Item | Value |
---|---|
geneid | 2202 |
ensemblid | ENSG00000115380.20 |
hgncid | 3218 |
symbol | EFEMP1 |
name | EGF containing fibulin extracellular matrix protein 1 |
refseq_nuc | NM_001039348.3 |
refseq_prot | NP_001034437.1 |
ensembl_nuc | ENST00000355426.8 |
ensembl_prot | ENSP00000347596.3 |
mane_status | MANE Select |
chr | chr2 |
start | 55865967 |
end | 55923782 |
strand | - |
ver | v1.2 |
region | chr2:55865967-55923782 |
region5000 | chr2:55860967-55928782 |
regionname0 | EFEMP1_chr2_55865967_55923782 |
regionname5000 | EFEMP1_chr2_55860967_55928782 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 493 | 348 | 91 | 58 | 150 | 13 | 34 | 116 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0002 | 0/0 | 493 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0003 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1482 | 323 | 73 | 52 | 150 | 13 | 33 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
c0002 | 0/0 | 1482 | 12 | 11 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
c0003 | 0/0 | 1482 | 7 | 6 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
c0004 | 0/0 | 1482 | 4 | 0 | 3 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
c0005 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
c0006 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
c0007 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
c0008 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1227 | 249 | 52 | 47 | 113 | 13 | 23 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0002 | 0/0 | 1227 | 21 | 20 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0003 | 0/0 | 1227 | 13 | 5 | 2 | 4 | 0 | 2 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0004 | 0/1 | 1227 | 12 | 0 | 4 | 2 | 1 | 4 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0005 | 0/0 | 1227 | 12 | 2 | 1 | 9 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0006 | 0/0 | 1227 | 9 | 9 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0007 | 0/0 | 1227 | 6 | 0 | 0 | 5 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0008 | 0/0 | 1227 | 5 | 0 | 0 | 5 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0009 | 0/0 | 1227 | 4 | 0 | 0 | 4 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0010 | 0/0 | 1226 | 4 | 0 | 3 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0011 | 0/0 | 1227 | 3 | 0 | 0 | 3 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0012 | 0/0 | 1227 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0013 | 0/0 | 1227 | 2 | 2 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0014 | 0/0 | 1227 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0015 | 0/0 | 1227 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0016 | 0/0 | 1226 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0017 | 0/0 | 1227 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0018 | 0/0 | 1227 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0019 | 0/0 | 1227 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0020 | 0/0 | 1227 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
t0021 | 0/0 | 1227 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0002 | 0/0 | 6 | 0 | 2 | 3 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0008 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1482 | 323 | 73 | 52 | 150 | 13 | 33 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0002 | 0/0 | 1482 | 12 | 11 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0003 | 0/0 | 1482 | 7 | 6 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0004 | 0/0 | 1482 | 4 | 0 | 3 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0006 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0008 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0002c0007 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0003c0005 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2708 | 235 | 41 | 45 | 113 | 12 | 23 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0002 | 0/0 | 2708 | 15 | 15 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0003 | 0/0 | 2708 | 13 | 5 | 2 | 4 | 0 | 2 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0004 | 0/1 | 2708 | 12 | 0 | 4 | 2 | 1 | 4 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0005 | 0/0 | 2708 | 12 | 2 | 1 | 9 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0006 | 0/0 | 2708 | 7 | 7 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0007 | 0/0 | 2708 | 6 | 0 | 0 | 5 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0008 | 0/0 | 2708 | 5 | 0 | 0 | 5 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0009 | 0/0 | 2708 | 4 | 0 | 0 | 4 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0011 | 0/0 | 2708 | 3 | 0 | 0 | 3 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0012 | 0/0 | 2708 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0013 | 0/0 | 2708 | 2 | 2 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0014 | 0/0 | 2708 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0015 | 0/0 | 2708 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0016 | 0/0 | 2707 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0017 | 0/0 | 2708 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0018 | 0/0 | 2708 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0019 | 0/0 | 2708 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0001t0020 | 0/0 | 2708 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0002t0001 | 0/0 | 2708 | 11 | 10 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0002t0006 | 0/0 | 2708 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0003t0002 | 0/0 | 2708 | 5 | 4 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0003t0006 | 0/0 | 2708 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0003t0021 | 0/0 | 2708 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0004t0010 | 0/0 | 2707 | 4 | 0 | 3 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0006t0002 | 0/0 | 2708 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0001c0008t0001 | 0/0 | 2708 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0002c0007t0001 | 0/0 | 2708 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
a0003c0005t0001 | 0/0 | 2708 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | copy fasta | chr2 | 55860967 | 55928782 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 3 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0004g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0004g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0006g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0007g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0008g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0008g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0008g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0008g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0009g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0009g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0009g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0011g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0012g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0012g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0013g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0014g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0015g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0016g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0017g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0018g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0019g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0001t0020g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0002t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0003t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0003t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0003t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0003t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0003t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0003t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0003t0021g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0004t0010g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0004t0010g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0004t0010g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0004t0010g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0006t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0001c0008t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0002c0007t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
a0003c0005t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | GBR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00140 | hp1 | a0002 | c0007 | t0001 | g0262 | EUR | GBR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | FIN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00408 | hp1 | a0001 | c0001 | t0009 | g0263 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0074 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01070 | hp1 | a0001 | c0004 | t0010 | g0298 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01081 | hp1 | a0001 | c0004 | t0010 | g0300 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01099 | hp2 | a0001 | c0004 | t0010 | g0299 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0165 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01167 | hp1 | a0001 | c0003 | t0002 | g0290 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0057 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01346 | hp1 | a0001 | c0008 | t0001 | g0268 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0053 | EUR | IBS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0052 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0129 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02129 | hp2 | a0001 | c0001 | t0009 | g0264 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02145 | hp2 | a0001 | c0001 | t0013 | g0015 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CDX | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02258 | hp2 | a0001 | c0001 | t0019 | g0259 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PEL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0109 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0048 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0100 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0101 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0062 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03017 | hp1 | a0001 | c0001 | t0007 | g0041 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03017 | hp2 | a0001 | c0004 | t0010 | g0297 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03041 | hp2 | a0001 | c0002 | t0006 | g0071 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03130 | hp1 | a0001 | c0003 | t0021 | g0288 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03139 | hp2 | a0001 | c0001 | t0013 | g0015 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03195 | hp1 | a0003 | c0005 | t0001 | g0273 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0095 | AFR | ESN | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03225 | hp1 | a0001 | c0003 | t0002 | g0289 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03486 | hp1 | a0001 | c0003 | t0002 | g0293 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03486 | hp2 | a0001 | c0006 | t0002 | g0285 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03491 | hp2 | a0001 | c0001 | t0016 | g0257 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03704 | hp2 | a0001 | c0001 | t0017 | g0090 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0050 | SAS | BEB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | STU | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | YRI | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18939 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18944 | hp1 | a0001 | c0001 | t0009 | g0223 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18946 | hp2 | a0001 | c0001 | t0020 | g0261 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18951 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18956 | hp1 | a0001 | c0001 | t0014 | g0055 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18959 | hp2 | a0001 | c0001 | t0012 | g0183 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18961 | hp1 | a0001 | c0001 | t0005 | g0253 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18972 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18978 | hp2 | a0001 | c0001 | t0007 | g0046 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18986 | hp1 | a0001 | c0001 | t0009 | g0258 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18999 | hp1 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19004 | hp2 | a0001 | c0001 | t0008 | g0031 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19005 | hp2 | a0001 | c0001 | t0008 | g0294 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19006 | hp2 | a0001 | c0001 | t0012 | g0179 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19007 | hp1 | a0001 | c0001 | t0008 | g0295 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19009 | hp1 | a0001 | c0001 | t0011 | g0007 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | LWK | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | LWK | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19054 | hp1 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19054 | hp2 | a0001 | c0001 | t0011 | g0007 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19058 | hp2 | a0001 | c0001 | t0011 | g0007 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19064 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19076 | hp1 | a0001 | c0001 | t0018 | g0195 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19081 | hp2 | a0001 | c0001 | t0005 | g0128 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19082 | hp1 | a0001 | c0001 | t0008 | g0296 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19087 | hp1 | a0001 | c0001 | t0007 | g0045 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19088 | hp1 | a0001 | c0001 | t0008 | g0031 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | YRI | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0088 | AFR | YRI | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0272 | AFR | ASW | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ASW | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | GIH | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA20905 | hp2 | a0001 | c0001 | t0015 | g0059 | SAS | GIH | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | MSL | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | USA | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
HG06807 | hp2 | a0001 | c0003 | t0002 | g0291 | AFR | USA | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | USA | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA20300 | hp2 | a0001 | c0003 | t0006 | g0061 | AFR | USA | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
NA21309 | hp2 | a0001 | c0003 | t0002 | g0292 | AFR | LWK | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0058 | REF | REF | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0177 | REF | REF | EFEMP1_chr2_55860967_55928782 | EFEMP1 | chr2 | 55860967 | 55928782 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55867219
|
T | G | 1 | a0003 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1336A>C | p.Ser446Arg | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 1456/2708 | 1336/1482 | 446/493 | chr2 | 55867219 | ||
chr2:55918036
|
T | G | 1 | a0002 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.146A>C | p.Asp49Ala | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/12 | 266/2708 | 146/1482 | 49/493 | chr2 | 55918036 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55877831
|
G | A | 1 | a0001c0006 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.675C>T | p.His225His | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 7/12 | 795/2708 | 675/1482 | 225/493 | chr2 | 55877831 | ||
chr2:55917795
|
T | C | 1 | a0001c0004 | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
synonymous_variant | LOW | c.387A>G | p.Glu129Glu | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/12 | 507/2708 | 387/1482 | 129/493 | chr2 | 55917795 | ||
chr2:55917936
|
T | C | 1 | a0001c0003 | 7 | HG01167.hp1 HG03130.hp1 HG03225.hp1 others(4): Show |
synonymous_variant | LOW | c.246A>G | p.Glu82Glu | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/12 | 366/2708 | 246/1482 | 82/493 | chr2 | 55917936 | ||
chr2:55917975
|
G | T | 2 | a0001c0002a0003c0005 | 13 | HG00738.hp2 HG02280.hp1 HG02886.hp2 others(10): Show |
synonymous_variant | LOW | c.207C>A | p.Leu69Leu | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/12 | 327/2708 | 207/1482 | 69/493 | chr2 | 55917975 | ||
chr2:55922423
|
G | A | 1 | a0001c0008 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.18C>T | p.Phe6Phe | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/12 | 138/2708 | 18/1482 | 6/493 | chr2 | 55922423 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55866010
|
C | T | 3 | a0001c0001t0006a0001c0002t0006a0001c0003t0006 | 9 | HG02257.hp2 HG02572.hp1 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1063G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 1063 | chr2 | 55866010 | |||||
chr2:55866069
|
G | C | 1 | a0001c0001t0004 | 12 | HG01074.hp1 HG01255.hp1 HG01257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1004C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 1004 | chr2 | 55866069 | |||||
chr2:55866111
|
G | T | 2 | a0001c0001t0005a0001c0001t0007 | 18 | HG00544.hp2 HG00597.hp1 HG01109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*962C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 962 | chr2 | 55866111 | |||||
chr2:55866273
|
G | A | 1 | a0001c0001t0013 | 2 | HG02145.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*800C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 800 | chr2 | 55866273 | |||||
chr2:55866378
|
A | G | 1 | a0001c0001t0012 | 2 | NA18959.hp2 NA19006.hp2 |
3_prime_UTR_variant | MODIFIER | c.*695T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 695 | chr2 | 55866378 | |||||
chr2:55866386
|
A | G | 2 | a0001c0001t0011a0001c0001t0018 | 4 | NA19009.hp1 NA19054.hp2 NA19058.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*687T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 687 | chr2 | 55866386 | |||||
chr2:55866405
|
G | A | 1 | a0001c0001t0015 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*668C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 668 | chr2 | 55866405 | |||||
chr2:55866424
|
G | A | 1 | a0001c0001t0019 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*649C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 649 | chr2 | 55866424 | |||||
chr2:55866566
|
G | A | 1 | a0001c0003t0021 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*507C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 507 | chr2 | 55866566 | |||||
chr2:55866738
|
T | C | 1 | a0001c0001t0020 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 335 | chr2 | 55866738 | |||||
chr2:55866825
|
T | G | 2 | a0001c0001t0009a0001c0001t0014 | 5 | HG00408.hp1 HG02129.hp2 NA18944.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*248A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 248 | chr2 | 55866825 | |||||
chr2:55866986
|
C | T | 1 | a0001c0001t0017 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 87 | chr2 | 55866986 | |||||
chr2:55867066
|
GA | G | 2 | a0001c0001t0016a0001c0004t0010 | 5 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6delT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 12/12 | 6 | chr2 | 55867066 | |||||
chr2:55922930
|
G | T | 1 | a0001c0001t0011 | 3 | NA19009.hp1 NA19054.hp2 NA19058.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-39C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 2/12 | chr2 | 55922930 | ||||||
chr2:55923714
|
T | C | 5 | a0001c0001t0002a0001c0003t0002a0001c0003t0021others(2): Show | 26 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-52A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 1/12 | 1274 | chr2 | 55923714 | |||||
chr2:55923722
|
C | T | 1 | a0001c0001t0015 | 1 | NA20905.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 1/12 | 1282 | chr2 | 55923722 | |||||
chr2:55923726
|
G | A | 1 | a0001c0001t0008 | 5 | NA19004.hp2 NA19005.hp2 NA19007.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-64C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 1/12 | 1286 | chr2 | 55923726 | |||||
chr2:55923729
|
C | T | 4 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(1): Show | 32 | HG00438.hp1 HG01074.hp1 HG01255.hp1 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-67G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 1/12 | 1289 | chr2 | 55923729 | |||||
chr2:55923750
|
G | A | 1 | a0001c0004t0010 | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-88C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 1/12 | 1310 | chr2 | 55923750 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55867259
|
G | A | 6 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0199others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1321-25C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55867259 | ||||||
chr2:55867443
|
C | CT | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1321-210dupA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55867443 | ||||||
chr2:55867443
|
CT | C | 57 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(54): Show | 63 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1321-210delA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55867443 | ||||||
chr2:55867457
|
T | TA | 4 | a0001c0001t0001g0157a0001c0001t0001g0230a0001c0001t0001g0241others(1): Show | 4 | NA18962.hp1 NA18968.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321-224dupT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55867457 | ||||||
chr2:55867458
|
A | T | 2 | a0001c0001t0001g0214a0001c0001t0003g0033 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1321-224T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55867458 | ||||||
chr2:55867462
|
A | C | 3 | a0001c0001t0002g0277a0001c0001t0002g0286a0001c0006t0002g0285 | 3 | HG02559.hp2 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1321-228T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55867462 | ||||||
chr2:55867864
|
T | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(26): Show | 34 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1321-630A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55867864 | ||||||
chr2:55867875
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 243 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.1321-641T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55867875 | ||||||
chr2:55867969
|
T | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 227 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1321-735A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55867969 | ||||||
chr2:55868074
|
G | A | 1 | a0001c0001t0007g0041 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1321-840C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55868074 | ||||||
chr2:55868113
|
C | T | 1 | a0001c0001t0003g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1321-879G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55868113 | ||||||
chr2:55868133
|
G | A | 10 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0091others(7): Show | 10 | HG02559.hp1 HG03704.hp1 HG03704.hp2 others(7): Show |
intron_variant | MODIFIER | c.1321-899C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55868133 | ||||||
chr2:55868180
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0126a0001c0001t0001g0138 | 3 | HG03942.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1321-946C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55868180 | ||||||
chr2:55868231
|
G | T | 10 | a0001c0001t0004g0005a0001c0001t0004g0032a0001c0001t0004g0039others(7): Show | 12 | HG01074.hp1 HG01255.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1321-997C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55868231 | ||||||
chr2:55868519
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1321-1285G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55868519 | ||||||
chr2:55868718
|
A | G | 5 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321-1484T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55868718 | ||||||
chr2:55868838
|
C | T | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321-1604G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55868838 | ||||||
chr2:55868859
|
C | G | 31 | a0001c0001t0001g0029a0001c0001t0003g0048a0001c0001t0004g0005others(28): Show | 35 | HG00544.hp2 HG00597.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1321-1625G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55868859 | ||||||
chr2:55869178
|
T | C | 1 | a0001c0001t0002g0278 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1320+1542A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55869178 | ||||||
chr2:55869374
|
G | A | 6 | a0001c0001t0001g0113a0001c0001t0006g0014a0001c0001t0006g0088others(3): Show | 7 | HG02257.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1320+1346C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55869374 | ||||||
chr2:55869377
|
A | C | 1 | a0001c0001t0013g0015 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1320+1343T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55869377 | ||||||
chr2:55869438
|
T | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(13): Show | 19 | HG02280.hp1 HG02559.hp1 HG02976.hp1 others(16): Show |
intron_variant | MODIFIER | c.1320+1282A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55869438 | ||||||
chr2:55869634
|
A | C | 1 | a0001c0001t0003g0043 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1320+1086T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55869634 | ||||||
chr2:55869757
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(107): Show | 132 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1320+963T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55869757 | ||||||
chr2:55869763
|
T | C | 5 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1320+957A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55869763 | ||||||
chr2:55869777
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1320+943G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55869777 | ||||||
chr2:55869893
|
T | G | 1 | a0001c0001t0001g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1320+827A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55869893 | ||||||
chr2:55869932
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1320+788G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55869932 | ||||||
chr2:55870259
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1320+461T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55870259 | ||||||
chr2:55870270
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1320+450C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55870270 | ||||||
chr2:55870315
|
T | C | 1 | a0001c0001t0003g0042 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1320+405A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55870315 | ||||||
chr2:55870379
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1320+341G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55870379 | ||||||
chr2:55870576
|
A | G | 40 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(37): Show | 44 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1320+144T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55870576 | ||||||
chr2:55870643
|
C | CACA | 3 | a0001c0001t0001g0026a0001c0001t0001g0082a0001c0003t0021g0288 | 4 | HG00642.hp1 HG01074.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1320+74_1320+76dup others(3): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55870643 | ||||||
chr2:55870643
|
CACA | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0073others(38): Show | 46 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.1320+74_1320+76del others(3): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55870643 | ||||||
chr2:55870696
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1320+24A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 11/11 | chr2 | 55870696 | ||||||
chr2:55871137
|
G | A | 10 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(7): Show | 10 | HG01168.hp1 HG01516.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1001-14C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55871137 | ||||||
chr2:55871265
|
C | T | 1 | a0001c0002t0001g0067 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1001-142G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55871265 | ||||||
chr2:55871351
|
A | C | 1 | a0001c0001t0001g0210 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1001-228T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55871351 | ||||||
chr2:55871361
|
T | C | 1 | a0001c0001t0001g0022 | 2 | NA18992.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1001-238A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55871361 | ||||||
chr2:55871434
|
G | C | 6 | a0001c0001t0001g0113a0001c0001t0006g0014a0001c0001t0006g0088others(3): Show | 7 | HG02257.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1001-311C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55871434 | ||||||
chr2:55871508
|
A | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0073others(14): Show | 20 | HG00438.hp1 HG00738.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1001-385T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55871508 | ||||||
chr2:55871559
|
G | C | 4 | a0001c0001t0008g0031a0001c0001t0008g0294a0001c0001t0008g0295others(1): Show | 5 | NA19004.hp2 NA19005.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-436C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55871559 | ||||||
chr2:55871616
|
G | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(37): Show | 44 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1001-493C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55871616 | ||||||
chr2:55871842
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0003g0042 | 2 | HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1001-719A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55871842 | ||||||
chr2:55872069
|
TAAC | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(13): Show | 19 | HG02280.hp1 HG02559.hp1 HG02976.hp1 others(16): Show |
intron_variant | MODIFIER | c.1001-949_1001-947d others(5): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872069 | ||||||
chr2:55872090
|
TA | T | 7 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0086others(4): Show | 7 | HG01346.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1001-968delT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872090 | ||||||
chr2:55872258
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1001-1135A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872258 | ||||||
chr2:55872308
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1001-1185A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872308 | ||||||
chr2:55872340
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1001-1217G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872340 | ||||||
chr2:55872341
|
T | C | 1 | a0001c0003t0002g0293 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1001-1218A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872341 | ||||||
chr2:55872405
|
T | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(13): Show | 19 | HG02280.hp1 HG02559.hp1 HG02976.hp1 others(16): Show |
intron_variant | MODIFIER | c.1001-1282A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872405 | ||||||
chr2:55872517
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1001-1394G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872517 | ||||||
chr2:55872530
|
G | A | 5 | a0001c0001t0001g0220a0001c0001t0001g0231a0001c0001t0002g0278others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-1407C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872530 | ||||||
chr2:55872537
|
G | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0199others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-1414C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872537 | ||||||
chr2:55872609
|
C | G | 1 | a0001c0001t0005g0118 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1001-1486G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872609 | ||||||
chr2:55872617
|
T | G | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-1494A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872617 | ||||||
chr2:55872874
|
A | G | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-1751T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55872874 | ||||||
chr2:55873066
|
C | CCA | 15 | a0001c0001t0001g0029a0001c0001t0001g0152a0001c0001t0001g0178others(12): Show | 18 | HG01255.hp1 HG01257.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.1000+1878_1000+187 others(6): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
C | CCACA | 49 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0016others(46): Show | 63 | HG00099.hp2 HG00642.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.1000+1876_1000+187 others(8): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
C | CCACACA | 43 | a0001c0001t0001g0027a0001c0001t0001g0108a0001c0001t0001g0110others(40): Show | 45 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1000+1874_1000+187 others(10): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
C | CCACACAC others(1): Show |
43 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0019others(40): Show | 52 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1000+1872_1000+187 others(12): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
C | CCACACAC others(3): Show |
66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(63): Show | 80 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.1000+1870_1000+187 others(14): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
C | CCACACAC others(5): Show |
18 | a0001c0001t0001g0020a0001c0001t0001g0114a0001c0001t0001g0123others(15): Show | 19 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(16): Show |
intron_variant | MODIFIER | c.1000+1868_1000+187 others(16): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
C | CCACACAC others(7): Show |
11 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0126others(8): Show | 12 | HG00323.hp2 HG00673.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1000+1866_1000+187 others(18): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
C | CCACACAC others(9): Show |
3 | a0001c0001t0006g0100a0001c0001t0013g0015a0001c0003t0006g0061 | 4 | HG02145.hp2 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+1864_1000+187 others(20): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
C | CCACACAC others(11): Show |
1 | a0001c0001t0009g0223 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1000+1862_1000+187 others(22): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
C | CCACACAC others(13): Show |
1 | a0001c0001t0001g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1000+1860_1000+187 others(24): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
C | CCACACAC others(17): Show |
1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1000+1856_1000+187 others(28): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
C | CCACACAC others(19): Show |
1 | a0001c0001t0001g0081 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1000+1854_1000+187 others(30): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
CCA | C | 4 | a0001c0001t0001g0159a0001c0001t0003g0035a0001c0001t0005g0165others(1): Show | 4 | HG01109.hp2 HG02129.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+1878_1000+187 others(6): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
CCACA | C | 9 | a0001c0001t0001g0084a0001c0001t0001g0113a0001c0001t0001g0185others(6): Show | 10 | HG02257.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1000+1876_1000+187 others(8): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
CCACACA | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0091others(7): Show | 13 | HG03704.hp1 HG03704.hp2 HG03710.hp1 others(10): Show |
intron_variant | MODIFIER | c.1000+1874_1000+187 others(10): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873066
|
CCACACAC others(9): Show |
C | 3 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0065 | 3 | HG02280.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1000+1864_1000+187 others(20): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873066 | ||||||
chr2:55873238
|
G | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(53): Show | 63 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.1000+1708C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873238 | ||||||
chr2:55873254
|
G | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0191 | 2 | NA18988.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1000+1692C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873254 | ||||||
chr2:55873426
|
G | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(10): Show | 16 | HG02559.hp1 HG03704.hp1 HG03704.hp2 others(13): Show |
intron_variant | MODIFIER | c.1000+1520C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873426 | ||||||
chr2:55873711
|
C | G | 13 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0199others(10): Show | 13 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1000+1235G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873711 | ||||||
chr2:55873718
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1000+1228G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873718 | ||||||
chr2:55873764
|
G | A | 1 | a0001c0001t0001g0026 | 2 | HG00642.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1000+1182C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873764 | ||||||
chr2:55873781
|
C | T | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+1165G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873781 | ||||||
chr2:55873796
|
C | T | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+1150G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873796 | ||||||
chr2:55873923
|
TA | T | 7 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0188others(4): Show | 7 | HG00140.hp2 HG01346.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000+1022delT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873923 | ||||||
chr2:55873983
|
T | TAAAAACA others(308): Show |
3 | a0001c0002t0001g0272a0001c0002t0006g0071a0003c0005t0001g0273 | 3 | HG03041.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1000+962_1000+963i others(317): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55873983
|
T | TAAAAACA others(319): Show |
2 | a0001c0001t0005g0077a0001c0001t0005g0095 | 2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1000+962_1000+963i others(328): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55873983
|
T | TAAAAACA others(321): Show |
1 | a0001c0001t0007g0012 | 2 | NA18951.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1000+962_1000+963i others(330): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55873983
|
T | TAAAAACA others(322): Show |
2 | a0001c0001t0007g0044a0001c0001t0007g0045 | 2 | NA18999.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1000+962_1000+963i others(331): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55873983
|
T | TAAAAACA others(331): Show |
2 | a0001c0001t0003g0048a0001c0001t0007g0041 | 2 | HG02602.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1000+962_1000+963i others(340): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55873983
|
T | TAAAAACA others(333): Show |
1 | a0001c0001t0005g0129 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1000+962_1000+963i others(342): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55873983
|
T | TAAAAACA others(336): Show |
2 | a0001c0001t0005g0118a0001c0001t0005g0243 | 2 | HG00597.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1000+962_1000+963i others(345): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55873983
|
T | TAAAAACA others(338): Show |
2 | a0001c0001t0005g0244a0001c0001t0005g0252 | 2 | NA18939.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1000+962_1000+963i others(347): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55873983
|
T | TAAAAACA others(339): Show |
2 | a0001c0001t0005g0074a0001c0001t0005g0253 | 2 | HG00544.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1000+962_1000+963i others(348): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55873983
|
T | TAAAAACA others(340): Show |
1 | a0001c0001t0007g0046 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1000+962_1000+963i others(349): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55873983
|
T | TAAAAACA others(343): Show |
1 | a0001c0001t0005g0128 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1000+962_1000+963i others(352): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55873983
|
T | TAAAAACA others(344): Show |
1 | a0001c0001t0005g0075 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1000+962_1000+963i others(353): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55873983 | ||||||
chr2:55874010
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1000+936A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874010 | ||||||
chr2:55874026
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1000+920A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874026 | ||||||
chr2:55874034
|
T | C | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+912A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874034 | ||||||
chr2:55874041
|
T | C | 3 | a0001c0001t0006g0100a0001c0001t0013g0015a0001c0003t0006g0061 | 4 | HG02145.hp2 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+905A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874041 | ||||||
chr2:55874404
|
TC | T | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+541delG | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874404 | ||||||
chr2:55874483
|
C | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(49): Show | 59 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1000+463G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874483 | ||||||
chr2:55874500
|
T | C | 1 | a0001c0001t0001g0021 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1000+446A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874500 | ||||||
chr2:55874609
|
T | G | 1 | a0001c0001t0003g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1000+337A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874609 | ||||||
chr2:55874655
|
T | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(13): Show | 19 | HG02280.hp1 HG02559.hp1 HG02976.hp1 others(16): Show |
intron_variant | MODIFIER | c.1000+291A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874655 | ||||||
chr2:55874691
|
G | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(49): Show | 59 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1000+255C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874691 | ||||||
chr2:55874841
|
T | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(10): Show | 16 | HG02559.hp1 HG03704.hp1 HG03704.hp2 others(13): Show |
intron_variant | MODIFIER | c.1000+105A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874841 | ||||||
chr2:55874884
|
T | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(49): Show | 59 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1000+62A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874884 | ||||||
chr2:55874920
|
A | G | 1 | a0001c0001t0002g0281 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1000+26T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874920 | ||||||
chr2:55874926
|
GA | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(49): Show | 59 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1000+19delT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 9/11 | chr2 | 55874926 | ||||||
chr2:55875090
|
A | C | 2 | a0001c0001t0001g0214a0001c0001t0003g0033 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.881-25T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875090 | ||||||
chr2:55875125
|
G | GAT | 42 | a0001c0001t0001g0029a0001c0001t0001g0079a0001c0001t0001g0080others(39): Show | 46 | HG00544.hp2 HG00597.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.881-62_881-61dupAT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875125 | ||||||
chr2:55875145
|
T | TTA | 5 | a0001c0001t0001g0135a0001c0001t0001g0220a0001c0001t0001g0225others(2): Show | 5 | HG01358.hp2 HG01884.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.881-82_881-81dupTA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875145 | ||||||
chr2:55875146
|
T | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(33): Show | 40 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.881-81A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875146 | ||||||
chr2:55875178
|
A | G | 5 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.881-113T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875178 | ||||||
chr2:55875183
|
T | C | 2 | a0001c0001t0001g0214a0001c0001t0003g0033 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.881-118A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875183 | ||||||
chr2:55875208
|
A | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0135a0001c0001t0001g0141others(1): Show | 7 | NA18945.hp1 NA18957.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.881-143T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875208 | ||||||
chr2:55875231
|
A | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-166T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875231 | ||||||
chr2:55875251
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.881-186T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875251 | ||||||
chr2:55875333
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.881-268A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875333 | ||||||
chr2:55875333
|
T | TACACACA others(7): Show |
1 | a0001c0001t0001g0227 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.881-269_881-268ins others(14): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875333 | ||||||
chr2:55875333
|
T | TACACACA others(11): Show |
1 | a0001c0002t0001g0065 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.881-269_881-268ins others(18): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875333 | ||||||
chr2:55875333
|
T | TACACACA others(13): Show |
1 | a0001c0002t0001g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.881-269_881-268ins others(20): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875333 | ||||||
chr2:55875333
|
T | TACACACA others(17): Show |
1 | a0001c0002t0001g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.881-269_881-268ins others(24): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875333 | ||||||
chr2:55875335
|
T | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(86): Show | 97 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.881-270A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875335 | ||||||
chr2:55875335
|
T | TAC | 48 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(45): Show | 59 | HG00323.hp2 HG00544.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.881-272_881-271dup others(2): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875335 | ||||||
chr2:55875335
|
T | TACAC | 3 | a0001c0001t0001g0155a0001c0001t0001g0182a0001c0001t0004g0052 | 3 | HG00323.hp1 HG01952.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.881-274_881-271dup others(4): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875335 | ||||||
chr2:55875335
|
TAC | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.881-272_881-271del others(2): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875335 | ||||||
chr2:55875361
|
C | T | 31 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(28): Show | 35 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.881-296G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875361 | ||||||
chr2:55875363
|
C | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(29): Show | 36 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.881-298G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875363 | ||||||
chr2:55875365
|
C | CACACACA others(15): Show |
1 | a0001c0001t0002g0277 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.881-301_881-300ins others(22): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875365 | ||||||
chr2:55875365
|
C | CACACACA others(13): Show |
7 | a0001c0001t0001g0084a0001c0001t0001g0202a0001c0001t0002g0281others(4): Show | 7 | HG02559.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.881-301_881-300ins others(20): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875365 | ||||||
chr2:55875365
|
C | CACACACA others(11): Show |
10 | a0001c0001t0001g0092a0001c0001t0001g0099a0001c0001t0001g0110others(7): Show | 10 | HG02015.hp1 HG02280.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.881-301_881-300ins others(18): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875365 | ||||||
chr2:55875365
|
C | CACACACA others(9): Show |
12 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0093others(9): Show | 15 | HG01884.hp2 HG02109.hp1 HG03041.hp2 others(12): Show |
intron_variant | MODIFIER | c.881-301_881-300ins others(16): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875365 | ||||||
chr2:55875365
|
C | CACACACA others(11): Show |
1 | a0001c0001t0005g0128 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.881-301_881-300ins others(18): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875365 | ||||||
chr2:55875365
|
C | CACACACA others(7): Show |
13 | a0001c0001t0001g0091a0001c0001t0005g0074a0001c0001t0005g0075others(10): Show | 14 | HG00544.hp2 HG00597.hp1 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.881-301_881-300ins others(14): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875365 | ||||||
chr2:55875365
|
C | CACACACA others(5): Show |
1 | a0001c0001t0003g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.881-301_881-300ins others(12): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875365 | ||||||
chr2:55875365
|
C | CACACATA others(1): Show |
3 | a0001c0004t0010g0297a0001c0004t0010g0299a0001c0004t0010g0300 | 3 | HG01081.hp1 HG01099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.881-301_881-300ins others(8): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875365 | ||||||
chr2:55875365
|
C | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(29): Show | 36 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.881-300G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875365 | ||||||
chr2:55875371
|
TA | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(27): Show | 34 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.881-307delT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875371 | ||||||
chr2:55875372
|
A | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(18): Show | 24 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.881-307T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875372 | ||||||
chr2:55875374
|
T | A | 5 | a0001c0001t0005g0074a0001c0001t0005g0075a0001c0001t0005g0077others(2): Show | 5 | HG00544.hp2 HG02109.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.881-309A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875374 | ||||||
chr2:55875417
|
T | C | 8 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0199others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.881-352A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875417 | ||||||
chr2:55875609
|
A | G | 9 | a0001c0001t0001g0029a0001c0001t0004g0005a0001c0001t0004g0050others(6): Show | 12 | HG01074.hp1 HG01255.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.881-544T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875609 | ||||||
chr2:55875788
|
G | A | 6 | a0001c0001t0001g0113a0001c0001t0006g0014a0001c0001t0006g0088others(3): Show | 7 | HG02257.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.881-723C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55875788 | ||||||
chr2:55876035
|
G | A | 37 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(34): Show | 41 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.880+588C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55876035 | ||||||
chr2:55876160
|
A | T | 1 | a0001c0001t0001g0148 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.880+463T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55876160 | ||||||
chr2:55876217
|
A | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(53): Show | 63 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.880+406T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55876217 | ||||||
chr2:55876323
|
C | T | 7 | a0001c0001t0001g0078a0001c0001t0001g0085a0001c0001t0001g0086others(4): Show | 7 | HG01346.hp2 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.880+300G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55876323 | ||||||
chr2:55876370
|
C | T | 1 | a0001c0001t0018g0195 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.880+253G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55876370 | ||||||
chr2:55876371
|
G | A | 2 | a0001c0001t0003g0036a0001c0002t0001g0068 | 2 | HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.880+252C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55876371 | ||||||
chr2:55876515
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0131others(5): Show | 10 | HG00544.hp1 HG02165.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.880+108T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55876515 | ||||||
chr2:55876547
|
T | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(49): Show | 59 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.880+76A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 8/11 | chr2 | 55876547 | ||||||
chr2:55876756
|
T | TTA | 20 | a0001c0001t0003g0048a0001c0001t0005g0074a0001c0001t0005g0075others(17): Show | 21 | HG00544.hp2 HG00597.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.761-16_761-15dupTA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 7/11 | chr2 | 55876756 | ||||||
chr2:55876787
|
T | TAC | 5 | a0001c0001t0006g0014a0001c0001t0006g0088a0001c0001t0006g0101others(2): Show | 6 | HG02257.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.761-47_761-46dupGT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 7/11 | chr2 | 55876787 | ||||||
chr2:55876941
|
A | T | 85 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(82): Show | 93 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.761-199T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 7/11 | chr2 | 55876941 | ||||||
chr2:55876958
|
A | C | 1 | a0001c0001t0002g0283 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.761-216T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 7/11 | chr2 | 55876958 | ||||||
chr2:55876962
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.761-220G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 7/11 | chr2 | 55876962 | ||||||
chr2:55877118
|
A | T | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(49): Show | 59 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.761-376T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 7/11 | chr2 | 55877118 | ||||||
chr2:55877176
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(17): Show | 23 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.761-434C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 7/11 | chr2 | 55877176 | ||||||
chr2:55877719
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.760+27T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 7/11 | chr2 | 55877719 | ||||||
chr2:55877721
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.760+25T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 7/11 | chr2 | 55877721 | ||||||
chr2:55878393
|
T | G | 3 | a0001c0002t0001g0272a0001c0002t0006g0071a0003c0005t0001g0273 | 3 | HG03041.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.641-528A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55878393 | ||||||
chr2:55878494
|
G | GCTCAACT | 5 | a0001c0001t0001g0220a0001c0001t0001g0231a0001c0001t0002g0278others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-636_641-630dup others(7): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55878494 | ||||||
chr2:55878500
|
C | A | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-635G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55878500 | ||||||
chr2:55878658
|
T | TAAAACAA others(3): Show |
56 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(53): Show | 63 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.641-803_641-794dup others(10): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55878658 | ||||||
chr2:55878770
|
G | A | 3 | a0001c0001t0002g0278a0001c0001t0002g0279a0001c0001t0002g0280 | 3 | HG02258.hp1 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.641-905C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55878770 | ||||||
chr2:55878781
|
T | A | 10 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(7): Show | 10 | HG01168.hp1 HG01516.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.641-916A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55878781 | ||||||
chr2:55878799
|
T | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(86): Show | 97 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.641-934A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55878799 | ||||||
chr2:55878804
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.641-939C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55878804 | ||||||
chr2:55878952
|
T | C | 1 | a0001c0001t0002g0030 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.641-1087A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55878952 | ||||||
chr2:55879132
|
G | A | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-1267C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879132 | ||||||
chr2:55879167
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.641-1302C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879167 | ||||||
chr2:55879283
|
C | T | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-1418G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879283 | ||||||
chr2:55879406
|
G | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(13): Show | 19 | HG02280.hp1 HG02559.hp1 HG02976.hp1 others(16): Show |
intron_variant | MODIFIER | c.641-1541C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879406 | ||||||
chr2:55879445
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.641-1580T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879445 | ||||||
chr2:55879506
|
C | T | 10 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(7): Show | 10 | HG01168.hp1 HG01516.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.641-1641G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879506 | ||||||
chr2:55879591
|
T | A | 1 | a0001c0001t0001g0152 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.641-1726A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879591 | ||||||
chr2:55879652
|
T | A | 5 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-1787A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879652 | ||||||
chr2:55879683
|
G | GTCCA | 8 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0199others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.641-1819_641-1818i others(6): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879683 | ||||||
chr2:55879685
|
A | T | 35 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(32): Show | 39 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.641-1820T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879685 | ||||||
chr2:55879697
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.641-1832C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879697 | ||||||
chr2:55879793
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(107): Show | 132 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.640+1819G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55879793 | ||||||
chr2:55880065
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0145 | 2 | HG00558.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.640+1547T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55880065 | ||||||
chr2:55880289
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.640+1323A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55880289 | ||||||
chr2:55880304
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.640+1308C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55880304 | ||||||
chr2:55880400
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.640+1212G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55880400 | ||||||
chr2:55880428
|
A | T | 19 | a0001c0001t0001g0021a0001c0001t0001g0072a0001c0001t0001g0079others(16): Show | 20 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.640+1184T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55880428 | ||||||
chr2:55880486
|
C | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(13): Show | 19 | HG02280.hp1 HG02559.hp1 HG02976.hp1 others(16): Show |
intron_variant | MODIFIER | c.640+1126G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55880486 | ||||||
chr2:55880538
|
A | G | 16 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(13): Show | 19 | HG02280.hp1 HG02559.hp1 HG02976.hp1 others(16): Show |
intron_variant | MODIFIER | c.640+1074T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55880538 | ||||||
chr2:55880625
|
C | T | 8 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0199others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.640+987G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55880625 | ||||||
chr2:55880769
|
A | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0199others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+843T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55880769 | ||||||
chr2:55880841
|
C | T | 13 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0199others(10): Show | 13 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.640+771G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55880841 | ||||||
chr2:55881006
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.640+606T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55881006 | ||||||
chr2:55881198
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(160): Show | 187 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.640+414G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55881198 | ||||||
chr2:55881242
|
A | G | 3 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0065 | 3 | HG02280.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.640+370T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55881242 | ||||||
chr2:55881430
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.640+182T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55881430 | ||||||
chr2:55881473
|
G | A | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+139C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55881473 | ||||||
chr2:55881554
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0072others(31): Show | 38 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.640+58C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55881554 | ||||||
chr2:55881557
|
T | A | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+55A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55881557 | ||||||
chr2:55881606
|
A | G | 1 | a0001c0001t0003g0036 | 1 | NA18522.hp1 | splice_region_variant&intron_variant | LOW | c.640+6T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 6/11 | chr2 | 55881606 | ||||||
chr2:55881739
|
C | T | 1 | a0001c0001t0005g0243 | 1 | NA19054.hp1 | splice_region_variant&intron_variant | LOW | c.518-5G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55881739 | ||||||
chr2:55881745
|
C | T | 3 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0065 | 3 | HG02280.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.518-11G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55881745 | ||||||
chr2:55881747
|
T | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0021others(69): Show | 80 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.518-13A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55881747 | ||||||
chr2:55881764
|
T | G | 5 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-30A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55881764 | ||||||
chr2:55882040
|
T | G | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-306A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55882040 | ||||||
chr2:55882096
|
T | C | 1 | a0001c0001t0005g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.518-362A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55882096 | ||||||
chr2:55882324
|
ATCTT | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0072others(31): Show | 38 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.518-594_518-591del others(4): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55882324 | ||||||
chr2:55882537
|
CA | C | 17 | a0001c0001t0003g0048a0001c0001t0005g0074a0001c0001t0005g0075others(14): Show | 18 | HG00544.hp2 HG00597.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.518-804delT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55882537 | ||||||
chr2:55882562
|
G | A | 1 | a0001c0003t0021g0288 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.518-828C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55882562 | ||||||
chr2:55882632
|
T | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(17): Show | 23 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.518-898A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55882632 | ||||||
chr2:55883034
|
A | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-1300T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883034 | ||||||
chr2:55883090
|
G | A | 1 | a0001c0001t0003g0056 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.518-1356C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883090 | ||||||
chr2:55883204
|
C | G | 5 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-1470G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883204 | ||||||
chr2:55883211
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.518-1477G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883211 | ||||||
chr2:55883417
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 281 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.518-1683A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883417 | ||||||
chr2:55883423
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.518-1689C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883423 | ||||||
chr2:55883448
|
G | A | 5 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-1714C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883448 | ||||||
chr2:55883535
|
C | A | 6 | a0001c0001t0001g0113a0001c0001t0006g0014a0001c0001t0006g0088others(3): Show | 7 | HG02257.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.518-1801G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883535 | ||||||
chr2:55883559
|
C | G | 2 | a0001c0001t0006g0100a0001c0003t0006g0061 | 2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.518-1825G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883559 | ||||||
chr2:55883685
|
C | G | 18 | a0001c0001t0001g0021a0001c0001t0001g0072a0001c0001t0001g0079others(15): Show | 19 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.518-1951G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883685 | ||||||
chr2:55883877
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0003g0033 | 2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.518-2143C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883877 | ||||||
chr2:55883964
|
C | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0072others(31): Show | 38 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.518-2230G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55883964 | ||||||
chr2:55884014
|
A | G | 5 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-2280T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55884014 | ||||||
chr2:55884174
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(105): Show | 129 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.518-2440G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55884174 | ||||||
chr2:55884209
|
A | G | 1 | a0001c0001t0005g0243 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.518-2475T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55884209 | ||||||
chr2:55884662
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.518-2928C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55884662 | ||||||
chr2:55884687
|
T | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0023others(33): Show | 40 | HG00099.hp1 HG00438.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.518-2953A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55884687 | ||||||
chr2:55884704
|
C | A | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-2970G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55884704 | ||||||
chr2:55884714
|
T | C | 4 | a0001c0001t0002g0030a0001c0001t0002g0287a0001c0001t0003g0036others(1): Show | 5 | HG01891.hp2 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-2980A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55884714 | ||||||
chr2:55884801
|
A | G | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-3067T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55884801 | ||||||
chr2:55885006
|
T | C | 1 | a0001c0002t0001g0067 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.518-3272A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55885006 | ||||||
chr2:55885033
|
G | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0199others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-3299C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55885033 | ||||||
chr2:55885305
|
C | A | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 249 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.518-3571G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55885305 | ||||||
chr2:55885540
|
G | A | 18 | a0001c0001t0001g0021a0001c0001t0001g0072a0001c0001t0001g0079others(15): Show | 19 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.518-3806C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55885540 | ||||||
chr2:55885581
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0198 | 3 | HG00741.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.518-3847A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55885581 | ||||||
chr2:55885670
|
G | A | 1 | a0001c0001t0004g0057 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.518-3936C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55885670 | ||||||
chr2:55885741
|
C | T | 5 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-4007G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55885741 | ||||||
chr2:55885754
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(17): Show | 23 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.518-4020C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55885754 | ||||||
chr2:55885824
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.518-4090G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55885824 | ||||||
chr2:55886344
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.518-4610C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55886344 | ||||||
chr2:55886403
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0084a0001c0001t0001g0089others(17): Show | 23 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.518-4669C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55886403 | ||||||
chr2:55886611
|
C | T | 8 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0199others(5): Show | 8 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.518-4877G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55886611 | ||||||
chr2:55886954
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.518-5220T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55886954 | ||||||
chr2:55886959
|
A | G | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-5225T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55886959 | ||||||
chr2:55887029
|
C | G | 5 | a0001c0001t0002g0277a0001c0001t0002g0281a0001c0001t0002g0282others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-5295G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55887029 | ||||||
chr2:55887268
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.518-5534A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55887268 | ||||||
chr2:55887369
|
A | C | 12 | a0001c0001t0001g0016a0001c0001t0001g0082a0001c0001t0001g0219others(9): Show | 13 | HG01109.hp2 HG02559.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.518-5635T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55887369 | ||||||
chr2:55887637
|
C | T | 3 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0065 | 3 | HG02280.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.518-5903G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55887637 | ||||||
chr2:55887905
|
A | G | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-6171T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55887905 | ||||||
chr2:55887928
|
T | C | 1 | a0001c0001t0019g0259 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.518-6194A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55887928 | ||||||
chr2:55888028
|
T | C | 3 | a0001c0001t0001g0214a0001c0001t0003g0033a0001c0002t0001g0067 | 3 | HG02615.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.518-6294A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888028 | ||||||
chr2:55888190
|
A | C | 1 | a0001c0001t0003g0038 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.518-6456T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888190 | ||||||
chr2:55888209
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.518-6475A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888209 | ||||||
chr2:55888283
|
T | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18961.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.518-6549A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888283 | ||||||
chr2:55888333
|
A | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(103): Show | 127 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.518-6599T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888333 | ||||||
chr2:55888334
|
C | CT | 45 | a0001c0001t0001g0021a0001c0001t0001g0072a0001c0001t0001g0078others(42): Show | 49 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.518-6601dupA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888334 | ||||||
chr2:55888334
|
C | CTT | 12 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0219others(9): Show | 12 | HG01070.hp1 HG01109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.518-6602_518-6601d others(4): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888334 | ||||||
chr2:55888334
|
CT | C | 9 | a0001c0001t0001g0093a0001c0001t0001g0201a0001c0001t0001g0202others(6): Show | 9 | HG01943.hp1 HG02622.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-6601delA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888334 | ||||||
chr2:55888334
|
CTT | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(102): Show | 126 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.518-6602_518-6601d others(4): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888334 | ||||||
chr2:55888335
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0245 | 2 | HG04115.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.518-6601A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888335 | ||||||
chr2:55888337
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.518-6603A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888337 | ||||||
chr2:55888411
|
C | A | 1 | a0001c0001t0001g0024 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.518-6677G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888411 | ||||||
chr2:55888440
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.518-6706G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888440 | ||||||
chr2:55888489
|
C | T | 43 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0060others(40): Show | 46 | HG00408.hp1 HG00609.hp1 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.518-6755G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888489 | ||||||
chr2:55888657
|
A | AAGAAAAC others(1): Show |
3 | a0001c0001t0001g0139a0001c0001t0001g0146a0001c0001t0001g0225 | 3 | HG00738.hp1 HG01175.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.518-6931_518-6924d others(10): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888657 | ||||||
chr2:55888693
|
C | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02622.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.518-6959G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888693 | ||||||
chr2:55888699
|
T | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 146 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.518-6965A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888699 | ||||||
chr2:55888724
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0200 | 3 | HG01884.hp2 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.518-6990C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888724 | ||||||
chr2:55888899
|
G | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | HG00673.hp1 HG02056.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-7165C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55888899 | ||||||
chr2:55889049
|
C | G | 1 | a0001c0003t0021g0288 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.518-7315G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889049 | ||||||
chr2:55889058
|
TTGATTCT others(13): Show |
T | 9 | a0001c0001t0003g0035a0001c0001t0004g0005a0001c0001t0004g0050others(6): Show | 11 | HG01074.hp1 HG01255.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.518-7344_518-7325d others(22): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889058 | ||||||
chr2:55889118
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0005g0165 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.518-7384T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889118 | ||||||
chr2:55889460
|
T | C | 39 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0119others(36): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.518-7726A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889460 | ||||||
chr2:55889526
|
G | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 12 | HG01167.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.518-7792C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889526 | ||||||
chr2:55889665
|
A | G | 39 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0119others(36): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.518-7931T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889665 | ||||||
chr2:55889688
|
G | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0192 | 3 | NA18944.hp2 NA18950.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.518-7954C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889688 | ||||||
chr2:55889824
|
T | TA | 21 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0084others(18): Show | 25 | HG00738.hp2 HG01346.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.518-8091dupT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889824 | ||||||
chr2:55889824
|
T | TAA | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(142): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.518-8092_518-8091d others(4): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889824 | ||||||
chr2:55889824
|
TA | T | 17 | a0001c0001t0001g0021a0001c0001t0001g0072a0001c0001t0001g0164others(14): Show | 19 | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.518-8091delT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889824 | ||||||
chr2:55889824
|
TAA | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 12 | HG01167.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.518-8092_518-8091d others(4): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889824 | ||||||
chr2:55889905
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 287 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.518-8171A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55889905 | ||||||
chr2:55890336
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.518-8602T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55890336 | ||||||
chr2:55890435
|
T | C | 7 | a0001c0001t0002g0278a0001c0001t0002g0279a0001c0001t0002g0280others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.518-8701A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55890435 | ||||||
chr2:55890479
|
T | C | 63 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(60): Show | 71 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(68): Show |
intron_variant | MODIFIER | c.518-8745A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55890479 | ||||||
chr2:55890690
|
C | T | 1 | a0001c0001t0001g0017 | 2 | HG02135.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.518-8956G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55890690 | ||||||
chr2:55890859
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.518-9125T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55890859 | ||||||
chr2:55890888
|
T | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0191 | 2 | NA18988.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.518-9154A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55890888 | ||||||
chr2:55890911
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.518-9177C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55890911 | ||||||
chr2:55891068
|
A | T | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-9334T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55891068 | ||||||
chr2:55891111
|
A | G | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-9377T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55891111 | ||||||
chr2:55891184
|
G | A | 1 | a0001c0001t0003g0035 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.518-9450C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55891184 | ||||||
chr2:55891546
|
T | C | 1 | a0001c0001t0005g0118 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.518-9812A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55891546 | ||||||
chr2:55891549
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.518-9815A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55891549 | ||||||
chr2:55891970
|
A | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 253 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.518-10236T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55891970 | ||||||
chr2:55892015
|
TCA | T | 51 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0079others(48): Show | 54 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.518-10283_518-1028 others(6): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892015 | ||||||
chr2:55892219
|
T | C | 5 | a0001c0001t0006g0100a0001c0002t0001g0067a0001c0002t0001g0272others(2): Show | 5 | HG02809.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-10485A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892219 | ||||||
chr2:55892278
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0164 | 3 | HG01069.hp1 HG01071.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.518-10544C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892278 | ||||||
chr2:55892375
|
A | T | 50 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(47): Show | 58 | HG00099.hp2 HG00140.hp1 HG01168.hp2 others(55): Show |
intron_variant | MODIFIER | c.518-10641T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892375 | ||||||
chr2:55892522
|
C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.518-10788G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892522 | ||||||
chr2:55892533
|
A | ATAGGATT others(12): Show |
52 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0079others(49): Show | 55 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.518-10818_518-1080 others(23): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892533 | ||||||
chr2:55892585
|
A | T | 52 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0079others(49): Show | 55 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.518-10851T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892585 | ||||||
chr2:55892609
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.518-10875G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892609 | ||||||
chr2:55892764
|
A | C | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-11030T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892764 | ||||||
chr2:55892811
|
A | C | 1 | a0001c0001t0001g0168 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.518-11077T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892811 | ||||||
chr2:55892832
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 251 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.518-11098C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892832 | ||||||
chr2:55892867
|
G | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0161 | 2 | NA18962.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.518-11133C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892867 | ||||||
chr2:55892908
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.518-11174G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892908 | ||||||
chr2:55892928
|
G | C | 1 | a0001c0001t0001g0158 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.518-11194C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892928 | ||||||
chr2:55892951
|
A | G | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0203others(6): Show | 11 | HG00642.hp1 HG01074.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.518-11217T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55892951 | ||||||
chr2:55893019
|
A | G | 39 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0119others(36): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.518-11285T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893019 | ||||||
chr2:55893020
|
T | G | 1 | a0001c0001t0003g0047 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.518-11286A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893020 | ||||||
chr2:55893040
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0214a0001c0001t0001g0219 | 3 | HG02615.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.518-11306A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893040 | ||||||
chr2:55893102
|
A | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.518-11368T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893102 | ||||||
chr2:55893153
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.518-11419A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893153 | ||||||
chr2:55893262
|
C | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-11528G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893262 | ||||||
chr2:55893485
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.518-11751C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893485 | ||||||
chr2:55893563
|
T | C | 1 | a0001c0001t0002g0277 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.518-11829A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893563 | ||||||
chr2:55893570
|
G | A | 1 | a0001c0003t0006g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.518-11836C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893570 | ||||||
chr2:55893654
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.518-11920C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893654 | ||||||
chr2:55893718
|
A | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 254 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.518-11984T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893718 | ||||||
chr2:55893744
|
G | C | 2 | a0001c0001t0001g0082a0001c0003t0021g0288 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.518-12010C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893744 | ||||||
chr2:55893909
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0220 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.518-12175G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55893909 | ||||||
chr2:55894185
|
A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 254 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.518-12451T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55894185 | ||||||
chr2:55894311
|
G | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.518-12577C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55894311 | ||||||
chr2:55894346
|
C | T | 1 | a0001c0003t0006g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.518-12612G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55894346 | ||||||
chr2:55894358
|
T | C | 2 | a0001c0001t0006g0100a0001c0002t0001g0067 | 2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.518-12624A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55894358 | ||||||
chr2:55894433
|
TG | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.518-12700delC | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55894433 | ||||||
chr2:55894640
|
T | C | 1 | a0001c0001t0018g0195 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.518-12906A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55894640 | ||||||
chr2:55894733
|
A | C | 9 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0084others(6): Show | 9 | HG00738.hp2 HG01346.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-12999T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55894733 | ||||||
chr2:55894762
|
G | GT | 39 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0119others(36): Show | 41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.518-13029dupA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55894762 | ||||||
chr2:55894858
|
T | C | 52 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0079others(49): Show | 55 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.518-13124A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55894858 | ||||||
chr2:55895033
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | NA18940.hp2 NA18969.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.518-13299C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55895033 | ||||||
chr2:55895079
|
C | A | 2 | a0001c0001t0001g0082a0001c0003t0021g0288 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.518-13345G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55895079 | ||||||
chr2:55895118
|
C | G | 1 | a0001c0003t0006g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.518-13384G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55895118 | ||||||
chr2:55895446
|
C | T | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-13712G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55895446 | ||||||
chr2:55895544
|
C | CT | 88 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0072others(85): Show | 93 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.518-13811dupA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55895544 | ||||||
chr2:55895544
|
C | CTT | 5 | a0001c0001t0004g0005a0001c0001t0004g0050a0001c0001t0004g0052others(2): Show | 7 | HG01257.hp1 HG01952.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-13812_518-1381 others(6): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55895544 | ||||||
chr2:55895757
|
T | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 201 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.518-14023A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55895757 | ||||||
chr2:55895763
|
T | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 264 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.518-14029A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55895763 | ||||||
chr2:55895792
|
T | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 195 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.518-14058A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55895792 | ||||||
chr2:55895808
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 271 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.518-14074G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55895808 | ||||||
chr2:55895869
|
C | A | 1 | a0001c0001t0008g0031 | 2 | NA19004.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.518-14135G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55895869 | ||||||
chr2:55896080
|
T | A | 2 | a0001c0001t0001g0082a0001c0003t0021g0288 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.518-14346A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55896080 | ||||||
chr2:55896196
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(222): Show | 262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.518-14462G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55896196 | ||||||
chr2:55896231
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 266 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.518-14497T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55896231 | ||||||
chr2:55896337
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.518-14603G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55896337 | ||||||
chr2:55896423
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.518-14689A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55896423 | ||||||
chr2:55896792
|
T | C | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 12 | HG01167.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.518-15058A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55896792 | ||||||
chr2:55896793
|
A | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0229a0001c0001t0001g0265others(1): Show | 4 | HG00738.hp2 HG01346.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-15059T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55896793 | ||||||
chr2:55896996
|
C | T | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-15262G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55896996 | ||||||
chr2:55897025
|
T | C | 41 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0119others(38): Show | 43 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.518-15291A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55897025 | ||||||
chr2:55897074
|
C | T | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG00673.hp1 HG02056.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-15340G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55897074 | ||||||
chr2:55897149
|
G | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 260 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.518-15415C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55897149 | ||||||
chr2:55897378
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.518-15644A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55897378 | ||||||
chr2:55897383
|
C | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.518-15649G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55897383 | ||||||
chr2:55897394
|
T | TAA | 254 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 294 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.518-15662_518-1566 others(6): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55897394 | ||||||
chr2:55897820
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.518-16086A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55897820 | ||||||
chr2:55897972
|
C | T | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-16238G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55897972 | ||||||
chr2:55898069
|
T | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0200 | 3 | HG01884.hp2 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.518-16335A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55898069 | ||||||
chr2:55898070
|
ATTCCTT | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0200 | 3 | HG01884.hp2 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.518-16342_518-1633 others(10): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55898070 | ||||||
chr2:55898077
|
C | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0200 | 3 | HG01884.hp2 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.518-16343G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55898077 | ||||||
chr2:55898171
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.518-16437T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55898171 | ||||||
chr2:55898184
|
T | C | 36 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0115others(33): Show | 40 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.518-16450A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55898184 | ||||||
chr2:55898241
|
G | C | 2 | a0001c0001t0001g0082a0001c0003t0021g0288 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.518-16507C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55898241 | ||||||
chr2:55898563
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.518-16829A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55898563 | ||||||
chr2:55898684
|
C | T | 1 | a0001c0001t0007g0041 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.518-16950G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55898684 | ||||||
chr2:55898691
|
A | C | 1 | a0001c0001t0001g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.518-16957T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55898691 | ||||||
chr2:55898949
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 129 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.518-17215A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55898949 | ||||||
chr2:55899243
|
CT | C | 1 | a0001c0001t0011g0007 | 3 | NA19009.hp1 NA19054.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.518-17510delA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55899243 | ||||||
chr2:55899374
|
C | T | 40 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0119others(37): Show | 42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.518-17640G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55899374 | ||||||
chr2:55899375
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.518-17641C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55899375 | ||||||
chr2:55899518
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.518-17784T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55899518 | ||||||
chr2:55899544
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.518-17810C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55899544 | ||||||
chr2:55899593
|
T | A | 1 | a0001c0001t0001g0142 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.518-17859A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55899593 | ||||||
chr2:55899594
|
G | T | 1 | a0001c0001t0001g0142 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.518-17860C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55899594 | ||||||
chr2:55899704
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.517+17961T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55899704 | ||||||
chr2:55899956
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 121 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.517+17709A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55899956 | ||||||
chr2:55899964
|
AT | A | 9 | a0001c0001t0003g0035a0001c0001t0004g0005a0001c0001t0004g0050others(6): Show | 11 | HG01074.hp1 HG01255.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.517+17700delA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55899964 | ||||||
chr2:55900592
|
T | C | 1 | a0001c0001t0005g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.517+17073A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55900592 | ||||||
chr2:55900669
|
T | TTC | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 288 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.517+16994_517+1699 others(6): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55900669 | ||||||
chr2:55900699
|
T | C | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+16966A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55900699 | ||||||
chr2:55900892
|
T | C | 150 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(147): Show | 166 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.517+16773A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55900892 | ||||||
chr2:55900956
|
C | A | 22 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(19): Show | 25 | HG01074.hp1 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.517+16709G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55900956 | ||||||
chr2:55901003
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02622.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.517+16662T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901003 | ||||||
chr2:55901034
|
T | C | 6 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0287others(3): Show | 6 | HG02647.hp1 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.517+16631A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901034 | ||||||
chr2:55901165
|
A | T | 150 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(147): Show | 166 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.517+16500T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901165 | ||||||
chr2:55901206
|
T | A | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+16459A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901206 | ||||||
chr2:55901292
|
C | A | 4 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0286others(1): Show | 4 | HG02559.hp2 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+16373G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901292 | ||||||
chr2:55901391
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(57): Show | 77 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.517+16274C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901391 | ||||||
chr2:55901550
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0220 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.517+16115G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901550 | ||||||
chr2:55901709
|
G | C | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+15956C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901709 | ||||||
chr2:55901722
|
A | G | 11 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0214others(8): Show | 11 | HG00738.hp2 HG01346.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.517+15943T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901722 | ||||||
chr2:55901766
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.517+15899G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901766 | ||||||
chr2:55901803
|
T | C | 1 | a0001c0001t0001g0021 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.517+15862A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901803 | ||||||
chr2:55901812
|
G | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0220 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.517+15853C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901812 | ||||||
chr2:55901817
|
T | G | 1 | a0001c0001t0001g0161 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.517+15848A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901817 | ||||||
chr2:55901925
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.517+15740T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901925 | ||||||
chr2:55901950
|
T | C | 10 | a0001c0001t0001g0078a0001c0001t0001g0214a0001c0001t0001g0219others(7): Show | 10 | HG00738.hp2 HG01346.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+15715A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55901950 | ||||||
chr2:55902036
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 119 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.517+15629G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55902036 | ||||||
chr2:55902331
|
C | CAT | 150 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(147): Show | 166 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.517+15333_517+1533 others(6): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55902331 | ||||||
chr2:55902498
|
C | T | 149 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(146): Show | 165 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.517+15167G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55902498 | ||||||
chr2:55902693
|
T | C | 1 | a0001c0001t0002g0277 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.517+14972A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55902693 | ||||||
chr2:55902735
|
A | C | 131 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(128): Show | 146 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.517+14930T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55902735 | ||||||
chr2:55902745
|
T | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 287 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.517+14920A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55902745 | ||||||
chr2:55902957
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.517+14708C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55902957 | ||||||
chr2:55902983
|
A | G | 1 | a0001c0001t0003g0040 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.517+14682T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55902983 | ||||||
chr2:55903245
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.517+14420T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55903245 | ||||||
chr2:55903366
|
A | T | 1 | a0001c0008t0001g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.517+14299T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55903366 | ||||||
chr2:55903505
|
A | G | 138 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(135): Show | 154 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.517+14160T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55903505 | ||||||
chr2:55903616
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.517+14049T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55903616 | ||||||
chr2:55903676
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.517+13989G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55903676 | ||||||
chr2:55903983
|
A | AG | 13 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0072others(10): Show | 16 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.517+13681dupC | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55903983 | ||||||
chr2:55904009
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(235): Show | 278 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.517+13656T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904009 | ||||||
chr2:55904012
|
A | G | 138 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(135): Show | 154 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.517+13653T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904012 | ||||||
chr2:55904089
|
A | G | 138 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(135): Show | 154 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.517+13576T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904089 | ||||||
chr2:55904217
|
G | C | 2 | a0001c0002t0001g0272a0003c0005t0001g0273 | 2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.517+13448C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904217 | ||||||
chr2:55904235
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.517+13430C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904235 | ||||||
chr2:55904352
|
T | C | 1 | a0001c0001t0002g0030 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.517+13313A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904352 | ||||||
chr2:55904364
|
T | C | 2 | a0001c0001t0004g0032a0001c0001t0004g0039 | 2 | NA19057.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.517+13301A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904364 | ||||||
chr2:55904467
|
G | C | 57 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(54): Show | 65 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.517+13198C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904467 | ||||||
chr2:55904481
|
C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 289 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.517+13184G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904481 | ||||||
chr2:55904606
|
G | C | 1 | a0001c0001t0001g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.517+13059C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904606 | ||||||
chr2:55904652
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0214a0001c0001t0001g0219 | 3 | HG02615.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.517+13013T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904652 | ||||||
chr2:55904966
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0082a0001c0003t0021g0288 | 2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.517+12689_517+1269 others(14): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904966 | ||||||
chr2:55904966
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0002g0279a0001c0003t0006g0061 | 2 | HG02258.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.517+12698_517+1269 others(18): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904966 | ||||||
chr2:55904966
|
C | CTTTTTTT others(8): Show |
4 | a0001c0001t0002g0278a0001c0001t0002g0280a0001c0002t0001g0087others(1): Show | 4 | HG00738.hp2 HG01070.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+12698_517+1269 others(19): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904966 | ||||||
chr2:55904966
|
C | CTTTTTTT others(9): Show |
5 | a0001c0001t0001g0078a0001c0001t0001g0229a0001c0001t0001g0265others(2): Show | 5 | HG01081.hp1 HG01346.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+12698_517+1269 others(20): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904966 | ||||||
chr2:55904966
|
C | CTTTTTTT others(10): Show |
1 | a0001c0004t0010g0299 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.517+12698_517+1269 others(21): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904966 | ||||||
chr2:55904970
|
TTTTTTTT others(8): Show |
T | 13 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0072others(10): Show | 16 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.517+12680_517+1269 others(19): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904970 | ||||||
chr2:55904971
|
TTTTTTTT others(7): Show |
T | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(172): Show | 207 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.517+12680_517+1269 others(18): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904971 | ||||||
chr2:55904972
|
TTTTTTTC others(6): Show |
T | 35 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0104others(32): Show | 35 | HG00558.hp1 HG01167.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.517+12680_517+1269 others(17): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904972 | ||||||
chr2:55904973
|
TTTTTTCT others(5): Show |
T | 13 | a0001c0001t0001g0003a0001c0001t0001g0079a0001c0001t0001g0080others(10): Show | 17 | HG01517.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.517+12680_517+1269 others(16): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904973 | ||||||
chr2:55904974
|
TTTTTCTT others(4): Show |
T | 1 | a0001c0001t0001g0089 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.517+12680_517+1269 others(15): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55904974 | ||||||
chr2:55905126
|
T | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0220 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.517+12539A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55905126 | ||||||
chr2:55905141
|
A | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 276 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.517+12524T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55905141 | ||||||
chr2:55905236
|
A | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 276 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.517+12429T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55905236 | ||||||
chr2:55905285
|
G | A | 1 | a0001c0001t0005g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.517+12380C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55905285 | ||||||
chr2:55905677
|
G | A | 1 | a0001c0001t0016g0257 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.517+11988C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55905677 | ||||||
chr2:55905763
|
T | C | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | NA18949.hp2 NA18956.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.517+11902A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55905763 | ||||||
chr2:55905905
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 272 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.517+11760G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55905905 | ||||||
chr2:55906098
|
C | T | 2 | a0001c0001t0006g0100a0001c0002t0001g0067 | 2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.517+11567G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55906098 | ||||||
chr2:55906196
|
T | C | 10 | a0001c0001t0002g0276a0001c0001t0006g0088a0001c0002t0001g0062others(7): Show | 10 | HG02280.hp1 HG02723.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+11469A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55906196 | ||||||
chr2:55906222
|
CT | C | 12 | a0001c0001t0001g0089a0001c0001t0001g0121a0001c0001t0001g0138others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.517+11442delA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55906222 | ||||||
chr2:55906222
|
CTT | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 262 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.517+11441_517+1144 others(6): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55906222 | ||||||
chr2:55906381
|
G | A | 122 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(119): Show | 135 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.517+11284C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55906381 | ||||||
chr2:55906405
|
G | T | 1 | a0001c0001t0001g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.517+11260C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55906405 | ||||||
chr2:55906550
|
A | T | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.517+11115T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55906550 | ||||||
chr2:55906633
|
G | C | 2 | a0001c0004t0010g0299a0001c0004t0010g0300 | 2 | HG01081.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.517+11032C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55906633 | ||||||
chr2:55906722
|
T | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 119 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.517+10943A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55906722 | ||||||
chr2:55906747
|
T | A | 2 | a0001c0001t0001g0073a0001c0001t0006g0109 | 2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.517+10918A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55906747 | ||||||
chr2:55907077
|
T | C | 12 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0072others(9): Show | 14 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.517+10588A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55907077 | ||||||
chr2:55907160
|
C | T | 1 | a0001c0001t0003g0056 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.517+10505G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55907160 | ||||||
chr2:55907247
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02622.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.517+10418C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55907247 | ||||||
chr2:55907258
|
T | C | 7 | a0001c0001t0001g0086a0001c0001t0001g0196a0001c0003t0002g0289others(4): Show | 7 | HG01167.hp1 HG02622.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.517+10407A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55907258 | ||||||
chr2:55907665
|
C | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0027others(31): Show | 41 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.517+10000G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55907665 | ||||||
chr2:55907692
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 190 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.517+9973C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55907692 | ||||||
chr2:55907897
|
T | C | 21 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(18): Show | 22 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.517+9768A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55907897 | ||||||
chr2:55907963
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.517+9702G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55907963 | ||||||
chr2:55907964
|
G | A | 8 | a0001c0001t0004g0005a0001c0001t0004g0050a0001c0001t0004g0051others(5): Show | 10 | HG01074.hp1 HG01255.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.517+9701C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55907964 | ||||||
chr2:55908048
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG02622.hp1 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.517+9617C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908048 | ||||||
chr2:55908146
|
T | C | 22 | a0001c0001t0002g0030a0001c0001t0002g0274a0001c0001t0002g0275others(19): Show | 23 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.517+9519A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908146 | ||||||
chr2:55908200
|
T | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0203others(6): Show | 11 | HG00642.hp1 HG01074.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.517+9465A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908200 | ||||||
chr2:55908362
|
T | C | 31 | a0001c0001t0001g0013a0001c0001t0001g0112a0001c0001t0003g0034others(28): Show | 35 | HG00438.hp1 HG01074.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.517+9303A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908362 | ||||||
chr2:55908374
|
A | G | 17 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(14): Show | 18 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.517+9291T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908374 | ||||||
chr2:55908378
|
T | A | 1 | a0001c0001t0008g0294 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.517+9287A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908378 | ||||||
chr2:55908439
|
A | G | 17 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(14): Show | 18 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.517+9226T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908439 | ||||||
chr2:55908586
|
A | T | 3 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276 | 3 | HG02723.hp2 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.517+9079T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908586 | ||||||
chr2:55908699
|
A | G | 11 | a0001c0003t0002g0289a0001c0003t0002g0290a0001c0003t0002g0291others(8): Show | 11 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+8966T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908699 | ||||||
chr2:55908759
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.517+8906G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908759 | ||||||
chr2:55908902
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.517+8763G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908902 | ||||||
chr2:55908967
|
T | C | 17 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(14): Show | 18 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.517+8698A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55908967 | ||||||
chr2:55909093
|
T | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(79): Show | 92 | HG00438.hp1 HG01070.hp1 HG01074.hp1 others(89): Show |
intron_variant | MODIFIER | c.517+8572A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55909093 | ||||||
chr2:55909343
|
C | G | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+8322G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55909343 | ||||||
chr2:55909344
|
G | T | 17 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(14): Show | 18 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.517+8321C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55909344 | ||||||
chr2:55909383
|
G | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02622.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.517+8282C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55909383 | ||||||
chr2:55909509
|
C | T | 3 | a0001c0001t0003g0035a0001c0001t0003g0036a0001c0001t0003g0037 | 3 | HG02647.hp1 HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.517+8156G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55909509 | ||||||
chr2:55909556
|
T | C | 17 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(14): Show | 18 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.517+8109A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55909556 | ||||||
chr2:55909681
|
C | T | 1 | a0001c0001t0008g0294 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.517+7984G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55909681 | ||||||
chr2:55909841
|
T | G | 11 | a0001c0003t0002g0289a0001c0003t0002g0290a0001c0003t0002g0291others(8): Show | 11 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+7824A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55909841 | ||||||
chr2:55909875
|
A | G | 1 | a0001c0002t0001g0066 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.517+7790T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55909875 | ||||||
chr2:55910026
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0117a0001c0001t0001g0120others(3): Show | 8 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+7639A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55910026 | ||||||
chr2:55910073
|
T | C | 1 | a0001c0001t0005g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.517+7592A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55910073 | ||||||
chr2:55910497
|
C | A | 1 | a0001c0001t0019g0259 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.517+7168G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55910497 | ||||||
chr2:55910525
|
C | A | 5 | a0001c0001t0002g0278a0001c0001t0002g0279a0001c0001t0002g0280others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+7140G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55910525 | ||||||
chr2:55910543
|
G | C | 6 | a0001c0003t0002g0289a0001c0003t0002g0290a0001c0003t0002g0291others(3): Show | 6 | HG01167.hp1 HG03130.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.517+7122C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55910543 | ||||||
chr2:55910615
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.517+7050G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55910615 | ||||||
chr2:55910715
|
G | A | 3 | a0001c0001t0006g0014a0001c0001t0006g0101a0001c0001t0006g0102 | 4 | HG02257.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+6950C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55910715 | ||||||
chr2:55910812
|
G | A | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+6853C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55910812 | ||||||
chr2:55910912
|
C | G | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+6753G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55910912 | ||||||
chr2:55910938
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.517+6727G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55910938 | ||||||
chr2:55911164
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0093 | 5 | NA18945.hp2 NA18953.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+6501A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55911164 | ||||||
chr2:55911338
|
A | G | 1 | a0001c0001t0003g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.517+6327T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55911338 | ||||||
chr2:55911340
|
A | C | 6 | a0001c0003t0002g0289a0001c0003t0002g0290a0001c0003t0002g0291others(3): Show | 6 | HG01167.hp1 HG03130.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.517+6325T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55911340 | ||||||
chr2:55911446
|
T | C | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+6219A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55911446 | ||||||
chr2:55911550
|
AT | A | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+6114delA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55911550 | ||||||
chr2:55911589
|
G | C | 17 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(14): Show | 18 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.517+6076C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55911589 | ||||||
chr2:55911674
|
T | C | 1 | a0001c0001t0019g0259 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.517+5991A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55911674 | ||||||
chr2:55911704
|
C | A | 10 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(7): Show | 11 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+5961G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55911704 | ||||||
chr2:55911728
|
G | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0078others(6): Show | 9 | HG00544.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+5937C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55911728 | ||||||
chr2:55911786
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+5879G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55911786 | ||||||
chr2:55912077
|
G | A | 5 | a0001c0001t0002g0278a0001c0001t0002g0279a0001c0001t0002g0280others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+5588C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55912077 | ||||||
chr2:55912103
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.517+5562C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55912103 | ||||||
chr2:55912301
|
G | A | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+5364C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55912301 | ||||||
chr2:55912402
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.517+5263A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55912402 | ||||||
chr2:55912455
|
A | G | 4 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+5210T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55912455 | ||||||
chr2:55912782
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02622.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.517+4883T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55912782 | ||||||
chr2:55913053
|
G | T | 9 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0078others(6): Show | 9 | HG00544.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+4612C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55913053 | ||||||
chr2:55913396
|
A | G | 76 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(73): Show | 85 | HG00438.hp1 HG01070.hp1 HG01074.hp1 others(82): Show |
intron_variant | MODIFIER | c.517+4269T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55913396 | ||||||
chr2:55913604
|
C | CT | 116 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0013others(113): Show | 129 | HG00438.hp1 HG00544.hp2 HG00738.hp2 others(126): Show |
intron_variant | MODIFIER | c.517+4060dupA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55913604 | ||||||
chr2:55913778
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0209a0001c0001t0001g0210 | 5 | NA18939.hp1 NA19004.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+3887C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55913778 | ||||||
chr2:55913831
|
GA | G | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+3833delT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55913831 | ||||||
chr2:55913938
|
A | T | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+3727T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55913938 | ||||||
chr2:55913995
|
G | A | 55 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(52): Show | 64 | HG00438.hp1 HG01074.hp1 HG01168.hp1 others(61): Show |
intron_variant | MODIFIER | c.517+3670C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55913995 | ||||||
chr2:55914009
|
C | CA | 9 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(6): Show | 9 | HG02258.hp1 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.517+3655dupT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914009 | ||||||
chr2:55914074
|
T | C | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+3591A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914074 | ||||||
chr2:55914170
|
G | A | 1 | a0001c0001t0014g0055 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.517+3495C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914170 | ||||||
chr2:55914315
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.517+3350T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914315 | ||||||
chr2:55914336
|
C | T | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+3329G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914336 | ||||||
chr2:55914367
|
C | T | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+3298G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914367 | ||||||
chr2:55914444
|
C | G | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+3221G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914444 | ||||||
chr2:55914474
|
A | G | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+3191T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914474 | ||||||
chr2:55914587
|
A | G | 34 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0115others(31): Show | 38 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.517+3078T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914587 | ||||||
chr2:55914818
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.517+2847C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914818 | ||||||
chr2:55914963
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(85): Show | 107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.517+2702C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914963 | ||||||
chr2:55914990
|
T | A | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+2675A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55914990 | ||||||
chr2:55915010
|
T | C | 17 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(14): Show | 18 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.517+2655A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915010 | ||||||
chr2:55915121
|
T | C | 1 | a0001c0001t0003g0056 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.517+2544A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915121 | ||||||
chr2:55915258
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG02622.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.517+2407A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915258 | ||||||
chr2:55915282
|
A | G | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+2383T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915282 | ||||||
chr2:55915398
|
C | T | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+2267G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915398 | ||||||
chr2:55915433
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.517+2232A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915433 | ||||||
chr2:55915521
|
A | T | 1 | a0001c0003t0006g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.517+2144T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915521 | ||||||
chr2:55915573
|
A | C | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+2092T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915573 | ||||||
chr2:55915627
|
G | T | 1 | a0001c0001t0001g0168 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.517+2038C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915627 | ||||||
chr2:55915863
|
C | A | 54 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(51): Show | 63 | HG00438.hp1 HG01074.hp1 HG01168.hp1 others(60): Show |
intron_variant | MODIFIER | c.517+1802G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915863 | ||||||
chr2:55915901
|
A | G | 1 | a0001c0001t0006g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.517+1764T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915901 | ||||||
chr2:55915934
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.517+1731T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55915934 | ||||||
chr2:55916039
|
G | A | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+1626C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916039 | ||||||
chr2:55916107
|
A | AT | 33 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0076others(30): Show | 36 | HG00544.hp2 HG00738.hp2 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.517+1557dupA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916107 | ||||||
chr2:55916107
|
AT | A | 10 | a0001c0001t0001g0113a0001c0001t0001g0159a0001c0001t0001g0160others(7): Show | 11 | HG01891.hp2 HG02129.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+1557delA | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916107 | ||||||
chr2:55916108
|
T | TG | 4 | a0001c0001t0006g0014a0001c0001t0006g0088a0001c0001t0006g0101others(1): Show | 5 | HG02257.hp2 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+1556_517+1557i others(3): Show |
EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916108 | ||||||
chr2:55916109
|
T | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0103others(9): Show | 16 | HG01168.hp1 HG01516.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.517+1556A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916109 | ||||||
chr2:55916241
|
T | C | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+1424A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916241 | ||||||
chr2:55916347
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.517+1318A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916347 | ||||||
chr2:55916390
|
G | A | 1 | a0001c0001t0006g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.517+1275C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916390 | ||||||
chr2:55916689
|
G | C | 4 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+976C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916689 | ||||||
chr2:55916735
|
T | G | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+930A>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916735 | ||||||
chr2:55916872
|
T | C | 4 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+793A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916872 | ||||||
chr2:55916886
|
C | T | 10 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(7): Show | 11 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+779G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916886 | ||||||
chr2:55916994
|
C | A | 10 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(7): Show | 11 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+671G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55916994 | ||||||
chr2:55917018
|
T | C | 4 | a0001c0004t0010g0297a0001c0004t0010g0298a0001c0004t0010g0299others(1): Show | 4 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+647A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55917018 | ||||||
chr2:55917045
|
C | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 7 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+620G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55917045 | ||||||
chr2:55917120
|
A | C | 2 | a0001c0001t0001g0119a0001c0001t0004g0032 | 2 | NA18979.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.517+545T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55917120 | ||||||
chr2:55917244
|
T | A | 1 | a0001c0001t0004g0057 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.517+421A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55917244 | ||||||
chr2:55917263
|
C | G | 15 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0103others(12): Show | 20 | HG01168.hp1 HG01516.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.517+402G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55917263 | ||||||
chr2:55917303
|
A | G | 5 | a0001c0001t0002g0278a0001c0001t0002g0279a0001c0001t0002g0280others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+362T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55917303 | ||||||
chr2:55917370
|
G | C | 6 | a0001c0001t0002g0030a0001c0001t0002g0283a0001c0001t0002g0284others(3): Show | 7 | HG01891.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+295C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55917370 | ||||||
chr2:55917573
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.517+92G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 5/11 | chr2 | 55917573 | ||||||
chr2:55918135
|
A | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0103others(13): Show | 21 | HG01168.hp1 HG01516.hp1 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.130+84T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 4/11 | chr2 | 55918135 | ||||||
chr2:55918406
|
T | C | 34 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0115others(31): Show | 38 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.82-139A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55918406 | ||||||
chr2:55918460
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.82-193C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55918460 | ||||||
chr2:55918567
|
C | G | 3 | a0001c0002t0001g0063a0001c0002t0001g0064a0001c0002t0001g0065 | 3 | HG02280.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.82-300G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55918567 | ||||||
chr2:55918613
|
T | TA | 75 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(72): Show | 85 | HG01070.hp1 HG01074.hp1 HG01081.hp1 others(82): Show |
intron_variant | MODIFIER | c.82-347dupT | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55918613 | ||||||
chr2:55918654
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.82-387G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55918654 | ||||||
chr2:55918679
|
C | A | 26 | a0001c0001t0002g0030a0001c0001t0002g0274a0001c0001t0002g0275others(23): Show | 27 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.82-412G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55918679 | ||||||
chr2:55918715
|
A | T | 13 | a0001c0001t0002g0274a0001c0001t0002g0275a0001c0001t0002g0276others(10): Show | 13 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.82-448T>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55918715 | ||||||
chr2:55918775
|
C | T | 1 | a0001c0001t0005g0118 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.82-508G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55918775 | ||||||
chr2:55919101
|
G | T | 1 | a0001c0003t0006g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.82-834C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919101 | ||||||
chr2:55919149
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.82-882A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919149 | ||||||
chr2:55919236
|
G | T | 1 | a0001c0001t0005g0165 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.82-969C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919236 | ||||||
chr2:55919390
|
TG | T | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG02486.hp2 HG02602.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-1124delC | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919390 | ||||||
chr2:55919393
|
G | T | 6 | a0001c0003t0002g0289a0001c0003t0002g0290a0001c0003t0002g0291others(3): Show | 6 | HG01167.hp1 HG03130.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-1126C>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919393 | ||||||
chr2:55919484
|
A | G | 5 | a0001c0001t0002g0278a0001c0001t0002g0279a0001c0001t0002g0280others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-1217T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919484 | ||||||
chr2:55919563
|
G | A | 1 | a0002c0007t0001g0262 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.82-1296C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919563 | ||||||
chr2:55919658
|
T | A | 1 | a0001c0001t0004g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.82-1391A>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919658 | ||||||
chr2:55919758
|
G | A | 6 | a0001c0003t0002g0289a0001c0003t0002g0290a0001c0003t0002g0291others(3): Show | 6 | HG01167.hp1 HG03130.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-1491C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919758 | ||||||
chr2:55919848
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.82-1581C>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919848 | ||||||
chr2:55919915
|
T | C | 20 | a0001c0001t0001g0114a0001c0001t0002g0030a0001c0001t0002g0274others(17): Show | 21 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.82-1648A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919915 | ||||||
chr2:55919954
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0091others(3): Show | 9 | HG03704.hp2 HG03710.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-1687G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55919954 | ||||||
chr2:55920229
|
A | G | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG02486.hp2 HG02602.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-1962T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55920229 | ||||||
chr2:55920251
|
T | C | 2 | a0001c0001t0009g0263a0001c0001t0009g0264 | 2 | HG00408.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.82-1984A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55920251 | ||||||
chr2:55920354
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0089a0001c0001t0001g0091others(4): Show | 10 | HG01433.hp1 HG03704.hp2 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+2006A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55920354 | ||||||
chr2:55920388
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.81+1972G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55920388 | ||||||
chr2:55920535
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.81+1825C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55920535 | ||||||
chr2:55920537
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.81+1823C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55920537 | ||||||
chr2:55920538
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0164 | 3 | HG01069.hp1 HG01071.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.81+1822G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55920538 | ||||||
chr2:55920658
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.81+1702C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55920658 | ||||||
chr2:55920764
|
G | A | 76 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(73): Show | 86 | HG00438.hp1 HG01070.hp1 HG01074.hp1 others(83): Show |
intron_variant | MODIFIER | c.81+1596C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55920764 | ||||||
chr2:55920799
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.81+1561G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55920799 | ||||||
chr2:55920937
|
C | A | 3 | a0001c0001t0002g0286a0001c0001t0002g0287a0001c0006t0002g0285 | 3 | HG02559.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.81+1423G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55920937 | ||||||
chr2:55921487
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.81+873T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55921487 | ||||||
chr2:55921706
|
A | C | 1 | a0001c0002t0001g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.81+654T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55921706 | ||||||
chr2:55921795
|
C | T | 1 | a0001c0001t0001g0013 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.81+565G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55921795 | ||||||
chr2:55922024
|
G | A | 6 | a0001c0003t0002g0289a0001c0003t0002g0290a0001c0003t0002g0291others(3): Show | 6 | HG01167.hp1 HG03130.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+336C>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55922024 | ||||||
chr2:55922296
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.81+64T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55922296 | ||||||
chr2:55922340
|
C | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(56): Show | 75 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.81+20G>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 3/11 | chr2 | 55922340 | ||||||
chr2:55922574
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0115 | 4 | HG01433.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-127G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 2/11 | chr2 | 55922574 | ||||||
chr2:55922739
|
C | T | 1 | a0001c0003t0006g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-8+160G>A | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 2/11 | chr2 | 55922739 | ||||||
chr2:55923214
|
T | C | 3 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271 | 3 | HG00642.hp2 HG01069.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-48-275A>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 1/11 | chr2 | 55923214 | ||||||
chr2:55923267
|
A | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0013others(114): Show | 130 | HG00438.hp1 HG00544.hp2 HG00738.hp2 others(127): Show |
intron_variant | MODIFIER | c.-48-328T>C | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 1/11 | chr2 | 55923267 | ||||||
chr2:55923302
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-48-363T>G | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 1/11 | chr2 | 55923302 | ||||||
chr2:55923637
|
C | A | 2 | a0001c0002t0001g0272a0003c0005t0001g0273 | 2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-49+74G>T | EFEMP1 | ENSG00000115380.20 | transcript | ENST00000355426.8 | protein_coding | 1/11 | chr2 | 55923637 |