||||||
chr4:108082891
|
A | G | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.638+465T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108082891 | ||||||
chr4:108082970
|
A | C | 205 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.638+386T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108082970 | ||||||
chr4:108083056
|
A | G | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0184 | 3 | NA18950.hp2 NA18962.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.638+300T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108083056 | ||||||
chr4:108083064
|
T | C | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.638+292A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108083064 | ||||||
chr4:108083163
|
G | A | 3 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0224 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.638+193C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108083163 | ||||||
chr4:108083223
|
T | C | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.638+133A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108083223 | ||||||
chr4:108083230
|
T | C | 2 | a0001c0001t0004g0094a0001c0001t0019g0095 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.638+126A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 5/11 | chr4 | 108083230 | ||||||
chr4:108083819
|
G | A | 83 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(80): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.548-373C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108083819 | ||||||
chr4:108083998
|
G | A | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.548-552C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108083998 | ||||||
chr4:108084512
|
A | G | 2 | a0001c0001t0004g0094a0001c0001t0019g0095 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.548-1066T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108084512 | ||||||
chr4:108084531
|
C | G | 13 | a0001c0001t0003g0169a0001c0001t0003g0171a0001c0001t0003g0174others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.548-1085G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108084531 | ||||||
chr4:108084808
|
T | G | 221 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.548-1362A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108084808 | ||||||
chr4:108085076
|
C | CTATTT | 3 | a0001c0001t0004g0016a0001c0001t0004g0030a0001c0001t0004g0031 | 3 | HG02451.hp2 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.548-1635_548-1631d others(7): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108085076 | ||||||
chr4:108085225
|
T | C | 213 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.548-1779A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108085225 | ||||||
chr4:108085233
|
C | T | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.548-1787G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108085233 | ||||||
chr4:108085234
|
G | A | 2 | a0001c0001t0003g0218a0001c0001t0003g0219 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.548-1788C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108085234 | ||||||
chr4:108085331
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.548-1885C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108085331 | ||||||
chr4:108085544
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.548-2098G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108085544 | ||||||
chr4:108085623
|
T | C | 1 | a0001c0001t0004g0091 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.548-2177A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108085623 | ||||||
chr4:108085678
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.548-2232C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108085678 | ||||||
chr4:108085703
|
C | CTCTA | 203 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.548-2261_548-2258d others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108085703 | ||||||
chr4:108085762
|
T | C | 90 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.548-2316A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108085762 | ||||||
chr4:108085823
|
T | C | 28 | a0001c0001t0001g0208a0001c0001t0001g0227a0001c0001t0003g0122others(25): Show | 28 | HG00558.hp1 HG01099.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.548-2377A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108085823 | ||||||
chr4:108086127
|
A | T | 205 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.548-2681T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086127 | ||||||
chr4:108086266
|
T | G | 3 | a0001c0002t0001g0121a0001c0002t0001g0129a0001c0002t0001g0130 | 3 | HG00735.hp2 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.548-2820A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086266 | ||||||
chr4:108086692
|
G | C | 2 | a0001c0001t0005g0135a0001c0001t0005g0164 | 2 | HG01952.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.547+2433C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086692 | ||||||
chr4:108086758
|
C | T | 5 | a0001c0001t0001g0252a0001c0001t0003g0247a0001c0001t0003g0249others(2): Show | 5 | HG02922.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.547+2367G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086758 | ||||||
chr4:108086829
|
T | TACACACA others(1): Show |
7 | a0001c0001t0001g0128a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG01515.hp2 HG02129.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.547+2288_547+2295d others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086829 | ||||||
chr4:108086829
|
T | TACACACA others(3): Show |
71 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.547+2286_547+2295d others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086829 | ||||||
chr4:108086829
|
T | TACACACA others(5): Show |
3 | a0001c0001t0001g0231a0001c0001t0003g0178a0001c0001t0003g0250 | 3 | HG03139.hp1 NA18906.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.547+2284_547+2295d others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086829 | ||||||
chr4:108086829
|
T | TACACACA others(7): Show |
17 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0244others(14): Show | 17 | HG01255.hp1 HG02572.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.547+2282_547+2295d others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086829 | ||||||
chr4:108086829
|
T | TACACACA others(9): Show |
16 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0002g0041others(13): Show | 16 | HG01109.hp2 HG01192.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.547+2280_547+2295d others(18): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086829 | ||||||
chr4:108086829
|
T | TACACACA others(11): Show |
15 | a0001c0001t0001g0260a0001c0001t0002g0018a0001c0001t0002g0032others(12): Show | 15 | HG00609.hp1 HG00642.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.547+2278_547+2295d others(20): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086829 | ||||||
chr4:108086829
|
T | TACACACA others(13): Show |
20 | a0001c0001t0002g0022a0001c0001t0002g0029a0001c0001t0002g0033others(17): Show | 20 | HG00621.hp1 HG00735.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.547+2276_547+2295d others(22): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086829 | ||||||
chr4:108086829
|
T | TACACACA others(15): Show |
36 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.547+2295_547+2296i others(24): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086829 | ||||||
chr4:108086829
|
T | TACACACA others(17): Show |
5 | a0001c0001t0002g0051a0001c0001t0002g0087a0001c0001t0002g0090others(2): Show | 5 | HG02004.hp1 HG02004.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+2295_547+2296i others(26): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086829 | ||||||
chr4:108086829
|
T | TACACACA others(19): Show |
12 | a0001c0001t0002g0071a0001c0001t0002g0078a0001c0001t0002g0079others(9): Show | 12 | HG00140.hp2 HG01099.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.547+2295_547+2296i others(28): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086829 | ||||||
chr4:108086955
|
T | C | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.547+2170A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108086955 | ||||||
chr4:108087088
|
G | C | 1 | a0001c0001t0026g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.547+2037C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087088 | ||||||
chr4:108087110
|
G | T | 115 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.547+2015C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087110 | ||||||
chr4:108087383
|
G | A | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.547+1742C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087383 | ||||||
chr4:108087407
|
G | C | 1 | a0001c0001t0013g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.547+1718C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087407 | ||||||
chr4:108087430
|
T | A | 200 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.547+1695A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087430 | ||||||
chr4:108087431
|
A | T | 3 | a0001c0001t0003g0123a0001c0001t0004g0094a0001c0001t0019g0095 | 3 | HG02559.hp2 HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.547+1694T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087431 | ||||||
chr4:108087452
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.547+1673C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087452 | ||||||
chr4:108087630
|
G | A | 200 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.547+1495C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087630 | ||||||
chr4:108087745
|
C | T | 1 | a0001c0001t0004g0031 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.547+1380G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087745 | ||||||
chr4:108087746
|
G | A | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.547+1379C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087746 | ||||||
chr4:108087749
|
T | C | 3 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0086 | 3 | HG01257.hp1 HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.547+1376A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087749 | ||||||
chr4:108087931
|
A | G | 208 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.547+1194T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087931 | ||||||
chr4:108087958
|
G | C | 3 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0224 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.547+1167C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108087958 | ||||||
chr4:108088020
|
G | T | 9 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.547+1105C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088020 | ||||||
chr4:108088034
|
G | A | 1 | a0001c0001t0013g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.547+1091C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088034 | ||||||
chr4:108088293
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0001g0150a0001c0001t0002g0023 | 3 | HG00544.hp2 NA18957.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.547+832A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088293 | ||||||
chr4:108088395
|
C | A | 3 | a0001c0001t0002g0017a0001c0001t0002g0020a0001c0001t0002g0038 | 3 | NA19004.hp2 NA19056.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.547+730G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088395 | ||||||
chr4:108088474
|
C | T | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.547+651G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088474 | ||||||
chr4:108088499
|
C | T | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.547+626G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088499 | ||||||
chr4:108088540
|
C | T | 89 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.547+585G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088540 | ||||||
chr4:108088565
|
T | C | 1 | a0001c0001t0003g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.547+560A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088565 | ||||||
chr4:108088615
|
G | T | 90 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.547+510C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088615 | ||||||
chr4:108088745
|
T | TAACATCT others(7): Show |
199 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.547+379_547+380ins others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088745 | ||||||
chr4:108088955
|
T | C | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.547+170A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088955 | ||||||
chr4:108088970
|
G | T | 1 | a0001c0001t0002g0079 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.547+155C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108088970 | ||||||
chr4:108089051
|
A | G | 212 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.547+74T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108089051 | ||||||
chr4:108089089
|
C | CA | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.547+35dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 4/11 | chr4 | 108089089 | ||||||
chr4:108089515
|
G | A | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.415-258C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108089515 | ||||||
chr4:108089562
|
T | C | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.415-305A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108089562 | ||||||
chr4:108089688
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.415-431G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108089688 | ||||||
chr4:108089934
|
T | C | 2 | a0001c0001t0004g0094a0001c0001t0019g0095 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.415-677A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108089934 | ||||||
chr4:108090020
|
G | A | 4 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-763C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108090020 | ||||||
chr4:108090133
|
C | T | 5 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(2): Show | 5 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-876G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108090133 | ||||||
chr4:108090146
|
T | C | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.415-889A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108090146 | ||||||
chr4:108090220
|
T | C | 202 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.415-963A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108090220 | ||||||
chr4:108090289
|
TTAA | T | 7 | a0001c0001t0003g0174a0001c0001t0003g0209a0001c0001t0003g0210others(4): Show | 7 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-1035_415-1033d others(5): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108090289 | ||||||
chr4:108090416
|
T | C | 26 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(23): Show | 26 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.415-1159A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108090416 | ||||||
chr4:108090564
|
A | G | 7 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(4): Show | 7 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-1307T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108090564 | ||||||
chr4:108090760
|
G | A | 219 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.415-1503C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108090760 | ||||||
chr4:108090920
|
T | C | 1 | a0001c0001t0022g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-1663A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108090920 | ||||||
chr4:108091025
|
C | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260 | 3 | HG01109.hp2 HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.415-1768G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091025 | ||||||
chr4:108091027
|
T | C | 26 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0192others(23): Show | 26 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.415-1770A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091027 | ||||||
chr4:108091197
|
T | C | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.415-1940A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091197 | ||||||
chr4:108091404
|
C | A | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415-2147G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091404 | ||||||
chr4:108091445
|
CG | C | 130 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0127others(127): Show | 130 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.415-2189delC | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091445 | ||||||
chr4:108091453
|
G | C | 4 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-2196C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091453 | ||||||
chr4:108091453
|
GGA | G | 85 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.415-2198_415-2197d others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091453 | ||||||
chr4:108091454
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.415-2197C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091454 | ||||||
chr4:108091454
|
GA | G | 4 | a0001c0001t0003g0192a0003c0004t0001g0114a0003c0004t0001g0115others(1): Show | 4 | HG00642.hp2 HG02602.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-2198delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091454 | ||||||
chr4:108091455
|
A | G | 4 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-2198T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091455 | ||||||
chr4:108091460
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.415-2203T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091460 | ||||||
chr4:108091462
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0013g0110 | 2 | HG03453.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.415-2205T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091462 | ||||||
chr4:108091464
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0013g0110 | 2 | HG03453.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.415-2207C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091464 | ||||||
chr4:108091811
|
G | A | 140 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.415-2554C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091811 | ||||||
chr4:108091999
|
T | C | 1 | a0001c0001t0026g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.415-2742A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108091999 | ||||||
chr4:108092157
|
C | T | 7 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0065others(4): Show | 7 | HG00140.hp1 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-2900G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092157 | ||||||
chr4:108092381
|
T | C | 85 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.415-3124A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092381 | ||||||
chr4:108092442
|
C | A | 1 | a0001c0001t0002g0085 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.415-3185G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092442 | ||||||
chr4:108092528
|
T | C | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-3271A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092528 | ||||||
chr4:108092589
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0077 | 2 | HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.415-3332C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092589 | ||||||
chr4:108092692
|
ACTAT | A | 85 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.415-3439_415-3436d others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092692 | ||||||
chr4:108092888
|
G | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0145a0001c0001t0001g0149 | 3 | NA18970.hp2 NA18982.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.415-3631C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092888 | ||||||
chr4:108092917
|
TA | T | 94 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.415-3661delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092917 | ||||||
chr4:108092917
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0001g0116 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.415-3672_415-3661d others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092917 | ||||||
chr4:108092926
|
A | AC | 23 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(20): Show | 23 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.415-3670_415-3669i others(3): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092926 | ||||||
chr4:108092927
|
A | AC | 5 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0224others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-3671_415-3670i others(3): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092927 | ||||||
chr4:108092928
|
A | AAC | 6 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(3): Show | 6 | HG01891.hp2 HG02602.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-3672_415-3671i others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092928 | ||||||
chr4:108092928
|
A | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0156 | 2 | NA18983.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.415-3671T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092928 | ||||||
chr4:108092939
|
A | AAAC | 13 | a0001c0001t0002g0029a0001c0001t0002g0043a0001c0001t0002g0049others(10): Show | 13 | HG00544.hp1 HG01192.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-3683_415-3682i others(5): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092939 | ||||||
chr4:108092939
|
A | AAC | 77 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(74): Show | 77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.415-3683_415-3682i others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092939 | ||||||
chr4:108092939
|
A | AC | 5 | a0001c0001t0002g0038a0001c0001t0004g0030a0001c0001t0011g0106others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-3683_415-3682i others(3): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092939 | ||||||
chr4:108092939
|
A | C | 119 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0127others(116): Show | 119 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.415-3682T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092939 | ||||||
chr4:108092942
|
A | C | 1 | a0001c0001t0002g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.415-3685T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092942 | ||||||
chr4:108092979
|
A | G | 11 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.415-3722T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108092979 | ||||||
chr4:108093565
|
A | T | 2 | a0001c0001t0002g0024a0001c0001t0002g0051 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.415-4308T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108093565 | ||||||
chr4:108094195
|
C | T | 1 | a0001c0001t0022g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-4938G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108094195 | ||||||
chr4:108094468
|
C | G | 2 | a0001c0001t0002g0064a0001c0001t0002g0092 | 2 | NA18952.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.415-5211G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108094468 | ||||||
chr4:108094614
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.415-5357G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108094614 | ||||||
chr4:108094669
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.415-5412A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108094669 | ||||||
chr4:108094959
|
C | A | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.415-5702G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108094959 | ||||||
chr4:108094977
|
A | G | 15 | a0001c0001t0003g0123a0001c0001t0003g0218a0001c0001t0003g0219others(12): Show | 15 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-5720T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108094977 | ||||||
chr4:108095023
|
T | C | 1 | a0001c0001t0022g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-5766A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108095023 | ||||||
chr4:108095169
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.415-5912G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108095169 | ||||||
chr4:108095668
|
C | A | 145 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.415-6411G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108095668 | ||||||
chr4:108095780
|
C | T | 12 | a0001c0001t0003g0122a0001c0001t0003g0170a0001c0001t0003g0180others(9): Show | 12 | HG00558.hp1 HG01099.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-6523G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108095780 | ||||||
chr4:108095954
|
T | G | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415-6697A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108095954 | ||||||
chr4:108096372
|
G | A | 146 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0236others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.415-7115C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108096372 | ||||||
chr4:108096612
|
T | G | 3 | a0001c0001t0002g0052a0001c0001t0002g0060a0001c0001t0002g0081 | 3 | HG00642.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.415-7355A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108096612 | ||||||
chr4:108096720
|
A | T | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | NA18971.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.415-7463T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108096720 | ||||||
chr4:108096793
|
A | G | 1 | a0001c0001t0013g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.415-7536T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108096793 | ||||||
chr4:108096874
|
T | A | 16 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(13): Show | 16 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.415-7617A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108096874 | ||||||
chr4:108096906
|
G | C | 119 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.415-7649C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108096906 | ||||||
chr4:108097182
|
C | T | 16 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(13): Show | 16 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.415-7925G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108097182 | ||||||
chr4:108097295
|
T | C | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415-8038A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108097295 | ||||||
chr4:108097551
|
G | A | 14 | a0001c0001t0003g0123a0001c0001t0003g0218a0001c0001t0003g0219others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.415-8294C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108097551 | ||||||
chr4:108097643
|
G | C | 1 | a0001c0001t0003g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.415-8386C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108097643 | ||||||
chr4:108097661
|
T | A | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.415-8404A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108097661 | ||||||
chr4:108097742
|
A | AT | 119 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.415-8486dupA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108097742 | ||||||
chr4:108098169
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.415-8912C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108098169 | ||||||
chr4:108098502
|
A | AAGGGGGG others(2): Show |
7 | a0001c0001t0002g0058a0001c0001t0002g0080a0001c0001t0002g0082others(4): Show | 7 | HG01069.hp1 HG03490.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-9254_415-9246d others(11): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108098502 | ||||||
chr4:108098603
|
C | A | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.415-9346G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108098603 | ||||||
chr4:108098641
|
C | T | 16 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(13): Show | 16 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.415-9384G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108098641 | ||||||
chr4:108098673
|
A | G | 145 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.415-9416T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108098673 | ||||||
chr4:108098757
|
T | C | 1 | a0001c0001t0020g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.415-9500A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108098757 | ||||||
chr4:108098821
|
C | T | 81 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(78): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.415-9564G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108098821 | ||||||
chr4:108098826
|
A | G | 10 | a0001c0001t0001g0243a0001c0001t0003g0238a0001c0001t0003g0239others(7): Show | 10 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.415-9569T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108098826 | ||||||
chr4:108098828
|
C | G | 1 | a0001c0001t0002g0027 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.415-9571G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108098828 | ||||||
chr4:108099073
|
C | T | 1 | a0001c0001t0025g0262 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.415-9816G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099073 | ||||||
chr4:108099086
|
T | C | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-9829A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099086 | ||||||
chr4:108099125
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.415-9868G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099125 | ||||||
chr4:108099363
|
G | A | 141 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(138): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.415-10106C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099363 | ||||||
chr4:108099512
|
G | A | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.415-10255C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099512 | ||||||
chr4:108099516
|
A | G | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.415-10259T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099516 | ||||||
chr4:108099518
|
G | A | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.415-10261C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099518 | ||||||
chr4:108099518
|
GTA | G | 107 | a0001c0001t0001g0187a0001c0001t0001g0243a0001c0001t0001g0252others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.415-10263_415-1026 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099518 | ||||||
chr4:108099518
|
GTATA | G | 18 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0043others(15): Show | 18 | HG00140.hp2 HG00609.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.415-10265_415-1026 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099518 | ||||||
chr4:108099520
|
A | G | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.415-10263T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099520 | ||||||
chr4:108099532
|
A | G | 12 | a0001c0001t0001g0201a0001c0001t0002g0024a0001c0001t0002g0057others(9): Show | 12 | HG00280.hp1 HG01069.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-10275T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099532 | ||||||
chr4:108099534
|
A | G | 194 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.415-10277T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099534 | ||||||
chr4:108099538
|
G | A | 11 | a0001c0001t0001g0201a0001c0001t0002g0024a0001c0001t0002g0057others(8): Show | 11 | HG00280.hp1 HG01069.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.415-10281C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099538 | ||||||
chr4:108099540
|
A | G | 18 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0043others(15): Show | 18 | HG00140.hp2 HG00609.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.415-10283T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099540 | ||||||
chr4:108099542
|
A | G | 11 | a0001c0001t0001g0201a0001c0001t0002g0024a0001c0001t0002g0057others(8): Show | 11 | HG00280.hp1 HG01069.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.415-10285T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099542 | ||||||
chr4:108099544
|
G | A | 18 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0043others(15): Show | 18 | HG00140.hp2 HG00609.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.415-10287C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099544 | ||||||
chr4:108099550
|
G | GCA | 4 | a0001c0001t0001g0257a0001c0001t0003g0247a0001c0001t0026g0264others(1): Show | 4 | HG01243.hp2 HG02809.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-10294_415-1029 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099550 | ||||||
chr4:108099550
|
G | GCATA | 3 | a0001c0001t0001g0256a0001c0001t0003g0244a0001c0001t0006g0255 | 3 | HG01109.hp2 HG01255.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.415-10294_415-1029 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099550 | ||||||
chr4:108099550
|
G | GCATATA | 3 | a0001c0001t0001g0260a0001c0001t0006g0254a0001c0001t0006g0259 | 3 | HG02280.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.415-10294_415-1029 others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099550 | ||||||
chr4:108099550
|
GTGTGTAT others(15): Show |
G | 3 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242 | 3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415-10315_415-1029 others(26): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099550 | ||||||
chr4:108099551
|
T | C | 15 | a0001c0001t0001g0252a0001c0001t0003g0238a0001c0001t0003g0239others(12): Show | 15 | HG01192.hp2 HG02004.hp2 HG02886.hp2 others(12): Show |
intron_variant | MODIFIER | c.415-10294A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099551 | ||||||
chr4:108099552
|
G | A | 36 | a0001c0001t0001g0201a0001c0001t0001g0252a0001c0001t0001g0256others(33): Show | 36 | HG00280.hp1 HG01069.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.415-10295C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099552 | ||||||
chr4:108099554
|
G | A | 85 | a0001c0001t0001g0187a0001c0001t0001g0252a0001c0001t0001g0256others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.415-10297C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099554 | ||||||
chr4:108099556
|
A | ATG | 3 | a0001c0001t0001g0128a0001c0001t0001g0188a0001c0001t0002g0021 | 3 | HG02602.hp2 NA19070.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.415-10301_415-1030 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099556 | ||||||
chr4:108099556
|
A | ATGTG | 3 | a0001c0001t0001g0125a0001c0001t0003g0192a0001c0001t0004g0094 | 3 | HG02559.hp2 HG02976.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.415-10303_415-1030 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099556 | ||||||
chr4:108099556
|
A | G | 71 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.415-10299T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099556 | ||||||
chr4:108099556
|
ATGTGTGT others(5): Show |
A | 1 | a0001c0001t0003g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.415-10311_415-1030 others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099556 | ||||||
chr4:108099558
|
G | A | 24 | a0001c0001t0001g0252a0001c0001t0001g0256a0001c0001t0001g0257others(21): Show | 24 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.415-10301C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099558 | ||||||
chr4:108099560
|
G | A | 21 | a0001c0001t0001g0252a0001c0001t0001g0256a0001c0001t0001g0257others(18): Show | 21 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.415-10303C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099560 | ||||||
chr4:108099562
|
G | A | 19 | a0001c0001t0001g0252a0001c0001t0001g0257a0001c0001t0003g0238others(16): Show | 19 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(16): Show |
intron_variant | MODIFIER | c.415-10305C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099562 | ||||||
chr4:108099562
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0004g0091 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.415-10306_415-1030 others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099562 | ||||||
chr4:108099562
|
G | GTATATAT others(5): Show |
10 | a0001c0001t0001g0201a0001c0001t0002g0024a0001c0001t0002g0057others(7): Show | 10 | HG00280.hp1 HG01069.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.415-10306_415-1030 others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099562 | ||||||
chr4:108099564
|
G | A | 12 | a0001c0001t0001g0252a0001c0001t0003g0238a0001c0001t0003g0239others(9): Show | 12 | HG01192.hp2 HG02004.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-10307C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099564 | ||||||
chr4:108099564
|
G | GTATATAT others(3): Show |
18 | a0001c0001t0002g0014a0001c0001t0002g0018a0001c0001t0002g0022others(15): Show | 18 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.415-10308_415-1030 others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099564 | ||||||
chr4:108099564
|
G | GTATATAT others(5): Show |
15 | a0001c0001t0002g0027a0001c0001t0002g0036a0001c0001t0002g0037others(12): Show | 15 | HG01257.hp1 HG01258.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-10308_415-1030 others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099564 | ||||||
chr4:108099564
|
G | GTATATAT others(7): Show |
1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.415-10308_415-1030 others(18): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099564 | ||||||
chr4:108099566
|
G | A | 44 | a0001c0001t0001g0187a0001c0001t0002g0010a0001c0001t0002g0014others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.415-10309C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099566 | ||||||
chr4:108099568
|
G | A | 44 | a0001c0001t0001g0187a0001c0001t0002g0010a0001c0001t0002g0017others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.415-10311C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099568 | ||||||
chr4:108099570
|
G | A | 54 | a0001c0001t0001g0187a0001c0001t0002g0010a0001c0001t0002g0017others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.415-10313C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
G | GTA | 7 | a0001c0001t0001g0119a0001c0001t0001g0141a0001c0001t0001g0156others(4): Show | 7 | HG01192.hp1 HG02559.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-10315_415-1031 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
G | GTATA | 5 | a0001c0001t0001g0138a0001c0001t0001g0154a0001c0001t0001g0194others(2): Show | 5 | HG02004.hp1 HG02083.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-10317_415-1031 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0003g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.415-10325_415-1031 others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
G | GTGTGTAT others(5): Show |
1 | a0003c0004t0001g0114 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.415-10314_415-1031 others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
G | GTGTGTGT others(7): Show |
1 | a0003c0004t0001g0115 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.415-10314_415-1031 others(18): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
GTA | G | 15 | a0001c0001t0001g0132a0001c0001t0001g0137a0001c0001t0001g0139others(12): Show | 15 | HG01081.hp1 HG01358.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-10315_415-1031 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
GTATA | G | 18 | a0001c0001t0001g0120a0001c0001t0001g0152a0001c0001t0001g0160others(15): Show | 18 | HG00558.hp2 HG00642.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.415-10317_415-1031 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
GTATATA | G | 12 | a0001c0001t0001g0118a0001c0001t0001g0133a0001c0001t0001g0143others(9): Show | 12 | HG01070.hp2 HG01257.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-10319_415-1031 others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
GTATATAT others(1): Show |
G | 12 | a0001c0001t0001g0127a0001c0001t0001g0136a0001c0001t0001g0173others(9): Show | 12 | HG00544.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-10321_415-1031 others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
GTATATAT others(3): Show |
G | 5 | a0001c0001t0001g0175a0001c0001t0003g0124a0001c0001t0003g0250others(2): Show | 5 | HG01891.hp2 HG02615.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-10323_415-1031 others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
GTATATAT others(5): Show |
G | 10 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0181others(7): Show | 10 | HG02280.hp2 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-10325_415-1031 others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
GTATATAT others(7): Show |
G | 9 | a0001c0001t0003g0170a0001c0001t0003g0180a0001c0001t0003g0222others(6): Show | 9 | HG00558.hp1 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-10327_415-1031 others(18): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
GTATATAT others(9): Show |
G | 21 | a0001c0001t0003g0122a0001c0001t0003g0169a0001c0001t0003g0171others(18): Show | 21 | HG01099.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.415-10329_415-1031 others(20): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
GTATATAT others(11): Show |
G | 3 | a0001c0001t0003g0221a0001c0001t0013g0107a0001c0001t0023g0166 | 3 | HG03017.hp2 HG03486.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.415-10331_415-1031 others(22): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
GTATATAT others(13): Show |
G | 4 | a0001c0001t0001g0147a0001c0001t0001g0165a0001c0001t0001g0232others(1): Show | 4 | HG00099.hp2 HG01256.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-10333_415-1031 others(24): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099570
|
GTATATAT others(21): Show |
G | 2 | a0001c0001t0001g0134a0001c0001t0001g0216 | 2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.415-10341_415-1031 others(32): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099570 | ||||||
chr4:108099572
|
A | G | 35 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0236others(32): Show | 35 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.415-10315T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099572 | ||||||
chr4:108099573
|
T | C | 3 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242 | 3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415-10316A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099573 | ||||||
chr4:108099574
|
A | ATATGTGT others(1): Show |
11 | a0001c0001t0001g0187a0001c0001t0002g0010a0001c0001t0002g0017others(8): Show | 11 | HG00609.hp2 HG01081.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-10318_415-1031 others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099574 | ||||||
chr4:108099574
|
A | G | 11 | a0001c0001t0001g0182a0001c0001t0001g0236a0001c0001t0001g0257others(8): Show | 11 | HG00280.hp2 HG00735.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.415-10317T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099574 | ||||||
chr4:108099576
|
A | ATATGTGT others(31): Show |
1 | a0001c0001t0002g0063 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.415-10320_415-1031 others(42): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099576 | ||||||
chr4:108099576
|
A | ATGTGTG | 11 | a0001c0001t0002g0050a0001c0001t0002g0052a0001c0001t0002g0054others(8): Show | 11 | HG00621.hp1 HG01255.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-10320_415-1031 others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099576 | ||||||
chr4:108099576
|
A | G | 12 | a0001c0001t0001g0236a0001c0001t0003g0123a0001c0001t0003g0245others(9): Show | 12 | HG00642.hp2 HG01192.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-10319T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099576 | ||||||
chr4:108099578
|
A | ATGTG | 9 | a0001c0001t0002g0026a0001c0001t0002g0043a0001c0001t0002g0045others(6): Show | 9 | HG00140.hp2 HG01099.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-10322_415-1032 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099578 | ||||||
chr4:108099578
|
A | ATGTGTG | 6 | a0001c0001t0002g0034a0001c0001t0002g0067a0001c0001t0002g0081others(3): Show | 6 | HG00609.hp1 HG02129.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-10322_415-1032 others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099578 | ||||||
chr4:108099578
|
A | G | 16 | a0001c0001t0002g0044a0001c0001t0002g0047a0001c0001t0002g0075others(13): Show | 16 | HG00099.hp1 HG00642.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.415-10321T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099578 | ||||||
chr4:108099580
|
A | G | 23 | a0001c0001t0001g0252a0001c0001t0002g0026a0001c0001t0002g0043others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.415-10323T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099580 | ||||||
chr4:108099582
|
A | G | 17 | a0001c0001t0001g0175a0001c0001t0001g0252a0001c0001t0002g0044others(14): Show | 17 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.415-10325T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099582 | ||||||
chr4:108099584
|
A | G | 9 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0224others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.415-10327T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099584 | ||||||
chr4:108099586
|
A | G | 13 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0224others(10): Show | 13 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-10329T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099586 | ||||||
chr4:108099588
|
A | G | 13 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242others(10): Show | 13 | HG01884.hp1 HG02257.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.415-10331T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099588 | ||||||
chr4:108099590
|
A | G | 12 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242others(9): Show | 12 | HG01884.hp1 HG02257.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-10333T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099590 | ||||||
chr4:108099592
|
A | G | 6 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242others(3): Show | 6 | HG02257.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-10335T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099592 | ||||||
chr4:108099594
|
A | G | 5 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242others(2): Show | 5 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-10337T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099594 | ||||||
chr4:108099596
|
A | G | 3 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242 | 3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415-10339T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099596 | ||||||
chr4:108099619
|
A | T | 2 | a0001c0001t0001g0188a0001c0001t0013g0110 | 2 | HG02602.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.415-10362T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099619 | ||||||
chr4:108099646
|
G | A | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-10389C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099646 | ||||||
chr4:108099725
|
A | G | 2 | a0001c0001t0002g0083a0001c0001t0002g0087 | 2 | HG02622.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.415-10468T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099725 | ||||||
chr4:108099819
|
T | TA | 9 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(6): Show | 9 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-10563dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099819 | ||||||
chr4:108099853
|
C | T | 7 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(4): Show | 7 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-10596G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108099853 | ||||||
chr4:108100113
|
A | G | 90 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.415-10856T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108100113 | ||||||
chr4:108100300
|
A | C | 1 | a0001c0001t0002g0078 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.415-11043T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108100300 | ||||||
chr4:108100342
|
T | C | 10 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(7): Show | 10 | HG01109.hp2 HG01255.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-11085A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108100342 | ||||||
chr4:108100790
|
T | C | 1 | a0001c0001t0009g0015 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.415-11533A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108100790 | ||||||
chr4:108101008
|
A | G | 2 | a0001c0001t0002g0050a0001c0001t0002g0069 | 2 | HG00621.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.415-11751T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108101008 | ||||||
chr4:108101139
|
AT | A | 3 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206 | 3 | HG01891.hp1 HG02148.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.415-11883delA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108101139 | ||||||
chr4:108101296
|
A | G | 90 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.415-12039T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108101296 | ||||||
chr4:108101582
|
T | C | 2 | a0001c0001t0012g0100a0001c0001t0012g0108 | 2 | HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.415-12325A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108101582 | ||||||
chr4:108101781
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.415-12524A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108101781 | ||||||
chr4:108102019
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.415-12762G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108102019 | ||||||
chr4:108102058
|
G | A | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-12801C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108102058 | ||||||
chr4:108102063
|
C | CA | 45 | a0001c0001t0001g0148a0001c0001t0001g0173a0001c0001t0001g0243others(42): Show | 45 | HG00621.hp2 HG00642.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.415-12807dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108102063 | ||||||
chr4:108102439
|
T | C | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.415-13182A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108102439 | ||||||
chr4:108102440
|
C | T | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.415-13183G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108102440 | ||||||
chr4:108102508
|
A | G | 2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.415-13251T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108102508 | ||||||
chr4:108102528
|
G | T | 2 | a0001c0001t0003g0170a0001c0001t0003g0180 | 2 | HG00558.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.415-13271C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108102528 | ||||||
chr4:108102939
|
G | A | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-13682C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108102939 | ||||||
chr4:108103166
|
G | A | 1 | a0001c0001t0003g0206 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.415-13909C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108103166 | ||||||
chr4:108103196
|
C | A | 6 | a0001c0001t0003g0123a0001c0001t0003g0218a0001c0001t0003g0219others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-13939G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108103196 | ||||||
chr4:108103263
|
A | C | 1 | a0001c0001t0007g0101 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.415-14006T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108103263 | ||||||
chr4:108103347
|
T | C | 1 | a0001c0001t0022g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-14090A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108103347 | ||||||
chr4:108103494
|
G | A | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.415-14237C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108103494 | ||||||
chr4:108104043
|
C | T | 136 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.415-14786G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104043 | ||||||
chr4:108104174
|
T | C | 15 | a0001c0001t0003g0123a0001c0001t0003g0218a0001c0001t0003g0219others(12): Show | 15 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-14917A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104174 | ||||||
chr4:108104223
|
A | C | 121 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.415-14966T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104223 | ||||||
chr4:108104264
|
T | A | 10 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(7): Show | 10 | HG01109.hp2 HG01255.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-15007A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104264 | ||||||
chr4:108104304
|
T | C | 1 | a0001c0001t0013g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.415-15047A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104304 | ||||||
chr4:108104328
|
G | A | 85 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0002g0010others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.415-15071C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104328 | ||||||
chr4:108104448
|
AAAT | A | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-15194_415-1519 others(7): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104448 | ||||||
chr4:108104473
|
T | A | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-15216A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104473 | ||||||
chr4:108104475
|
A | T | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.415-15218T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104475 | ||||||
chr4:108104476
|
A | AAT | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-15221_415-1522 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104476 | ||||||
chr4:108104503
|
AT | A | 24 | a0001c0001t0001g0127a0001c0001t0001g0132a0001c0001t0001g0133others(21): Show | 24 | HG00621.hp2 HG01070.hp2 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.415-15247delA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104503 | ||||||
chr4:108104570
|
A | T | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.415-15313T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104570 | ||||||
chr4:108104654
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.415-15397G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104654 | ||||||
chr4:108104709
|
T | C | 136 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.415-15452A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104709 | ||||||
chr4:108104804
|
T | C | 15 | a0001c0001t0003g0123a0001c0001t0003g0218a0001c0001t0003g0219others(12): Show | 15 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-15547A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104804 | ||||||
chr4:108104805
|
G | A | 1 | a0001c0001t0013g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.415-15548C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104805 | ||||||
chr4:108104825
|
G | T | 139 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.415-15568C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108104825 | ||||||
chr4:108105079
|
A | G | 139 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.415-15822T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105079 | ||||||
chr4:108105122
|
G | A | 4 | a0001c0001t0008g0006a0001c0001t0008g0007a0001c0001t0008g0008others(1): Show | 4 | HG00140.hp2 HG01099.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-15865C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105122 | ||||||
chr4:108105181
|
C | CT | 118 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.415-15925dupA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105181 | ||||||
chr4:108105258
|
A | G | 136 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(133): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.415-16001T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105258 | ||||||
chr4:108105347
|
A | C | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-16090T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105347 | ||||||
chr4:108105456
|
C | T | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415-16199G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105456 | ||||||
chr4:108105458
|
G | A | 1 | a0004c0009t0002g0096 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.415-16201C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105458 | ||||||
chr4:108105463
|
G | C | 1 | a0001c0006t0006g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.415-16206C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105463 | ||||||
chr4:108105472
|
C | T | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415-16215G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105472 | ||||||
chr4:108105522
|
G | C | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.415-16265C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105522 | ||||||
chr4:108105645
|
C | T | 9 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0004g0016others(6): Show | 9 | HG00280.hp1 HG00323.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-16388G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105645 | ||||||
chr4:108105873
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.415-16616T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108105873 | ||||||
chr4:108106004
|
G | A | 18 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(15): Show | 18 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.415-16747C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108106004 | ||||||
chr4:108106143
|
C | T | 1 | a0003c0004t0001g0114 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.415-16886G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108106143 | ||||||
chr4:108106241
|
C | G | 15 | a0001c0001t0003g0123a0001c0001t0003g0218a0001c0001t0003g0219others(12): Show | 15 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-16984G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108106241 | ||||||
chr4:108106355
|
G | C | 15 | a0001c0001t0003g0123a0001c0001t0003g0218a0001c0001t0003g0219others(12): Show | 15 | HG01069.hp2 HG01071.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-17098C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108106355 | ||||||
chr4:108106502
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0216 | 2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.415-17245C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108106502 | ||||||
chr4:108106757
|
T | G | 71 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0128others(68): Show | 71 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.415-17500A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108106757 | ||||||
chr4:108106883
|
G | A | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-17626C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108106883 | ||||||
chr4:108107065
|
C | A | 3 | a0001c0002t0001g0121a0001c0002t0001g0129a0001c0002t0001g0130 | 3 | HG00735.hp2 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.415-17808G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107065 | ||||||
chr4:108107087
|
T | C | 4 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-17830A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107087 | ||||||
chr4:108107106
|
G | C | 262 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.415-17849C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107106 | ||||||
chr4:108107266
|
G | GT | 17 | a0001c0001t0002g0071a0001c0001t0003g0204a0001c0001t0003g0205others(14): Show | 17 | HG01099.hp1 HG01884.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.415-18010dupA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107266 | ||||||
chr4:108107406
|
T | A | 1 | a0001c0001t0004g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415-18149A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107406 | ||||||
chr4:108107458
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.415-18201T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107458 | ||||||
chr4:108107459
|
T | G | 1 | a0001c0001t0004g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.415-18202A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107459 | ||||||
chr4:108107503
|
T | A | 1 | a0001c0001t0003g0247 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.415-18246A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107503 | ||||||
chr4:108107507
|
A | AT | 137 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.415-18251dupA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107507 | ||||||
chr4:108107550
|
TA | T | 14 | a0001c0001t0001g0120a0001c0001t0001g0172a0001c0001t0001g0173others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.415-18294delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107550 | ||||||
chr4:108107769
|
C | T | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-18512G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107769 | ||||||
chr4:108107857
|
A | C | 25 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(22): Show | 25 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.415-18600T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108107857 | ||||||
chr4:108108194
|
C | G | 3 | a0001c0001t0001g0186a0001c0001t0001g0189a0001c0001t0001g0193 | 3 | HG01081.hp1 HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.415-18937G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108108194 | ||||||
chr4:108108544
|
G | T | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-19287C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108108544 | ||||||
chr4:108108616
|
T | C | 28 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(25): Show | 28 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.415-19359A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108108616 | ||||||
chr4:108108734
|
A | G | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-19477T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108108734 | ||||||
chr4:108108892
|
T | C | 1 | a0001c0001t0022g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-19635A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108108892 | ||||||
chr4:108109128
|
G | A | 3 | a0001c0001t0001g0252a0001c0001t0003g0247a0001c0001t0003g0251 | 3 | HG02922.hp1 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.415-19871C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108109128 | ||||||
chr4:108109164
|
G | T | 111 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.415-19907C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108109164 | ||||||
chr4:108109323
|
T | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0003g0117 | 3 | HG01109.hp1 HG01257.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.415-20066A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108109323 | ||||||
chr4:108109326
|
C | T | 139 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0243others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.415-20069G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108109326 | ||||||
chr4:108109556
|
A | G | 10 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(7): Show | 10 | HG01109.hp2 HG01255.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-20299T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108109556 | ||||||
chr4:108109859
|
G | C | 1 | a0001c0001t0017g0035 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.415-20602C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108109859 | ||||||
chr4:108109870
|
C | G | 1 | a0001c0001t0003g0234 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.415-20613G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108109870 | ||||||
chr4:108110270
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.415-21013T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108110270 | ||||||
chr4:108110450
|
T | C | 24 | a0001c0001t0001g0236a0001c0001t0001g0256a0001c0001t0001g0257others(21): Show | 24 | HG01109.hp2 HG01255.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.415-21193A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108110450 | ||||||
chr4:108110578
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0003g0117 | 3 | HG01109.hp1 HG01257.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.415-21321G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108110578 | ||||||
chr4:108110814
|
C | G | 1 | a0001c0001t0026g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.415-21557G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108110814 | ||||||
chr4:108111179
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.415-21922C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108111179 | ||||||
chr4:108111293
|
A | C | 9 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(6): Show | 9 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-22036T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108111293 | ||||||
chr4:108111541
|
T | A | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-22284A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108111541 | ||||||
chr4:108111559
|
C | T | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.415-22302G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108111559 | ||||||
chr4:108111621
|
T | C | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.415-22364A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108111621 | ||||||
chr4:108112204
|
T | C | 8 | a0001c0001t0003g0124a0001c0001t0003g0192a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-22947A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108112204 | ||||||
chr4:108112234
|
G | C | 1 | a0001c0001t0003g0235 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.415-22977C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108112234 | ||||||
chr4:108112351
|
G | A | 13 | a0001c0001t0001g0236a0001c0001t0004g0094a0001c0001t0007g0101others(10): Show | 13 | HG01515.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-23094C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108112351 | ||||||
chr4:108112728
|
G | A | 113 | a0001c0001t0001g0236a0001c0001t0002g0010a0001c0001t0002g0014others(110): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.415-23471C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108112728 | ||||||
chr4:108112823
|
T | C | 184 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0201others(181): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.415-23566A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108112823 | ||||||
chr4:108112866
|
A | T | 1 | a0001c0001t0019g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.415-23609T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108112866 | ||||||
chr4:108112867
|
C | G | 1 | a0001c0001t0019g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.415-23610G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108112867 | ||||||
chr4:108112870
|
G | A | 1 | a0001c0001t0019g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.415-23613C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108112870 | ||||||
chr4:108112941
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.415-23684A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108112941 | ||||||
chr4:108113469
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.415-24212C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108113469 | ||||||
chr4:108113790
|
G | C | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-24533C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108113790 | ||||||
chr4:108113801
|
T | C | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-24544A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108113801 | ||||||
chr4:108113865
|
A | G | 7 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(4): Show | 7 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-24608T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108113865 | ||||||
chr4:108114246
|
CA | C | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-24990delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108114246 | ||||||
chr4:108114483
|
G | A | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-25226C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108114483 | ||||||
chr4:108114672
|
C | T | 13 | a0001c0001t0001g0236a0001c0001t0004g0094a0001c0001t0007g0101others(10): Show | 13 | HG01515.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-25415G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108114672 | ||||||
chr4:108114789
|
G | T | 5 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(2): Show | 5 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-25532C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108114789 | ||||||
chr4:108114801
|
T | G | 1 | a0001c0001t0005g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.415-25544A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108114801 | ||||||
chr4:108114829
|
T | C | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.415-25572A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108114829 | ||||||
chr4:108114843
|
G | A | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-25586C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108114843 | ||||||
chr4:108114969
|
G | A | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.415-25712C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108114969 | ||||||
chr4:108115005
|
G | T | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-25748C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115005 | ||||||
chr4:108115343
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.415-26086A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115343 | ||||||
chr4:108115344
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.415-26087T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115344 | ||||||
chr4:108115374
|
A | C | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.415-26117T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115374 | ||||||
chr4:108115491
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.415-26234G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115491 | ||||||
chr4:108115845
|
A | C | 3 | a0001c0001t0011g0099a0001c0001t0011g0109a0001c0001t0013g0110 | 3 | HG02630.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.415-26588T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115845 | ||||||
chr4:108115846
|
T | C | 1 | a0001c0001t0011g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.415-26589A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TAC | 40 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0144others(37): Show | 40 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.415-26591_415-2659 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TACAC | 48 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0143others(45): Show | 48 | HG00558.hp1 HG00621.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.415-26593_415-2659 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TACACAC | 46 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(43): Show | 46 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.415-26595_415-2659 others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TACACACA others(1): Show |
18 | a0001c0001t0002g0020a0001c0001t0002g0027a0001c0001t0002g0045others(15): Show | 18 | HG00544.hp1 HG00735.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.415-26597_415-2659 others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TACACACA others(3): Show |
11 | a0001c0001t0002g0017a0001c0001t0002g0044a0001c0001t0002g0066others(8): Show | 11 | HG01243.hp1 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.415-26599_415-2659 others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TACACACA others(5): Show |
5 | a0001c0001t0002g0077a0001c0001t0002g0080a0001c0001t0003g0214others(2): Show | 5 | HG00642.hp2 HG01975.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-26601_415-2659 others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TACACACA others(7): Show |
4 | a0001c0001t0001g0252a0001c0001t0003g0235a0001c0001t0003g0247others(1): Show | 4 | HG02922.hp1 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-26603_415-2659 others(18): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TACACACA others(9): Show |
2 | a0001c0001t0003g0239a0001c0001t0026g0264 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.415-26605_415-2659 others(20): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TACACACA others(11): Show |
2 | a0001c0001t0003g0238a0001c0001t0003g0240 | 2 | HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.415-26607_415-2659 others(22): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TACACACA others(15): Show |
5 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242others(2): Show | 5 | HG01255.hp1 HG02004.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-26611_415-2659 others(26): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TACACACA others(17): Show |
1 | a0001c0001t0003g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.415-26613_415-2659 others(28): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
T | TACACACA others(21): Show |
1 | a0001c0001t0003g0246 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.415-26617_415-2659 others(32): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
TAC | T | 8 | a0001c0001t0001g0120a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01358.hp1 HG01952.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-26591_415-2659 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
TACAC | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0187a0001c0001t0002g0021 | 3 | HG00609.hp2 NA20300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.415-26593_415-2659 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115846
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0090 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.415-26599_415-2659 others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115846 | ||||||
chr4:108115892
|
T | C | 1 | a0001c0001t0003g0221 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.415-26635A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108115892 | ||||||
chr4:108116521
|
A | C | 3 | a0001c0001t0002g0052a0001c0001t0002g0060a0001c0001t0002g0081 | 3 | HG00642.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.415-27264T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108116521 | ||||||
chr4:108116779
|
A | C | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | NA18971.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.415-27522T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108116779 | ||||||
chr4:108116785
|
G | C | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.415-27528C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108116785 | ||||||
chr4:108116942
|
G | C | 1 | a0001c0001t0003g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.415-27685C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108116942 | ||||||
chr4:108117140
|
C | T | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-27883G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108117140 | ||||||
chr4:108117251
|
A | T | 130 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0252others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.415-27994T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108117251 | ||||||
chr4:108117311
|
C | T | 6 | a0001c0001t0003g0169a0001c0001t0003g0171a0001c0001t0003g0202others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-28054G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108117311 | ||||||
chr4:108117487
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.415-28230C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108117487 | ||||||
chr4:108117498
|
G | A | 104 | a0001c0001t0001g0236a0001c0001t0002g0010a0001c0001t0002g0014others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.415-28241C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108117498 | ||||||
chr4:108117528
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.415-28271T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108117528 | ||||||
chr4:108117602
|
G | A | 43 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0201others(40): Show | 43 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.415-28345C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108117602 | ||||||
chr4:108117718
|
G | T | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.415-28461C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108117718 | ||||||
chr4:108118263
|
G | T | 127 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.415-29006C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108118263 | ||||||
chr4:108118428
|
C | T | 29 | a0001c0001t0001g0201a0001c0001t0001g0208a0001c0001t0001g0227others(26): Show | 29 | HG00558.hp1 HG01099.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.415-29171G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108118428 | ||||||
chr4:108118526
|
T | A | 2 | a0001c0001t0002g0018a0001c0001t0018g0019 | 2 | HG01358.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.415-29269A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108118526 | ||||||
chr4:108118978
|
T | C | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.415-29721A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108118978 | ||||||
chr4:108118998
|
ATACCGCA others(3): Show |
A | 5 | a0001c0001t0002g0022a0001c0001t0002g0029a0001c0001t0002g0036others(2): Show | 5 | NA18951.hp1 NA18959.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-29751_415-2974 others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108118998 | ||||||
chr4:108119392
|
C | A | 2 | a0001c0001t0002g0065a0001c0001t0002g0070 | 2 | HG01081.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.415-30135G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119392 | ||||||
chr4:108119398
|
T | C | 1 | a0001c0001t0004g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.415-30141A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119398 | ||||||
chr4:108119437
|
A | C | 1 | a0001c0001t0002g0084 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.415-30180T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119437 | ||||||
chr4:108119989
|
A | T | 30 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0132others(27): Show | 30 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.415-30732T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119989 | ||||||
chr4:108119993
|
A | ATG | 6 | a0001c0001t0001g0138a0001c0001t0001g0181a0001c0001t0001g0184others(3): Show | 6 | HG00735.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-30738_415-3073 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119993 | ||||||
chr4:108119993
|
ATG | A | 52 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0120others(49): Show | 52 | HG00280.hp2 HG00558.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.415-30738_415-3073 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119993 | ||||||
chr4:108119993
|
ATGTG | A | 15 | a0001c0001t0001g0153a0001c0001t0001g0256a0001c0001t0001g0257others(12): Show | 15 | HG01109.hp2 HG01255.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.415-30740_415-3073 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119993 | ||||||
chr4:108119993
|
ATGTGTG | A | 90 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0128others(87): Show | 90 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.415-30742_415-3073 others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119993 | ||||||
chr4:108119993
|
ATGTGTGT others(1): Show |
A | 92 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.415-30744_415-3073 others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119993 | ||||||
chr4:108119993
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0001g0237a0001c0001t0013g0110 | 2 | HG01256.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.415-30746_415-3073 others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119993 | ||||||
chr4:108119995
|
G | A | 4 | a0001c0001t0001g0236a0001c0001t0003g0204a0001c0001t0003g0205others(1): Show | 4 | HG01515.hp2 HG01891.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-30738C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119995 | ||||||
chr4:108119997
|
G | A | 42 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0201others(39): Show | 42 | HG00558.hp1 HG00642.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.415-30740C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119997 | ||||||
chr4:108119999
|
G | A | 14 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(11): Show | 14 | HG01109.hp2 HG01255.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.415-30742C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108119999 | ||||||
chr4:108120001
|
G | A | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(25): Show | 28 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.415-30744C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108120001 | ||||||
chr4:108120003
|
G | A | 90 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.415-30746C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108120003 | ||||||
chr4:108120005
|
G | A | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.415-30748C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108120005 | ||||||
chr4:108120031
|
G | A | 137 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0252others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.415-30774C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108120031 | ||||||
chr4:108120172
|
C | A | 91 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.415-30915G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108120172 | ||||||
chr4:108120594
|
T | C | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-31337A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108120594 | ||||||
chr4:108120709
|
A | C | 1 | a0001c0001t0001g0145 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.415-31452T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108120709 | ||||||
chr4:108120739
|
A | C | 1 | a0001c0001t0001g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.415-31482T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108120739 | ||||||
chr4:108120835
|
A | T | 1 | a0001c0001t0001g0149 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.415-31578T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108120835 | ||||||
chr4:108120916
|
T | G | 2 | a0001c0001t0012g0100a0001c0001t0012g0108 | 2 | HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.415-31659A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108120916 | ||||||
chr4:108121005
|
A | C | 1 | a0001c0001t0022g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-31748T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108121005 | ||||||
chr4:108121538
|
G | A | 3 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0003g0117 | 3 | HG01109.hp1 HG01257.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.415-32281C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108121538 | ||||||
chr4:108122199
|
T | G | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-32942A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108122199 | ||||||
chr4:108122433
|
G | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.415-33176C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108122433 | ||||||
chr4:108122527
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.415-33270C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108122527 | ||||||
chr4:108122555
|
G | A | 7 | a0001c0001t0002g0043a0001c0001t0002g0045a0001c0001t0002g0046others(4): Show | 7 | HG00099.hp1 HG00735.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-33298C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108122555 | ||||||
chr4:108122963
|
T | A | 1 | a0001c0001t0008g0008 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.415-33706A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108122963 | ||||||
chr4:108122995
|
T | C | 10 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(7): Show | 10 | HG01109.hp2 HG01255.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-33738A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108122995 | ||||||
chr4:108123096
|
A | T | 2 | a0001c0001t0003g0170a0001c0001t0003g0180 | 2 | HG00558.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.415-33839T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123096 | ||||||
chr4:108123327
|
A | C | 1 | a0001c0001t0002g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.415-34070T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123327 | ||||||
chr4:108123432
|
G | GT | 44 | a0001c0001t0001g0119a0001c0001t0001g0148a0001c0001t0001g0156others(41): Show | 44 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.415-34176dupA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123432 | ||||||
chr4:108123432
|
G | GTT | 21 | a0001c0001t0001g0116a0001c0001t0001g0133a0001c0001t0001g0208others(18): Show | 21 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.415-34177_415-3417 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123432 | ||||||
chr4:108123432
|
GT | G | 31 | a0001c0001t0001g0177a0001c0001t0001g0186a0001c0001t0001g0256others(28): Show | 31 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.415-34176delA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123432 | ||||||
chr4:108123432
|
GTT | G | 71 | a0001c0001t0001g0236a0001c0001t0001g0252a0001c0001t0002g0010others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.415-34177_415-3417 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123432 | ||||||
chr4:108123432
|
GTTT | G | 7 | a0001c0001t0002g0038a0001c0001t0002g0067a0001c0001t0002g0082others(4): Show | 7 | HG00140.hp1 HG00609.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-34178_415-3417 others(7): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123432 | ||||||
chr4:108123435
|
T | G | 1 | a0004c0009t0002g0096 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.415-34178A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123435 | ||||||
chr4:108123630
|
C | T | 2 | a0001c0001t0004g0094a0001c0001t0019g0095 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.415-34373G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123630 | ||||||
chr4:108123712
|
G | A | 110 | a0001c0001t0001g0236a0001c0001t0002g0010a0001c0001t0002g0014others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.415-34455C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123712 | ||||||
chr4:108123715
|
T | A | 1 | a0001c0001t0002g0087 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.415-34458A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123715 | ||||||
chr4:108123720
|
A | G | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.415-34463T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123720 | ||||||
chr4:108123743
|
A | T | 1 | a0003c0004t0001g0115 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.415-34486T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123743 | ||||||
chr4:108123905
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.415-34648C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108123905 | ||||||
chr4:108124157
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.415-34900T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108124157 | ||||||
chr4:108124374
|
A | AT | 21 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0003g0238others(18): Show | 21 | HG01192.hp2 HG01515.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.415-35118dupA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108124374 | ||||||
chr4:108124393
|
G | A | 87 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.415-35136C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108124393 | ||||||
chr4:108124523
|
C | A | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.415-35266G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108124523 | ||||||
chr4:108124534
|
T | G | 1 | a0001c0001t0004g0091 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.415-35277A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108124534 | ||||||
chr4:108124679
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.415-35422G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108124679 | ||||||
chr4:108124727
|
A | G | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-35470T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108124727 | ||||||
chr4:108124874
|
C | T | 5 | a0001c0001t0001g0236a0001c0001t0004g0094a0001c0001t0015g0001others(2): Show | 5 | HG01515.hp2 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-35617G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108124874 | ||||||
chr4:108124892
|
G | A | 1 | a0001c0001t0019g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.415-35635C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108124892 | ||||||
chr4:108125202
|
C | T | 80 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.415-35945G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108125202 | ||||||
chr4:108125224
|
C | T | 29 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(26): Show | 29 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.415-35967G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108125224 | ||||||
chr4:108125343
|
A | G | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-36086T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108125343 | ||||||
chr4:108125463
|
G | A | 1 | a0001c0001t0002g0084 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.415-36206C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108125463 | ||||||
chr4:108125724
|
T | TG | 15 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(12): Show | 15 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.415-36468_415-3646 others(5): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108125724 | ||||||
chr4:108125728
|
T | G | 46 | a0001c0001t0002g0017a0001c0001t0002g0020a0001c0001t0002g0022others(43): Show | 46 | HG00544.hp1 HG00609.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.415-36471A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108125728 | ||||||
chr4:108125804
|
G | A | 91 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.415-36547C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108125804 | ||||||
chr4:108125833
|
G | A | 7 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(4): Show | 7 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-36576C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108125833 | ||||||
chr4:108126445
|
A | C | 1 | a0001c0001t0005g0146 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.414+37123T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126445 | ||||||
chr4:108126558
|
C | T | 149 | a0001c0001t0001g0125a0001c0001t0001g0201a0001c0001t0001g0208others(146): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.414+37010G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126558 | ||||||
chr4:108126755
|
T | A | 129 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(126): Show | 129 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.414+36813A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126755 | ||||||
chr4:108126761
|
C | T | 1 | a0001c0001t0026g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414+36807G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126761 | ||||||
chr4:108126788
|
A | T | 91 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.414+36780T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126788 | ||||||
chr4:108126804
|
C | CA | 94 | a0001c0001t0001g0236a0001c0001t0001g0252a0001c0001t0002g0010others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.414+36763dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126804 | ||||||
chr4:108126804
|
CA | C | 88 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(85): Show | 88 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.414+36763delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126804 | ||||||
chr4:108126869
|
A | ATG | 25 | a0001c0001t0001g0160a0001c0001t0001g0236a0001c0001t0002g0052others(22): Show | 25 | HG00642.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.414+36697_414+3669 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126869 | ||||||
chr4:108126869
|
A | ATGTG | 9 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(6): Show | 9 | HG01884.hp1 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.414+36695_414+3669 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126869 | ||||||
chr4:108126869
|
ATG | A | 85 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.414+36697_414+3669 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126869 | ||||||
chr4:108126869
|
ATGTG | A | 29 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(26): Show | 29 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.414+36695_414+3669 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126869 | ||||||
chr4:108126895
|
A | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0081 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.414+36673T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108126895 | ||||||
chr4:108127143
|
GA | G | 139 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0252others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.414+36424delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108127143 | ||||||
chr4:108127368
|
G | A | 3 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0021g0098 | 3 | HG01192.hp2 HG02004.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.414+36200C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108127368 | ||||||
chr4:108127435
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG00323.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.414+36133C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108127435 | ||||||
chr4:108127437
|
T | C | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.414+36131A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108127437 | ||||||
chr4:108127439
|
G | A | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.414+36129C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108127439 | ||||||
chr4:108127525
|
G | A | 28 | a0001c0001t0001g0201a0001c0001t0001g0208a0001c0001t0001g0227others(25): Show | 28 | HG00558.hp1 HG01099.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.414+36043C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108127525 | ||||||
chr4:108127579
|
C | T | 26 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(23): Show | 26 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.414+35989G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108127579 | ||||||
chr4:108127767
|
G | C | 2 | a0001c0001t0002g0024a0001c0001t0002g0051 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.414+35801C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108127767 | ||||||
chr4:108127832
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.414+35736C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108127832 | ||||||
chr4:108128096
|
G | T | 1 | a0001c0001t0003g0230 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.414+35472C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108128096 | ||||||
chr4:108128218
|
G | A | 91 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.414+35350C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108128218 | ||||||
chr4:108128228
|
A | G | 1 | a0001c0001t0003g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.414+35340T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108128228 | ||||||
chr4:108128508
|
CT | C | 28 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(25): Show | 28 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.414+35059delA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108128508 | ||||||
chr4:108128525
|
G | A | 3 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242 | 3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+35043C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108128525 | ||||||
chr4:108128563
|
T | C | 92 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.414+35005A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108128563 | ||||||
chr4:108128637
|
C | T | 1 | a0003c0004t0001g0115 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.414+34931G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108128637 | ||||||
chr4:108128675
|
C | T | 1 | a0001c0001t0003g0234 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414+34893G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108128675 | ||||||
chr4:108128926
|
C | A | 1 | a0001c0001t0001g0196 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.414+34642G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108128926 | ||||||
chr4:108129061
|
A | C | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.414+34507T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108129061 | ||||||
chr4:108129103
|
C | G | 1 | a0001c0001t0002g0084 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.414+34465G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108129103 | ||||||
chr4:108129410
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.414+34158A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108129410 | ||||||
chr4:108129459
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0216 | 2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.414+34109A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108129459 | ||||||
chr4:108129496
|
A | C | 87 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.414+34072T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108129496 | ||||||
chr4:108129637
|
T | C | 1 | a0001c0001t0003g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.414+33931A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108129637 | ||||||
chr4:108130002
|
G | A | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.414+33566C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130002 | ||||||
chr4:108130007
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.414+33561A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130007 | ||||||
chr4:108130014
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.414+33554G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130014 | ||||||
chr4:108130030
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.414+33538C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130030 | ||||||
chr4:108130205
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.414+33363C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130205 | ||||||
chr4:108130464
|
A | G | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+33104T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130464 | ||||||
chr4:108130469
|
T | C | 92 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.414+33099A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130469 | ||||||
chr4:108130564
|
C | CA | 17 | a0001c0001t0001g0127a0001c0001t0001g0161a0001c0001t0001g0175others(14): Show | 17 | HG01934.hp2 HG02109.hp2 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.414+33003dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130564 | ||||||
chr4:108130564
|
CA | C | 24 | a0001c0001t0001g0139a0001c0001t0001g0236a0001c0001t0002g0024others(21): Show | 24 | HG00642.hp2 HG01515.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.414+33003delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130564 | ||||||
chr4:108130729
|
C | A | 1 | a0001c0001t0002g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.414+32839G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130729 | ||||||
chr4:108130729
|
C | CA | 11 | a0001c0001t0001g0139a0001c0001t0002g0052a0001c0001t0002g0060others(8): Show | 11 | HG00642.hp1 HG00642.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.414+32838dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130729 | ||||||
chr4:108130745
|
A | T | 1 | a0001c0001t0002g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.414+32823T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130745 | ||||||
chr4:108130764
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.414+32804T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130764 | ||||||
chr4:108130865
|
T | C | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.414+32703A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108130865 | ||||||
chr4:108131069
|
G | A | 29 | a0001c0001t0001g0201a0001c0001t0001g0208a0001c0001t0001g0227others(26): Show | 29 | HG00558.hp1 HG01099.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.414+32499C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108131069 | ||||||
chr4:108131246
|
G | A | 13 | a0001c0001t0001g0236a0001c0001t0004g0094a0001c0001t0007g0101others(10): Show | 13 | HG01515.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.414+32322C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108131246 | ||||||
chr4:108131370
|
A | C | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+32198T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108131370 | ||||||
chr4:108131388
|
TA | T | 106 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0002g0010others(103): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.414+32179delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108131388 | ||||||
chr4:108131947
|
A | G | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414+31621T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108131947 | ||||||
chr4:108131953
|
A | T | 1 | a0001c0001t0003g0204 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.414+31615T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108131953 | ||||||
chr4:108131994
|
C | T | 3 | a0001c0002t0001g0121a0001c0002t0001g0129a0001c0002t0001g0130 | 3 | HG00735.hp2 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.414+31574G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108131994 | ||||||
chr4:108132412
|
C | G | 1 | a0001c0001t0003g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.414+31156G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132412 | ||||||
chr4:108132496
|
C | T | 57 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0132others(54): Show | 57 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.414+31072G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132496 | ||||||
chr4:108132598
|
T | G | 111 | a0001c0001t0001g0236a0001c0001t0002g0010a0001c0001t0002g0014others(108): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.414+30970A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132598 | ||||||
chr4:108132659
|
C | CT | 20 | a0001c0001t0001g0177a0001c0001t0001g0236a0001c0001t0003g0169others(17): Show | 20 | HG00558.hp2 HG01069.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.414+30908dupA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTT | 5 | a0001c0001t0002g0037a0001c0001t0002g0045a0001c0001t0002g0075others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+30906_414+3090 others(7): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTT | 50 | a0001c0001t0002g0014a0001c0001t0002g0020a0001c0001t0002g0022others(47): Show | 50 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.414+30905_414+3090 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTT | 29 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0032others(26): Show | 29 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.414+30904_414+3090 others(9): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTT | 8 | a0001c0001t0002g0010a0001c0001t0002g0053a0001c0001t0002g0080others(5): Show | 8 | HG01192.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+30903_414+3090 others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT | 7 | a0001c0001t0001g0243a0001c0001t0001g0257a0001c0001t0001g0260others(4): Show | 7 | HG01255.hp1 HG02280.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+30902_414+3090 others(11): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(1): Show |
11 | a0001c0001t0001g0252a0001c0001t0001g0256a0001c0001t0003g0245others(8): Show | 11 | HG01109.hp2 HG01192.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.414+30901_414+3090 others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240 | 3 | HG02965.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.414+30899_414+3090 others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0022g0248a0001c0001t0026g0264 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.414+30898_414+3090 others(15): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.414+30895_414+3090 others(18): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0127a0001c0001t0001g0168 | 2 | HG00323.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.414+30894_414+3090 others(19): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(9): Show |
15 | a0001c0001t0001g0120a0001c0001t0001g0134a0001c0001t0001g0137others(12): Show | 15 | HG00280.hp2 HG00609.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.414+30893_414+3090 others(20): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(10): Show |
32 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0139others(29): Show | 32 | HG00735.hp2 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.414+30892_414+3090 others(21): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(11): Show |
17 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0142others(14): Show | 17 | HG00099.hp2 HG02083.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.414+30891_414+3090 others(22): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0159 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.414+30890_414+3090 others(23): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(13): Show |
3 | a0001c0001t0001g0143a0001c0001t0001g0186a0001c0001t0001g0191 | 3 | HG01070.hp2 HG01516.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.414+30889_414+3090 others(24): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(14): Show |
3 | a0001c0001t0001g0179a0001c0001t0001g0215a0001c0001t0005g0146 | 3 | NA18963.hp2 NA18968.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.414+30888_414+3090 others(25): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.414+30884_414+3090 others(29): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132659
|
CT | C | 11 | a0001c0001t0004g0094a0001c0001t0007g0101a0001c0001t0007g0103others(8): Show | 11 | HG00642.hp2 HG01884.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.414+30908delA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132659 | ||||||
chr4:108132863
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414+30705C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132863 | ||||||
chr4:108132984
|
C | G | 1 | a0001c0001t0003g0234 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414+30584G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108132984 | ||||||
chr4:108133035
|
G | A | 1 | a0001c0001t0002g0038 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.414+30533C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133035 | ||||||
chr4:108133055
|
C | G | 1 | a0001c0001t0005g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.414+30513G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133055 | ||||||
chr4:108133100
|
A | C | 1 | a0001c0001t0002g0043 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.414+30468T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133100 | ||||||
chr4:108133125
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.414+30443G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133125 | ||||||
chr4:108133258
|
T | C | 1 | a0001c0001t0012g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.414+30310A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133258 | ||||||
chr4:108133483
|
C | G | 13 | a0001c0001t0001g0236a0001c0001t0004g0094a0001c0001t0007g0101others(10): Show | 13 | HG01515.hp2 HG01884.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.414+30085G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133483 | ||||||
chr4:108133491
|
T | A | 2 | a0001c0001t0004g0055a0001c0001t0004g0056 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.414+30077A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133491 | ||||||
chr4:108133587
|
G | A | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.414+29981C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133587 | ||||||
chr4:108133607
|
G | A | 6 | a0001c0001t0007g0102a0001c0001t0007g0103a0001c0001t0007g0104others(3): Show | 6 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+29961C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133607 | ||||||
chr4:108133710
|
C | T | 3 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240 | 3 | HG02965.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.414+29858G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133710 | ||||||
chr4:108133726
|
A | C | 11 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(8): Show | 11 | HG01109.hp2 HG01255.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+29842T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133726 | ||||||
chr4:108133959
|
G | A | 16 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(13): Show | 16 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.414+29609C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108133959 | ||||||
chr4:108134166
|
C | CA | 214 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(211): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.414+29401dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108134166 | ||||||
chr4:108134166
|
CA | C | 7 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0214others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+29401delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108134166 | ||||||
chr4:108134411
|
A | G | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.414+29157T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108134411 | ||||||
chr4:108134592
|
G | A | 5 | a0001c0001t0002g0057a0001c0001t0002g0059a0001c0001t0002g0063others(2): Show | 5 | HG00609.hp1 HG02015.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+28976C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108134592 | ||||||
chr4:108134713
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.414+28855T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108134713 | ||||||
chr4:108134773
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.414+28795A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108134773 | ||||||
chr4:108134795
|
C | A | 16 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(13): Show | 16 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.414+28773G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108134795 | ||||||
chr4:108134830
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.414+28738G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108134830 | ||||||
chr4:108134939
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.414+28629G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108134939 | ||||||
chr4:108135087
|
G | C | 1 | a0001c0001t0005g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.414+28481C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108135087 | ||||||
chr4:108135169
|
G | A | 1 | a0001c0001t0020g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.414+28399C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108135169 | ||||||
chr4:108135176
|
A | T | 1 | a0001c0001t0003g0250 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.414+28392T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108135176 | ||||||
chr4:108135572
|
C | T | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.414+27996G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108135572 | ||||||
chr4:108135601
|
T | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0142a0001c0001t0001g0159 | 3 | HG02129.hp1 NA18968.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.414+27967A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108135601 | ||||||
chr4:108135635
|
G | T | 46 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0252others(43): Show | 46 | HG00642.hp2 HG01109.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.414+27933C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108135635 | ||||||
chr4:108135871
|
G | T | 5 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(2): Show | 5 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+27697C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108135871 | ||||||
chr4:108136213
|
A | C | 3 | a0001c0001t0001g0236a0001c0001t0015g0001a0001c0001t0016g0005 | 3 | HG01515.hp2 HG02257.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.414+27355T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108136213 | ||||||
chr4:108136248
|
C | T | 80 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.414+27320G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108136248 | ||||||
chr4:108136282
|
T | C | 1 | a0001c0001t0002g0032 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.414+27286A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108136282 | ||||||
chr4:108136465
|
C | CT | 14 | a0001c0001t0001g0236a0001c0001t0002g0088a0001c0001t0004g0094others(11): Show | 14 | HG01515.hp2 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.414+27102dupA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108136465 | ||||||
chr4:108136465
|
CT | C | 89 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.414+27102delA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108136465 | ||||||
chr4:108136465
|
CTT | C | 32 | a0001c0001t0001g0152a0001c0001t0001g0243a0001c0001t0001g0252others(29): Show | 32 | HG00642.hp2 HG01109.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.414+27101_414+2710 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108136465 | ||||||
chr4:108136549
|
G | A | 2 | a0001c0001t0006g0254a0001c0001t0006g0259 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.414+27019C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108136549 | ||||||
chr4:108136842
|
T | C | 2 | a0001c0001t0002g0067a0001c0001t0002g0089 | 2 | HG00609.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.414+26726A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108136842 | ||||||
chr4:108136944
|
T | C | 26 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(23): Show | 26 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.414+26624A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108136944 | ||||||
chr4:108136977
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.414+26591C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108136977 | ||||||
chr4:108137287
|
G | C | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+26281C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108137287 | ||||||
chr4:108137303
|
C | T | 135 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0252others(132): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.414+26265G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108137303 | ||||||
chr4:108137374
|
TC | T | 10 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189others(7): Show | 10 | HG01081.hp1 HG01106.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.414+26193delG | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108137374 | ||||||
chr4:108137492
|
C | A | 1 | a0001c0001t0001g0231 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.414+26076G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108137492 | ||||||
chr4:108137530
|
G | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0031 | 2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.414+26038C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108137530 | ||||||
chr4:108137562
|
G | T | 89 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.414+26006C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108137562 | ||||||
chr4:108137963
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.414+25605C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108137963 | ||||||
chr4:108138338
|
T | C | 1 | a0001c0001t0013g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.414+25230A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108138338 | ||||||
chr4:108138358
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.414+25210C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108138358 | ||||||
chr4:108138424
|
T | C | 3 | a0001c0001t0001g0188a0001c0001t0001g0217a0001c0001t0001g0232 | 3 | HG02258.hp1 HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.414+25144A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108138424 | ||||||
chr4:108138506
|
T | TACAC | 15 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(12): Show | 15 | HG01192.hp2 HG02004.hp2 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.414+25058_414+2506 others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108138506 | ||||||
chr4:108138506
|
T | TACACAC | 115 | a0001c0001t0001g0236a0001c0001t0001g0256a0001c0001t0001g0257others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.414+25056_414+2506 others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108138506 | ||||||
chr4:108138506
|
TAC | T | 4 | a0001c0001t0001g0125a0001c0001t0011g0099a0001c0001t0011g0106others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+25060_414+2506 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108138506 | ||||||
chr4:108138531
|
G | C | 1 | a0001c0001t0004g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.414+25037C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108138531 | ||||||
chr4:108138851
|
G | T | 26 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(23): Show | 26 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.414+24717C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108138851 | ||||||
chr4:108138901
|
A | G | 80 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.414+24667T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108138901 | ||||||
chr4:108138960
|
C | A | 220 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.414+24608G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108138960 | ||||||
chr4:108139193
|
G | A | 1 | a0002c0003t0002g0072 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.414+24375C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108139193 | ||||||
chr4:108139208
|
C | T | 79 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.414+24360G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108139208 | ||||||
chr4:108139384
|
C | G | 1 | a0001c0001t0002g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.414+24184G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108139384 | ||||||
chr4:108139411
|
A | G | 79 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.414+24157T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108139411 | ||||||
chr4:108139616
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0003g0192 | 2 | HG03490.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.414+23952C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108139616 | ||||||
chr4:108139675
|
T | G | 2 | a0001c0001t0004g0094a0001c0001t0019g0095 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.414+23893A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108139675 | ||||||
chr4:108140220
|
C | G | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.414+23348G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108140220 | ||||||
chr4:108140327
|
T | G | 1 | a0004c0009t0002g0096 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.414+23241A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108140327 | ||||||
chr4:108140367
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.414+23201G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108140367 | ||||||
chr4:108140462
|
G | C | 9 | a0001c0001t0001g0119a0001c0001t0001g0136a0001c0001t0001g0137others(6): Show | 9 | HG00544.hp2 HG00609.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+23106C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108140462 | ||||||
chr4:108140524
|
C | T | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+23044G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108140524 | ||||||
chr4:108140525
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.414+23043C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108140525 | ||||||
chr4:108140593
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.414+22975G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108140593 | ||||||
chr4:108140918
|
A | G | 2 | a0001c0001t0004g0094a0001c0001t0019g0095 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.414+22650T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108140918 | ||||||
chr4:108141309
|
A | G | 1 | a0001c0001t0026g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414+22259T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108141309 | ||||||
chr4:108141354
|
C | T | 94 | a0001c0001t0001g0189a0001c0001t0001g0256a0001c0001t0001g0257others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.414+22214G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108141354 | ||||||
chr4:108141387
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.414+22181G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108141387 | ||||||
chr4:108141462
|
C | T | 3 | a0001c0001t0003g0223a0001c0001t0003g0225a0001c0001t0003g0226 | 3 | HG01884.hp2 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.414+22106G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108141462 | ||||||
chr4:108141529
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.414+22039T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108141529 | ||||||
chr4:108141682
|
T | C | 6 | a0001c0001t0003g0169a0001c0001t0003g0171a0001c0001t0003g0202others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+21886A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108141682 | ||||||
chr4:108141685
|
G | C | 1 | a0001c0001t0005g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.414+21883C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108141685 | ||||||
chr4:108142245
|
G | A | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+21323C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108142245 | ||||||
chr4:108142305
|
T | C | 10 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(7): Show | 10 | HG01109.hp2 HG01255.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+21263A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108142305 | ||||||
chr4:108142596
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.414+20972G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108142596 | ||||||
chr4:108142628
|
G | A | 1 | a0001c0001t0003g0234 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414+20940C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108142628 | ||||||
chr4:108142956
|
C | A | 2 | a0001c0001t0004g0094a0001c0001t0019g0095 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.414+20612G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108142956 | ||||||
chr4:108143042
|
C | T | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+20526G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108143042 | ||||||
chr4:108143078
|
G | A | 6 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+20490C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108143078 | ||||||
chr4:108143416
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.414+20152G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108143416 | ||||||
chr4:108143490
|
T | A | 1 | a0001c0001t0004g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.414+20078A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108143490 | ||||||
chr4:108143647
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.414+19921G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108143647 | ||||||
chr4:108143666
|
C | T | 4 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+19902G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108143666 | ||||||
chr4:108143901
|
A | C | 1 | a0001c0001t0002g0065 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.414+19667T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108143901 | ||||||
chr4:108144218
|
A | G | 5 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(2): Show | 5 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+19350T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108144218 | ||||||
chr4:108144238
|
C | A | 13 | a0001c0001t0003g0169a0001c0001t0003g0171a0001c0001t0003g0174others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+19330G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108144238 | ||||||
chr4:108144397
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.414+19171G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108144397 | ||||||
chr4:108144470
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.414+19098T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108144470 | ||||||
chr4:108144571
|
T | C | 1 | a0001c0001t0003g0223 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.414+18997A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108144571 | ||||||
chr4:108144785
|
A | G | 1 | a0001c0001t0003g0123 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.414+18783T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108144785 | ||||||
chr4:108144865
|
C | CA | 198 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0120others(195): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.414+18702dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108144865 | ||||||
chr4:108144865
|
C | CAA | 28 | a0001c0001t0001g0127a0001c0001t0001g0138a0001c0001t0001g0156others(25): Show | 28 | HG00558.hp2 HG00642.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.414+18701_414+1870 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108144865 | ||||||
chr4:108144927
|
T | C | 263 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.414+18641A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108144927 | ||||||
chr4:108145002
|
G | A | 139 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0252others(136): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.414+18566C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108145002 | ||||||
chr4:108145128
|
C | T | 135 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0252others(132): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.414+18440G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108145128 | ||||||
chr4:108145186
|
C | T | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414+18382G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108145186 | ||||||
chr4:108145210
|
C | T | 140 | a0001c0001t0001g0176a0001c0001t0001g0236a0001c0001t0001g0243others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.414+18358G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108145210 | ||||||
chr4:108145378
|
A | G | 25 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(22): Show | 25 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.414+18190T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108145378 | ||||||
chr4:108145386
|
G | A | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+18182C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108145386 | ||||||
chr4:108145575
|
T | C | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+17993A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108145575 | ||||||
chr4:108146410
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.414+17158A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108146410 | ||||||
chr4:108146679
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.414+16889T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108146679 | ||||||
chr4:108146690
|
T | C | 3 | a0001c0002t0001g0121a0001c0002t0001g0129a0001c0002t0001g0130 | 3 | HG00735.hp2 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.414+16878A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108146690 | ||||||
chr4:108146742
|
G | T | 101 | a0001c0001t0001g0236a0001c0001t0002g0010a0001c0001t0002g0014others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.414+16826C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108146742 | ||||||
chr4:108146805
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.414+16763A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108146805 | ||||||
chr4:108147096
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.414+16472G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108147096 | ||||||
chr4:108147122
|
G | C | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.414+16446C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108147122 | ||||||
chr4:108147239
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0185 | 2 | HG02015.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.414+16329C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108147239 | ||||||
chr4:108147259
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.414+16309A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108147259 | ||||||
chr4:108147692
|
A | G | 1 | a0001c0001t0013g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.414+15876T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108147692 | ||||||
chr4:108148121
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.414+15447C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108148121 | ||||||
chr4:108148245
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.414+15323G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108148245 | ||||||
chr4:108148254
|
C | T | 1 | a0001c0001t0003g0251 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.414+15314G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108148254 | ||||||
chr4:108148256
|
T | C | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+15312A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108148256 | ||||||
chr4:108148288
|
A | AAC | 16 | a0001c0001t0001g0136a0001c0001t0001g0243a0001c0001t0001g0252others(13): Show | 16 | HG00544.hp2 HG01192.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.414+15279_414+1528 others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108148288 | ||||||
chr4:108148288
|
A | AC | 190 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.414+15279_414+1528 others(5): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108148288 | ||||||
chr4:108148288
|
A | C | 13 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+15280T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108148288 | ||||||
chr4:108148420
|
A | G | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.414+15148T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108148420 | ||||||
chr4:108148854
|
T | C | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.414+14714A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108148854 | ||||||
chr4:108148963
|
T | C | 4 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+14605A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108148963 | ||||||
chr4:108149176
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.414+14392A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149176 | ||||||
chr4:108149231
|
G | A | 79 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.414+14337C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149231 | ||||||
chr4:108149288
|
C | T | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414+14280G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149288 | ||||||
chr4:108149314
|
C | A | 4 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+14254G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149314 | ||||||
chr4:108149325
|
G | A | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414+14243C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149325 | ||||||
chr4:108149328
|
G | A | 49 | a0001c0001t0002g0017a0001c0001t0002g0020a0001c0001t0002g0022others(46): Show | 49 | HG00544.hp1 HG00609.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.414+14240C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149328 | ||||||
chr4:108149338
|
G | A | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414+14230C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149338 | ||||||
chr4:108149344
|
G | A | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414+14224C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149344 | ||||||
chr4:108149458
|
C | CA | 5 | a0001c0001t0003g0221a0001c0001t0011g0099a0001c0001t0011g0106others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+14109dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0002g0020a0001c0001t0002g0078a0001c0001t0002g0085others(2): Show | 5 | HG00140.hp1 HG01070.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+14100_414+1410 others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(4): Show |
69 | a0001c0001t0001g0236a0001c0001t0002g0014a0001c0001t0002g0018others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.414+14099_414+1410 others(15): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(5): Show |
18 | a0001c0001t0002g0010a0001c0001t0002g0017a0001c0001t0002g0026others(15): Show | 18 | HG00544.hp1 HG00642.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.414+14098_414+1410 others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0006g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.414+14094_414+1410 others(20): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(12): Show |
4 | a0001c0001t0003g0249a0001c0001t0010g0002a0001c0001t0010g0003others(1): Show | 4 | HG02896.hp1 HG02897.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+14109_414+1411 others(23): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0001g0252a0001c0001t0003g0250 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.414+14109_414+1411 others(24): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(14): Show |
2 | a0001c0001t0003g0247a0001c0001t0003g0251 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.414+14109_414+1411 others(25): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(15): Show |
9 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0241others(6): Show | 9 | HG00642.hp2 HG01243.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.414+14109_414+1411 others(26): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(16): Show |
5 | a0001c0001t0001g0243a0001c0001t0003g0240a0001c0001t0003g0245others(2): Show | 5 | HG01192.hp2 HG02004.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+14109_414+1411 others(27): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(25): Show |
4 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(1): Show | 4 | HG01109.hp2 HG01255.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+14109_414+1411 others(36): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(32): Show |
1 | a0001c0001t0006g0254 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.414+14109_414+1411 others(43): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(4): Show |
7 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(4): Show | 7 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+14109_414+1411 others(15): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149458
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0013g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.414+14109_414+1411 others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149458 | ||||||
chr4:108149477
|
T | A | 8 | a0001c0001t0003g0124a0001c0001t0003g0245a0001c0001t0010g0002others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+14091A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149477 | ||||||
chr4:108149516
|
G | A | 135 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0252others(132): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.414+14052C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149516 | ||||||
chr4:108149540
|
A | T | 1 | a0001c0001t0022g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.414+14028T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149540 | ||||||
chr4:108149611
|
A | T | 1 | a0001c0001t0002g0049 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.414+13957T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149611 | ||||||
chr4:108149635
|
G | GTACATAT others(21): Show |
2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.414+13905_414+1393 others(32): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149635 | ||||||
chr4:108149658
|
T | C | 2 | a0001c0001t0004g0094a0001c0001t0019g0095 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.414+13910A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149658 | ||||||
chr4:108149971
|
A | G | 16 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(13): Show | 16 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.414+13597T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108149971 | ||||||
chr4:108150077
|
T | A | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414+13491A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108150077 | ||||||
chr4:108150084
|
A | G | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414+13484T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108150084 | ||||||
chr4:108150131
|
T | C | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.414+13437A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108150131 | ||||||
chr4:108150649
|
T | C | 10 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(7): Show | 10 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+12919A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108150649 | ||||||
chr4:108150737
|
A | G | 4 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+12831T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108150737 | ||||||
chr4:108150748
|
C | T | 10 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(7): Show | 10 | HG01109.hp2 HG01255.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+12820G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108150748 | ||||||
chr4:108150768
|
A | C | 1 | a0001c0001t0020g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.414+12800T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108150768 | ||||||
chr4:108150800
|
T | G | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.414+12768A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108150800 | ||||||
chr4:108151181
|
A | AC | 29 | a0001c0001t0001g0201a0001c0001t0001g0208a0001c0001t0001g0227others(26): Show | 29 | HG00558.hp1 HG01099.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.414+12386dupG | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108151181 | ||||||
chr4:108151500
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.414+12068T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108151500 | ||||||
chr4:108151600
|
T | C | 3 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242 | 3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+11968A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108151600 | ||||||
chr4:108151885
|
G | A | 2 | a0001c0001t0004g0094a0001c0001t0019g0095 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.414+11683C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108151885 | ||||||
chr4:108152093
|
A | G | 16 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(13): Show | 16 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.414+11475T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108152093 | ||||||
chr4:108152110
|
G | A | 2 | a0001c0001t0002g0078a0001c0001t0002g0079 | 2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.414+11458C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108152110 | ||||||
chr4:108152127
|
C | G | 14 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(11): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.414+11441G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108152127 | ||||||
chr4:108152142
|
G | A | 2 | a0001c0001t0003g0199a0001c0001t0003g0200 | 2 | HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.414+11426C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108152142 | ||||||
chr4:108152293
|
T | A | 1 | a0001c0001t0001g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.414+11275A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108152293 | ||||||
chr4:108152501
|
T | A | 14 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(11): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.414+11067A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108152501 | ||||||
chr4:108152708
|
C | T | 14 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(11): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.414+10860G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108152708 | ||||||
chr4:108152942
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.414+10626C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108152942 | ||||||
chr4:108153343
|
T | C | 14 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(11): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.414+10225A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108153343 | ||||||
chr4:108153644
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.414+9924G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108153644 | ||||||
chr4:108153865
|
T | G | 1 | a0001c0001t0003g0250 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.414+9703A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108153865 | ||||||
chr4:108153877
|
A | G | 260 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.414+9691T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108153877 | ||||||
chr4:108154361
|
C | T | 1 | a0001c0001t0011g0099 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.414+9207G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108154361 | ||||||
chr4:108154362
|
A | G | 14 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(11): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.414+9206T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108154362 | ||||||
chr4:108154443
|
C | CA | 114 | a0001c0001t0001g0118a0001c0001t0001g0201a0001c0001t0001g0208others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.414+9124dupT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108154443 | ||||||
chr4:108154443
|
C | CAA | 47 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0001g0172others(44): Show | 47 | HG00280.hp2 HG00544.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.414+9123_414+9124d others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108154443 | ||||||
chr4:108154443
|
C | CAAA | 69 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0132others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.414+9122_414+9124d others(5): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108154443 | ||||||
chr4:108154443
|
C | CAAAA | 13 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0141others(10): Show | 13 | HG00323.hp2 HG00544.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.414+9121_414+9124d others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108154443 | ||||||
chr4:108154443
|
CA | C | 7 | a0001c0001t0007g0101a0001c0001t0012g0100a0001c0001t0012g0108others(4): Show | 7 | HG01884.hp1 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+9124delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108154443 | ||||||
chr4:108154502
|
A | C | 16 | a0001c0001t0001g0236a0001c0001t0003g0122a0001c0001t0004g0094others(13): Show | 16 | HG01515.hp2 HG01884.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.414+9066T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108154502 | ||||||
chr4:108154562
|
AT | A | 5 | a0001c0001t0001g0252a0001c0001t0003g0247a0001c0001t0003g0249others(2): Show | 5 | HG02922.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+9005delA | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108154562 | ||||||
chr4:108155095
|
T | C | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.414+8473A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108155095 | ||||||
chr4:108155145
|
GA | G | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+8422delT | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108155145 | ||||||
chr4:108155171
|
A | G | 5 | a0001c0001t0001g0252a0001c0001t0003g0247a0001c0001t0003g0249others(2): Show | 5 | HG02922.hp1 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+8397T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108155171 | ||||||
chr4:108155202
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.414+8366A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108155202 | ||||||
chr4:108155425
|
A | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0184 | 3 | NA18950.hp2 NA18962.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.414+8143T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108155425 | ||||||
chr4:108155666
|
C | A | 79 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0125others(76): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.414+7902G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108155666 | ||||||
chr4:108155726
|
T | C | 1 | a0001c0001t0004g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.414+7842A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108155726 | ||||||
chr4:108155809
|
A | G | 9 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(6): Show | 9 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+7759T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108155809 | ||||||
chr4:108155992
|
AG | A | 4 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+7575delC | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108155992 | ||||||
chr4:108156275
|
C | G | 1 | a0001c0001t0026g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414+7293G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108156275 | ||||||
chr4:108156377
|
A | G | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.414+7191T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108156377 | ||||||
chr4:108156768
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.414+6800G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108156768 | ||||||
chr4:108156823
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.414+6745C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108156823 | ||||||
chr4:108156893
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.414+6675T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108156893 | ||||||
chr4:108156978
|
G | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.414+6590C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108156978 | ||||||
chr4:108157148
|
TTC | T | 6 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0218others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+6418_414+6419d others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157148 | ||||||
chr4:108157148
|
TTCTC | T | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.414+6416_414+6419d others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157148 | ||||||
chr4:108157164
|
C | A | 3 | a0001c0001t0008g0009a0001c0001t0019g0095a0002c0003t0002g0074 | 3 | HG00140.hp2 HG02895.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.414+6404G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157164 | ||||||
chr4:108157164
|
C | CTA | 7 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 7 | HG02015.hp1 HG02523.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+6403_414+6404i others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157164 | ||||||
chr4:108157164
|
CTCTCTA | C | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.414+6398_414+6403d others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157164 | ||||||
chr4:108157166
|
C | A | 66 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0128others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.414+6402G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157166 | ||||||
chr4:108157166
|
C | CTA | 6 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0181others(3): Show | 6 | HG00280.hp2 HG03579.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+6401_414+6402i others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157166 | ||||||
chr4:108157168
|
C | A | 166 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.414+6400G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157168 | ||||||
chr4:108157170
|
A | C | 27 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0169others(24): Show | 27 | HG00642.hp2 HG01099.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.414+6398T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157170 | ||||||
chr4:108157171
|
T | TACACACA others(3): Show |
1 | a0001c0001t0002g0090 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.414+6396_414+6397i others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157171 | ||||||
chr4:108157172
|
A | C | 12 | a0001c0001t0001g0252a0001c0001t0003g0238a0001c0001t0003g0239others(9): Show | 12 | HG01192.hp2 HG01243.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.414+6396T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157172 | ||||||
chr4:108157173
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.414+6395A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157173 | ||||||
chr4:108157173
|
T | TACACACA others(5): Show |
1 | a0001c0001t0002g0084 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.414+6394_414+6395i others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157173 | ||||||
chr4:108157175
|
T | C | 7 | a0001c0001t0002g0018a0001c0001t0002g0022a0001c0001t0002g0029others(4): Show | 7 | HG01358.hp1 HG02004.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+6393A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157175 | ||||||
chr4:108157175
|
T | TACAC | 10 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0053others(7): Show | 10 | HG01192.hp1 HG01255.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+6392_414+6393i others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157175 | ||||||
chr4:108157175
|
T | TACACAC | 15 | a0001c0001t0002g0032a0001c0001t0002g0033a0001c0001t0002g0034others(12): Show | 15 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.414+6392_414+6393i others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157175 | ||||||
chr4:108157175
|
T | TACACACA others(1): Show |
19 | a0001c0001t0002g0014a0001c0001t0002g0021a0001c0001t0002g0024others(16): Show | 19 | HG00323.hp1 HG01069.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+6392_414+6393i others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157175 | ||||||
chr4:108157175
|
T | TACACACA others(3): Show |
14 | a0001c0001t0002g0026a0001c0001t0002g0039a0001c0001t0002g0065others(11): Show | 14 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.414+6392_414+6393i others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157175 | ||||||
chr4:108157175
|
T | TACACACA others(5): Show |
6 | a0001c0001t0002g0010a0001c0001t0002g0020a0001c0001t0002g0068others(3): Show | 6 | HG01106.hp1 HG01496.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+6392_414+6393i others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157175 | ||||||
chr4:108157175
|
T | TACACACA others(9): Show |
3 | a0001c0001t0002g0017a0001c0001t0002g0071a0001c0001t0002g0085 | 3 | HG00140.hp1 HG03927.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.414+6392_414+6393i others(18): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157175 | ||||||
chr4:108157175
|
T | TACACACA others(11): Show |
1 | a0001c0001t0002g0050 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.414+6392_414+6393i others(20): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157175 | ||||||
chr4:108157177
|
T | C | 80 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(77): Show | 80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.414+6391A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157177 | ||||||
chr4:108157177
|
T | TACAC | 3 | a0001c0001t0002g0052a0001c0001t0002g0081a0001c0001t0003g0245 | 3 | HG02717.hp1 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.414+6390_414+6391i others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157177 | ||||||
chr4:108157177
|
T | TACACAC | 4 | a0001c0001t0002g0047a0001c0001t0002g0075a0001c0001t0002g0076others(1): Show | 4 | HG00099.hp1 HG00735.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+6390_414+6391i others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157177 | ||||||
chr4:108157177
|
T | TACACACA others(1): Show |
9 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(6): Show | 9 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+6390_414+6391i others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157177 | ||||||
chr4:108157177
|
T | TACACACA others(3): Show |
3 | a0001c0001t0003g0124a0001c0001t0010g0004a0003c0004t0001g0115 | 3 | HG01891.hp2 NA19076.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.414+6390_414+6391i others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157177 | ||||||
chr4:108157177
|
T | TACACACA others(5): Show |
2 | a0001c0001t0007g0102a0001c0001t0022g0248 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.414+6390_414+6391i others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157177 | ||||||
chr4:108157177
|
T | TACACACA others(9): Show |
3 | a0001c0001t0007g0103a0001c0001t0007g0104a0001c0008t0007g0105 | 3 | HG01884.hp1 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.414+6390_414+6391i others(18): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157177 | ||||||
chr4:108157177
|
TATACACA others(7): Show |
T | 3 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260 | 3 | HG01109.hp2 HG02280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.414+6377_414+6390d others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157177 | ||||||
chr4:108157179
|
T | C | 105 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0017others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.414+6389A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157179 | ||||||
chr4:108157179
|
T | TATAC | 5 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0175others(2): Show | 5 | HG00609.hp2 HG01070.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+6388_414+6389i others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157179 | ||||||
chr4:108157179
|
T | TATACAC | 33 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0132others(30): Show | 33 | HG00558.hp2 HG00621.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.414+6388_414+6389i others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157179 | ||||||
chr4:108157179
|
T | TATACACA others(1): Show |
16 | a0001c0001t0001g0125a0001c0001t0001g0165a0001c0001t0001g0167others(13): Show | 16 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.414+6388_414+6389i others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157179 | ||||||
chr4:108157179
|
T | TATACACA others(3): Show |
9 | a0001c0001t0001g0119a0001c0001t0001g0177a0001c0001t0001g0243others(6): Show | 9 | HG01255.hp1 HG02004.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+6388_414+6389i others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157179 | ||||||
chr4:108157179
|
T | TATACACA others(5): Show |
3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0252 | 3 | HG01106.hp2 HG01358.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.414+6388_414+6389i others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157179 | ||||||
chr4:108157179
|
T | TATATAC | 3 | a0001c0001t0001g0120a0001c0001t0001g0145a0001c0001t0001g0237 | 3 | HG01256.hp2 HG03195.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.414+6388_414+6389i others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157179 | ||||||
chr4:108157179
|
T | TATATACA others(1): Show |
4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0215others(1): Show | 4 | HG01934.hp2 HG01952.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+6388_414+6389i others(10): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157179 | ||||||
chr4:108157179
|
T | TATATATA others(3): Show |
1 | a0001c0001t0005g0163 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.414+6388_414+6389i others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157179 | ||||||
chr4:108157179
|
TAC | T | 3 | a0001c0001t0001g0201a0001c0001t0003g0122a0001c0001t0003g0221 | 3 | NA18960.hp2 NA18991.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.414+6387_414+6388d others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157179 | ||||||
chr4:108157181
|
C | T | 33 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0172others(30): Show | 33 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.414+6387G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157181 | ||||||
chr4:108157183
|
C | T | 5 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0218others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+6385G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157183 | ||||||
chr4:108157189
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.414+6379G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157189 | ||||||
chr4:108157191
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.414+6377G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157191 | ||||||
chr4:108157207
|
CACACACA others(7): Show |
C | 6 | a0001c0001t0006g0254a0001c0001t0006g0255a0001c0001t0006g0258others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+6347_414+6360d others(16): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157207 | ||||||
chr4:108157221
|
A | C | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(4): Show | 7 | HG00621.hp1 HG01109.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+6347T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157221 | ||||||
chr4:108157240
|
C | T | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.414+6328G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157240 | ||||||
chr4:108157534
|
C | G | 1 | a0001c0001t0001g0132 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.414+6034G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157534 | ||||||
chr4:108157549
|
G | A | 14 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(11): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.414+6019C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157549 | ||||||
chr4:108157825
|
G | A | 3 | a0001c0001t0001g0252a0001c0001t0003g0247a0001c0001t0003g0251 | 3 | HG02922.hp1 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.414+5743C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157825 | ||||||
chr4:108157985
|
T | A | 1 | a0001c0001t0003g0214 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.414+5583A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108157985 | ||||||
chr4:108158009
|
C | T | 7 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(4): Show | 7 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+5559G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108158009 | ||||||
chr4:108158048
|
C | A | 3 | a0001c0002t0001g0121a0001c0002t0001g0129a0001c0002t0001g0130 | 3 | HG00735.hp2 HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.414+5520G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108158048 | ||||||
chr4:108158418
|
A | AAG | 65 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0128others(62): Show | 65 | HG00099.hp2 HG00323.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.414+5148_414+5149d others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108158418 | ||||||
chr4:108158437
|
C | A | 39 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(36): Show | 39 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.414+5131G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108158437 | ||||||
chr4:108158439
|
C | T | 1 | a0001c0002t0001g0129 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.414+5129G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108158439 | ||||||
chr4:108158444
|
C | T | 2 | a0001c0001t0002g0048a0001c0001t0002g0049 | 2 | HG00544.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.414+5124G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108158444 | ||||||
chr4:108158610
|
G | A | 14 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(11): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.414+4958C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108158610 | ||||||
chr4:108158705
|
T | C | 1 | a0001c0006t0006g0253 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.414+4863A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108158705 | ||||||
chr4:108158942
|
T | C | 1 | a0001c0001t0003g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.414+4626A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108158942 | ||||||
chr4:108159345
|
A | C | 10 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(7): Show | 10 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+4223T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108159345 | ||||||
chr4:108159398
|
C | T | 1 | a0001c0001t0022g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.414+4170G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108159398 | ||||||
chr4:108159853
|
A | T | 1 | a0001c0001t0005g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.414+3715T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108159853 | ||||||
chr4:108159962
|
G | A | 4 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+3606C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108159962 | ||||||
chr4:108160110
|
G | A | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+3458C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108160110 | ||||||
chr4:108160173
|
T | G | 1 | a0001c0001t0002g0044 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.414+3395A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108160173 | ||||||
chr4:108160294
|
C | A | 4 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+3274G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108160294 | ||||||
chr4:108160369
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.414+3199C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108160369 | ||||||
chr4:108160463
|
G | A | 3 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242 | 3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+3105C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108160463 | ||||||
chr4:108160571
|
T | A | 26 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(23): Show | 26 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.414+2997A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108160571 | ||||||
chr4:108160895
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0003g0117 | 3 | HG01109.hp1 HG01257.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.414+2673G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108160895 | ||||||
chr4:108161080
|
T | C | 9 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0260others(6): Show | 9 | HG01109.hp2 HG02280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+2488A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108161080 | ||||||
chr4:108161159
|
G | C | 19 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(16): Show | 19 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+2409C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108161159 | ||||||
chr4:108161180
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0018g0019 | 2 | HG01358.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.414+2388A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108161180 | ||||||
chr4:108161375
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.414+2193T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108161375 | ||||||
chr4:108161389
|
G | A | 3 | a0001c0001t0001g0243a0001c0001t0003g0241a0001c0001t0003g0242 | 3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+2179C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108161389 | ||||||
chr4:108161837
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG00280.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.414+1731G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108161837 | ||||||
chr4:108161966
|
A | G | 1 | a0001c0001t0020g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.414+1602T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108161966 | ||||||
chr4:108162149
|
T | C | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+1419A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108162149 | ||||||
chr4:108162573
|
AGT | A | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+993_414+994del others(2): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108162573 | ||||||
chr4:108162589
|
T | C | 11 | a0001c0001t0001g0243a0001c0001t0003g0238a0001c0001t0003g0239others(8): Show | 11 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+979A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108162589 | ||||||
chr4:108162595
|
C | T | 2 | a0001c0001t0004g0094a0001c0001t0019g0095 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.414+973G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108162595 | ||||||
chr4:108162609
|
G | T | 14 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(11): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.414+959C>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108162609 | ||||||
chr4:108163117
|
C | T | 14 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(11): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.414+451G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108163117 | ||||||
chr4:108163155
|
A | T | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.414+413T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108163155 | ||||||
chr4:108163187
|
T | C | 1 | a0001c0001t0003g0180 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.414+381A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108163187 | ||||||
chr4:108163336
|
ATC | A | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+230_414+231del others(2): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 3/11 | chr4 | 108163336 | ||||||
chr4:108163945
|
T | C | 7 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-244A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/11 | chr4 | 108163945 | ||||||
chr4:108164037
|
T | A | 2 | a0001c0001t0002g0041a0001c0001t0002g0042 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.281-336A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/11 | chr4 | 108164037 | ||||||
chr4:108164120
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.281-419A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/11 | chr4 | 108164120 | ||||||
chr4:108164231
|
T | C | 8 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(5): Show | 8 | HG00099.hp1 HG00735.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-530A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/11 | chr4 | 108164231 | ||||||
chr4:108164390
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.281-689A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/11 | chr4 | 108164390 | ||||||
chr4:108164391
|
T | A | 2 | a0001c0001t0001g0236a0001c0001t0015g0001 | 2 | HG01515.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.281-690A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/11 | chr4 | 108164391 | ||||||
chr4:108164420
|
G | C | 1 | a0001c0001t0003g0230 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.280+677C>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/11 | chr4 | 108164420 | ||||||
chr4:108164835
|
T | C | 9 | a0001c0001t0001g0236a0001c0001t0003g0124a0001c0001t0010g0002others(6): Show | 9 | HG00642.hp2 HG01515.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+262A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/11 | chr4 | 108164835 | ||||||
chr4:108165000
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.280+97G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/11 | chr4 | 108165000 | ||||||
chr4:108165068
|
A | T | 1 | a0001c0001t0001g0128 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.280+29T>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 2/11 | chr4 | 108165068 | ||||||
chr4:108165191
|
A | G | 26 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(23): Show | 26 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.214-28T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108165191 | ||||||
chr4:108165339
|
A | G | 14 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(11): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.214-176T>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108165339 | ||||||
chr4:108165412
|
T | C | 1 | a0001c0001t0002g0020 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.214-249A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108165412 | ||||||
chr4:108165418
|
A | C | 1 | a0001c0001t0004g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214-255T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108165418 | ||||||
chr4:108165508
|
T | C | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214-345A>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108165508 | ||||||
chr4:108165655
|
T | G | 4 | a0001c0001t0003g0124a0001c0001t0010g0002a0001c0001t0010g0003others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-492A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108165655 | ||||||
chr4:108165938
|
C | T | 1 | a0001c0001t0002g0022 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.214-775G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108165938 | ||||||
chr4:108166175
|
C | T | 17 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0003g0238others(14): Show | 17 | HG01192.hp2 HG01243.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.214-1012G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108166175 | ||||||
chr4:108166223
|
A | C | 14 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(11): Show | 14 | HG01884.hp1 HG02572.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.214-1060T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108166223 | ||||||
chr4:108166277
|
C | A | 1 | a0001c0001t0002g0021 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.214-1114G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108166277 | ||||||
chr4:108166489
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.213+1066C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108166489 | ||||||
chr4:108166655
|
T | G | 2 | a0001c0001t0024g0263a0001c0001t0025g0262 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.213+900A>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108166655 | ||||||
chr4:108166673
|
C | A | 3 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0004g0091 | 3 | NA18962.hp1 NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.213+882G>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108166673 | ||||||
chr4:108166695
|
A | C | 8 | a0001c0001t0007g0101a0001c0001t0007g0102a0001c0001t0007g0103others(5): Show | 8 | HG01884.hp1 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+860T>G | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108166695 | ||||||
chr4:108166882
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.213+673G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108166882 | ||||||
chr4:108166946
|
C | T | 1 | a0001c0001t0016g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.213+609G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108166946 | ||||||
chr4:108166984
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0003g0126 | 2 | NA18945.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.213+571G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108166984 | ||||||
chr4:108167064
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.213+491G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167064 | ||||||
chr4:108167099
|
T | A | 1 | a0001c0001t0020g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.213+456A>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167099 | ||||||
chr4:108167262
|
G | A | 3 | a0001c0001t0004g0094a0001c0001t0016g0005a0001c0001t0019g0095 | 3 | HG02257.hp1 HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.213+293C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167262 | ||||||
chr4:108167272
|
G | A | 3 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0021g0098 | 3 | HG01192.hp2 HG02004.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.213+283C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167272 | ||||||
chr4:108167334
|
C | T | 3 | a0001c0001t0011g0099a0001c0001t0011g0106a0001c0001t0011g0109 | 3 | HG02572.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.213+221G>A | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167334 | ||||||
chr4:108167351
|
T | TAC | 25 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0227others(22): Show | 25 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.213+202_213+203dup others(2): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167351 | ||||||
chr4:108167351
|
T | TACAC | 10 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0002g0087others(7): Show | 10 | HG01099.hp1 HG01515.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+200_213+203dup others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167351 | ||||||
chr4:108167351
|
T | TACACAC | 4 | a0001c0001t0001g0236a0001c0001t0002g0092a0001c0001t0002g0093others(1): Show | 4 | HG01069.hp1 HG02965.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+198_213+203dup others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167351 | ||||||
chr4:108167351
|
TAC | T | 98 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0128others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.213+202_213+203del others(2): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167351 | ||||||
chr4:108167351
|
TACAC | T | 31 | a0001c0001t0001g0237a0001c0001t0002g0014a0001c0001t0002g0017others(28): Show | 31 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.213+200_213+203del others(4): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167351 | ||||||
chr4:108167351
|
TACACAC | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0003g0247others(2): Show | 5 | HG03195.hp2 HG03453.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+198_213+203del others(6): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167351 | ||||||
chr4:108167351
|
TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0003g0117 | 3 | HG01109.hp1 HG01257.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.213+196_213+203del others(8): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167351 | ||||||
chr4:108167351
|
TACACACA others(5): Show |
T | 4 | a0001c0001t0003g0244a0001c0001t0003g0245a0001c0001t0003g0246others(1): Show | 4 | HG01192.hp2 HG01255.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+192_213+203del others(12): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167351 | ||||||
chr4:108167351
|
TACACACA others(7): Show |
T | 7 | a0001c0001t0001g0243a0001c0001t0003g0238a0001c0001t0003g0239others(4): Show | 7 | HG01243.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.213+190_213+203del others(14): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167351 | ||||||
chr4:108167351
|
TACACACA others(23): Show |
T | 1 | a0001c0001t0002g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.213+174_213+203del others(30): Show |
LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167351 | ||||||
chr4:108167437
|
C | G | 3 | a0003c0004t0001g0114a0003c0004t0001g0115a0005c0005t0003g0113 | 3 | HG00642.hp2 HG02602.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.213+118G>C | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167437 | ||||||
chr4:108167438
|
G | A | 2 | a0001c0001t0004g0094a0001c0001t0019g0095 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.213+117C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167438 | ||||||
chr4:108167464
|
G | A | 1 | a0001c0001t0013g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.213+91C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167464 | ||||||
chr4:108167472
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.213+83C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167472 | ||||||
chr4:108167518
|
G | A | 26 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0256others(23): Show | 26 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.213+37C>T | LEF1 | ENSG00000138795.10 | transcript | ENST00000265165.6 | protein_coding | 1/11 | chr4 | 108167518 |