Item | Value |
---|---|
geneid | 392617 |
ensemblid | ENSG00000225968.8 |
hgncid | 33154 |
symbol | ELFN1 |
name | extracellular leucine rich repeat and fibronectin type III domain containing 1 |
refseq_nuc | NM_001128636.4 |
refseq_prot | NP_001122108.1 |
ensembl_nuc | ENST00000424383.5 |
ensembl_prot | ENSP00000456548.1 |
mane_status | MANE Select |
chr | chr7 |
start | 1670277 |
end | 1747946 |
strand | + |
ver | v1.2 |
region | chr7:1670277-1747946 |
region5000 | chr7:1665277-1752946 |
regionname0 | ELFN1_chr7_1670277_1747946 |
regionname5000 | ELFN1_chr7_1665277_1752946 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 828 | 277 | 79 | 55 | 92 | 13 | 36 | 63 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0002 | 0/0 | 828 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0003 | 0/0 | 828 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0004 | 0/0 | 828 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0005 | 0/0 | 828 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0006 | 0/0 | 828 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0007 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0008 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0009 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0010 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0011 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0012 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0013 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0014 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0015 | 0/0 | 828 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2487 | 223 | 67 | 49 | 71 | 12 | 23 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0002 | 0/1 | 2487 | 34 | 0 | 4 | 15 | 1 | 13 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0003 | 0/0 | 2487 | 6 | 6 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0004 | 0/0 | 2487 | 5 | 1 | 0 | 4 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0005 | 0/0 | 2487 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0006 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0007 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0008 | 0/0 | 2487 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0009 | 0/0 | 2487 | 2 | 0 | 0 | 0 | 0 | 2 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0010 | 0/0 | 2487 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0011 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0012 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0013 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0014 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0015 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0016 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0017 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0018 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0019 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0020 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0021 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0022 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0023 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0024 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0025 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0026 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
c0027 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1493 | 85 | 19 | 21 | 27 | 6 | 12 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0002 | 1/0 | 1490 | 25 | 1 | 7 | 10 | 2 | 4 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0003 | 0/1 | 1495 | 21 | 7 | 1 | 6 | 2 | 4 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0004 | 0/0 | 1493 | 19 | 0 | 3 | 11 | 0 | 5 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0005 | 0/0 | 1496 | 15 | 10 | 1 | 4 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0006 | 0/0 | 1493 | 9 | 8 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0007 | 0/0 | 1497 | 6 | 0 | 1 | 4 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0008 | 0/0 | 1498 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0009 | 0/0 | 1498 | 5 | 1 | 3 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0010 | 0/0 | 1497 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0011 | 0/0 | 1494 | 5 | 0 | 0 | 4 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0012 | 0/0 | 1486 | 5 | 1 | 4 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0013 | 0/0 | 1493 | 5 | 0 | 0 | 5 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0014 | 0/0 | 1490 | 4 | 0 | 3 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0015 | 0/0 | 1498 | 4 | 0 | 0 | 1 | 0 | 3 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0016 | 0/0 | 1497 | 4 | 4 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0017 | 0/0 | 1493 | 4 | 0 | 4 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0018 | 0/0 | 1489 | 4 | 1 | 0 | 2 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0019 | 0/0 | 1499 | 3 | 0 | 1 | 0 | 1 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0020 | 0/0 | 1495 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0021 | 0/0 | 1494 | 3 | 0 | 1 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0022 | 0/0 | 1494 | 3 | 1 | 2 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0023 | 0/0 | 1490 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0024 | 0/0 | 1489 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0025 | 0/0 | 1500 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0026 | 0/0 | 1499 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0027 | 0/0 | 1497 | 2 | 0 | 0 | 1 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0028 | 0/0 | 1497 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0029 | 0/0 | 1496 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0030 | 0/0 | 1494 | 2 | 1 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0031 | 0/0 | 1494 | 2 | 0 | 0 | 1 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0032 | 0/0 | 1492 | 2 | 1 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0033 | 0/0 | 1489 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0034 | 0/0 | 1490 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0035 | 0/0 | 1493 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0036 | 0/0 | 1490 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0037 | 0/0 | 1492 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0038 | 0/0 | 1499 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0039 | 0/0 | 1489 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0040 | 0/0 | 1501 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0041 | 0/0 | 1500 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0042 | 0/0 | 1501 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0043 | 0/0 | 1499 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0044 | 0/0 | 1496 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0045 | 0/0 | 1495 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0046 | 0/0 | 1495 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0047 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0048 | 0/0 | 1504 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0049 | 0/0 | 1499 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0050 | 0/0 | 1498 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0051 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0052 | 0/0 | 1495 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0053 | 0/0 | 1493 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0054 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0055 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0056 | 0/0 | 1492 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0057 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0058 | 0/0 | 1490 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0059 | 0/0 | 1493 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0060 | 0/0 | 1492 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0061 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0062 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0063 | 0/0 | 1493 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0064 | 0/0 | 1497 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
t0065 | 0/0 | 1496 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2487 | 223 | 67 | 49 | 71 | 12 | 23 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0002 | 0/1 | 2487 | 34 | 0 | 4 | 15 | 1 | 13 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0004 | 0/0 | 2487 | 5 | 1 | 0 | 4 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0005 | 0/0 | 2487 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0007 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0011 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0014 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0018 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0021 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0025 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0026 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0027 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0002c0003 | 0/0 | 2487 | 6 | 6 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0002c0024 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0003c0006 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0004c0009 | 0/0 | 2487 | 2 | 0 | 0 | 0 | 0 | 2 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0005c0010 | 0/0 | 2487 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0006c0008 | 0/0 | 2487 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0007c0012 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0008c0013 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0009c0015 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0010c0016 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0011c0020 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0012c0019 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0013c0017 | 0/0 | 2487 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0014c0022 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0015c0023 | 0/0 | 2487 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3979 | 76 | 18 | 18 | 25 | 6 | 9 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0002 | 1/0 | 3976 | 24 | 1 | 7 | 9 | 2 | 4 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0003 | 0/0 | 3981 | 7 | 6 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0004 | 0/0 | 3979 | 7 | 0 | 0 | 7 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0005 | 0/0 | 3982 | 12 | 7 | 1 | 4 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0006 | 0/0 | 3979 | 8 | 7 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0007 | 0/0 | 3983 | 5 | 0 | 0 | 4 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0008 | 0/0 | 3984 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0009 | 0/0 | 3984 | 5 | 1 | 3 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0011 | 0/0 | 3980 | 5 | 0 | 0 | 4 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0012 | 0/0 | 3972 | 5 | 1 | 4 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0013 | 0/0 | 3979 | 5 | 0 | 0 | 5 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0014 | 0/0 | 3976 | 4 | 0 | 3 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0015 | 0/0 | 3984 | 4 | 0 | 0 | 1 | 0 | 3 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0016 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0017 | 0/0 | 3979 | 4 | 0 | 4 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0018 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0019 | 0/0 | 3985 | 3 | 0 | 1 | 0 | 1 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0020 | 0/0 | 3981 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0021 | 0/0 | 3980 | 3 | 0 | 1 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0022 | 0/0 | 3980 | 3 | 1 | 2 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0023 | 0/0 | 3976 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0025 | 0/0 | 3986 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0026 | 0/0 | 3985 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0028 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0029 | 0/0 | 3982 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0031 | 0/0 | 3980 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0033 | 0/0 | 3975 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0035 | 0/0 | 3979 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0036 | 0/0 | 3976 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0038 | 0/0 | 3985 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0039 | 0/0 | 3975 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0040 | 0/0 | 3987 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0041 | 0/0 | 3986 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0042 | 0/0 | 3987 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0043 | 0/0 | 3985 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0044 | 0/0 | 3982 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0047 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0048 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0049 | 0/0 | 3985 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0051 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0052 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0055 | 0/0 | 3979 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0056 | 0/0 | 3978 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0059 | 0/0 | 3979 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0060 | 0/0 | 3978 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0063 | 0/0 | 3979 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0064 | 0/0 | 3983 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0001t0065 | 0/0 | 3982 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0002t0001 | 0/0 | 3979 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0002t0003 | 0/1 | 3981 | 12 | 0 | 0 | 6 | 1 | 4 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0002t0004 | 0/0 | 3979 | 12 | 0 | 3 | 4 | 0 | 5 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0002t0007 | 0/0 | 3983 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0002t0018 | 0/0 | 3975 | 3 | 0 | 0 | 2 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0002t0027 | 0/0 | 3983 | 2 | 0 | 0 | 1 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0002t0030 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0002t0031 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0002t0053 | 0/0 | 3979 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0004t0034 | 0/0 | 3976 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0004t0037 | 0/0 | 3978 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0004t0054 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0004t0061 | 0/0 | 3977 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0005t0010 | 0/0 | 3983 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0007t0005 | 0/0 | 3982 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0011t0034 | 0/0 | 3976 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0014t0001 | 0/0 | 3979 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0018t0001 | 0/0 | 3979 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0021t0023 | 0/0 | 3976 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0025t0058 | 0/0 | 3976 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0026t0057 | 0/0 | 3977 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0001c0027t0062 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0002c0003t0003 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0002c0003t0006 | 0/0 | 3979 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0002c0003t0024 | 0/0 | 3975 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0002c0003t0050 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0002c0024t0030 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0003c0006t0016 | 0/0 | 3983 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0004c0009t0001 | 0/0 | 3979 | 2 | 0 | 0 | 0 | 0 | 2 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0005c0010t0045 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0005c0010t0046 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0006c0008t0028 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0006c0008t0029 | 0/0 | 3982 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0007c0012t0032 | 0/0 | 3978 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0008c0013t0020 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0009c0015t0032 | 0/0 | 3978 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0010c0016t0001 | 0/0 | 3979 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0011c0020t0002 | 0/0 | 3976 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0012c0019t0001 | 0/0 | 3979 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0013c0017t0001 | 0/0 | 3979 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0014c0022t0001 | 0/0 | 3979 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
a0015c0023t0003 | 0/0 | 3981 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | copy fasta | chr7 | 1665277 | 1752946 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0007g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0007g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0007g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0009g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0009g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0009g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0011g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0011g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0011g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0011g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0012g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0012g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0012g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0012g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0012g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0013g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0013g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0013g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0013g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0014g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0014g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0014g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0014g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0015g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0015g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0015g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0015g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0016g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0017g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0017g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0017g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0017g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0018g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0019g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0019g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0019g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0020g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0020g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0021g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0021g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0021g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0022g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0022g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0022g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0023g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0023g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0025g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0025g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0026g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0026g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0028g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0029g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0031g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0033g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0033g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0035g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0035g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0036g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0036g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0038g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0039g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0040g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0041g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0042g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0043g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0044g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0047g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0048g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0049g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0051g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0052g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0055g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0056g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0059g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0060g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0063g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0064g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0001t0065g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0007g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0018g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0018g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0018g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0027g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0027g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0030g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0031g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0002t0053g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0004t0034g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0004t0037g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0004t0037g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0004t0054g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0004t0061g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0005t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0005t0010g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0005t0010g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0005t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0005t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0007t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0007t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0007t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0011t0034g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0014t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0018t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0021t0023g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0025t0058g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0026t0057g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0001c0027t0062g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0002c0003t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0002c0003t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0002c0003t0024g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0002c0003t0024g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0002c0003t0024g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0002c0003t0050g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0002c0024t0030g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0003c0006t0016g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0003c0006t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0003c0006t0016g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0004c0009t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0004c0009t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0005c0010t0045g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0005c0010t0046g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0006c0008t0028g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0006c0008t0029g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0007c0012t0032g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0008c0013t0020g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0009c0015t0032g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0010c0016t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0011c0020t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0012c0019t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0013c0017t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0014c0022t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
a0015c0023t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0258 | EUR | GBR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00280 | hp1 | a0001 | c0001 | t0019 | g0154 | EUR | FIN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00408 | hp1 | a0001 | c0001 | t0013 | g0093 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0301 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00423 | hp1 | a0001 | c0002 | t0018 | g0032 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00423 | hp2 | a0001 | c0001 | t0013 | g0274 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00438 | hp1 | a0001 | c0001 | t0007 | g0166 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00544 | hp2 | a0013 | c0017 | t0001 | g0217 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00558 | hp1 | a0001 | c0001 | t0023 | g0196 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00558 | hp2 | a0001 | c0001 | t0056 | g0195 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00621 | hp1 | a0001 | c0001 | t0007 | g0202 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00639 | hp2 | a0001 | c0001 | t0012 | g0013 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00733 | hp1 | a0001 | c0002 | t0004 | g0255 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00733 | hp2 | a0001 | c0018 | t0001 | g0065 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00735 | hp1 | a0001 | c0001 | t0021 | g0082 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00735 | hp2 | a0001 | c0001 | t0022 | g0253 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00738 | hp1 | a0001 | c0001 | t0014 | g0097 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01070 | hp1 | a0012 | c0019 | t0001 | g0256 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01071 | hp1 | a0001 | c0001 | t0014 | g0074 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01074 | hp1 | a0001 | c0001 | t0014 | g0181 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01074 | hp2 | a0001 | c0001 | t0022 | g0073 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0036 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01099 | hp1 | a0001 | c0001 | t0017 | g0080 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01099 | hp2 | a0001 | c0001 | t0019 | g0122 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01106 | hp2 | a0001 | c0002 | t0004 | g0057 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01167 | hp1 | a0001 | c0001 | t0012 | g0212 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01167 | hp2 | a0001 | c0001 | t0012 | g0184 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01168 | hp1 | a0001 | c0001 | t0009 | g0044 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01169 | hp1 | a0001 | c0001 | t0012 | g0211 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01169 | hp2 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01175 | hp1 | a0001 | c0001 | t0009 | g0119 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01175 | hp2 | a0001 | c0002 | t0004 | g0153 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0156 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01243 | hp2 | a0001 | c0001 | t0048 | g0124 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01255 | hp1 | a0001 | c0001 | t0064 | g0006 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01358 | hp2 | a0001 | c0001 | t0017 | g0197 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01433 | hp1 | a0001 | c0001 | t0017 | g0101 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01433 | hp2 | a0001 | c0001 | t0059 | g0083 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01496 | hp1 | a0009 | c0015 | t0032 | g0191 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01515 | hp1 | a0001 | c0001 | t0014 | g0076 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01516 | hp1 | a0001 | c0002 | t0003 | g0110 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0172 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01517 | hp1 | a0001 | c0001 | t0039 | g0173 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0075 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01884 | hp1 | a0001 | c0001 | t0022 | g0264 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01884 | hp2 | a0001 | c0011 | t0034 | g0007 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0121 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01891 | hp2 | a0001 | c0001 | t0028 | g0079 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01975 | hp2 | a0001 | c0002 | t0007 | g0050 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01993 | hp1 | a0010 | c0016 | t0001 | g0286 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01993 | hp2 | a0001 | c0001 | t0017 | g0099 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02071 | hp1 | a0001 | c0014 | t0001 | g0001 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02074 | hp1 | a0001 | c0001 | t0015 | g0163 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02074 | hp2 | a0001 | c0002 | t0018 | g0229 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02083 | hp1 | a0001 | c0001 | t0021 | g0263 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0220 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02145 | hp1 | a0002 | c0003 | t0024 | g0183 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02145 | hp2 | a0001 | c0001 | t0012 | g0149 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | CDX | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | CDX | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CDX | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02257 | hp1 | a0002 | c0003 | t0006 | g0005 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02258 | hp1 | a0001 | c0001 | t0065 | g0295 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02258 | hp2 | a0001 | c0001 | t0020 | g0009 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02280 | hp1 | a0001 | c0027 | t0062 | g0200 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02280 | hp2 | a0001 | c0001 | t0055 | g0297 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02451 | hp1 | a0001 | c0001 | t0020 | g0132 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02572 | hp2 | a0008 | c0013 | t0020 | g0091 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02602 | hp2 | a0001 | c0002 | t0004 | g0262 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02615 | hp1 | a0001 | c0001 | t0018 | g0137 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02615 | hp2 | a0001 | c0001 | t0008 | g0021 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02622 | hp1 | a0001 | c0001 | t0025 | g0046 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02622 | hp2 | a0001 | c0001 | t0026 | g0135 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02630 | hp1 | a0001 | c0001 | t0051 | g0011 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02630 | hp2 | a0001 | c0005 | t0010 | g0147 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02647 | hp2 | a0003 | c0006 | t0016 | g0182 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02698 | hp1 | a0001 | c0002 | t0018 | g0033 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02698 | hp2 | a0001 | c0002 | t0004 | g0042 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02723 | hp1 | a0001 | c0004 | t0034 | g0126 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02723 | hp2 | a0001 | c0001 | t0029 | g0023 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02735 | hp1 | a0001 | c0001 | t0040 | g0040 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02735 | hp2 | a0001 | c0002 | t0004 | g0277 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0118 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02818 | hp2 | a0001 | c0001 | t0025 | g0004 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02886 | hp1 | a0001 | c0005 | t0010 | g0148 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0222 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02896 | hp1 | a0001 | c0001 | t0035 | g0047 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02976 | hp1 | a0006 | c0008 | t0029 | g0292 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02976 | hp2 | a0001 | c0001 | t0038 | g0296 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03041 | hp2 | a0001 | c0001 | t0008 | g0193 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03098 | hp2 | a0001 | c0005 | t0010 | g0143 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03139 | hp2 | a0003 | c0006 | t0016 | g0201 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03195 | hp1 | a0001 | c0007 | t0005 | g0129 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0131 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03209 | hp2 | a0014 | c0022 | t0001 | g0025 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03225 | hp1 | a0001 | c0001 | t0049 | g0017 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03225 | hp2 | a0001 | c0005 | t0010 | g0146 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0136 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0123 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03486 | hp2 | a0002 | c0003 | t0003 | g0014 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03491 | hp1 | a0001 | c0002 | t0003 | g0244 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03491 | hp2 | a0001 | c0001 | t0019 | g0058 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03516 | hp2 | a0002 | c0003 | t0024 | g0144 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03540 | hp1 | a0001 | c0001 | t0026 | g0012 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03540 | hp2 | a0001 | c0005 | t0010 | g0141 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03579 | hp1 | a0001 | c0001 | t0052 | g0026 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03579 | hp2 | a0007 | c0012 | t0032 | g0159 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03669 | hp1 | a0001 | c0001 | t0015 | g0170 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03704 | hp1 | a0001 | c0001 | t0011 | g0102 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03704 | hp2 | a0001 | c0002 | t0003 | g0103 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03710 | hp1 | a0004 | c0009 | t0001 | g0109 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03710 | hp2 | a0001 | c0001 | t0015 | g0271 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03831 | hp1 | a0001 | c0002 | t0003 | g0272 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03927 | hp1 | a0001 | c0002 | t0027 | g0049 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03942 | hp1 | a0001 | c0002 | t0004 | g0289 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03942 | hp2 | a0001 | c0002 | t0003 | g0189 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG04115 | hp1 | a0001 | c0001 | t0042 | g0165 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG04115 | hp2 | a0001 | c0001 | t0007 | g0273 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG04199 | hp2 | a0001 | c0002 | t0053 | g0117 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG04204 | hp1 | a0004 | c0009 | t0001 | g0250 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG04204 | hp2 | a0001 | c0001 | t0031 | g0100 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG04228 | hp1 | a0001 | c0001 | t0041 | g0171 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18522 | hp2 | a0002 | c0024 | t0030 | g0020 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18612 | hp1 | a0001 | c0001 | t0011 | g0241 | EAS | CHB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | CHB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0291 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18941 | hp1 | a0001 | c0001 | t0013 | g0087 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18943 | hp1 | a0001 | c0001 | t0033 | g0248 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18943 | hp2 | a0001 | c0004 | t0037 | g0278 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18944 | hp1 | a0001 | c0001 | t0007 | g0168 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18944 | hp2 | a0001 | c0004 | t0037 | g0279 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18945 | hp2 | a0011 | c0020 | t0002 | g0054 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18947 | hp2 | a0001 | c0002 | t0004 | g0238 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18948 | hp1 | a0001 | c0001 | t0044 | g0218 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18948 | hp2 | a0001 | c0001 | t0011 | g0084 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18953 | hp2 | a0001 | c0021 | t0023 | g0194 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18959 | hp1 | a0001 | c0004 | t0061 | g0275 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18963 | hp1 | a0001 | c0001 | t0011 | g0213 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18963 | hp2 | a0001 | c0001 | t0007 | g0167 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18964 | hp1 | a0001 | c0001 | t0011 | g0105 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18964 | hp2 | a0001 | c0002 | t0030 | g0269 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18977 | hp1 | a0001 | c0001 | t0021 | g0276 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18977 | hp2 | a0001 | c0002 | t0003 | g0221 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18980 | hp1 | a0001 | c0002 | t0004 | g0249 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18980 | hp2 | a0001 | c0001 | t0023 | g0228 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18983 | hp1 | a0001 | c0002 | t0004 | g0094 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18993 | hp2 | a0001 | c0002 | t0003 | g0251 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18995 | hp1 | a0001 | c0002 | t0003 | g0267 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19000 | hp2 | a0001 | c0002 | t0004 | g0236 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19003 | hp1 | a0005 | c0010 | t0045 | g0151 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19003 | hp2 | a0001 | c0001 | t0060 | g0246 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19004 | hp2 | a0001 | c0002 | t0027 | g0190 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19009 | hp2 | a0001 | c0001 | t0043 | g0164 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19030 | hp1 | a0002 | c0003 | t0024 | g0037 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19030 | hp2 | a0001 | c0007 | t0005 | g0127 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19043 | hp1 | a0001 | c0025 | t0058 | g0038 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19043 | hp2 | a0001 | c0001 | t0016 | g0030 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19055 | hp1 | a0001 | c0004 | t0054 | g0169 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19055 | hp2 | a0001 | c0001 | t0033 | g0285 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19060 | hp1 | a0001 | c0002 | t0003 | g0270 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19060 | hp2 | a0005 | c0010 | t0046 | g0152 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19065 | hp1 | a0001 | c0001 | t0013 | g0199 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19065 | hp2 | a0001 | c0001 | t0013 | g0231 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19066 | hp2 | a0001 | c0002 | t0003 | g0268 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19074 | hp2 | a0001 | c0002 | t0031 | g0237 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19081 | hp2 | a0001 | c0002 | t0003 | g0215 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19082 | hp2 | a0001 | c0001 | t0036 | g0282 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19089 | hp2 | a0001 | c0001 | t0036 | g0138 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0162 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ASW | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA20129 | hp2 | a0002 | c0003 | t0050 | g0179 | AFR | ASW | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA20752 | hp1 | a0001 | c0001 | t0009 | g0120 | EUR | TSI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA20805 | hp2 | a0015 | c0023 | t0003 | g0130 | EUR | TSI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA20905 | hp1 | a0001 | c0001 | t0015 | g0176 | SAS | GIH | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA20905 | hp2 | a0001 | c0002 | t0004 | g0041 | SAS | GIH | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01123 | hp1 | a0001 | c0026 | t0057 | g0187 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02109 | hp2 | a0001 | c0007 | t0005 | g0185 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03471 | hp1 | a0003 | c0006 | t0016 | g0140 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG03471 | hp2 | a0006 | c0008 | t0028 | g0293 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG06807 | hp1 | a0001 | c0001 | t0063 | g0070 | AFR | USA | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | USA | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA20300 | hp1 | a0001 | c0001 | t0047 | g0051 | AFR | USA | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | USA | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
NA21309 | hp2 | a0001 | c0001 | t0035 | g0290 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0003 | g0111 | REF | REF | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0104 | REF | REF | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1744607
|
G | A | 1 | a0003 | 3 | HG02647.hp2 HG03139.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.11G>A | p.Arg4His | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 637/3976 | 11/2487 | 4/828 | chr7 | 1744607 | ||
chr7:1744885
|
G | A | 1 | a0006 | 2 | HG02976.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.289G>A | p.Gly97Ser | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 915/3976 | 289/2487 | 97/828 | chr7 | 1744885 | ||
chr7:1745543
|
G | A | 1 | a0007 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.947G>A | p.Arg316His | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1573/3976 | 947/2487 | 316/828 | chr7 | 1745543 | ||
chr7:1745902
|
G | A | 1 | a0008 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1306G>A | p.Val436Ile | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1932/3976 | 1306/2487 | 436/828 | chr7 | 1745902 | ||
chr7:1746026
|
C | T | 1 | a0015 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1430C>T | p.Ala477Val | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2056/3976 | 1430/2487 | 477/828 | chr7 | 1746026 | ||
chr7:1746484
|
G | A | 3 | a0002a0007a0009 | 9 | HG01496.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
missense_variant | MODERATE | c.1888G>A | p.Val630Met | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2514/3976 | 1888/2487 | 630/828 | chr7 | 1746484 | ||
chr7:1746494
|
C | G | 1 | a0014 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1898C>G | p.Ala633Gly | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2524/3976 | 1898/2487 | 633/828 | chr7 | 1746494 | ||
chr7:1746554
|
G | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.1958G>C | p.Arg653Pro | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2584/3976 | 1958/2487 | 653/828 | chr7 | 1746554 | ||
chr7:1746623
|
C | T | 1 | a0009 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.2027C>T | p.Ala676Val | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2653/3976 | 2027/2487 | 676/828 | chr7 | 1746623 | ||
chr7:1746661
|
G | A | 1 | a0004 | 2 | HG03710.hp1 HG04204.hp1 |
missense_variant | MODERATE | c.2065G>A | p.Val689Met | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2691/3976 | 2065/2487 | 689/828 | chr7 | 1746661 | ||
chr7:1746773
|
C | T | 1 | a0011 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.2177C>T | p.Pro726Leu | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2803/3976 | 2177/2487 | 726/828 | chr7 | 1746773 | ||
chr7:1746895
|
G | A | 1 | a0013 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.2299G>A | p.Glu767Lys | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2925/3976 | 2299/2487 | 767/828 | chr7 | 1746895 | ||
chr7:1746952
|
C | T | 1 | a0012 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.2356C>T | p.Arg786Trp | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2982/3976 | 2356/2487 | 786/828 | chr7 | 1746952 | ||
chr7:1746968
|
A | T | 1 | a0005 | 2 | NA19003.hp1 NA19060.hp2 |
missense_variant | MODERATE | c.2372A>T | p.Glu791Val | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2998/3976 | 2372/2487 | 791/828 | chr7 | 1746968 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1744656
|
C | T | 1 | a0001c0027 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.60C>T | p.His20His | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 686/3976 | 60/2487 | 20/828 | chr7 | 1744656 | ||
chr7:1744911
|
G | A | 2 | a0001c0004a0001c0011 | 6 | HG01884.hp2 HG02723.hp1 NA18943.hp2 others(3): Show |
synonymous_variant | LOW | c.315G>A | p.Ser105Ser | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 941/3976 | 315/2487 | 105/828 | chr7 | 1744911 | ||
chr7:1745280
|
C | G | 1 | a0001c0026 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.684C>G | p.Gly228Gly | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1310/3976 | 684/2487 | 228/828 | chr7 | 1745280 | ||
chr7:1745355
|
C | T | 1 | a0001c0025 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.759C>T | p.Asp253Asp | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1385/3976 | 759/2487 | 253/828 | chr7 | 1745355 | ||
chr7:1745361
|
C | T | 1 | a0001c0011 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.765C>T | p.Tyr255Tyr | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1391/3976 | 765/2487 | 255/828 | chr7 | 1745361 | ||
chr7:1745592
|
C | T | 1 | a0002c0024 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.996C>T | p.Thr332Thr | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1622/3976 | 996/2487 | 332/828 | chr7 | 1745592 | ||
chr7:1745832
|
C | T | 1 | a0001c0027 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1236C>T | p.Pro412Pro | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1862/3976 | 1236/2487 | 412/828 | chr7 | 1745832 | ||
chr7:1746066
|
C | A | 1 | a0001c0014 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1470C>A | p.Gly490Gly | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2096/3976 | 1470/2487 | 490/828 | chr7 | 1746066 | ||
chr7:1746102
|
G | A | 3 | a0001c0002a0001c0026a0015c0023 | 36 | HG00423.hp1 HG00733.hp1 HG01106.hp2 others(33): Show |
synonymous_variant | LOW | c.1506G>A | p.Ala502Ala | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2132/3976 | 1506/2487 | 502/828 | chr7 | 1746102 | ||
chr7:1746537
|
C | T | 1 | a0001c0007 | 3 | HG02109.hp2 HG03195.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1941C>T | p.Arg647Arg | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2567/3976 | 1941/2487 | 647/828 | chr7 | 1746537 | ||
chr7:1746558
|
C | T | 1 | a0001c0021 | 1 | NA18953.hp2 | synonymous_variant | LOW | c.1962C>T | p.Ala654Ala | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2588/3976 | 1962/2487 | 654/828 | chr7 | 1746558 | ||
chr7:1746987
|
C | T | 1 | a0001c0018 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.2391C>T | p.Gly797Gly | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 3017/3976 | 2391/2487 | 797/828 | chr7 | 1746987 | ||
chr7:1747065
|
G | A | 1 | a0001c0005 | 5 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
synonymous_variant | LOW | c.2469G>A | p.Ser823Ser | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 3095/3976 | 2469/2487 | 823/828 | chr7 | 1747065 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1688063
|
G | A | 1 | a0001c0001t0038 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-543G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/4 | 56534 | chr7 | 1688063 | |||||
chr7:1688110
|
C | T | 1 | a0001c0001t0065 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-496C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/4 | 56487 | chr7 | 1688110 | |||||
chr7:1688121
|
C | T | 1 | a0001c0001t0064 | 1 | HG01255.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-485C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/4 | chr7 | 1688121 | ||||||
chr7:1709095
|
A | G | 1 | a0001c0001t0063 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-451A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/4 | 35502 | chr7 | 1709095 | |||||
chr7:1709106
|
C | T | 1 | a0001c0027t0062 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-440C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/4 | 35491 | chr7 | 1709106 | |||||
chr7:1744490
|
C | A | 2 | a0001c0001t0014a0001c0001t0039 | 5 | HG00738.hp1 HG01071.hp1 HG01074.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-107C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 107 | chr7 | 1744490 | |||||
chr7:1744518
|
C | T | 2 | a0001c0004t0037a0001c0004t0061 | 3 | NA18943.hp2 NA18944.hp2 NA18959.hp1 |
5_prime_UTR_variant | MODIFIER | c.-79C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 79 | chr7 | 1744518 | |||||
chr7:1747132
|
C | T | 1 | a0001c0001t0036 | 2 | NA19082.hp2 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*49C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 49 | chr7 | 1747132 | |||||
chr7:1747182
|
T | C | 13 | a0001c0001t0007a0001c0001t0015a0001c0001t0016others(10): Show | 24 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*99T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 99 | chr7 | 1747182 | |||||
chr7:1747208
|
C | T | 1 | a0002c0003t0024 | 3 | HG02145.hp1 HG03516.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*125C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 125 | chr7 | 1747208 | |||||
chr7:1747209
|
G | A | 11 | a0001c0001t0007a0001c0001t0015a0001c0001t0017others(8): Show | 23 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*126G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 126 | chr7 | 1747209 | |||||
chr7:1747249
|
C | T | 1 | a0001c0001t0035 | 2 | HG02896.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*166C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 166 | chr7 | 1747249 | |||||
chr7:1747283
|
C | T | 2 | a0001c0001t0023a0001c0021t0023 | 3 | HG00558.hp1 NA18953.hp2 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*200C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 200 | chr7 | 1747283 | |||||
chr7:1747289
|
G | A | 1 | a0001c0001t0047 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*206G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 206 | chr7 | 1747289 | |||||
chr7:1747302
|
C | CCA | 4 | a0001c0001t0056a0001c0004t0037a0001c0004t0061others(1): Show | 5 | HG00558.hp2 HG01123.hp1 NA18943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*251_*252dupAC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | ||||
chr7:1747302
|
C | CCACA | 15 | a0001c0001t0004a0001c0001t0011a0001c0001t0031others(12): Show | 37 | HG00408.hp2 HG00544.hp1 HG00733.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*249_*252dupACAC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | ||||
chr7:1747302
|
C | CCACACA | 18 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(15): Show | 56 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*247_*252dupACACAC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | ||||
chr7:1747302
|
C | CCACACAC others(1): Show |
10 | a0001c0001t0008a0001c0001t0009a0001c0001t0015others(7): Show | 26 | HG00280.hp1 HG01099.hp2 HG01168.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*245_*252dupACACAC others(2): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | ||||
chr7:1747302
|
C | CCACACAC others(3): Show |
8 | a0001c0001t0025a0001c0001t0026a0001c0001t0038others(5): Show | 10 | HG02622.hp1 HG02622.hp2 HG02735.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*243_*252dupACACAC others(4): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | ||||
chr7:1747302
|
C | CCACACAC others(7): Show |
1 | a0001c0001t0048 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239_*252dupACACAC others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | ||||
chr7:1747302
|
CCACA | C | 1 | a0001c0001t0012 | 5 | HG00639.hp2 HG01167.hp1 HG01167.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*249_*252delACAC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 249 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | ||||
chr7:1747313
|
C | CACAG | 20 | a0001c0001t0001a0001c0001t0006a0001c0001t0013others(17): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*233_*234insGACA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 234 | INFO_REALIGN_3_PRIME | chr7 | 1747313 | ||||
chr7:1747361
|
A | C | 1 | a0001c0001t0035 | 2 | HG02896.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*278A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 278 | chr7 | 1747361 | |||||
chr7:1747367
|
G | C | 20 | a0001c0001t0001a0001c0001t0013a0001c0001t0017others(17): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*284G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 284 | chr7 | 1747367 | |||||
chr7:1747465
|
T | A | 1 | a0001c0025t0058 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*382T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 382 | chr7 | 1747465 | |||||
chr7:1747570
|
G | A | 1 | a0001c0001t0013 | 5 | HG00408.hp1 HG00423.hp2 NA18941.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*487G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 487 | chr7 | 1747570 | |||||
chr7:1747600
|
A | G | 29 | a0001c0001t0001a0001c0001t0006a0001c0001t0013others(26): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*517A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 517 | chr7 | 1747600 | |||||
chr7:1747765
|
G | A | 1 | a0001c0001t0059 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*682G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 682 | chr7 | 1747765 | |||||
chr7:1747790
|
T | C | 6 | a0001c0001t0031a0001c0001t0040a0001c0001t0041others(3): Show | 7 | HG02735.hp1 HG04204.hp2 HG04228.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*707T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 707 | chr7 | 1747790 | |||||
chr7:1747823
|
A | G | 1 | a0001c0005t0010 | 5 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*740A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 740 | chr7 | 1747823 | |||||
chr7:1747883
|
T | TA | 13 | a0001c0001t0007a0001c0001t0019a0001c0001t0020others(10): Show | 24 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*817dupA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 818 | INFO_REALIGN_3_PRIME | chr7 | 1747883 | ||||
chr7:1747883
|
TA | T | 40 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(37): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*817delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 817 | INFO_REALIGN_3_PRIME | chr7 | 1747883 | ||||
chr7:1747883
|
TAA | T | 6 | a0001c0001t0060a0001c0002t0030a0002c0003t0050others(3): Show | 6 | HG01496.hp1 HG03579.hp2 NA18522.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*816_*817delAA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 816 | INFO_REALIGN_3_PRIME | chr7 | 1747883 | ||||
chr7:1747938
|
C | A | 71 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(68): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*855C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 855 | chr7 | 1747938 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:1670395
|
T | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01361.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-549+41T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670395 | ||||||
chr7:1670531
|
G | A | 2 | a0001c0001t0025g0004a0002c0003t0006g0005 | 2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-549+177G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670531 | ||||||
chr7:1670595
|
G | T | 1 | a0001c0001t0004g0301 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-549+241G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670595 | ||||||
chr7:1670630
|
GC | G | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0003g0300others(2): Show | 5 | HG02280.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-549+280delC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1670630 | |||||
chr7:1670831
|
C | G | 2 | a0001c0001t0005g0294a0001c0001t0065g0295 | 2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-549+477C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670831 | ||||||
chr7:1670880
|
C | T | 2 | a0006c0008t0028g0293a0006c0008t0029g0292 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-549+526C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670880 | ||||||
chr7:1670922
|
C | T | 2 | a0001c0001t0006g0291a0001c0001t0035g0290 | 2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-549+568C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670922 | ||||||
chr7:1670929
|
C | G | 1 | a0001c0002t0004g0289 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-549+575C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670929 | ||||||
chr7:1670983
|
AC | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0239a0001c0001t0001g0240others(49): Show | 52 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.-549+633delC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1670983 | |||||
chr7:1671170
|
G | GC | 50 | a0001c0001t0001g0142a0001c0001t0001g0145a0001c0001t0001g0155others(47): Show | 50 | HG00280.hp1 HG00438.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.-549+827dupC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671170 | |||||
chr7:1671170
|
G | GCC | 14 | a0001c0001t0001g0188a0001c0001t0001g0192a0001c0001t0002g0198others(11): Show | 14 | HG00558.hp1 HG00558.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.-549+826_-549+827d others(4): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671170 | |||||
chr7:1671170
|
G | GCCC | 23 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0210others(20): Show | 23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-549+825_-549+827d others(5): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671170 | |||||
chr7:1671170
|
G | GCCCC | 15 | a0001c0001t0001g0230a0001c0001t0001g0234a0001c0001t0001g0235others(12): Show | 15 | HG00438.hp2 HG02074.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.-549+824_-549+827d others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671170 | |||||
chr7:1671170
|
GC | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(67): Show | 70 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-549+827delC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671170 | |||||
chr7:1671362
|
G | C | 2 | a0001c0001t0025g0004a0002c0003t0006g0005 | 2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-549+1008G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671362 | ||||||
chr7:1671403
|
T | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(76): Show | 79 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-549+1049T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671403 | ||||||
chr7:1671406
|
A | G | 1 | a0001c0026t0057g0187 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-549+1052A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671406 | ||||||
chr7:1671426
|
T | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(78): Show | 81 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-549+1072T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671426 | ||||||
chr7:1671637
|
GA | G | 9 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0003g0024others(6): Show | 9 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-549+1286delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671637 | |||||
chr7:1671958
|
T | G | 38 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0155others(35): Show | 38 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.-549+1604T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671958 | ||||||
chr7:1671990
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.-549+1636T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671990 | ||||||
chr7:1671992
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.-549+1638T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671992 | ||||||
chr7:1671993
|
C | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.-549+1639C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671993 | ||||||
chr7:1671995
|
A | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.-549+1641A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671995 | ||||||
chr7:1672061
|
C | G | 1 | a0001c0001t0002g0223 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-549+1707C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672061 | ||||||
chr7:1672066
|
G | A | 2 | a0001c0001t0006g0031a0001c0025t0058g0038 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-549+1712G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672066 | ||||||
chr7:1672072
|
G | C | 3 | a0001c0001t0001g0188a0001c0001t0003g0039a0001c0001t0005g0150 | 3 | HG01109.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-549+1718G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672072 | ||||||
chr7:1672077
|
G | A | 1 | a0001c0001t0006g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-549+1723G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672077 | ||||||
chr7:1672145
|
G | C | 1 | a0009c0015t0032g0191 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-549+1791G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672145 | ||||||
chr7:1672418
|
C | T | 3 | a0001c0001t0003g0186a0001c0005t0010g0141a0003c0006t0016g0140 | 3 | HG03471.hp1 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-549+2064C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672418 | ||||||
chr7:1672460
|
C | T | 2 | a0001c0001t0001g0283a0001c0001t0003g0039 | 2 | HG01109.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-549+2106C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672460 | ||||||
chr7:1672494
|
T | C | 7 | a0001c0001t0001g0142a0001c0001t0001g0145a0001c0005t0010g0143others(4): Show | 7 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-549+2140T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672494 | ||||||
chr7:1672699
|
C | T | 3 | a0001c0001t0001g0139a0001c0001t0036g0138a0001c0001t0036g0282 | 3 | NA18970.hp1 NA19082.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.-549+2345C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672699 | ||||||
chr7:1672735
|
C | A | 2 | a0001c0002t0018g0032a0001c0002t0018g0033 | 2 | HG00423.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-549+2381C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672735 | ||||||
chr7:1672737
|
C | T | 1 | a0001c0001t0003g0300 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-549+2383C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672737 | ||||||
chr7:1672850
|
A | G | 41 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0125others(38): Show | 41 | HG01099.hp2 HG01167.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.-549+2496A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672850 | ||||||
chr7:1672923
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-549+2569C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672923 | ||||||
chr7:1672934
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-549+2580C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672934 | ||||||
chr7:1672997
|
G | A | 1 | a0001c0001t0040g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-549+2643G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672997 | ||||||
chr7:1673054
|
G | A | 1 | a0001c0001t0003g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-549+2700G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673054 | ||||||
chr7:1673093
|
C | CCT | 128 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(125): Show | 128 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-549+2740_-549+274 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1673093 | |||||
chr7:1673093
|
C | CT | 83 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(80): Show | 83 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-549+2739_-549+274 others(5): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673093 | ||||||
chr7:1673093
|
C | T | 4 | a0001c0001t0013g0199a0001c0002t0004g0236a0001c0002t0004g0238others(1): Show | 4 | NA18947.hp2 NA19000.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-549+2739C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673093 | ||||||
chr7:1673184
|
G | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(170): Show | 173 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.-549+2830G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673184 | ||||||
chr7:1673234
|
C | G | 1 | a0001c0001t0003g0300 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-549+2880C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673234 | ||||||
chr7:1673250
|
G | A | 1 | a0001c0001t0006g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-549+2896G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673250 | ||||||
chr7:1673303
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0142a0001c0001t0003g0039others(2): Show | 5 | HG01109.hp2 HG02055.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-549+2949A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673303 | ||||||
chr7:1673373
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-549+3019G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673373 | ||||||
chr7:1673519
|
C | A | 1 | a0001c0001t0019g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-549+3165C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673519 | ||||||
chr7:1673584
|
G | A | 19 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0155others(16): Show | 19 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-549+3230G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673584 | ||||||
chr7:1673639
|
C | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108 | 3 | HG00140.hp2 HG03831.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-549+3285C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673639 | ||||||
chr7:1673804
|
T | C | 1 | a0002c0003t0024g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-549+3450T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673804 | ||||||
chr7:1673813
|
G | A | 1 | a0004c0009t0001g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-549+3459G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673813 | ||||||
chr7:1673996
|
G | A | 3 | a0001c0001t0005g0294a0001c0001t0048g0124a0001c0001t0055g0297 | 3 | HG01243.hp2 HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-549+3642G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673996 | ||||||
chr7:1674053
|
G | A | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-549+3699G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674053 | ||||||
chr7:1674082
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0142 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-549+3728C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674082 | ||||||
chr7:1674250
|
G | A | 1 | a0001c0002t0003g0110 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-549+3896G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674250 | ||||||
chr7:1674401
|
G | A | 3 | a0001c0001t0001g0192a0001c0001t0008g0193a0009c0015t0032g0191 | 3 | HG01496.hp1 HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-549+4047G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674401 | ||||||
chr7:1674439
|
G | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(168): Show | 171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-549+4085G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674439 | ||||||
chr7:1674500
|
A | G | 1 | a0001c0027t0062g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-549+4146A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674500 | ||||||
chr7:1674629
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0047g0051 | 2 | HG01109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-549+4275G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674629 | ||||||
chr7:1674636
|
C | G | 1 | a0001c0001t0012g0184 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-549+4282C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674636 | ||||||
chr7:1674641
|
G | A | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-549+4287G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674641 | ||||||
chr7:1674812
|
G | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(138): Show | 141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-549+4458G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674812 | ||||||
chr7:1674844
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0053others(2): Show | 5 | HG00741.hp2 HG01361.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-549+4490G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674844 | ||||||
chr7:1674878
|
T | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0005g0162others(3): Show | 6 | HG01081.hp1 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-549+4524T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674878 | ||||||
chr7:1674911
|
A | G | 1 | a0001c0001t0011g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-549+4557A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674911 | ||||||
chr7:1674949
|
G | A | 1 | a0001c0027t0062g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-549+4595G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674949 | ||||||
chr7:1675023
|
G | A | 1 | a0001c0021t0023g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-549+4669G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675023 | ||||||
chr7:1675027
|
T | TCCCCACA others(24): Show |
169 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(166): Show | 169 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-549+4674_-549+470 others(35): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1675027 | |||||
chr7:1675043
|
C | CCGGGCTC others(24): Show |
1 | a0001c0001t0013g0231 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-549+4704_-549+470 others(35): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1675043 | |||||
chr7:1675067
|
T | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(170): Show | 173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-549+4713T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675067 | ||||||
chr7:1675094
|
C | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0015others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.-549+4740C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675094 | ||||||
chr7:1675208
|
T | A | 48 | a0001c0001t0001g0008a0001c0001t0001g0239a0001c0001t0001g0240others(45): Show | 48 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.-549+4854T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675208 | ||||||
chr7:1675215
|
T | C | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(298): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.-549+4861T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675215 | ||||||
chr7:1675272
|
G | A | 4 | a0001c0001t0008g0123a0001c0001t0008g0131a0001c0001t0020g0132others(1): Show | 4 | HG02451.hp1 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-549+4918G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675272 | ||||||
chr7:1675326
|
T | C | 21 | a0001c0001t0001g0125a0001c0001t0001g0145a0001c0001t0001g0298others(18): Show | 21 | HG01168.hp1 HG01169.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-549+4972T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675326 | ||||||
chr7:1675332
|
G | A | 3 | a0001c0001t0006g0118a0001c0001t0016g0030a0002c0003t0024g0037 | 3 | HG02818.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-549+4978G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675332 | ||||||
chr7:1675360
|
C | T | 2 | a0001c0001t0012g0184a0002c0003t0024g0183 | 2 | HG01167.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-549+5006C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675360 | ||||||
chr7:1675406
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-549+5052C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675406 | ||||||
chr7:1675477
|
C | T | 1 | a0001c0011t0034g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-549+5123C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675477 | ||||||
chr7:1675556
|
C | T | 1 | a0001c0002t0004g0238 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-549+5202C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675556 | ||||||
chr7:1675708
|
G | A | 3 | a0001c0001t0001g0192a0001c0001t0008g0193a0009c0015t0032g0191 | 3 | HG01496.hp1 HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-549+5354G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675708 | ||||||
chr7:1675735
|
C | T | 1 | a0003c0006t0016g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-549+5381C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675735 | ||||||
chr7:1675738
|
T | C | 1 | a0002c0003t0050g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-549+5384T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675738 | ||||||
chr7:1675841
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-549+5487C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675841 | ||||||
chr7:1675855
|
C | T | 11 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0186others(8): Show | 11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-549+5501C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675855 | ||||||
chr7:1675883
|
C | T | 1 | a0001c0002t0003g0103 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-549+5529C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675883 | ||||||
chr7:1676011
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-549+5657A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676011 | ||||||
chr7:1676029
|
C | T | 3 | a0001c0001t0001g0299a0001c0001t0003g0300a0001c0001t0038g0296 | 3 | HG02559.hp1 HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-549+5675C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676029 | ||||||
chr7:1676156
|
G | C | 1 | a0011c0020t0002g0054 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-549+5802G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676156 | ||||||
chr7:1676263
|
C | T | 1 | a0001c0001t0011g0102 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-549+5909C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676263 | ||||||
chr7:1676435
|
C | T | 3 | a0001c0001t0006g0118a0001c0001t0016g0030a0002c0003t0050g0179 | 3 | HG02818.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-549+6081C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676435 | ||||||
chr7:1676448
|
G | A | 1 | a0001c0001t0016g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-549+6094G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676448 | ||||||
chr7:1676580
|
G | T | 1 | a0001c0011t0034g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-549+6226G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676580 | ||||||
chr7:1676642
|
C | A | 1 | a0001c0001t0001g0288 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-549+6288C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676642 | ||||||
chr7:1676718
|
G | A | 3 | a0001c0001t0005g0150a0001c0001t0019g0122a0001c0001t0020g0009 | 3 | HG01099.hp2 HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-549+6364G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676718 | ||||||
chr7:1676854
|
C | T | 1 | a0002c0003t0003g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-549+6500C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676854 | ||||||
chr7:1676934
|
C | T | 1 | a0001c0001t0005g0220 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-549+6580C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676934 | ||||||
chr7:1677025
|
C | A | 51 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0158others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-549+6671C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677025 | ||||||
chr7:1677037
|
G | A | 1 | a0001c0001t0006g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-549+6683G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677037 | ||||||
chr7:1677043
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-549+6689A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677043 | ||||||
chr7:1677114
|
T | C | 2 | a0005c0010t0045g0151a0005c0010t0046g0152 | 2 | NA19003.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-549+6760T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677114 | ||||||
chr7:1677203
|
C | A | 2 | a0001c0001t0001g0299a0001c0001t0038g0296 | 2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-549+6849C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677203 | ||||||
chr7:1677346
|
T | C | 11 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0186others(8): Show | 11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-549+6992T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677346 | ||||||
chr7:1677415
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-549+7061T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677415 | ||||||
chr7:1677478
|
G | T | 3 | a0001c0001t0025g0004a0001c0001t0065g0295a0002c0003t0006g0005 | 3 | HG02257.hp1 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-549+7124G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677478 | ||||||
chr7:1677554
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-549+7200G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677554 | ||||||
chr7:1677577
|
C | G | 1 | a0001c0011t0034g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-549+7223C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677577 | ||||||
chr7:1677650
|
C | T | 2 | a0001c0025t0058g0038a0002c0003t0024g0037 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-549+7296C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677650 | ||||||
chr7:1677686
|
GCCGATGT others(8): Show |
G | 1 | a0001c0001t0001g0008 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-549+7333_-549+734 others(19): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677686 | ||||||
chr7:1677871
|
G | A | 19 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0045others(16): Show | 19 | HG01099.hp2 HG01255.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-549+7517G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677871 | ||||||
chr7:1677955
|
A | G | 1 | a0001c0001t0005g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-549+7601A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677955 | ||||||
chr7:1678042
|
C | A | 9 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0186others(6): Show | 9 | HG02451.hp1 HG02622.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-549+7688C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678042 | ||||||
chr7:1678081
|
G | T | 2 | a0001c0001t0021g0276a0001c0004t0061g0275 | 2 | NA18959.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-549+7727G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678081 | ||||||
chr7:1678096
|
C | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0192others(56): Show | 59 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.-549+7742C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678096 | ||||||
chr7:1678148
|
G | A | 1 | a0001c0001t0013g0231 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-549+7794G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678148 | ||||||
chr7:1678243
|
A | C | 1 | a0001c0001t0005g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-549+7889A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678243 | ||||||
chr7:1678355
|
G | A | 2 | a0001c0025t0058g0038a0002c0003t0024g0037 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-549+8001G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678355 | ||||||
chr7:1678457
|
T | C | 1 | a0002c0003t0050g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-549+8103T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678457 | ||||||
chr7:1678746
|
C | T | 1 | a0001c0002t0031g0237 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-549+8392C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678746 | ||||||
chr7:1678759
|
C | T | 1 | a0001c0001t0017g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-549+8405C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678759 | ||||||
chr7:1679085
|
G | T | 1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-549+8731G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679085 | ||||||
chr7:1679147
|
G | A | 1 | a0002c0003t0024g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-549+8793G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679147 | ||||||
chr7:1679158
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-549+8804C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679158 | ||||||
chr7:1679173
|
ACG | A | 7 | a0001c0001t0012g0184a0001c0001t0016g0030a0001c0001t0025g0004others(4): Show | 7 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-549+8825_-549+882 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1679173 | |||||
chr7:1679177
|
G | GCA | 23 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(20): Show | 23 | HG00408.hp2 HG01106.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.-549+8824_-549+882 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1679177 | |||||
chr7:1679179
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(174): Show | 177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.-549+8825G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679179 | ||||||
chr7:1679179
|
G | GCA | 19 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0045others(16): Show | 19 | HG00639.hp2 HG01099.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-549+8842_-549+884 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1679179 | |||||
chr7:1679181
|
A | G | 2 | a0001c0001t0047g0051a0001c0002t0007g0050 | 2 | HG01975.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-549+8827A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679181 | ||||||
chr7:1679297
|
G | A | 1 | a0001c0001t0016g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-548-8761G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679297 | ||||||
chr7:1679332
|
G | A | 1 | a0001c0001t0015g0163 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-548-8726G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679332 | ||||||
chr7:1679451
|
G | A | 2 | a0001c0001t0003g0133a0001c0001t0003g0134 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-548-8607G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679451 | ||||||
chr7:1679541
|
C | T | 1 | a0002c0003t0006g0005 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-548-8517C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679541 | ||||||
chr7:1679556
|
C | A | 1 | a0001c0001t0033g0285 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-548-8502C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679556 | ||||||
chr7:1679651
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-548-8407C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679651 | ||||||
chr7:1679685
|
C | T | 11 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0186others(8): Show | 11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-548-8373C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679685 | ||||||
chr7:1679704
|
C | T | 1 | a0002c0003t0024g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-548-8354C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679704 | ||||||
chr7:1679726
|
T | C | 3 | a0001c0001t0006g0028a0001c0001t0016g0030a0002c0003t0050g0179 | 3 | HG02896.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-548-8332T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679726 | ||||||
chr7:1679753
|
C | T | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-548-8305C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679753 | ||||||
chr7:1679919
|
G | A | 2 | a0001c0001t0012g0211a0001c0001t0012g0212 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-548-8139G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679919 | ||||||
chr7:1680088
|
C | T | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-548-7970C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680088 | ||||||
chr7:1680097
|
G | A | 25 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0002g0242others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-548-7961G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680097 | ||||||
chr7:1680120
|
C | T | 5 | a0001c0001t0012g0184a0001c0001t0025g0004a0001c0001t0065g0295others(2): Show | 5 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-548-7938C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680120 | ||||||
chr7:1680304
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-548-7754C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680304 | ||||||
chr7:1680313
|
C | T | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-548-7745C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680313 | ||||||
chr7:1680616
|
T | G | 42 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0158others(39): Show | 42 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-548-7442T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680616 | ||||||
chr7:1680618
|
A | G | 5 | a0001c0002t0003g0267a0001c0002t0003g0268a0001c0002t0003g0270others(2): Show | 5 | NA18964.hp2 NA18995.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-548-7440A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680618 | ||||||
chr7:1680655
|
A | G | 2 | a0001c0001t0031g0100a0004c0009t0001g0109 | 2 | HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-548-7403A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680655 | ||||||
chr7:1680686
|
C | T | 3 | a0001c0001t0006g0128a0001c0001t0009g0121a0001c0007t0005g0129 | 3 | HG01891.hp1 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-548-7372C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680686 | ||||||
chr7:1680706
|
C | T | 63 | a0001c0001t0001g0008a0001c0001t0001g0239a0001c0001t0001g0240others(60): Show | 63 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.-548-7352C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680706 | ||||||
chr7:1680737
|
A | AT | 8 | a0001c0001t0001g0142a0001c0001t0001g0230a0001c0001t0001g0266others(5): Show | 8 | HG00438.hp2 HG00621.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-548-7299dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1680737 | |||||
chr7:1680737
|
AT | A | 29 | a0001c0001t0001g0008a0001c0001t0001g0045a0001c0001t0001g0059others(26): Show | 29 | HG00140.hp2 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.-548-7299delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1680737 | |||||
chr7:1681122
|
A | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-548-6936A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681122 | ||||||
chr7:1681178
|
G | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-548-6880G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681178 | ||||||
chr7:1681207
|
T | C | 2 | a0001c0001t0012g0184a0002c0003t0024g0183 | 2 | HG01167.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-548-6851T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681207 | ||||||
chr7:1681222
|
G | A | 2 | a0001c0001t0002g0172a0001c0001t0039g0173 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-548-6836G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681222 | ||||||
chr7:1681333
|
A | AG | 21 | a0001c0001t0001g0125a0001c0001t0001g0145a0001c0001t0001g0298others(18): Show | 21 | HG01168.hp1 HG01169.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-548-6723dupG | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1681333 | |||||
chr7:1681384
|
A | G | 3 | a0001c0001t0001g0299a0001c0001t0003g0300a0001c0001t0038g0296 | 3 | HG02559.hp1 HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-548-6674A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681384 | ||||||
chr7:1681694
|
C | T | 4 | a0001c0001t0012g0184a0001c0001t0025g0004a0002c0003t0006g0005others(1): Show | 4 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-548-6364C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681694 | ||||||
chr7:1681744
|
G | C | 2 | a0001c0001t0001g0299a0001c0001t0003g0300 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-548-6314G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681744 | ||||||
chr7:1681910
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-548-6148T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681910 | ||||||
chr7:1682266
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-548-5792A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682266 | ||||||
chr7:1682440
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-548-5618T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682440 | ||||||
chr7:1682561
|
C | T | 15 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(12): Show | 15 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-548-5497C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682561 | ||||||
chr7:1682574
|
G | A | 1 | a0001c0001t0052g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-548-5484G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682574 | ||||||
chr7:1682608
|
AT | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(286): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-548-5432delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1682608 | |||||
chr7:1682633
|
A | G | 17 | a0001c0001t0001g0145a0001c0001t0003g0133a0001c0001t0003g0134others(14): Show | 17 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.-548-5425A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682633 | ||||||
chr7:1682916
|
G | A | 2 | a0001c0001t0001g0066a0001c0018t0001g0065 | 2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-548-5142G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682916 | ||||||
chr7:1683055
|
T | C | 15 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(12): Show | 15 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-548-5003T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683055 | ||||||
chr7:1683076
|
T | C | 3 | a0001c0001t0065g0295a0001c0025t0058g0038a0002c0003t0050g0179 | 3 | HG02258.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-548-4982T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683076 | ||||||
chr7:1683175
|
C | CT | 30 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0002g0115others(27): Show | 30 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-548-4872dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1683175 | |||||
chr7:1683466
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-548-4592G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683466 | ||||||
chr7:1683502
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-548-4556T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683502 | ||||||
chr7:1683569
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-548-4489A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683569 | ||||||
chr7:1683753
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-548-4305G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683753 | ||||||
chr7:1684070
|
A | C | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-548-3988A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684070 | ||||||
chr7:1684154
|
A | G | 1 | a0001c0001t0006g0291 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-548-3904A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684154 | ||||||
chr7:1684247
|
C | T | 2 | a0001c0007t0005g0127a0001c0007t0005g0185 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-548-3811C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684247 | ||||||
chr7:1684388
|
A | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-548-3670A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684388 | ||||||
chr7:1684454
|
A | G | 29 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0002g0242others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-548-3604A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684454 | ||||||
chr7:1684657
|
C | T | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-548-3401C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684657 | ||||||
chr7:1684837
|
A | G | 1 | a0003c0006t0016g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-548-3221A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684837 | ||||||
chr7:1684896
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-548-3162A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684896 | ||||||
chr7:1684904
|
A | T | 1 | a0001c0001t0005g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-548-3154A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684904 | ||||||
chr7:1684934
|
A | G | 10 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(7): Show | 10 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-548-3124A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684934 | ||||||
chr7:1685119
|
G | C | 1 | a0001c0002t0004g0153 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-548-2939G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1685119 | ||||||
chr7:1685221
|
A | G | 1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-548-2837A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1685221 | ||||||
chr7:1685312
|
G | A | 1 | a0001c0001t0009g0121 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-548-2746G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1685312 | ||||||
chr7:1685774
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0060g0246 | 2 | NA18946.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-548-2284G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1685774 | ||||||
chr7:1686020
|
A | G | 44 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0158others(41): Show | 44 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.-548-2038A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686020 | ||||||
chr7:1686059
|
CT | C | 58 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(55): Show | 58 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-548-1989delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1686059 | |||||
chr7:1686097
|
C | T | 9 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0055g0297others(6): Show | 9 | HG01884.hp2 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-548-1961C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686097 | ||||||
chr7:1686115
|
T | C | 24 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0002g0242others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.-548-1943T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686115 | ||||||
chr7:1686311
|
G | GT | 12 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0001g0235others(9): Show | 12 | HG00621.hp2 HG00738.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.-548-1728dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1686311 | |||||
chr7:1686313
|
T | TC | 54 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(51): Show | 54 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-548-1745_-548-174 others(5): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686313 | ||||||
chr7:1686314
|
T | C | 1 | a0001c0001t0040g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-548-1744T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686314 | ||||||
chr7:1686924
|
A | C | 1 | a0001c0001t0014g0097 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-548-1134A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686924 | ||||||
chr7:1686935
|
G | T | 1 | a0003c0006t0016g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-548-1123G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686935 | ||||||
chr7:1687135
|
G | A | 4 | a0001c0001t0001g0299a0001c0001t0003g0300a0001c0001t0006g0031others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-548-923G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1687135 | ||||||
chr7:1687348
|
A | AT | 10 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(7): Show | 10 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-548-698dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1687348 | |||||
chr7:1687348
|
AT | A | 13 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0186others(10): Show | 13 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-548-698delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1687348 | |||||
chr7:1687417
|
A | T | 1 | a0001c0002t0001g0243 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-548-641A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1687417 | ||||||
chr7:1687465
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0053 | 2 | HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-548-593C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1687465 | ||||||
chr7:1687502
|
C | G | 3 | a0001c0001t0065g0295a0001c0025t0058g0038a0002c0003t0050g0179 | 3 | HG02258.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-548-556C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1687502 | ||||||
chr7:1688031
|
A | AT | 31 | a0001c0001t0001g0015a0001c0001t0001g0096a0001c0001t0001g0125others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG01168.hp1 others(28): Show |
splice_region_variant&intron_variant | LOW | c.-548-5dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1688031 | |||||
chr7:1688031
|
AT | A | 15 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(12): Show | 15 | HG01167.hp2 HG02145.hp1 HG02451.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.-548-5delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1688031 | |||||
chr7:1688031
|
ATTTTTTT others(1): Show |
A | 26 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0003g0039others(23): Show | 26 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(23): Show |
splice_region_variant&intron_variant | LOW | c.-548-12_-548-5delT others(7): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1688031 | |||||
chr7:1688031
|
ATTTTTTT others(2): Show |
A | 16 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0003g0133others(13): Show | 16 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.-548-13_-548-5delT others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1688031 | |||||
chr7:1688352
|
G | C | 3 | a0001c0001t0002g0247a0001c0002t0003g0244a0001c0002t0004g0277 | 3 | HG02735.hp2 HG03491.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-456+202G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1688352 | ||||||
chr7:1688509
|
G | A | 2 | a0001c0001t0065g0295a0001c0025t0058g0038 | 2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-456+359G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1688509 | ||||||
chr7:1688567
|
C | A | 1 | a0001c0001t0005g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-456+417C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1688567 | ||||||
chr7:1688686
|
A | G | 1 | a0001c0027t0062g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-456+536A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1688686 | ||||||
chr7:1689157
|
G | A | 1 | a0003c0006t0016g0140 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-456+1007G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689157 | ||||||
chr7:1689255
|
T | C | 68 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(65): Show | 68 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-456+1105T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689255 | ||||||
chr7:1689417
|
G | A | 1 | a0001c0001t0008g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-456+1267G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689417 | ||||||
chr7:1689448
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-456+1298C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689448 | ||||||
chr7:1689740
|
C | T | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+1590C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689740 | ||||||
chr7:1689997
|
C | T | 14 | a0001c0001t0002g0209a0001c0001t0004g0205a0001c0001t0004g0206others(11): Show | 14 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.-456+1847C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689997 | ||||||
chr7:1690009
|
A | G | 15 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(12): Show | 15 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-456+1859A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690009 | ||||||
chr7:1690046
|
T | C | 47 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-456+1896T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690046 | ||||||
chr7:1690060
|
A | C | 3 | a0001c0001t0006g0028a0001c0001t0016g0030a0002c0003t0050g0179 | 3 | HG02896.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-456+1910A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690060 | ||||||
chr7:1690065
|
A | T | 15 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(12): Show | 15 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-456+1915A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690065 | ||||||
chr7:1690118
|
C | T | 2 | a0001c0001t0065g0295a0001c0025t0058g0038 | 2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-456+1968C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690118 | ||||||
chr7:1690217
|
T | A | 159 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0018others(156): Show | 159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.-456+2067T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690217 | ||||||
chr7:1690333
|
G | C | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+2183G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690333 | ||||||
chr7:1690450
|
G | C | 1 | a0001c0001t0011g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-456+2300G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690450 | ||||||
chr7:1690495
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-456+2345A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690495 | ||||||
chr7:1690522
|
G | A | 2 | a0001c0001t0006g0028a0001c0001t0016g0030 | 2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-456+2372G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690522 | ||||||
chr7:1690726
|
C | T | 75 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(72): Show | 75 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.-456+2576C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690726 | ||||||
chr7:1690927
|
T | C | 2 | a0001c0001t0006g0028a0001c0001t0016g0030 | 2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-456+2777T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690927 | ||||||
chr7:1690947
|
G | T | 2 | a0001c0001t0005g0136a0001c0001t0048g0124 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-456+2797G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690947 | ||||||
chr7:1690966
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-456+2816A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690966 | ||||||
chr7:1691049
|
TAA | T | 4 | a0001c0001t0001g0299a0001c0001t0003g0300a0001c0001t0038g0296others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-456+2901_-456+290 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1691049 | |||||
chr7:1691116
|
C | T | 2 | a0001c0001t0065g0295a0001c0025t0058g0038 | 2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-456+2966C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691116 | ||||||
chr7:1691133
|
G | T | 2 | a0001c0001t0006g0028a0001c0001t0016g0030 | 2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-456+2983G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691133 | ||||||
chr7:1691568
|
T | G | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-456+3418T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691568 | ||||||
chr7:1691637
|
T | A | 1 | a0015c0023t0003g0130 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-456+3487T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691637 | ||||||
chr7:1691651
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-456+3501C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691651 | ||||||
chr7:1691876
|
C | T | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+3726C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691876 | ||||||
chr7:1692044
|
G | A | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+3894G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692044 | ||||||
chr7:1692055
|
G | A | 1 | a0001c0001t0043g0164 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-456+3905G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692055 | ||||||
chr7:1692230
|
A | G | 29 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0003g0039others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-456+4080A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692230 | ||||||
chr7:1692300
|
C | T | 6 | a0001c0001t0003g0016a0001c0001t0003g0186a0001c0001t0012g0149others(3): Show | 6 | HG02145.hp2 HG02647.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-456+4150C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692300 | ||||||
chr7:1692326
|
C | T | 2 | a0001c0001t0001g0018a0001c0001t0008g0010 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-456+4176C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692326 | ||||||
chr7:1692374
|
A | G | 65 | a0001c0001t0001g0008a0001c0001t0001g0239a0001c0001t0001g0240others(62): Show | 65 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.-456+4224A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692374 | ||||||
chr7:1692470
|
C | A | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-456+4320C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692470 | ||||||
chr7:1692491
|
G | T | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+4341G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692491 | ||||||
chr7:1692509
|
A | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-456+4359A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692509 | ||||||
chr7:1692811
|
G | A | 1 | a0001c0001t0060g0246 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-456+4661G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692811 | ||||||
chr7:1693029
|
A | G | 11 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0186others(8): Show | 11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-456+4879A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693029 | ||||||
chr7:1693306
|
C | T | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-456+5156C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693306 | ||||||
chr7:1693346
|
G | A | 1 | a0001c0001t0013g0274 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-456+5196G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693346 | ||||||
chr7:1693460
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-456+5310C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693460 | ||||||
chr7:1693466
|
G | T | 56 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0252others(53): Show | 56 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.-456+5316G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693466 | ||||||
chr7:1693546
|
C | T | 45 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0158others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-456+5396C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693546 | ||||||
chr7:1693556
|
C | T | 25 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-456+5406C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693556 | ||||||
chr7:1693591
|
G | T | 1 | a0001c0002t0004g0094 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-456+5441G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693591 | ||||||
chr7:1693624
|
C | T | 1 | a0001c0001t0012g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-456+5474C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693624 | ||||||
chr7:1693670
|
C | T | 1 | a0001c0001t0005g0294 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-456+5520C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693670 | ||||||
chr7:1693788
|
G | C | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-456+5638G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693788 | ||||||
chr7:1693838
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG01934.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-456+5688G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693838 | ||||||
chr7:1693997
|
C | T | 1 | a0001c0001t0006g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-456+5847C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693997 | ||||||
chr7:1694009
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+5859C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694009 | ||||||
chr7:1694142
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+5992C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694142 | ||||||
chr7:1694159
|
T | C | 2 | a0001c0001t0012g0149a0003c0006t0016g0182 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-456+6009T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694159 | ||||||
chr7:1694179
|
C | T | 3 | a0001c0001t0007g0273a0001c0002t0003g0272a0001c0002t0027g0049 | 3 | HG03831.hp1 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-456+6029C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694179 | ||||||
chr7:1694310
|
C | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0053others(2): Show | 5 | HG00741.hp2 HG01361.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-456+6160C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694310 | ||||||
chr7:1694370
|
C | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+6220C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694370 | ||||||
chr7:1694413
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-456+6263A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694413 | ||||||
chr7:1694555
|
G | A | 1 | a0001c0001t0014g0181 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-456+6405G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694555 | ||||||
chr7:1694559
|
C | T | 46 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0158others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-456+6409C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694559 | ||||||
chr7:1694587
|
G | A | 1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+6437G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694587 | ||||||
chr7:1694665
|
C | T | 2 | a0001c0002t0003g0103a0001c0002t0003g0110 | 2 | HG01516.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-456+6515C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694665 | ||||||
chr7:1694724
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-456+6574G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694724 | ||||||
chr7:1694868
|
A | G | 19 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(16): Show | 19 | HG01167.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-456+6718A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694868 | ||||||
chr7:1694874
|
A | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+6724A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694874 | ||||||
chr7:1695039
|
T | C | 11 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0186others(8): Show | 11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-456+6889T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695039 | ||||||
chr7:1695072
|
AGACGGCT others(3): Show |
A | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+6925_-456+693 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1695072 | |||||
chr7:1695076
|
G | A | 11 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0186others(8): Show | 11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-456+6926G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695076 | ||||||
chr7:1695134
|
G | C | 2 | a0001c0001t0006g0118a0003c0006t0016g0140 | 2 | HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-456+6984G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695134 | ||||||
chr7:1695680
|
G | A | 1 | a0001c0001t0006g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-456+7530G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695680 | ||||||
chr7:1695703
|
G | A | 2 | a0001c0001t0012g0149a0003c0006t0016g0182 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-456+7553G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695703 | ||||||
chr7:1695747
|
C | CA | 140 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0029others(137): Show | 140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-456+7622dupA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1695747 | |||||
chr7:1695747
|
C | CAA | 67 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0019others(64): Show | 67 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-456+7621_-456+762 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1695747 | |||||
chr7:1695747
|
C | CAAA | 12 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0158others(9): Show | 12 | HG00544.hp1 HG02145.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-456+7620_-456+762 others(7): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1695747 | |||||
chr7:1695762
|
A | C | 10 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0186others(7): Show | 10 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-456+7612A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695762 | ||||||
chr7:1695786
|
G | T | 1 | a0001c0001t0001g0299 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-456+7636G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695786 | ||||||
chr7:1695836
|
T | A | 11 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0186others(8): Show | 11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-456+7686T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695836 | ||||||
chr7:1695919
|
C | T | 1 | a0001c0001t0005g0219 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-456+7769C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695919 | ||||||
chr7:1695970
|
C | A | 74 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-456+7820C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695970 | ||||||
chr7:1695977
|
C | T | 1 | a0001c0002t0003g0189 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-456+7827C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695977 | ||||||
chr7:1696015
|
C | T | 1 | a0001c0002t0004g0153 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-456+7865C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696015 | ||||||
chr7:1696146
|
G | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0204others(31): Show | 34 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.-456+7996G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696146 | ||||||
chr7:1696160
|
C | CAG | 10 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0006g0028others(7): Show | 10 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-456+8025_-456+802 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696160 | |||||
chr7:1696175
|
A | AGT | 16 | a0001c0001t0001g0018a0001c0001t0003g0039a0001c0001t0003g0133others(13): Show | 16 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-456+8043_-456+804 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696175 | |||||
chr7:1696175
|
A | AGTGTGTG others(3): Show |
3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8035_-456+804 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696175 | |||||
chr7:1696175
|
A | T | 1 | a0001c0004t0034g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-456+8025A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696175 | ||||||
chr7:1696191
|
T | C | 1 | a0001c0027t0062g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-456+8041T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696191 | ||||||
chr7:1696195
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8045C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696195 | ||||||
chr7:1696219
|
A | C | 24 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0006g0291others(21): Show | 24 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.-456+8069A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696219 | ||||||
chr7:1696266
|
G | C | 1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+8116G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696266 | ||||||
chr7:1696277
|
G | GGA | 4 | a0001c0001t0001g0298a0001c0001t0035g0290a0001c0001t0055g0297others(1): Show | 4 | HG02280.hp2 NA19003.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-456+8145_-456+814 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696277 | |||||
chr7:1696277
|
GGAGA | G | 16 | a0001c0001t0001g0018a0001c0001t0001g0158a0001c0001t0001g0160others(13): Show | 16 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.-456+8143_-456+814 others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696277 | |||||
chr7:1696352
|
G | C | 1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+8202G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696352 | ||||||
chr7:1696367
|
G | A | 2 | a0001c0001t0006g0291a0001c0001t0035g0290 | 2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-456+8217G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696367 | ||||||
chr7:1696392
|
C | CT | 7 | a0001c0001t0001g0077a0001c0001t0002g0071a0001c0001t0002g0115others(4): Show | 7 | HG00423.hp2 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-456+8258dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696392 | |||||
chr7:1696514
|
C | A | 1 | a0001c0001t0047g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-456+8364C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696514 | ||||||
chr7:1696562
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8412C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696562 | ||||||
chr7:1696613
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8463G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696613 | ||||||
chr7:1696665
|
G | C | 3 | a0001c0001t0001g0254a0001c0001t0001g0283a0001c0001t0060g0246 | 3 | HG02135.hp1 HG02165.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-456+8515G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696665 | ||||||
chr7:1696735
|
C | G | 4 | a0001c0001t0012g0149a0001c0001t0065g0295a0002c0003t0050g0179others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-456+8585C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696735 | ||||||
chr7:1696736
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8586G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696736 | ||||||
chr7:1696766
|
T | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8616T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696766 | ||||||
chr7:1696785
|
A | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8635A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696785 | ||||||
chr7:1696809
|
G | A | 13 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(10): Show | 13 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-456+8659G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696809 | ||||||
chr7:1696846
|
T | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8696T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696846 | ||||||
chr7:1697022
|
G | A | 45 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-456+8872G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697022 | ||||||
chr7:1697043
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-456+8893C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697043 | ||||||
chr7:1697048
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-456+8898G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697048 | ||||||
chr7:1697052
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+8902C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697052 | ||||||
chr7:1697269
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+9119C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697269 | ||||||
chr7:1697293
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-456+9143C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697293 | ||||||
chr7:1697422
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-456+9272A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697422 | ||||||
chr7:1697456
|
G | C | 10 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0006g0028others(7): Show | 10 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-456+9306G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697456 | ||||||
chr7:1697489
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0142 | 2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-456+9339C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697489 | ||||||
chr7:1697490
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+9340G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697490 | ||||||
chr7:1697568
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-456+9418C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697568 | ||||||
chr7:1697576
|
C | T | 13 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0006g0028others(10): Show | 13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-456+9426C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697576 | ||||||
chr7:1697733
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-456+9583C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697733 | ||||||
chr7:1697766
|
C | T | 1 | a0001c0001t0017g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-456+9616C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697766 | ||||||
chr7:1697849
|
A | G | 2 | a0001c0001t0002g0075a0001c0001t0014g0076 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-456+9699A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697849 | ||||||
chr7:1697860
|
C | T | 2 | a0006c0008t0028g0293a0006c0008t0029g0292 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-456+9710C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697860 | ||||||
chr7:1697861
|
G | T | 60 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(57): Show | 60 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-456+9711G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697861 | ||||||
chr7:1697947
|
G | A | 1 | a0001c0001t0048g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-456+9797G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697947 | ||||||
chr7:1697982
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-456+9832C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697982 | ||||||
chr7:1698180
|
A | G | 16 | a0001c0001t0001g0145a0001c0001t0001g0158a0001c0001t0001g0160others(13): Show | 16 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-456+10030A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698180 | ||||||
chr7:1698231
|
T | A | 29 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-456+10081T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698231 | ||||||
chr7:1698274
|
T | C | 1 | a0001c0002t0053g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-456+10124T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698274 | ||||||
chr7:1698459
|
C | T | 1 | a0002c0003t0003g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-456+10309C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698459 | ||||||
chr7:1698491
|
A | G | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-456+10341A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698491 | ||||||
chr7:1698737
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-455-10354T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698737 | ||||||
chr7:1699048
|
A | G | 1 | a0001c0001t0002g0198 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-455-10043A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699048 | ||||||
chr7:1699295
|
A | G | 1 | a0001c0001t0038g0296 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-455-9796A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699295 | ||||||
chr7:1699714
|
T | C | 3 | a0001c0001t0001g0299a0001c0001t0003g0300a0002c0024t0030g0020 | 3 | HG02559.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-455-9377T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699714 | ||||||
chr7:1699738
|
C | T | 2 | a0001c0001t0025g0004a0001c0001t0038g0296 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-455-9353C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699738 | ||||||
chr7:1699828
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-455-9263C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699828 | ||||||
chr7:1699849
|
G | A | 4 | a0001c0001t0003g0039a0001c0001t0005g0150a0001c0001t0006g0028others(1): Show | 4 | HG01109.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-9242G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699849 | ||||||
chr7:1699930
|
G | C | 30 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(27): Show | 30 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-455-9161G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699930 | ||||||
chr7:1700193
|
C | T | 28 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-455-8898C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700193 | ||||||
chr7:1700223
|
G | A | 28 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-455-8868G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700223 | ||||||
chr7:1700253
|
AC | A | 28 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-455-8836delC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1700253 | |||||
chr7:1700280
|
A | G | 28 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-455-8811A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700280 | ||||||
chr7:1700298
|
A | G | 28 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-455-8793A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700298 | ||||||
chr7:1700326
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-455-8765C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700326 | ||||||
chr7:1700449
|
C | A | 2 | a0001c0001t0012g0211a0001c0001t0012g0212 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-455-8642C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700449 | ||||||
chr7:1700488
|
C | G | 29 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-455-8603C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700488 | ||||||
chr7:1700505
|
G | A | 1 | a0001c0001t0044g0218 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-455-8586G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700505 | ||||||
chr7:1700635
|
C | T | 1 | a0003c0006t0016g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-455-8456C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700635 | ||||||
chr7:1700726
|
G | A | 1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-455-8365G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700726 | ||||||
chr7:1700739
|
C | T | 50 | a0001c0001t0001g0008a0001c0001t0001g0245a0001c0001t0001g0252others(47): Show | 50 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.-455-8352C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700739 | ||||||
chr7:1700746
|
C | T | 1 | a0001c0002t0027g0049 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-455-8345C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700746 | ||||||
chr7:1700767
|
C | G | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-8324C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700767 | ||||||
chr7:1700793
|
T | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(8): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-455-8298T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700793 | ||||||
chr7:1700797
|
C | T | 3 | a0001c0001t0005g0150a0001c0001t0006g0028a0001c0026t0057g0187 | 3 | HG01123.hp1 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-8294C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700797 | ||||||
chr7:1700827
|
C | G | 30 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(27): Show | 30 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-455-8264C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700827 | ||||||
chr7:1700893
|
G | A | 2 | a0006c0008t0028g0293a0006c0008t0029g0292 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-455-8198G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700893 | ||||||
chr7:1700895
|
C | A | 1 | a0001c0001t0001g0245 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-455-8196C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700895 | ||||||
chr7:1701063
|
G | T | 1 | a0001c0001t0006g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-455-8028G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701063 | ||||||
chr7:1701071
|
ATGTGTGC others(17): Show |
A | 2 | a0001c0001t0012g0211a0001c0001t0012g0212 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-455-8011_-455-798 others(28): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1701071 | |||||
chr7:1701092
|
C | T | 4 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0002t0003g0103others(1): Show | 4 | HG01516.hp1 HG01934.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-7999C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701092 | ||||||
chr7:1701107
|
A | G | 29 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-455-7984A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701107 | ||||||
chr7:1701111
|
G | A | 2 | a0001c0001t0025g0004a0001c0001t0038g0296 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-455-7980G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701111 | ||||||
chr7:1701135
|
ATG | A | 3 | a0001c0001t0005g0294a0001c0001t0012g0184a0002c0003t0024g0183 | 3 | HG01167.hp2 HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-455-7945_-455-794 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1701135 | |||||
chr7:1701154
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-455-7937G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701154 | ||||||
chr7:1701334
|
C | T | 29 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(26): Show | 29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-455-7757C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701334 | ||||||
chr7:1701378
|
G | C | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-7713G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701378 | ||||||
chr7:1701689
|
C | T | 2 | a0001c0001t0025g0004a0001c0001t0038g0296 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-455-7402C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701689 | ||||||
chr7:1701787
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-455-7304A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701787 | ||||||
chr7:1701877
|
T | A | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-7214T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701877 | ||||||
chr7:1701990
|
T | C | 14 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(11): Show | 14 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-455-7101T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701990 | ||||||
chr7:1702121
|
T | G | 1 | a0001c0001t0005g0156 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-455-6970T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702121 | ||||||
chr7:1702177
|
C | T | 1 | a0001c0002t0003g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-455-6914C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702177 | ||||||
chr7:1702220
|
T | C | 1 | a0001c0001t0028g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-455-6871T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702220 | ||||||
chr7:1702371
|
C | T | 1 | a0001c0001t0012g0013 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-455-6720C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702371 | ||||||
chr7:1702394
|
T | G | 10 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(7): Show | 10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6697T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702394 | ||||||
chr7:1702401
|
C | T | 1 | a0001c0001t0019g0122 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-455-6690C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702401 | ||||||
chr7:1702408
|
A | G | 10 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(7): Show | 10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6683A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702408 | ||||||
chr7:1702410
|
G | A | 15 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0142others(12): Show | 15 | HG01255.hp1 HG02055.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-455-6681G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702410 | ||||||
chr7:1702418
|
G | A | 1 | a0001c0001t0002g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-455-6673G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702418 | ||||||
chr7:1702421
|
G | T | 3 | a0001c0001t0006g0028a0001c0005t0010g0147a0001c0005t0010g0148 | 3 | HG02630.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-6670G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702421 | ||||||
chr7:1702422
|
G | C | 3 | a0001c0001t0006g0028a0001c0005t0010g0147a0001c0005t0010g0148 | 3 | HG02630.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-6669G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702422 | ||||||
chr7:1702423
|
G | A | 3 | a0001c0001t0006g0028a0001c0005t0010g0147a0001c0005t0010g0148 | 3 | HG02630.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-6668G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702423 | ||||||
chr7:1702424
|
G | A | 3 | a0001c0001t0006g0028a0001c0005t0010g0147a0001c0005t0010g0148 | 3 | HG02630.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-6667G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702424 | ||||||
chr7:1702424
|
G | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0298 | 2 | NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-455-6667G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702424 | ||||||
chr7:1702425
|
G | A | 3 | a0001c0001t0006g0028a0001c0005t0010g0147a0001c0005t0010g0148 | 3 | HG02630.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-6666G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702425 | ||||||
chr7:1702425
|
G | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0298 | 2 | NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-455-6666G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702425 | ||||||
chr7:1702425
|
G | T | 4 | a0001c0001t0055g0297a0001c0005t0010g0143a0001c0005t0010g0146others(1): Show | 4 | HG02280.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-6666G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702425 | ||||||
chr7:1702426
|
G | A | 5 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0006g0028others(2): Show | 5 | HG02630.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-455-6665G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702426 | ||||||
chr7:1702426
|
G | C | 4 | a0001c0001t0055g0297a0001c0005t0010g0143a0001c0005t0010g0146others(1): Show | 4 | HG02280.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-6665G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702426 | ||||||
chr7:1702426
|
G | T | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-455-6665G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702426 | ||||||
chr7:1702427
|
G | A | 13 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0006g0028others(10): Show | 13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-455-6664G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702427 | ||||||
chr7:1702427
|
G | C | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-455-6664G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702427 | ||||||
chr7:1702427
|
GA | G | 22 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0142others(19): Show | 22 | HG01109.hp2 HG01255.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-455-6653delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1702427 | |||||
chr7:1702439
|
G | A | 10 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(7): Show | 10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6652G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702439 | ||||||
chr7:1702442
|
G | A | 10 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(7): Show | 10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6649G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702442 | ||||||
chr7:1702444
|
AGACCCTC others(87): Show |
A | 4 | a0001c0001t0005g0150a0001c0001t0006g0028a0001c0005t0010g0147others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-455-6646_-455-655 others(98): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702444 | ||||||
chr7:1702445
|
G | A | 6 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0055g0297others(3): Show | 6 | HG02280.hp2 HG03098.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-455-6646G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702445 | ||||||
chr7:1702446
|
ACCCTCCC others(85): Show |
A | 6 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0055g0297others(3): Show | 6 | HG02280.hp2 HG03098.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-455-6644_-455-655 others(96): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702446 | ||||||
chr7:1702540
|
C | A | 10 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(7): Show | 10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6551C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702540 | ||||||
chr7:1702546
|
G | A | 10 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(7): Show | 10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6545G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702546 | ||||||
chr7:1702554
|
ATGGATTG others(391): Show |
A | 1 | a0001c0001t0006g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-455-6535_-455-613 others(4): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1702554 | |||||
chr7:1702554
|
ATGGATTG others(392): Show |
A | 9 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(6): Show | 9 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-455-6536_-455-613 others(4): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702554 | ||||||
chr7:1702607
|
C | G | 4 | a0001c0001t0012g0149a0001c0001t0065g0295a0002c0003t0050g0179others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-6484C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702607 | ||||||
chr7:1702613
|
A | G | 41 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0239others(38): Show | 41 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.-455-6478A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702613 | ||||||
chr7:1702739
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0077 | 2 | NA18967.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-455-6352G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702739 | ||||||
chr7:1702744
|
T | G | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-6347T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702744 | ||||||
chr7:1702921
|
G | A | 1 | a0001c0001t0029g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-455-6170G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702921 | ||||||
chr7:1702953
|
T | A | 1 | a0001c0001t0006g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-455-6138T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702953 | ||||||
chr7:1703016
|
C | T | 2 | a0001c0001t0012g0149a0001c0002t0004g0289 | 2 | HG02145.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-455-6075C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703016 | ||||||
chr7:1703055
|
T | C | 46 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0239others(43): Show | 46 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.-455-6036T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703055 | ||||||
chr7:1703258
|
C | T | 1 | a0003c0006t0016g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-455-5833C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703258 | ||||||
chr7:1703278
|
G | C | 40 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0239others(37): Show | 40 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.-455-5813G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703278 | ||||||
chr7:1703305
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-455-5786G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703305 | ||||||
chr7:1703385
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-455-5706G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703385 | ||||||
chr7:1703581
|
C | G | 6 | a0001c0001t0002g0071a0001c0001t0002g0075a0001c0001t0014g0074others(3): Show | 6 | HG00738.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.-455-5510C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703581 | ||||||
chr7:1703696
|
T | C | 65 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0145others(62): Show | 65 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-455-5395T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703696 | ||||||
chr7:1703788
|
G | A | 4 | a0001c0001t0012g0149a0001c0001t0065g0295a0002c0003t0050g0179others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-5303G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703788 | ||||||
chr7:1703815
|
C | A | 3 | a0001c0001t0001g0299a0001c0001t0003g0300a0002c0024t0030g0020 | 3 | HG02559.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-455-5276C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703815 | ||||||
chr7:1703846
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-455-5245T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703846 | ||||||
chr7:1704139
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-455-4952C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704139 | ||||||
chr7:1704146
|
G | A | 1 | a0001c0011t0034g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-455-4945G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704146 | ||||||
chr7:1704241
|
G | A | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-4850G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704241 | ||||||
chr7:1704272
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0002g0242 | 2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-455-4819G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704272 | ||||||
chr7:1704383
|
A | T | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-4708A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704383 | ||||||
chr7:1704544
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-455-4547C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704544 | ||||||
chr7:1704578
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-455-4513G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704578 | ||||||
chr7:1704657
|
G | T | 51 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-455-4434G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704657 | ||||||
chr7:1704701
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-455-4390C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704701 | ||||||
chr7:1704757
|
A | T | 4 | a0001c0001t0012g0149a0001c0001t0065g0295a0002c0003t0050g0179others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-4334A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704757 | ||||||
chr7:1704784
|
C | T | 3 | a0001c0001t0001g0299a0001c0001t0003g0300a0002c0024t0030g0020 | 3 | HG02559.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-455-4307C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704784 | ||||||
chr7:1704785
|
G | A | 30 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(27): Show | 30 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-455-4306G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704785 | ||||||
chr7:1704822
|
G | T | 1 | a0001c0001t0007g0168 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-455-4269G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704822 | ||||||
chr7:1704844
|
A | C | 12 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(9): Show | 12 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-455-4247A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704844 | ||||||
chr7:1704879
|
G | A | 1 | a0001c0004t0054g0169 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-455-4212G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704879 | ||||||
chr7:1704937
|
G | A | 48 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-455-4154G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704937 | ||||||
chr7:1705410
|
G | A | 1 | a0001c0001t0064g0006 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-455-3681G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705410 | ||||||
chr7:1705461
|
C | A | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-3630C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705461 | ||||||
chr7:1705799
|
G | A | 2 | a0001c0001t0001g0299a0001c0001t0003g0300 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-455-3292G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705799 | ||||||
chr7:1705813
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-455-3278C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705813 | ||||||
chr7:1705893
|
C | T | 1 | a0001c0001t0013g0093 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-455-3198C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705893 | ||||||
chr7:1705921
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-455-3170C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705921 | ||||||
chr7:1706049
|
G | A | 1 | a0001c0001t0019g0058 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-455-3042G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706049 | ||||||
chr7:1706143
|
G | C | 1 | a0001c0002t0027g0190 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-455-2948G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706143 | ||||||
chr7:1706163
|
G | A | 3 | a0001c0001t0012g0149a0001c0001t0065g0295a0003c0006t0016g0182 | 3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-455-2928G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706163 | ||||||
chr7:1706191
|
G | A | 1 | a0009c0015t0032g0191 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-455-2900G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706191 | ||||||
chr7:1706334
|
A | G | 1 | a0002c0024t0030g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-455-2757A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706334 | ||||||
chr7:1706424
|
A | AAAAAC | 5 | a0001c0001t0001g0114a0001c0001t0001g0261a0001c0001t0002g0174others(2): Show | 5 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-455-2625_-455-262 others(9): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | |||||
chr7:1706424
|
A | AAAAACAA others(3): Show |
1 | a0001c0001t0031g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-455-2630_-455-262 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | |||||
chr7:1706424
|
AAAAAC | A | 93 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(90): Show | 93 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-455-2625_-455-262 others(9): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | |||||
chr7:1706424
|
AAAAACAA others(3): Show |
A | 15 | a0001c0001t0001g0145a0001c0001t0001g0158a0001c0001t0001g0160others(12): Show | 15 | HG02280.hp2 HG02630.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-455-2630_-455-262 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | |||||
chr7:1706424
|
AAAAACAA others(8): Show |
A | 2 | a0001c0001t0003g0039a0001c0025t0058g0038 | 2 | HG01109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-455-2635_-455-262 others(19): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | |||||
chr7:1706424
|
AAAAACAA others(13): Show |
A | 4 | a0001c0001t0012g0149a0001c0001t0065g0295a0002c0003t0024g0144others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-2640_-455-262 others(24): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | |||||
chr7:1706469
|
C | A | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-2622C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706469 | ||||||
chr7:1706496
|
T | C | 126 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0019others(123): Show | 126 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-455-2595T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706496 | ||||||
chr7:1706549
|
C | T | 1 | a0001c0001t0005g0294 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-455-2542C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706549 | ||||||
chr7:1706713
|
A | G | 16 | a0001c0001t0001g0125a0001c0001t0005g0294a0001c0001t0006g0128others(13): Show | 16 | HG01099.hp2 HG01167.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-455-2378A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706713 | ||||||
chr7:1706820
|
C | T | 3 | a0001c0001t0005g0156a0001c0001t0006g0157a0002c0003t0006g0005 | 3 | HG01243.hp1 HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-455-2271C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706820 | ||||||
chr7:1706903
|
T | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-455-2188T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706903 | ||||||
chr7:1707005
|
C | CAACACAC others(20): Show |
1 | a0009c0015t0032g0191 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-455-2085_-455-205 others(31): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1707005 | |||||
chr7:1707073
|
C | T | 3 | a0001c0001t0005g0294a0001c0001t0012g0184a0002c0003t0024g0183 | 3 | HG01167.hp2 HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-455-2018C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707073 | ||||||
chr7:1707077
|
G | A | 1 | a0002c0024t0030g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-455-2014G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707077 | ||||||
chr7:1707186
|
C | T | 1 | a0001c0001t0015g0163 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-455-1905C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707186 | ||||||
chr7:1707273
|
C | T | 2 | a0001c0001t0021g0276a0001c0004t0061g0275 | 2 | NA18959.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-455-1818C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707273 | ||||||
chr7:1707293
|
A | C | 1 | a0001c0001t0016g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-455-1798A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707293 | ||||||
chr7:1707501
|
G | A | 10 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(7): Show | 10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-1590G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707501 | ||||||
chr7:1707550
|
G | A | 35 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0158others(32): Show | 35 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-455-1541G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707550 | ||||||
chr7:1707569
|
C | A | 32 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0005g0156others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-455-1522C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707569 | ||||||
chr7:1707595
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-455-1496A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707595 | ||||||
chr7:1707688
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0003g0300 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-455-1403C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707688 | ||||||
chr7:1707975
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-455-1116C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707975 | ||||||
chr7:1708026
|
C | G | 83 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0045others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-455-1065C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708026 | ||||||
chr7:1708055
|
A | AC | 13 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(10): Show | 13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-455-1030dupC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1708055 | |||||
chr7:1708136
|
C | T | 3 | a0001c0001t0005g0294a0001c0001t0012g0184a0002c0003t0024g0183 | 3 | HG01167.hp2 HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-455-955C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708136 | ||||||
chr7:1708161
|
GC | G | 3 | a0001c0001t0005g0294a0001c0001t0012g0184a0002c0003t0024g0183 | 3 | HG01167.hp2 HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-455-929delC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708161 | ||||||
chr7:1708167
|
C | G | 2 | a0001c0001t0017g0099a0001c0001t0059g0083 | 2 | HG01433.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-455-924C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708167 | ||||||
chr7:1708262
|
C | T | 1 | a0001c0001t0007g0167 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-455-829C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708262 | ||||||
chr7:1708335
|
G | A | 33 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0003g0039others(30): Show | 33 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.-455-756G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708335 | ||||||
chr7:1708370
|
A | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(8): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-455-721A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708370 | ||||||
chr7:1708389
|
G | A | 2 | a0001c0001t0002g0172a0001c0001t0039g0173 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-455-702G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708389 | ||||||
chr7:1708518
|
A | C | 77 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(74): Show | 77 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-455-573A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708518 | ||||||
chr7:1708697
|
CAGCCCCA others(16): Show |
C | 3 | a0001c0001t0012g0149a0001c0001t0065g0295a0003c0006t0016g0182 | 3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-455-384_-455-362d others(25): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1708697 | |||||
chr7:1708709
|
CTCTGGGG others(16): Show |
C | 4 | a0001c0001t0012g0013a0001c0001t0025g0004a0001c0001t0038g0296others(1): Show | 4 | HG00639.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-381_-455-359d others(25): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708709 | ||||||
chr7:1708785
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-455-306G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708785 | ||||||
chr7:1708790
|
G | A | 1 | a0001c0001t0011g0102 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-455-301G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708790 | ||||||
chr7:1708842
|
A | G | 13 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(10): Show | 13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-455-249A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708842 | ||||||
chr7:1708915
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(8): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-455-176T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708915 | ||||||
chr7:1708929
|
C | G | 2 | a0001c0001t0016g0030a0008c0013t0020g0091 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-455-162C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708929 | ||||||
chr7:1709069
|
C | G | 2 | a0001c0001t0026g0012a0001c0001t0051g0011 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-455-22C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1709069 | ||||||
chr7:1709284
|
G | A | 1 | a0003c0006t0016g0182 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-294+32G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709284 | ||||||
chr7:1709303
|
G | A | 1 | a0001c0007t0005g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-294+51G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709303 | ||||||
chr7:1709389
|
G | A | 2 | a0001c0001t0025g0004a0001c0001t0038g0296 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-294+137G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709389 | ||||||
chr7:1709415
|
A | G | 1 | a0001c0001t0025g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-294+163A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709415 | ||||||
chr7:1709506
|
G | A | 2 | a0001c0001t0043g0164a0001c0001t0044g0218 | 2 | NA18948.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-294+254G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709506 | ||||||
chr7:1709680
|
C | T | 1 | a0001c0002t0003g0189 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-294+428C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709680 | ||||||
chr7:1709696
|
C | T | 3 | a0001c0001t0019g0058a0001c0001t0031g0100a0004c0009t0001g0109 | 3 | HG03491.hp2 HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-294+444C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709696 | ||||||
chr7:1709807
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(8): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+555A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709807 | ||||||
chr7:1709963
|
C | G | 2 | a0001c0001t0006g0291a0001c0001t0035g0290 | 2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-294+711C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709963 | ||||||
chr7:1710014
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-294+762G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710014 | ||||||
chr7:1710219
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(8): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+967G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710219 | ||||||
chr7:1710386
|
T | C | 1 | a0001c0001t0019g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-294+1134T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710386 | ||||||
chr7:1710510
|
C | A | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-294+1258C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710510 | ||||||
chr7:1710542
|
C | T | 32 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0003g0039others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-294+1290C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710542 | ||||||
chr7:1710629
|
G | A | 64 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.-294+1377G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710629 | ||||||
chr7:1710712
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-294+1460C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710712 | ||||||
chr7:1710891
|
A | G | 1 | a0001c0001t0011g0102 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-294+1639A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710891 | ||||||
chr7:1710918
|
G | A | 1 | a0002c0024t0030g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-294+1666G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710918 | ||||||
chr7:1711024
|
C | T | 1 | a0001c0001t0005g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-294+1772C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711024 | ||||||
chr7:1711068
|
T | A | 1 | a0001c0001t0059g0083 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-294+1816T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711068 | ||||||
chr7:1711117
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-294+1865C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711117 | ||||||
chr7:1711161
|
C | T | 58 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-294+1909C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711161 | ||||||
chr7:1711492
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-294+2240T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711492 | ||||||
chr7:1711575
|
T | TGA | 9 | a0001c0001t0001g0107a0001c0001t0002g0061a0001c0001t0002g0062others(6): Show | 9 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.-294+2374_-294+237 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711575
|
T | TGAGA | 10 | a0001c0001t0001g0090a0001c0001t0007g0167a0001c0001t0007g0168others(7): Show | 10 | HG00735.hp1 HG01255.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.-294+2372_-294+237 others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711575
|
T | TGAGAGAG others(3): Show |
1 | a0001c0002t0018g0033 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-294+2366_-294+237 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711575
|
TGA | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0045others(50): Show | 53 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-294+2374_-294+237 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711575
|
TGAGA | T | 51 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0066others(48): Show | 51 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-294+2372_-294+237 others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711575
|
TGAGAGA | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0053others(43): Show | 46 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.-294+2370_-294+237 others(10): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711575
|
TGAGAGAG others(1): Show |
T | 55 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0067others(52): Show | 55 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.-294+2368_-294+237 others(12): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711575
|
TGAGAGAG others(3): Show |
T | 18 | a0001c0001t0001g0008a0001c0001t0002g0071a0001c0001t0002g0075others(15): Show | 18 | HG01071.hp1 HG01515.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.-294+2366_-294+237 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711575
|
TGAGAGAG others(5): Show |
T | 13 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0072others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-294+2364_-294+237 others(16): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711575
|
TGAGAGAG others(7): Show |
T | 3 | a0001c0001t0001g0177a0001c0001t0022g0073a0001c0002t0004g0262 | 3 | HG01074.hp2 HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-294+2362_-294+237 others(18): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711575
|
TGAGAGAG others(9): Show |
T | 3 | a0001c0001t0002g0115a0001c0002t0018g0229a0012c0019t0001g0256 | 3 | HG01070.hp1 HG02074.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-294+2360_-294+237 others(20): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711575
|
TGAGAGAG others(15): Show |
T | 2 | a0001c0001t0001g0257a0002c0024t0030g0020 | 2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-294+2354_-294+237 others(26): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | |||||
chr7:1711615
|
A | C | 3 | a0001c0001t0012g0149a0001c0001t0065g0295a0003c0006t0016g0182 | 3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+2363A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711615 | ||||||
chr7:1711617
|
A | C | 3 | a0001c0001t0012g0149a0001c0001t0065g0295a0003c0006t0016g0182 | 3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+2365A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711617 | ||||||
chr7:1711618
|
GAGAGAGA others(3): Show |
G | 1 | a0001c0001t0001g0113 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-294+2367_-294+237 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711618 | ||||||
chr7:1711619
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(8): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+2367A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711619 | ||||||
chr7:1711658
|
C | T | 1 | a0001c0001t0006g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-294+2406C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711658 | ||||||
chr7:1711699
|
T | C | 13 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(10): Show | 13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-294+2447T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711699 | ||||||
chr7:1711858
|
G | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(8): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+2606G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711858 | ||||||
chr7:1712063
|
G | A | 1 | a0001c0001t0011g0102 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-294+2811G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712063 | ||||||
chr7:1712146
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+2894G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712146 | ||||||
chr7:1712261
|
A | G | 54 | a0001c0001t0001g0008a0001c0001t0001g0230a0001c0001t0001g0245others(51): Show | 54 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-294+3009A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712261 | ||||||
chr7:1712372
|
G | A | 13 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(10): Show | 13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-294+3120G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712372 | ||||||
chr7:1712408
|
C | T | 69 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0045others(66): Show | 69 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-294+3156C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712408 | ||||||
chr7:1712427
|
CT | C | 60 | a0001c0001t0001g0008a0001c0001t0001g0230a0001c0001t0001g0245others(57): Show | 60 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-294+3186delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1712427 | |||||
chr7:1712477
|
G | A | 1 | a0001c0001t0028g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-294+3225G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712477 | ||||||
chr7:1712640
|
C | T | 3 | a0001c0001t0012g0149a0001c0001t0065g0295a0003c0006t0016g0182 | 3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+3388C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712640 | ||||||
chr7:1712651
|
C | CA | 13 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(10): Show | 13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-294+3402dupA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1712651 | |||||
chr7:1712706
|
A | G | 2 | a0001c0001t0012g0184a0002c0003t0024g0183 | 2 | HG01167.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-294+3454A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712706 | ||||||
chr7:1712711
|
T | C | 43 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0239others(40): Show | 43 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.-294+3459T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712711 | ||||||
chr7:1712812
|
T | A | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-294+3560T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712812 | ||||||
chr7:1712827
|
T | G | 14 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(11): Show | 14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+3575T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712827 | ||||||
chr7:1713108
|
C | T | 1 | a0001c0001t0016g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-294+3856C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713108 | ||||||
chr7:1713264
|
A | G | 1 | a0001c0002t0003g0111 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-294+4012A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713264 | ||||||
chr7:1713280
|
G | A | 1 | a0001c0027t0062g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-294+4028G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713280 | ||||||
chr7:1713401
|
G | A | 1 | a0001c0001t0016g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-294+4149G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713401 | ||||||
chr7:1713447
|
C | T | 44 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0158others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.-294+4195C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713447 | ||||||
chr7:1713605
|
C | G | 66 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(63): Show | 66 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-294+4353C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713605 | ||||||
chr7:1713679
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-294+4427C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713679 | ||||||
chr7:1713752
|
G | T | 14 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0012g0149others(11): Show | 14 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-294+4500G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713752 | ||||||
chr7:1713753
|
G | T | 1 | a0001c0011t0034g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-294+4501G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713753 | ||||||
chr7:1713754
|
G | A | 37 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0158others(34): Show | 37 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.-294+4502G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713754 | ||||||
chr7:1713831
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0053others(10): Show | 13 | HG00140.hp2 HG00544.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.-294+4579C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713831 | ||||||
chr7:1713850
|
C | T | 2 | a0001c0001t0026g0012a0001c0001t0051g0011 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-294+4598C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713850 | ||||||
chr7:1713876
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-294+4624C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713876 | ||||||
chr7:1713963
|
C | T | 16 | a0001c0001t0001g0018a0001c0001t0001g0299a0001c0001t0003g0133others(13): Show | 16 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-294+4711C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713963 | ||||||
chr7:1714038
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(294): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-294+4786T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714038 | ||||||
chr7:1714090
|
C | T | 22 | a0001c0001t0001g0204a0001c0001t0001g0214a0001c0001t0001g0216others(19): Show | 22 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.-294+4838C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714090 | ||||||
chr7:1714308
|
G | A | 35 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0158others(32): Show | 35 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-294+5056G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714308 | ||||||
chr7:1714392
|
C | A | 1 | a0001c0001t0025g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-294+5140C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714392 | ||||||
chr7:1714480
|
A | G | 16 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(13): Show | 16 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-294+5228A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714480 | ||||||
chr7:1714482
|
A | C | 90 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-294+5230A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714482 | ||||||
chr7:1714632
|
C | G | 3 | a0001c0001t0025g0004a0001c0001t0038g0296a0002c0024t0030g0020 | 3 | HG02818.hp2 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-294+5380C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714632 | ||||||
chr7:1714778
|
C | A | 2 | a0001c0001t0012g0149a0003c0006t0016g0182 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+5526C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714778 | ||||||
chr7:1714818
|
C | G | 1 | a0001c0001t0006g0161 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-294+5566C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714818 | ||||||
chr7:1714845
|
G | A | 1 | a0001c0002t0018g0229 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-294+5593G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714845 | ||||||
chr7:1714864
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-294+5612C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714864 | ||||||
chr7:1714872
|
C | T | 14 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(11): Show | 14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+5620C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714872 | ||||||
chr7:1714873
|
A | G | 188 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0018others(185): Show | 188 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.-294+5621A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714873 | ||||||
chr7:1714875
|
C | T | 5 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0001g0261others(2): Show | 5 | HG00741.hp1 HG01109.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-294+5623C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714875 | ||||||
chr7:1714894
|
C | A | 1 | a0001c0001t0006g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-294+5642C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714894 | ||||||
chr7:1714905
|
G | A | 1 | a0001c0001t0006g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-294+5653G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714905 | ||||||
chr7:1714907
|
T | C | 3 | a0001c0001t0012g0149a0001c0001t0065g0295a0003c0006t0016g0182 | 3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+5655T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714907 | ||||||
chr7:1714917
|
T | C | 89 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-294+5665T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714917 | ||||||
chr7:1715189
|
C | A | 1 | a0001c0002t0004g0277 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-294+5937C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715189 | ||||||
chr7:1715480
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0005g0162a0001c0001t0006g0031others(1): Show | 4 | HG01081.hp1 HG03209.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-294+6228G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715480 | ||||||
chr7:1715524
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0002g0284a0001c0001t0002g0287others(2): Show | 5 | NA18943.hp1 NA19009.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-294+6272C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715524 | ||||||
chr7:1715544
|
C | T | 1 | a0001c0001t0009g0121 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-294+6292C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715544 | ||||||
chr7:1715805
|
C | G | 3 | a0001c0001t0001g0245a0001c0001t0001g0283a0001c0001t0060g0246 | 3 | HG02135.hp1 NA18946.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-294+6553C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715805 | ||||||
chr7:1715821
|
T | C | 17 | a0001c0001t0001g0018a0001c0001t0001g0299a0001c0001t0003g0133others(14): Show | 17 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-294+6569T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715821 | ||||||
chr7:1715821
|
T | G | 1 | a0001c0002t0004g0236 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-294+6569T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715821 | ||||||
chr7:1715858
|
C | T | 2 | a0001c0001t0001g0066a0001c0018t0001g0065 | 2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-294+6606C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715858 | ||||||
chr7:1716103
|
A | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-294+6851A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716103 | ||||||
chr7:1716331
|
A | G | 16 | a0001c0001t0001g0018a0001c0001t0001g0299a0001c0001t0003g0133others(13): Show | 16 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-294+7079A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716331 | ||||||
chr7:1716341
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-294+7089G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716341 | ||||||
chr7:1716349
|
G | A | 1 | a0001c0011t0034g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-294+7097G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716349 | ||||||
chr7:1716370
|
C | T | 1 | a0001c0002t0004g0255 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-294+7118C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716370 | ||||||
chr7:1716372
|
T | G | 2 | a0001c0001t0025g0046a0001c0001t0035g0047 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-294+7120T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716372 | ||||||
chr7:1716648
|
G | A | 51 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0145others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-294+7396G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716648 | ||||||
chr7:1716850
|
G | C | 6 | a0001c0001t0001g0257a0001c0001t0013g0199a0001c0002t0004g0236others(3): Show | 6 | HG00639.hp1 NA18947.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-294+7598G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716850 | ||||||
chr7:1716862
|
G | A | 10 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(7): Show | 10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-294+7610G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716862 | ||||||
chr7:1716908
|
A | G | 1 | a0001c0001t0008g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-294+7656A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716908 | ||||||
chr7:1717010
|
A | G | 1 | a0002c0003t0003g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-294+7758A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717010 | ||||||
chr7:1717153
|
G | A | 8 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0055g0297others(5): Show | 8 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-294+7901G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717153 | ||||||
chr7:1717156
|
C | T | 1 | a0001c0001t0025g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-294+7904C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717156 | ||||||
chr7:1717398
|
G | A | 14 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(11): Show | 14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+8146G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717398 | ||||||
chr7:1717490
|
G | A | 51 | a0001c0001t0001g0008a0001c0001t0001g0245a0001c0001t0001g0252others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.-294+8238G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717490 | ||||||
chr7:1717506
|
C | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(8): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+8254C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717506 | ||||||
chr7:1717600
|
T | C | 65 | a0001c0001t0001g0018a0001c0001t0001g0055a0001c0001t0001g0056others(62): Show | 65 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.-294+8348T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717600 | ||||||
chr7:1717615
|
G | A | 64 | a0001c0001t0001g0018a0001c0001t0001g0055a0001c0001t0001g0056others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.-294+8363G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717615 | ||||||
chr7:1717663
|
C | T | 1 | a0002c0003t0050g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-294+8411C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717663 | ||||||
chr7:1717823
|
G | A | 1 | a0008c0013t0020g0091 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-294+8571G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717823 | ||||||
chr7:1717873
|
G | T | 2 | a0001c0002t0018g0032a0001c0002t0018g0033 | 2 | HG00423.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-294+8621G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717873 | ||||||
chr7:1717969
|
A | C | 53 | a0001c0001t0001g0008a0001c0001t0001g0245a0001c0001t0001g0252others(50): Show | 53 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.-294+8717A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717969 | ||||||
chr7:1718229
|
C | T | 1 | a0005c0010t0045g0151 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-294+8977C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718229 | ||||||
chr7:1718250
|
G | A | 1 | a0001c0001t0015g0176 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-294+8998G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718250 | ||||||
chr7:1718322
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-294+9070C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718322 | ||||||
chr7:1718340
|
C | A | 1 | a0001c0021t0023g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-294+9088C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718340 | ||||||
chr7:1718620
|
C | T | 1 | a0001c0001t0009g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-294+9368C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718620 | ||||||
chr7:1718657
|
G | A | 1 | a0001c0001t0038g0296 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+9405G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718657 | ||||||
chr7:1718674
|
A | G | 1 | a0002c0003t0003g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-294+9422A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718674 | ||||||
chr7:1718734
|
A | C | 1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-294+9482A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718734 | ||||||
chr7:1718825
|
G | A | 14 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(11): Show | 14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+9573G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718825 | ||||||
chr7:1718861
|
G | A | 1 | a0001c0001t0038g0296 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+9609G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718861 | ||||||
chr7:1719036
|
T | C | 113 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(110): Show | 113 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-294+9784T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719036 | ||||||
chr7:1719083
|
C | G | 14 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(11): Show | 14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+9831C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719083 | ||||||
chr7:1719118
|
ACCCCGCC others(119): Show |
A | 1 | a0001c0021t0023g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-294+9974_-294+100 others(5): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719118 | |||||
chr7:1719123
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-294+9871G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719123 | ||||||
chr7:1719142
|
GCCACCAA others(11): Show |
G | 1 | a0001c0001t0001g0092 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-294+9920_-294+993 others(22): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719142 | |||||
chr7:1719146
|
C | G | 1 | a0001c0001t0038g0296 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+9894C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719146 | ||||||
chr7:1719160
|
C | CCCACCAA others(29): Show |
1 | a0001c0002t0004g0289 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-294+10010_-294+10 others(42): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719160 | |||||
chr7:1719160
|
CCCACCAA others(29): Show |
C | 1 | a0001c0001t0002g0062 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-294+10010_-294+10 others(42): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719160 | |||||
chr7:1719163
|
A | ACCAACAG others(61): Show |
14 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(11): Show | 14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+9919_-294+992 others(72): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719163 | |||||
chr7:1719163
|
A | ACCAACAG others(43): Show |
1 | a0001c0001t0038g0296 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+9919_-294+992 others(54): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719163 | |||||
chr7:1719163
|
A | ACCAACAG others(61): Show |
11 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(8): Show | 11 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+9919_-294+992 others(72): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719163 | |||||
chr7:1719226
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+9974A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719226 | ||||||
chr7:1719230
|
A | C | 1 | a0001c0001t0001g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+9978A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719230 | ||||||
chr7:1719231
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+9979A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719231 | ||||||
chr7:1719232
|
G | C | 1 | a0001c0001t0001g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+9980G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719232 | ||||||
chr7:1719232
|
GCCACCAA others(47): Show |
G | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-294+10085_-294+10 others(60): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719232 | |||||
chr7:1719260
|
GGACCCAA others(28): Show |
G | 1 | a0001c0001t0001g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+10010_-294+10 others(41): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719260 | |||||
chr7:1719262
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-294+10010A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719262 | ||||||
chr7:1719266
|
A | C | 1 | a0001c0001t0001g0266 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-294+10014A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719266 | ||||||
chr7:1719267
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-294+10015A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719267 | ||||||
chr7:1719268
|
G | C | 1 | a0001c0001t0001g0266 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-294+10016G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719268 | ||||||
chr7:1719268
|
G | GCCACCAA others(11): Show |
103 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0022others(100): Show | 103 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-294+10046_-294+10 others(24): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719268 | |||||
chr7:1719268
|
G | GCCACCAA others(83): Show |
1 | a0001c0002t0003g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-294+10045_-294+10 others(96): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719268 | |||||
chr7:1719268
|
G | GCCACCAA others(29): Show |
2 | a0001c0001t0012g0149a0001c0001t0065g0295 | 2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-294+10028_-294+10 others(42): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719268 | |||||
chr7:1719268
|
G | GCCACCAA others(137): Show |
1 | a0001c0001t0001g0015 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-294+10063_-294+10 others(150): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719268 | |||||
chr7:1719289
|
A | ACCAACAG others(7): Show |
10 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0005g0150others(7): Show | 10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-294+10040_-294+10 others(20): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719289 | |||||
chr7:1719289
|
A | ACCAACAG others(25): Show |
16 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(13): Show | 16 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-294+10063_-294+10 others(38): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719289 | |||||
chr7:1719298
|
G | C | 1 | a0001c0001t0001g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+10046G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719298 | ||||||
chr7:1719298
|
G | GCCCCGCC others(12): Show |
1 | a0001c0001t0003g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-294+10063_-294+10 others(25): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719298 | |||||
chr7:1719298
|
G | GCCCCGCC others(30): Show |
38 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0239others(35): Show | 38 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.-294+10063_-294+10 others(43): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719298 | |||||
chr7:1719315
|
G | GGCCCCGC others(11): Show |
1 | a0001c0001t0007g0273 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-294+10063_-294+10 others(24): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719315 | ||||||
chr7:1719316
|
A | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+10064A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719316 | ||||||
chr7:1719320
|
A | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+10068A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719320 | ||||||
chr7:1719321
|
A | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+10069A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719321 | ||||||
chr7:1719322
|
G | C | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+10070G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719322 | ||||||
chr7:1719340
|
C | CCCACCAA others(11): Show |
3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+10099_-294+10 others(24): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719340 | |||||
chr7:1719340
|
C | CCCACCAA others(65): Show |
26 | a0001c0001t0001g0018a0001c0001t0001g0145a0001c0001t0001g0298others(23): Show | 26 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.-294+10099_-294+10 others(78): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719340 | |||||
chr7:1719447
|
C | G | 1 | a0001c0001t0005g0136 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-294+10195C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719447 | ||||||
chr7:1719753
|
G | A | 98 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0045others(95): Show | 98 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-294+10501G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719753 | ||||||
chr7:1719759
|
G | A | 1 | a0014c0022t0001g0025 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-294+10507G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719759 | ||||||
chr7:1719904
|
C | T | 1 | a0001c0026t0057g0187 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-294+10652C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719904 | ||||||
chr7:1719914
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-294+10662T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719914 | ||||||
chr7:1720007
|
A | G | 1 | a0001c0002t0053g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-294+10755A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720007 | ||||||
chr7:1720151
|
G | C | 1 | a0001c0001t0025g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-294+10899G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720151 | ||||||
chr7:1720226
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-294+10974C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720226 | ||||||
chr7:1720255
|
C | T | 56 | a0001c0001t0001g0018a0001c0001t0001g0055a0001c0001t0001g0056others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-294+11003C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720255 | ||||||
chr7:1720334
|
T | C | 44 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0239others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.-294+11082T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720334 | ||||||
chr7:1720338
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-294+11086C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720338 | ||||||
chr7:1720441
|
C | A | 1 | a0001c0001t0005g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-294+11189C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720441 | ||||||
chr7:1720542
|
C | G | 1 | a0001c0001t0042g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-294+11290C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720542 | ||||||
chr7:1720733
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+11481C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720733 | ||||||
chr7:1720928
|
C | G | 56 | a0001c0001t0001g0018a0001c0001t0001g0055a0001c0001t0001g0056others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-294+11676C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720928 | ||||||
chr7:1720935
|
T | G | 2 | a0001c0001t0043g0164a0001c0001t0044g0218 | 2 | NA18948.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-294+11683T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720935 | ||||||
chr7:1721030
|
T | C | 4 | a0001c0001t0001g0299a0001c0001t0003g0300a0002c0003t0050g0179others(1): Show | 4 | HG02559.hp1 HG02717.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-294+11778T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721030 | ||||||
chr7:1721193
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+11941C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721193 | ||||||
chr7:1721516
|
C | T | 1 | a0001c0001t0038g0296 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+12264C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721516 | ||||||
chr7:1721570
|
G | A | 1 | a0001c0001t0012g0184 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-294+12318G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721570 | ||||||
chr7:1721623
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(8): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+12371G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721623 | ||||||
chr7:1721745
|
C | T | 14 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(11): Show | 14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+12493C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721745 | ||||||
chr7:1722265
|
C | CT | 7 | a0001c0001t0001g0035a0001c0001t0001g0234a0001c0001t0015g0163others(4): Show | 7 | HG01175.hp2 HG02074.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-294+13032dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1722265 | |||||
chr7:1722265
|
CT | C | 11 | a0001c0001t0001g0158a0001c0001t0001g0180a0001c0001t0002g0227others(8): Show | 11 | HG01168.hp1 HG01891.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+13032delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1722265 | |||||
chr7:1722290
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+13038G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722290 | ||||||
chr7:1722303
|
G | C | 1 | a0001c0001t0001g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-294+13051G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722303 | ||||||
chr7:1722423
|
C | T | 1 | a0001c0001t0005g0162 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-294+13171C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722423 | ||||||
chr7:1722492
|
C | G | 1 | a0001c0001t0012g0013 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-294+13240C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722492 | ||||||
chr7:1722560
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+13308C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722560 | ||||||
chr7:1722611
|
A | C | 43 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0239others(40): Show | 43 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.-294+13359A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722611 | ||||||
chr7:1722864
|
G | C | 2 | a0001c0001t0001g0090a0001c0001t0021g0082 | 2 | HG00735.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-294+13612G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722864 | ||||||
chr7:1723060
|
G | A | 1 | a0001c0001t0006g0161 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-294+13808G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723060 | ||||||
chr7:1723087
|
G | A | 2 | a0001c0001t0001g0066a0001c0018t0001g0065 | 2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-294+13835G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723087 | ||||||
chr7:1723202
|
A | T | 3 | a0001c0001t0012g0149a0001c0001t0065g0295a0003c0006t0016g0182 | 3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+13950A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723202 | ||||||
chr7:1723298
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0025g0046a0001c0001t0035g0047 | 3 | HG02622.hp1 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-294+14046G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723298 | ||||||
chr7:1723311
|
A | G | 1 | a0015c0023t0003g0130 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-294+14059A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723311 | ||||||
chr7:1723358
|
C | T | 1 | a0001c0001t0051g0011 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-294+14106C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723358 | ||||||
chr7:1723486
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-294+14234C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723486 | ||||||
chr7:1723528
|
G | A | 50 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0204others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-294+14276G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723528 | ||||||
chr7:1723548
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0085 | 2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-294+14296T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723548 | ||||||
chr7:1723591
|
C | T | 1 | a0015c0023t0003g0130 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-294+14339C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723591 | ||||||
chr7:1723657
|
G | T | 1 | a0001c0027t0062g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-294+14405G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723657 | ||||||
chr7:1723683
|
C | T | 1 | a0001c0002t0004g0262 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-294+14431C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723683 | ||||||
chr7:1723809
|
A | G | 15 | a0001c0001t0001g0145a0001c0001t0001g0298a0001c0001t0006g0028others(12): Show | 15 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-294+14557A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723809 | ||||||
chr7:1723810
|
C | T | 3 | a0001c0001t0012g0149a0001c0001t0065g0295a0003c0006t0016g0182 | 3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+14558C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723810 | ||||||
chr7:1723819
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-294+14567G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723819 | ||||||
chr7:1723877
|
A | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0178a0001c0018t0001g0065 | 3 | HG00733.hp2 HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-294+14625A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723877 | ||||||
chr7:1723911
|
G | A | 1 | a0001c0001t0038g0296 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+14659G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723911 | ||||||
chr7:1724087
|
G | A | 14 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(11): Show | 14 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+14835G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724087 | ||||||
chr7:1724099
|
C | G | 76 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(73): Show | 76 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.-294+14847C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724099 | ||||||
chr7:1724103
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+14851C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724103 | ||||||
chr7:1724187
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-294+14935C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724187 | ||||||
chr7:1724393
|
T | C | 3 | a0001c0001t0001g0067a0001c0001t0002g0069a0001c0001t0063g0070 | 3 | HG01106.hp1 HG01168.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-294+15141T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724393 | ||||||
chr7:1724550
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-294+15298A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724550 | ||||||
chr7:1724674
|
A | G | 1 | a0001c0001t0008g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-294+15422A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724674 | ||||||
chr7:1724704
|
G | C | 1 | a0011c0020t0002g0054 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-294+15452G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724704 | ||||||
chr7:1724709
|
T | TC | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(8): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+15463dupC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1724709 | |||||
chr7:1724714
|
C | G | 10 | a0001c0001t0002g0209a0001c0001t0004g0205a0001c0001t0004g0206others(7): Show | 10 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.-294+15462C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724714 | ||||||
chr7:1724806
|
A | G | 1 | a0001c0001t0012g0013 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-294+15554A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724806 | ||||||
chr7:1724807
|
A | G | 66 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(63): Show | 66 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-294+15555A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724807 | ||||||
chr7:1724836
|
G | C | 48 | a0001c0001t0001g0018a0001c0001t0001g0055a0001c0001t0001g0056others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-294+15584G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724836 | ||||||
chr7:1724863
|
C | T | 1 | a0001c0001t0012g0013 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-294+15611C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724863 | ||||||
chr7:1724915
|
T | TA | 14 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(11): Show | 14 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+15664dupA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1724915 | |||||
chr7:1724949
|
G | C | 181 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0018others(178): Show | 181 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.-294+15697G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724949 | ||||||
chr7:1724957
|
A | C | 3 | a0001c0001t0025g0004a0001c0001t0038g0296a0002c0024t0030g0020 | 3 | HG02818.hp2 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-294+15705A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724957 | ||||||
chr7:1724977
|
G | A | 1 | a0001c0001t0026g0135 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-294+15725G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724977 | ||||||
chr7:1725279
|
G | A | 1 | a0001c0011t0034g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-294+16027G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725279 | ||||||
chr7:1725523
|
G | A | 1 | a0001c0001t0056g0195 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-294+16271G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725523 | ||||||
chr7:1725547
|
A | AGTCACTC others(8): Show |
1 | a0001c0001t0011g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-294+16298_-294+16 others(21): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1725547 | |||||
chr7:1725648
|
C | T | 1 | a0001c0001t0016g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-294+16396C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725648 | ||||||
chr7:1725705
|
G | A | 12 | a0001c0001t0001g0245a0001c0001t0001g0252a0001c0001t0001g0283others(9): Show | 12 | HG02083.hp1 HG02135.hp1 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.-294+16453G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725705 | ||||||
chr7:1725849
|
CA | C | 9 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-294+16601delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1725849 | |||||
chr7:1725929
|
C | T | 1 | a0001c0011t0034g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-294+16677C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725929 | ||||||
chr7:1725940
|
A | C | 1 | a0001c0001t0011g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-294+16688A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725940 | ||||||
chr7:1725947
|
C | T | 2 | a0001c0001t0009g0043a0001c0001t0009g0044 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-294+16695C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725947 | ||||||
chr7:1725956
|
G | A | 172 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0018others(169): Show | 172 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.-294+16704G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725956 | ||||||
chr7:1725959
|
A | ACACT | 100 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(97): Show | 100 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-294+16710_-294+16 others(10): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1725959 | |||||
chr7:1726024
|
A | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0142a0001c0001t0012g0013others(1): Show | 4 | HG00639.hp2 HG01496.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-294+16772A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726024 | ||||||
chr7:1726124
|
T | C | 2 | a0001c0001t0005g0162a0001c0001t0055g0297 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-294+16872T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726124 | ||||||
chr7:1726256
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-294+17004T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726256 | ||||||
chr7:1726446
|
A | G | 62 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(59): Show | 62 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-294+17194A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726446 | ||||||
chr7:1726459
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-294+17207G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726459 | ||||||
chr7:1726659
|
T | C | 19 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(16): Show | 19 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-294+17407T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726659 | ||||||
chr7:1726676
|
C | G | 12 | a0001c0001t0001g0045a0001c0001t0001g0298a0001c0001t0008g0010others(9): Show | 12 | HG00639.hp2 HG01255.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-294+17424C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726676 | ||||||
chr7:1726715
|
A | T | 2 | a0001c0001t0001g0299a0001c0001t0005g0048 | 2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-294+17463A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726715 | ||||||
chr7:1726927
|
C | T | 12 | a0001c0001t0001g0045a0001c0001t0001g0298a0001c0001t0008g0010others(9): Show | 12 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-293-17377C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726927 | ||||||
chr7:1726986
|
C | G | 6 | a0001c0001t0008g0123a0001c0001t0008g0131a0001c0001t0020g0009others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-17318C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726986 | ||||||
chr7:1727034
|
C | T | 55 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(52): Show | 55 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-293-17270C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727034 | ||||||
chr7:1727113
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0160a0007c0012t0032g0159 | 3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-293-17191G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727113 | ||||||
chr7:1727264
|
C | T | 1 | a0001c0001t0003g0300 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-293-17040C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727264 | ||||||
chr7:1727389
|
C | G | 1 | a0001c0002t0004g0094 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-293-16915C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727389 | ||||||
chr7:1727437
|
G | A | 7 | a0001c0001t0001g0145a0001c0001t0005g0150a0001c0001t0025g0004others(4): Show | 7 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-293-16867G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727437 | ||||||
chr7:1727477
|
GTGCCCCT others(16): Show |
G | 19 | a0001c0001t0001g0045a0001c0001t0001g0298a0001c0001t0008g0010others(16): Show | 19 | HG01243.hp2 HG01255.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-293-16821_-293-16 others(29): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1727477 | |||||
chr7:1727518
|
C | A | 1 | a0001c0002t0001g0243 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-293-16786C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727518 | ||||||
chr7:1727547
|
G | T | 4 | a0001c0001t0001g0188a0001c0001t0003g0024a0001c0001t0006g0028others(1): Show | 4 | HG01884.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-16757G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727547 | ||||||
chr7:1727611
|
G | A | 11 | a0001c0001t0001g0045a0001c0001t0001g0298a0001c0001t0008g0010others(8): Show | 11 | HG01255.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-293-16693G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727611 | ||||||
chr7:1727792
|
T | G | 7 | a0001c0001t0003g0039a0001c0001t0038g0296a0001c0025t0058g0038others(4): Show | 7 | HG01109.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-16512T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727792 | ||||||
chr7:1727826
|
T | C | 1 | a0001c0001t0006g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-293-16478T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727826 | ||||||
chr7:1727972
|
C | T | 1 | a0001c0001t0015g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-293-16332C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727972 | ||||||
chr7:1727989
|
C | T | 16 | a0001c0001t0001g0125a0001c0001t0003g0016a0001c0001t0005g0294others(13): Show | 16 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-293-16315C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727989 | ||||||
chr7:1727994
|
T | C | 1 | a0001c0001t0008g0021 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-293-16310T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727994 | ||||||
chr7:1728070
|
C | T | 4 | a0001c0001t0003g0039a0001c0001t0038g0296a0001c0025t0058g0038others(1): Show | 4 | HG01109.hp2 HG02976.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-16234C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728070 | ||||||
chr7:1728169
|
C | CAG | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-293-16135_-293-16 others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728169 | ||||||
chr7:1728285
|
C | T | 6 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(3): Show | 6 | HG02622.hp2 HG02895.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-16019C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728285 | ||||||
chr7:1728286
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-293-16018G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728286 | ||||||
chr7:1728419
|
C | T | 7 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(4): Show | 7 | HG02622.hp2 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-15885C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728419 | ||||||
chr7:1728444
|
C | T | 6 | a0001c0001t0008g0123a0001c0001t0008g0131a0001c0001t0020g0009others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-15860C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728444 | ||||||
chr7:1728474
|
C | G | 13 | a0001c0001t0001g0045a0001c0001t0001g0298a0001c0001t0008g0010others(10): Show | 13 | HG01255.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-293-15830C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728474 | ||||||
chr7:1728859
|
G | A | 7 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(4): Show | 7 | HG02622.hp2 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-15445G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728859 | ||||||
chr7:1728903
|
T | TCATCATC others(10): Show |
2 | a0001c0001t0001g0204a0001c0001t0001g0216 | 2 | NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-293-15385_-293-15 others(23): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1728903 | |||||
chr7:1729023
|
C | T | 1 | a0001c0001t0015g0163 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-293-15281C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729023 | ||||||
chr7:1729024
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-293-15280G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729024 | ||||||
chr7:1729025
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-293-15279G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729025 | ||||||
chr7:1729129
|
C | T | 1 | a0001c0004t0061g0275 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-293-15175C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729129 | ||||||
chr7:1729153
|
A | G | 5 | a0001c0001t0003g0039a0001c0001t0038g0296a0001c0027t0062g0200others(2): Show | 5 | HG01109.hp2 HG02280.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-293-15151A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729153 | ||||||
chr7:1729267
|
T | G | 1 | a0001c0001t0006g0161 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-293-15037T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729267 | ||||||
chr7:1729403
|
G | A | 20 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(17): Show | 20 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-293-14901G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729403 | ||||||
chr7:1729532
|
G | A | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-293-14772G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729532 | ||||||
chr7:1729716
|
C | T | 2 | a0001c0001t0005g0136a0001c0001t0005g0156 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-293-14588C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729716 | ||||||
chr7:1729750
|
T | C | 11 | a0001c0001t0003g0039a0001c0001t0006g0118a0001c0001t0006g0291others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-293-14554T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729750 | ||||||
chr7:1729837
|
A | T | 57 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.-293-14467A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729837 | ||||||
chr7:1729914
|
G | A | 4 | a0001c0001t0003g0039a0001c0001t0038g0296a0001c0025t0058g0038others(1): Show | 4 | HG01109.hp2 HG02976.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-14390G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729914 | ||||||
chr7:1729948
|
C | T | 1 | a0001c0001t0006g0161 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-293-14356C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729948 | ||||||
chr7:1729996
|
C | G | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-293-14308C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729996 | ||||||
chr7:1730054
|
G | A | 3 | a0001c0001t0001g0298a0001c0001t0055g0297a0001c0001t0064g0006 | 3 | HG01255.hp1 HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-293-14250G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730054 | ||||||
chr7:1730067
|
C | T | 1 | a0001c0001t0005g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-293-14237C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730067 | ||||||
chr7:1730083
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-293-14221G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730083 | ||||||
chr7:1730182
|
G | A | 1 | a0001c0001t0047g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-293-14122G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730182 | ||||||
chr7:1730390
|
C | T | 1 | a0001c0001t0006g0161 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-293-13914C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730390 | ||||||
chr7:1730464
|
A | G | 10 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(7): Show | 10 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-293-13840A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730464 | ||||||
chr7:1730533
|
T | G | 2 | a0001c0001t0002g0198a0001c0001t0002g0223 | 2 | HG02155.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-293-13771T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730533 | ||||||
chr7:1730631
|
C | T | 1 | a0001c0001t0004g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-293-13673C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730631 | ||||||
chr7:1730905
|
A | G | 37 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(34): Show | 37 | HG00639.hp2 HG01243.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.-293-13399A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730905 | ||||||
chr7:1731164
|
T | C | 6 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(3): Show | 6 | HG02622.hp2 HG02895.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-13140T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731164 | ||||||
chr7:1731312
|
A | G | 57 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(54): Show | 57 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.-293-12992A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731312 | ||||||
chr7:1731618
|
G | A | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-293-12686G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731618 | ||||||
chr7:1731630
|
G | A | 1 | a0007c0012t0032g0159 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-293-12674G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731630 | ||||||
chr7:1731636
|
G | A | 56 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(53): Show | 56 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.-293-12668G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731636 | ||||||
chr7:1731727
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-293-12577C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731727 | ||||||
chr7:1731737
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-293-12567C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731737 | ||||||
chr7:1731753
|
G | A | 5 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0299others(2): Show | 5 | HG02559.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-293-12551G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731753 | ||||||
chr7:1731839
|
G | A | 19 | a0001c0001t0007g0166a0001c0001t0007g0167a0001c0001t0007g0168others(16): Show | 19 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.-293-12465G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731839 | ||||||
chr7:1731892
|
T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-293-12412T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731892 | ||||||
chr7:1732062
|
C | T | 3 | a0001c0001t0003g0039a0001c0001t0038g0296a0002c0003t0050g0179 | 3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-12242C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732062 | ||||||
chr7:1732124
|
G | A | 1 | a0001c0025t0058g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-293-12180G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732124 | ||||||
chr7:1732171
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-293-12133A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732171 | ||||||
chr7:1732172
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-293-12132G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732172 | ||||||
chr7:1732231
|
G | A | 3 | a0001c0001t0005g0136a0001c0001t0005g0156a0002c0003t0006g0005 | 3 | HG01243.hp1 HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-293-12073G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732231 | ||||||
chr7:1732440
|
C | T | 3 | a0001c0001t0003g0039a0001c0001t0038g0296a0002c0003t0050g0179 | 3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-11864C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732440 | ||||||
chr7:1732466
|
A | T | 1 | a0001c0001t0005g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-293-11838A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732466 | ||||||
chr7:1732559
|
T | C | 20 | a0001c0001t0001g0045a0001c0001t0001g0188a0001c0001t0001g0298others(17): Show | 20 | HG01243.hp2 HG01255.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-293-11745T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732559 | ||||||
chr7:1732993
|
T | C | 6 | a0001c0001t0008g0123a0001c0001t0008g0131a0001c0001t0020g0009others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-11311T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732993 | ||||||
chr7:1733003
|
C | A | 2 | a0001c0001t0001g0299a0001c0001t0005g0048 | 2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-293-11301C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733003 | ||||||
chr7:1733061
|
C | T | 2 | a0001c0001t0020g0009a0001c0001t0020g0132 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-293-11243C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733061 | ||||||
chr7:1733104
|
T | C | 7 | a0001c0001t0006g0118a0001c0001t0006g0291a0001c0001t0012g0184others(4): Show | 7 | HG01167.hp2 HG02145.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-11200T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733104 | ||||||
chr7:1733143
|
C | T | 1 | a0001c0002t0004g0255 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-293-11161C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733143 | ||||||
chr7:1733285
|
G | A | 8 | a0001c0001t0006g0118a0001c0001t0006g0291a0001c0001t0012g0184others(5): Show | 8 | HG01167.hp2 HG02145.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-293-11019G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733285 | ||||||
chr7:1733320
|
G | A | 2 | a0006c0008t0028g0293a0006c0008t0029g0292 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-293-10984G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733320 | ||||||
chr7:1733442
|
G | A | 14 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(11): Show | 14 | HG01167.hp2 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-293-10862G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733442 | ||||||
chr7:1733566
|
C | G | 1 | a0005c0010t0046g0152 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-293-10738C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733566 | ||||||
chr7:1733566
|
C | T | 3 | a0001c0001t0003g0039a0001c0001t0038g0296a0002c0003t0050g0179 | 3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-10738C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733566 | ||||||
chr7:1733626
|
C | T | 7 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(4): Show | 7 | HG02622.hp2 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-10678C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733626 | ||||||
chr7:1733744
|
T | C | 4 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0119others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-10560T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733744 | ||||||
chr7:1734044
|
C | A | 1 | a0001c0001t0025g0046 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-293-10260C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734044 | ||||||
chr7:1734092
|
C | G | 14 | a0001c0001t0001g0045a0001c0001t0001g0188a0001c0001t0001g0298others(11): Show | 14 | HG01255.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-293-10212C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734092 | ||||||
chr7:1734139
|
G | T | 2 | a0001c0025t0058g0038a0002c0024t0030g0020 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-293-10165G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734139 | ||||||
chr7:1734267
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0142a0002c0003t0024g0037others(2): Show | 5 | HG02055.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-293-10037C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734267 | ||||||
chr7:1734314
|
G | A | 1 | a0002c0003t0024g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-293-9990G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734314 | ||||||
chr7:1734360
|
C | T | 57 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(54): Show | 57 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.-293-9944C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734360 | ||||||
chr7:1734729
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-293-9575T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734729 | ||||||
chr7:1734784
|
A | G | 1 | a0001c0001t0004g0226 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-293-9520A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734784 | ||||||
chr7:1734842
|
C | T | 3 | a0001c0001t0003g0039a0001c0001t0038g0296a0002c0003t0050g0179 | 3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-9462C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734842 | ||||||
chr7:1734952
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-293-9352C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734952 | ||||||
chr7:1735054
|
G | A | 2 | a0002c0003t0024g0144a0002c0003t0024g0183 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-293-9250G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735054 | ||||||
chr7:1735109
|
C | G | 2 | a0001c0025t0058g0038a0002c0024t0030g0020 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-293-9195C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735109 | ||||||
chr7:1735135
|
C | T | 1 | a0001c0001t0011g0213 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-293-9169C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735135 | ||||||
chr7:1735167
|
T | A | 28 | a0001c0001t0001g0096a0001c0001t0001g0214a0001c0001t0002g0112others(25): Show | 28 | HG00558.hp1 HG00639.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-293-9137T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735167 | ||||||
chr7:1735170
|
A | G | 62 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(59): Show | 62 | HG00558.hp1 HG00639.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.-293-9134A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735170 | ||||||
chr7:1735175
|
G | T | 6 | a0001c0001t0008g0123a0001c0001t0008g0131a0001c0001t0020g0009others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-9129G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735175 | ||||||
chr7:1735191
|
G | A | 4 | a0001c0001t0005g0220a0001c0001t0005g0232a0001c0001t0005g0233others(1): Show | 4 | HG02083.hp2 NA18946.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-9113G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735191 | ||||||
chr7:1735199
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-293-9105G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735199 | ||||||
chr7:1735201
|
C | T | 1 | a0001c0001t0065g0295 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-293-9103C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735201 | ||||||
chr7:1735229
|
A | T | 1 | a0008c0013t0020g0091 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-293-9075A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735229 | ||||||
chr7:1735269
|
G | A | 1 | a0001c0001t0003g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-293-9035G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735269 | ||||||
chr7:1735276
|
T | C | 2 | a0001c0001t0026g0012a0001c0001t0051g0011 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-293-9028T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735276 | ||||||
chr7:1735312
|
A | C | 26 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(23): Show | 26 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-293-8992A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735312 | ||||||
chr7:1735460
|
G | C | 40 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(37): Show | 40 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.-293-8844G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735460 | ||||||
chr7:1735529
|
C | T | 1 | a0001c0001t0031g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-293-8775C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735529 | ||||||
chr7:1735607
|
A | G | 46 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(43): Show | 46 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.-293-8697A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735607 | ||||||
chr7:1735958
|
G | A | 1 | a0001c0001t0023g0196 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-293-8346G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735958 | ||||||
chr7:1736086
|
C | G | 1 | a0002c0024t0030g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-293-8218C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736086 | ||||||
chr7:1736092
|
C | G | 6 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0299others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-8212C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736092 | ||||||
chr7:1736272
|
T | TC | 6 | a0001c0001t0008g0123a0001c0001t0008g0131a0001c0001t0020g0009others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-8027dupC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1736272 | |||||
chr7:1736282
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-293-8022G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736282 | ||||||
chr7:1736325
|
G | A | 17 | a0001c0001t0007g0166a0001c0001t0007g0167a0001c0001t0007g0168others(14): Show | 17 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-7979G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736325 | ||||||
chr7:1736441
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0142a0003c0006t0016g0182others(1): Show | 4 | HG02055.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-7863G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736441 | ||||||
chr7:1736539
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-293-7765C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736539 | ||||||
chr7:1736572
|
C | G | 1 | a0002c0003t0050g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-293-7732C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736572 | ||||||
chr7:1736730
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-293-7574T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736730 | ||||||
chr7:1736796
|
G | A | 55 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(52): Show | 55 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-293-7508G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736796 | ||||||
chr7:1736851
|
C | T | 1 | a0001c0001t0022g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-293-7453C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736851 | ||||||
chr7:1736862
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-7442C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736862 | ||||||
chr7:1736945
|
GA | G | 17 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(14): Show | 17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-7358delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736945 | ||||||
chr7:1736947
|
T | C | 17 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(14): Show | 17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-7357T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736947 | ||||||
chr7:1736985
|
C | G | 1 | a0001c0001t0031g0100 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-293-7319C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736985 | ||||||
chr7:1737080
|
G | T | 1 | a0001c0001t0001g0210 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-293-7224G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737080 | ||||||
chr7:1737108
|
C | A | 5 | a0001c0001t0002g0062a0001c0001t0002g0075a0001c0001t0002g0172others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-293-7196C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737108 | ||||||
chr7:1737127
|
C | G | 1 | a0001c0001t0011g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-293-7177C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737127 | ||||||
chr7:1737330
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-293-6974T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737330 | ||||||
chr7:1737331
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-293-6973C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737331 | ||||||
chr7:1737332
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-293-6972A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737332 | ||||||
chr7:1737378
|
G | A | 3 | a0001c0001t0003g0039a0001c0001t0038g0296a0002c0003t0050g0179 | 3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-6926G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737378 | ||||||
chr7:1737709
|
G | A | 6 | a0001c0001t0008g0123a0001c0001t0008g0131a0001c0001t0020g0009others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-6595G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737709 | ||||||
chr7:1737777
|
T | C | 25 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0035others(22): Show | 25 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-293-6527T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737777 | ||||||
chr7:1737821
|
C | T | 4 | a0001c0001t0005g0220a0001c0001t0005g0232a0001c0001t0005g0233others(1): Show | 4 | HG02083.hp2 NA18946.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-6483C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737821 | ||||||
chr7:1737980
|
C | G | 1 | a0001c0001t0019g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-293-6324C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737980 | ||||||
chr7:1738001
|
C | T | 2 | a0001c0025t0058g0038a0002c0024t0030g0020 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-293-6303C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738001 | ||||||
chr7:1738030
|
G | A | 1 | a0008c0013t0020g0091 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-293-6274G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738030 | ||||||
chr7:1738050
|
C | T | 17 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(14): Show | 17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-6254C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738050 | ||||||
chr7:1738188
|
A | T | 1 | a0001c0001t0005g0294 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-293-6116A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738188 | ||||||
chr7:1738330
|
C | T | 1 | a0001c0001t0006g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-293-5974C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738330 | ||||||
chr7:1738392
|
A | G | 1 | a0015c0023t0003g0130 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-293-5912A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738392 | ||||||
chr7:1738406
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0139 | 2 | HG00621.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-293-5898C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738406 | ||||||
chr7:1738590
|
G | T | 17 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(14): Show | 17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-5714G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738590 | ||||||
chr7:1738710
|
C | T | 4 | a0001c0002t0003g0267a0001c0002t0003g0268a0001c0002t0003g0270others(1): Show | 4 | NA18964.hp2 NA18995.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-5594C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738710 | ||||||
chr7:1738720
|
G | A | 5 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0299others(2): Show | 5 | HG02559.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-293-5584G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738720 | ||||||
chr7:1738731
|
C | T | 1 | a0001c0001t0025g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-293-5573C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738731 | ||||||
chr7:1738746
|
C | T | 17 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(14): Show | 17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-5558C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738746 | ||||||
chr7:1738934
|
C | G | 1 | a0002c0003t0050g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-293-5370C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738934 | ||||||
chr7:1738968
|
C | T | 12 | a0001c0001t0005g0294a0001c0001t0006g0128a0001c0001t0009g0043others(9): Show | 12 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-293-5336C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738968 | ||||||
chr7:1739007
|
C | T | 3 | a0001c0001t0003g0039a0001c0001t0038g0296a0002c0003t0050g0179 | 3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-5297C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739007 | ||||||
chr7:1739071
|
C | T | 7 | a0001c0001t0007g0202a0001c0001t0008g0123a0001c0001t0008g0131others(4): Show | 7 | HG00621.hp1 HG01243.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-293-5233C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739071 | ||||||
chr7:1739105
|
C | T | 136 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0018others(133): Show | 136 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-293-5199C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739105 | ||||||
chr7:1739114
|
G | A | 2 | a0001c0025t0058g0038a0002c0024t0030g0020 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-293-5190G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739114 | ||||||
chr7:1739127
|
C | A | 2 | a0001c0001t0011g0084a0001c0001t0011g0241 | 2 | NA18612.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-293-5177C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739127 | ||||||
chr7:1739139
|
T | A | 1 | a0001c0001t0005g0220 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-293-5165T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739139 | ||||||
chr7:1739166
|
G | T | 1 | a0001c0001t0047g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-293-5138G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739166 | ||||||
chr7:1739221
|
T | C | 2 | a0001c0001t0012g0211a0001c0001t0012g0212 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-293-5083T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739221 | ||||||
chr7:1739248
|
C | T | 6 | a0001c0001t0008g0123a0001c0001t0008g0131a0001c0001t0020g0009others(3): Show | 6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-5056C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739248 | ||||||
chr7:1739265
|
G | A | 1 | a0002c0003t0003g0014 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-293-5039G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739265 | ||||||
chr7:1739317
|
T | G | 96 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0045others(93): Show | 96 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-293-4987T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739317 | ||||||
chr7:1739351
|
C | G | 1 | a0002c0003t0024g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-293-4953C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739351 | ||||||
chr7:1739448
|
C | T | 4 | a0001c0001t0001g0298a0001c0001t0029g0023a0001c0001t0055g0297others(1): Show | 4 | HG01255.hp1 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-4856C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739448 | ||||||
chr7:1739473
|
C | T | 103 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0018others(100): Show | 103 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-293-4831C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739473 | ||||||
chr7:1739611
|
G | A | 2 | a0001c0001t0001g0125a0001c0002t0003g0111 | 2 | HG01934.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-293-4693G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739611 | ||||||
chr7:1739733
|
C | T | 2 | a0001c0001t0011g0084a0001c0001t0011g0241 | 2 | NA18612.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-293-4571C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739733 | ||||||
chr7:1739757
|
G | C | 1 | a0001c0002t0004g0255 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-293-4547G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739757 | ||||||
chr7:1739828
|
G | A | 3 | a0001c0001t0012g0184a0002c0003t0024g0144a0002c0003t0024g0183 | 3 | HG01167.hp2 HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-293-4476G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739828 | ||||||
chr7:1740003
|
C | T | 3 | a0001c0001t0003g0039a0001c0001t0038g0296a0002c0003t0050g0179 | 3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-4301C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740003 | ||||||
chr7:1740161
|
G | A | 1 | a0001c0001t0002g0112 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-293-4143G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740161 | ||||||
chr7:1740303
|
G | A | 2 | a0001c0025t0058g0038a0002c0024t0030g0020 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-293-4001G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740303 | ||||||
chr7:1740430
|
C | T | 1 | a0001c0001t0003g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-293-3874C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740430 | ||||||
chr7:1740702
|
C | T | 17 | a0001c0001t0001g0018a0001c0001t0003g0133a0001c0001t0003g0134others(14): Show | 17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-3602C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740702 | ||||||
chr7:1740804
|
C | T | 1 | a0009c0015t0032g0191 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-293-3500C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740804 | ||||||
chr7:1740807
|
G | A | 2 | a0001c0001t0003g0300a0001c0001t0019g0058 | 2 | HG02559.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-293-3497G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740807 | ||||||
chr7:1740928
|
G | A | 1 | a0001c0002t0018g0229 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-293-3376G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740928 | ||||||
chr7:1741062
|
A | G | 1 | a0001c0001t0002g0198 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-293-3242A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741062 | ||||||
chr7:1741111
|
C | G | 1 | a0001c0001t0003g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-293-3193C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741111 | ||||||
chr7:1741129
|
C | CA | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.-293-3156dupA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1741129 | |||||
chr7:1741129
|
C | CAA | 17 | a0001c0001t0001g0077a0001c0001t0001g0092a0001c0001t0001g0214others(14): Show | 17 | HG01167.hp1 HG01169.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.-293-3157_-293-315 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1741129 | |||||
chr7:1741129
|
CA | C | 22 | a0001c0001t0001g0045a0001c0001t0001g0298a0001c0001t0002g0069others(19): Show | 22 | HG00639.hp2 HG01168.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.-293-3156delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1741129 | |||||
chr7:1741231
|
C | G | 3 | a0001c0001t0003g0039a0001c0001t0038g0296a0002c0003t0050g0179 | 3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-3073C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741231 | ||||||
chr7:1741252
|
C | T | 1 | a0001c0002t0004g0262 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-293-3052C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741252 | ||||||
chr7:1741263
|
C | T | 3 | a0001c0001t0003g0039a0001c0001t0038g0296a0002c0003t0050g0179 | 3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-3041C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741263 | ||||||
chr7:1741308
|
G | C | 1 | a0001c0011t0034g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-293-2996G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741308 | ||||||
chr7:1741318
|
C | T | 1 | a0001c0001t0006g0161 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-293-2986C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741318 | ||||||
chr7:1741340
|
G | T | 13 | a0001c0001t0001g0045a0001c0001t0003g0024a0001c0001t0005g0162others(10): Show | 13 | HG01255.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-293-2964G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741340 | ||||||
chr7:1741410
|
A | G | 1 | a0002c0024t0030g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-293-2894A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741410 | ||||||
chr7:1741463
|
C | T | 1 | a0001c0001t0005g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-293-2841C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741463 | ||||||
chr7:1741558
|
T | C | 33 | a0001c0001t0001g0045a0001c0001t0001g0214a0001c0001t0002g0089others(30): Show | 33 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.-293-2746T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741558 | ||||||
chr7:1741663
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0022others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-293-2641G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741663 | ||||||
chr7:1741767
|
G | C | 1 | a0001c0001t0002g0052 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-293-2537G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741767 | ||||||
chr7:1741786
|
T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-293-2518T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741786 | ||||||
chr7:1741805
|
C | G | 3 | a0001c0001t0005g0136a0001c0001t0020g0009a0001c0001t0020g0132 | 3 | HG02258.hp2 HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-293-2499C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741805 | ||||||
chr7:1741855
|
AGACAGGG others(1275): Show |
A | 1 | a0001c0001t0049g0017 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-293-2445_-293-116 others(4): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1741855 | |||||
chr7:1741913
|
G | A | 1 | a0001c0001t0052g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-293-2391G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741913 | ||||||
chr7:1741917
|
T | C | 5 | a0001c0001t0001g0160a0001c0001t0005g0048a0001c0001t0008g0021others(2): Show | 5 | HG01496.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-293-2387T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741917 | ||||||
chr7:1741975
|
CACAG | C | 16 | a0001c0001t0001g0059a0001c0001t0001g0085a0001c0001t0005g0220others(13): Show | 16 | HG01099.hp1 HG01261.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.-293-2325_-293-232 others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1741975 | |||||
chr7:1742000
|
G | A | 1 | a0001c0001t0052g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-293-2304G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742000 | ||||||
chr7:1742025
|
T | G | 1 | a0001c0001t0028g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-293-2279T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742025 | ||||||
chr7:1742151
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0145 | 2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-293-2153C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742151 | ||||||
chr7:1742176
|
G | A | 3 | a0001c0001t0001g0192a0002c0003t0050g0179a0009c0015t0032g0191 | 3 | HG01496.hp1 HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-2128G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742176 | ||||||
chr7:1742297
|
C | T | 1 | a0001c0001t0028g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-293-2007C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742297 | ||||||
chr7:1742376
|
G | A | 1 | a0001c0027t0062g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-293-1928G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742376 | ||||||
chr7:1742396
|
C | G | 43 | a0001c0001t0001g0265a0001c0001t0001g0298a0001c0001t0002g0052others(40): Show | 43 | HG00558.hp1 HG00642.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-293-1908C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742396 | ||||||
chr7:1742454
|
G | A | 1 | a0001c0001t0009g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-293-1850G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742454 | ||||||
chr7:1742542
|
C | T | 4 | a0001c0002t0003g0267a0001c0002t0003g0268a0001c0002t0003g0270others(1): Show | 4 | NA18964.hp2 NA18995.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-1762C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742542 | ||||||
chr7:1742578
|
G | A | 1 | a0001c0001t0005g0219 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-293-1726G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742578 | ||||||
chr7:1742656
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0142a0001c0001t0001g0145others(3): Show | 6 | HG02055.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-293-1648C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742656 | ||||||
chr7:1742711
|
G | A | 1 | a0001c0001t0012g0184 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-293-1593G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742711 | ||||||
chr7:1742796
|
C | T | 7 | a0001c0001t0031g0100a0001c0001t0040g0040a0001c0001t0041g0171others(4): Show | 7 | HG02735.hp1 HG04204.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-1508C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742796 | ||||||
chr7:1742888
|
G | T | 1 | a0001c0002t0004g0289 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-293-1416G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742888 | ||||||
chr7:1742967
|
G | A | 1 | a0006c0008t0029g0292 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-293-1337G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742967 | ||||||
chr7:1742970
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-293-1334G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742970 | ||||||
chr7:1743088
|
TG | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-293-1209delG | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1743088 | |||||
chr7:1743137
|
G | A | 139 | a0001c0001t0001g0116a0001c0001t0001g0188a0001c0001t0001g0265others(136): Show | 139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-293-1167G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743137 | ||||||
chr7:1743140
|
C | T | 1 | a0001c0002t0004g0277 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-293-1164C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743140 | ||||||
chr7:1743145
|
C | T | 3 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0052g0026 | 3 | HG03139.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-293-1159C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743145 | ||||||
chr7:1743412
|
A | C | 4 | a0001c0001t0017g0080a0001c0001t0017g0099a0001c0001t0017g0101others(1): Show | 4 | HG01099.hp1 HG01358.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-892A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743412 | ||||||
chr7:1743488
|
A | C | 1 | a0001c0001t0006g0161 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-293-816A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743488 | ||||||
chr7:1743503
|
T | G | 1 | a0001c0001t0016g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-293-801T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743503 | ||||||
chr7:1743528
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-293-776A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743528 | ||||||
chr7:1743544
|
TG | T | 3 | a0002c0003t0024g0037a0002c0003t0024g0144a0002c0003t0024g0183 | 3 | HG02145.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-293-756delG | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1743544 | |||||
chr7:1743624
|
G | A | 3 | a0001c0001t0001g0245a0001c0001t0001g0283a0001c0001t0060g0246 | 3 | HG02135.hp1 NA18946.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-293-680G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743624 | ||||||
chr7:1743668
|
G | T | 1 | a0001c0027t0062g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-293-636G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743668 | ||||||
chr7:1743683
|
G | T | 2 | a0006c0008t0028g0293a0006c0008t0029g0292 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-293-621G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743683 | ||||||
chr7:1743689
|
G | A | 1 | a0001c0001t0005g0294 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-293-615G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743689 | ||||||
chr7:1743737
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 104 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-293-567G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743737 | ||||||
chr7:1743737
|
G | T | 1 | a0001c0002t0003g0251 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-293-567G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743737 | ||||||
chr7:1743761
|
C | G | 1 | a0001c0027t0062g0200 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-293-543C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743761 | ||||||
chr7:1743769
|
G | A | 6 | a0001c0001t0026g0135a0001c0005t0010g0141a0001c0005t0010g0143others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-535G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743769 | ||||||
chr7:1743853
|
G | A | 1 | a0001c0001t0004g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-293-451G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743853 | ||||||
chr7:1743946
|
C | T | 1 | a0001c0001t0009g0119 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-293-358C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743946 | ||||||
chr7:1744022
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0155 | 3 | HG02451.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-293-282C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744022 | ||||||
chr7:1744118
|
GA | G | 4 | a0001c0001t0008g0021a0001c0001t0008g0123a0001c0001t0008g0131others(1): Show | 4 | HG02615.hp2 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-185delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744118 | ||||||
chr7:1744145
|
G | A | 47 | a0001c0001t0001g0067a0001c0001t0001g0116a0001c0001t0004g0205others(44): Show | 47 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.-293-159G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744145 | ||||||
chr7:1744215
|
G | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(293): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-293-89G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744215 | ||||||
chr7:1744215
|
G | T | 1 | a0001c0002t0003g0251 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-293-89G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744215 | ||||||
chr7:1744222
|
C | T | 1 | a0001c0001t0021g0276 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-293-82C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744222 | ||||||
chr7:1744242
|
CGTCCCCT others(19): Show |
C | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(97): Show | 100 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
splice_region_variant&intron_variant | LOW | c.-293-32_-293-7delC others(25): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1744242 | |||||
chr7:1744280
|
G | A | 11 | a0001c0001t0005g0027a0001c0001t0005g0048a0001c0001t0005g0150others(8): Show | 11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-293-24G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744280 |