Item | Value |
---|---|
geneid | 25975 |
ensemblid | ENSG00000198759.12 |
hgncid | 3235 |
symbol | EGFL6 |
name | EGF like domain multiple 6 |
refseq_nuc | NM_015507.4 |
refseq_prot | NP_056322.2 |
ensembl_nuc | ENST00000361306.6 |
ensembl_prot | ENSP00000355126.1 |
mane_status | MANE Select |
chr | chrX |
start | 13569601 |
end | 13633575 |
strand | + |
ver | v1.2 |
region | chrX:13569601-13633575 |
region5000 | chrX:13564601-13638575 |
regionname0 | EGFL6_chrX_13569601_13633575 |
regionname5000 | EGFL6_chrX_13564601_13638575 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 553 | 236 | 42 | 43 | 107 | 11 | 31 | 85 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0002 | 0/0 | 553 | 45 | 17 | 3 | 24 | 0 | 1 | 21 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0003 | 0/0 | 553 | 5 | 0 | 3 | 2 | 0 | 0 | 2 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0004 | 0/0 | 553 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0005 | 0/0 | 553 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0006 | 0/0 | 553 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0007 | 0/0 | 553 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0008 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0009 | 0/0 | 553 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0010 | 0/0 | 553 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0011 | 0/0 | 553 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0012 | 0/0 | 553 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0013 | 0/0 | 553 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1662 | 206 | 29 | 37 | 101 | 11 | 26 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0002 | 0/0 | 1662 | 24 | 0 | 0 | 24 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0003 | 0/0 | 1662 | 19 | 15 | 3 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0004 | 0/0 | 1662 | 12 | 2 | 3 | 5 | 0 | 2 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0005 | 0/0 | 1662 | 9 | 8 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0006 | 0/0 | 1662 | 5 | 0 | 3 | 2 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0007 | 0/0 | 1662 | 4 | 1 | 0 | 1 | 0 | 2 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0008 | 0/0 | 1662 | 3 | 2 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0009 | 0/0 | 1662 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0010 | 0/0 | 1662 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0011 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0012 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0013 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0014 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0015 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0016 | 0/0 | 1662 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0017 | 0/0 | 1665 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0018 | 0/0 | 1662 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0019 | 0/0 | 1662 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0020 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0021 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0022 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0023 | 0/0 | 1662 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0024 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0025 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
c0026 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 742 | 129 | 31 | 31 | 49 | 4 | 12 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0002 | 0/0 | 742 | 63 | 8 | 5 | 44 | 2 | 4 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0003 | 0/0 | 742 | 40 | 5 | 7 | 10 | 5 | 13 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0004 | 0/0 | 742 | 35 | 18 | 6 | 11 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0005 | 0/0 | 742 | 10 | 5 | 0 | 4 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0006 | 0/0 | 742 | 8 | 1 | 1 | 6 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0007 | 0/0 | 742 | 7 | 2 | 0 | 5 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0008 | 0/0 | 742 | 5 | 1 | 0 | 3 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0009 | 0/0 | 743 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0010 | 0/0 | 742 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0011 | 0/0 | 742 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0012 | 0/0 | 742 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
t0013 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0292 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1662 | 206 | 29 | 37 | 101 | 11 | 26 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0001c0004 | 0/0 | 1662 | 12 | 2 | 3 | 5 | 0 | 2 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0001c0005 | 0/0 | 1662 | 9 | 8 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0001c0007 | 0/0 | 1662 | 4 | 1 | 0 | 1 | 0 | 2 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0001c0008 | 0/0 | 1662 | 3 | 2 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0001c0018 | 0/0 | 1662 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0001c0019 | 0/0 | 1662 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0002c0002 | 0/0 | 1662 | 24 | 0 | 0 | 24 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0002c0003 | 0/0 | 1662 | 19 | 15 | 3 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0002c0025 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0002c0026 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0003c0006 | 0/0 | 1662 | 5 | 0 | 3 | 2 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0004c0010 | 0/0 | 1662 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0004c0021 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0004c0022 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0005c0012 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0005c0013 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0005c0014 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0006c0009 | 0/0 | 1662 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0007c0024 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0008c0017 | 0/0 | 1665 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0009c0020 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0010c0016 | 0/0 | 1662 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0011c0023 | 0/0 | 1662 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0012c0011 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 | |
a0013c0015 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2403 | 104 | 12 | 28 | 47 | 4 | 11 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0001t0002 | 0/0 | 2403 | 56 | 7 | 3 | 41 | 2 | 3 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0001t0003 | 0/0 | 2403 | 31 | 4 | 4 | 8 | 5 | 10 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0001t0004 | 0/0 | 2403 | 4 | 2 | 2 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0001t0005 | 0/0 | 2403 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0001t0008 | 0/0 | 2403 | 4 | 1 | 0 | 2 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0001t0009 | 0/0 | 2404 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0001t0010 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0001t0011 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0001t0012 | 0/0 | 2403 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0001t0013 | 0/0 | 2402 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0004t0001 | 0/0 | 2403 | 4 | 1 | 1 | 1 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0004t0002 | 0/0 | 2403 | 3 | 0 | 0 | 3 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0004t0003 | 0/0 | 2403 | 3 | 0 | 2 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0004t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0004t0008 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0005t0001 | 0/0 | 2403 | 8 | 7 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0005t0002 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0007t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0007t0003 | 0/0 | 2403 | 3 | 0 | 0 | 1 | 0 | 2 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0008t0001 | 0/0 | 2403 | 3 | 2 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0018t0003 | 0/0 | 2403 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0001c0019t0002 | 0/0 | 2403 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0002c0002t0004 | 0/0 | 2403 | 10 | 0 | 0 | 10 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0002c0002t0005 | 0/0 | 2403 | 4 | 0 | 0 | 4 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0002c0002t0006 | 0/0 | 2403 | 5 | 0 | 0 | 5 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0002c0002t0007 | 0/0 | 2403 | 5 | 0 | 0 | 5 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0002c0003t0004 | 0/0 | 2403 | 13 | 10 | 3 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0002c0003t0005 | 0/0 | 2403 | 4 | 3 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0002c0003t0006 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0002c0003t0007 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0002c0025t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0002c0026t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0003c0006t0002 | 0/0 | 2403 | 2 | 0 | 2 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0003c0006t0004 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0003c0006t0006 | 0/0 | 2403 | 2 | 0 | 1 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0004c0010t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0004c0010t0003 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0004c0021t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0004c0022t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0005c0012t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0005c0013t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0005c0014t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0006c0009t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0006c0009t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0007c0024t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0008c0017t0003 | 0/0 | 2406 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0009c0020t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0010c0016t0004 | 0/0 | 2403 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0011c0023t0001 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0012c0011t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
a0013c0015t0007 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | copy fasta | chrX | 13564601 | 13638575 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0001g0292 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0008g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0008g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0010g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0011g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0012g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0001t0013g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0004t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0004t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0004t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0004t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0004t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0004t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0004t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0004t0008g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0005t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0005t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0005t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0005t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0005t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0005t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0007t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0007t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0007t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0007t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0008t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0008t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0008t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0018t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0001c0019t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0002t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0003t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0025t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0002c0026t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0003c0006t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0003c0006t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0003c0006t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0003c0006t0006g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0004c0010t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0004c0010t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0004c0021t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0004c0022t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0005c0012t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0005c0013t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0005c0014t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0006c0009t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0006c0009t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0007c0024t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0008c0017t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0009c0020t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0010c0016t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0011c0023t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0012c0011t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
a0013c0015t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0239 | EUR | GBR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0096 | EUR | GBR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0224 | EUR | FIN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0245 | EUR | FIN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00544 | hp1 | a0001 | c0004 | t0008 | g0014 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00621 | hp1 | a0002 | c0002 | t0006 | g0168 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0194 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01070 | hp1 | a0002 | c0003 | t0004 | g0146 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0228 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01074 | hp1 | a0002 | c0003 | t0004 | g0147 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01106 | hp1 | a0001 | c0005 | t0001 | g0053 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01109 | hp1 | a0010 | c0016 | t0004 | g0025 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01167 | hp1 | a0001 | c0004 | t0003 | g0003 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01169 | hp2 | a0001 | c0004 | t0003 | g0003 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01243 | hp1 | a0002 | c0003 | t0004 | g0052 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01346 | hp2 | a0001 | c0018 | t0003 | g0075 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0089 | EUR | IBS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01891 | hp1 | a0002 | c0003 | t0004 | g0160 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0151 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01975 | hp1 | a0003 | c0006 | t0002 | g0128 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02004 | hp1 | a0003 | c0006 | t0002 | g0121 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02027 | hp1 | a0001 | c0007 | t0003 | g0297 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02132 | hp1 | a0001 | c0001 | t0011 | g0210 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02145 | hp1 | a0001 | c0005 | t0001 | g0219 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02148 | hp2 | a0003 | c0006 | t0006 | g0004 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CDX | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02155 | hp2 | a0002 | c0002 | t0007 | g0018 | EAS | CDX | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02258 | hp1 | a0005 | c0014 | t0001 | g0028 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02280 | hp2 | a0013 | c0015 | t0007 | g0009 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02293 | hp1 | a0001 | c0008 | t0001 | g0048 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02451 | hp1 | a0002 | c0003 | t0005 | g0047 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02451 | hp2 | a0001 | c0004 | t0001 | g0066 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02523 | hp2 | a0002 | c0002 | t0006 | g0144 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02572 | hp1 | a0001 | c0004 | t0004 | g0055 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02615 | hp2 | a0002 | c0003 | t0004 | g0152 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02622 | hp1 | a0001 | c0005 | t0001 | g0049 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02630 | hp1 | a0006 | c0009 | t0004 | g0033 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02630 | hp2 | a0012 | c0011 | t0004 | g0054 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02647 | hp1 | a0004 | c0022 | t0001 | g0175 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02717 | hp1 | a0001 | c0001 | t0008 | g0294 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02723 | hp2 | a0001 | c0007 | t0001 | g0272 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02809 | hp2 | a0009 | c0020 | t0001 | g0232 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02886 | hp1 | a0001 | c0005 | t0001 | g0280 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02895 | hp1 | a0001 | c0008 | t0001 | g0173 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02965 | hp1 | a0002 | c0003 | t0005 | g0042 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02970 | hp1 | a0002 | c0025 | t0004 | g0265 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02976 | hp1 | a0005 | c0012 | t0001 | g0050 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03017 | hp1 | a0001 | c0004 | t0001 | g0243 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03041 | hp1 | a0001 | c0005 | t0002 | g0119 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03041 | hp2 | a0004 | c0010 | t0001 | g0241 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03139 | hp1 | a0004 | c0010 | t0003 | g0086 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03195 | hp2 | a0001 | c0008 | t0001 | g0295 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03209 | hp1 | a0002 | c0003 | t0004 | g0030 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03239 | hp2 | a0001 | c0004 | t0003 | g0061 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03453 | hp1 | a0002 | c0003 | t0004 | g0240 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03453 | hp2 | a0002 | c0003 | t0004 | g0051 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03486 | hp1 | a0002 | c0026 | t0004 | g0029 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03491 | hp1 | a0001 | c0001 | t0008 | g0011 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03491 | hp2 | a0001 | c0007 | t0003 | g0171 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03492 | hp1 | a0001 | c0007 | t0003 | g0172 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03516 | hp2 | a0002 | c0003 | t0004 | g0285 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03540 | hp1 | a0002 | c0003 | t0004 | g0032 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03579 | hp1 | a0001 | c0005 | t0001 | g0246 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03654 | hp1 | a0002 | c0003 | t0005 | g0167 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03688 | hp1 | a0001 | c0019 | t0002 | g0065 | SAS | STU | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03834 | hp2 | a0001 | c0001 | t0012 | g0093 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | STU | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0293 | SAS | STU | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18522 | hp1 | a0002 | c0003 | t0005 | g0046 | AFR | YRI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18906 | hp2 | a0001 | c0005 | t0001 | g0231 | AFR | YRI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18939 | hp1 | a0002 | c0002 | t0006 | g0126 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18939 | hp2 | a0002 | c0002 | t0004 | g0021 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18941 | hp1 | a0002 | c0002 | t0004 | g0202 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18943 | hp1 | a0002 | c0002 | t0005 | g0017 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18944 | hp1 | a0002 | c0002 | t0006 | g0099 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18946 | hp2 | a0002 | c0002 | t0007 | g0001 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18949 | hp2 | a0008 | c0017 | t0003 | g0296 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18954 | hp2 | a0002 | c0002 | t0007 | g0001 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18956 | hp2 | a0002 | c0002 | t0004 | g0213 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18959 | hp1 | a0003 | c0006 | t0004 | g0289 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18964 | hp2 | a0002 | c0002 | t0005 | g0153 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18967 | hp1 | a0001 | c0001 | t0009 | g0057 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18968 | hp1 | a0002 | c0002 | t0004 | g0264 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18970 | hp1 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18974 | hp1 | a0002 | c0002 | t0004 | g0282 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18977 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18979 | hp2 | a0002 | c0002 | t0007 | g0016 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18983 | hp1 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18990 | hp1 | a0002 | c0002 | t0005 | g0154 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18993 | hp2 | a0003 | c0006 | t0006 | g0004 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18994 | hp1 | a0011 | c0023 | t0001 | g0176 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19002 | hp2 | a0002 | c0002 | t0007 | g0015 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19004 | hp1 | a0002 | c0002 | t0004 | g0263 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0270 | AFR | LWK | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | LWK | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19043 | hp1 | a0002 | c0003 | t0004 | g0036 | AFR | LWK | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19056 | hp1 | a0001 | c0004 | t0001 | g0019 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19057 | hp1 | a0001 | c0004 | t0002 | g0125 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19057 | hp2 | a0002 | c0002 | t0004 | g0091 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19064 | hp2 | a0002 | c0002 | t0004 | g0020 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19065 | hp1 | a0002 | c0002 | t0004 | g0209 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19066 | hp1 | a0002 | c0002 | t0005 | g0077 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19072 | hp1 | a0001 | c0004 | t0002 | g0123 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19074 | hp2 | a0002 | c0002 | t0006 | g0097 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19076 | hp1 | a0001 | c0001 | t0013 | g0006 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19084 | hp1 | a0001 | c0004 | t0002 | g0124 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | YRI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ASW | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA20129 | hp2 | a0002 | c0003 | t0004 | g0031 | AFR | ASW | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0085 | EUR | TSI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0164 | EUR | TSI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | GIH | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02109 | hp1 | a0002 | c0003 | t0004 | g0284 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02486 | hp1 | a0004 | c0021 | t0001 | g0041 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02559 | hp1 | a0001 | c0005 | t0001 | g0148 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG02559 | hp2 | a0007 | c0024 | t0001 | g0040 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG03471 | hp1 | a0002 | c0003 | t0007 | g0010 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG06807 | hp1 | a0001 | c0005 | t0001 | g0271 | AFR | USA | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
HG06807 | hp2 | a0002 | c0003 | t0006 | g0037 | AFR | USA | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA20300 | hp1 | a0006 | c0009 | t0001 | g0283 | AFR | USA | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA20300 | hp2 | a0005 | c0013 | t0004 | g0027 | AFR | USA | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | LWK | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | LWK | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0292 | REF | REF | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0035 | REF | REF | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:13594844 | G | A | 4 | a0005a0006a0012others(1): Show | 7 | HG02258.hp1 HG02280.hp2 HG02630.hp1 others(4): Show |
missense_variant | MODERATE | c.196G>A | p.Glu66Lys | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/12 | 457/2403 | 196/1662 | 66/553 | chrX | 13594844 | ||
chrX:13600001 | C | T | 2 | a0006a0013 | 3 | HG02280.hp2 HG02630.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.307C>T | p.Arg103Trp | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/12 | 568/2403 | 307/1662 | 103/553 | chrX | 13600001 | ||
chrX:13603406 | C | T | 1 | a0007 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.490C>T | p.Arg164Cys | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/12 | 751/2403 | 490/1662 | 164/553 | chrX | 13603406 | ||
chrX:13606379 | A | G | 1 | a0011 | 1 | NA18994.hp1 | missense_variant&splice_region_variant | MODERATE | c.521A>G | p.Asp174Gly | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/12 | 782/2403 | 521/1662 | 174/553 | chrX | 13606379 | ||
chrX:13606511 | T | A | 1 | a0010 | 1 | HG01109.hp1 | missense_variant&splice_region_variant | MODERATE | c.653T>A | p.Ile218Lys | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/12 | 914/2403 | 653/1662 | 218/553 | chrX | 13606511 | ||
chrX:13617826 | A | AAG | 1 | a0008 | 1 | NA18949.hp2 | frameshift_variant | HIGH | c.875_876insAG | p.Lys293fs | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/12 | 1137/2403 | 876/1662 | 292/553 | chrX | 13617826 | ||
chrX:13617839 | T | TA | 1 | a0008 | 1 | NA18949.hp2 | frameshift_variant | HIGH | c.893dupA | p.Asn298fs | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/12 | 1155/2403 | 894/1662 | 298/553 | INFO_REALIGN_3_PRIME | chrX | 13617839 | |
chrX:13617944 | T | TA | 1 | a0008 | 1 | NA18949.hp2 | frameshift_variant | HIGH | c.999dupA | p.Gly334fs | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/12 | 1261/2403 | 1000/1662 | 334/553 | INFO_REALIGN_3_PRIME | chrX | 13617944 | |
chrX:13617989 | GA | G | 1 | a0008 | 1 | NA18949.hp2 | frameshift_variant | HIGH | c.1042delA | p.Arg348fs | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/12 | 1303/2403 | 1042/1662 | 348/553 | INFO_REALIGN_3_PRIME | chrX | 13617989 | |
chrX:13619187 | A | G | 1 | a0003 | 5 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
missense_variant | MODERATE | c.1127A>G | p.Glu376Gly | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/12 | 1388/2403 | 1127/1662 | 376/553 | chrX | 13619187 | ||
chrX:13627249 | G | T | 2 | a0004a0007 | 5 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(2): Show |
missense_variant | MODERATE | c.1524G>T | p.Leu508Phe | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/12 | 1785/2403 | 1524/1662 | 508/553 | chrX | 13627249 | ||
chrX:13633006 | G | A | 1 | a0009 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1573G>A | p.Gly525Ser | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 1834/2403 | 1573/1662 | 525/553 | chrX | 13633006 | ||
chrX:13633036 | G | A | 3 | a0002a0010a0013 | 47 | HG00621.hp1 HG01070.hp1 HG01074.hp1 others(44): Show |
missense_variant | MODERATE | c.1603G>A | p.Asp535Asn | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 1864/2403 | 1603/1662 | 535/553 | chrX | 13633036 | ||
chrX:13633042 | G | A | 1 | a0012 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1609G>A | p.Val537Ile | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 1870/2403 | 1609/1662 | 537/553 | chrX | 13633042 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:13600018 | A | G | 5 | a0001c0005a0002c0026a0005c0014others(2): Show | 14 | HG01106.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
synonymous_variant | LOW | c.324A>G | p.Arg108Arg | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/12 | 585/2403 | 324/1662 | 108/553 | chrX | 13600018 | ||
chrX:13600042 | C | T | 3 | a0001c0008a0002c0025a0005c0013 | 5 | HG02293.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.348C>T | p.Tyr116Tyr | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/12 | 609/2403 | 348/1662 | 116/553 | chrX | 13600042 | ||
chrX:13600045 | G | A | 5 | a0001c0005a0002c0026a0005c0014others(2): Show | 14 | HG01106.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
synonymous_variant | LOW | c.351G>A | p.Lys117Lys | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/12 | 612/2403 | 351/1662 | 117/553 | chrX | 13600045 | ||
chrX:13606476 | C | T | 2 | a0001c0007a0004c0022 | 5 | HG02027.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
synonymous_variant | LOW | c.618C>T | p.Phe206Phe | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/12 | 879/2403 | 618/1662 | 206/553 | chrX | 13606476 | ||
chrX:13617818 | C | T | 3 | a0001c0004a0002c0002a0004c0010 | 38 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(35): Show |
synonymous_variant | LOW | c.867C>T | p.Ser289Ser | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/12 | 1128/2403 | 867/1662 | 289/553 | chrX | 13617818 | ||
chrX:13618038 | C | A | 1 | a0001c0018 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.1087C>A | p.Arg363Arg | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/12 | 1348/2403 | 1087/1662 | 363/553 | chrX | 13618038 | ||
chrX:13627072 | G | A | 1 | a0001c0019 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.1347G>A | p.Leu449Leu | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/12 | 1608/2403 | 1347/1662 | 449/553 | chrX | 13627072 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:13569646 | T | A | 10 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(7): Show | 51 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(48): Show |
5_prime_UTR_variant | MODIFIER | c.-216T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/12 | 216 | chrX | 13569646 | |||||
chrX:13569710 | T | G | 9 | a0001c0001t0002a0001c0001t0010a0001c0004t0002others(6): Show | 72 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
5_prime_UTR_variant | MODIFIER | c.-152T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/12 | 152 | chrX | 13569710 | |||||
chrX:13569733 | C | G | 5 | a0001c0001t0008a0001c0004t0008a0002c0002t0007others(2): Show | 12 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-129C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/12 | 129 | chrX | 13569733 | |||||
chrX:13569809 | G | GC | 1 | a0001c0001t0009 | 1 | NA18967.hp1 | 5_prime_UTR_variant | MODIFIER | c.-51dupC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/12 | 50 | INFO_REALIGN_3_PRIME | chrX | 13569809 | ||||
chrX:13633238 | G | A | 20 | a0001c0001t0004a0001c0001t0005a0001c0004t0004others(17): Show | 60 | HG00621.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 143 | chrX | 13633238 | |||||
chrX:13633416 | GA | G | 1 | a0001c0001t0013 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*329delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 329 | INFO_REALIGN_3_PRIME | chrX | 13633416 | ||||
chrX:13633417 | A | G | 1 | a0001c0001t0010 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 322 | chrX | 13633417 | |||||
chrX:13633507 | C | T | 1 | a0001c0001t0012 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*412C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 412 | chrX | 13633507 | |||||
chrX:13633572 | A | G | 1 | a0001c0001t0011 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*477A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 477 | chrX | 13633572 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:13569943 | TCTGA | T | 2 | a0001c0007t0003g0297a0008c0017t0003g0296 | 2 | HG02027.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.74+12_74+15delACTG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13569943 | |||||
chrX:13570095 | C | T | 1 | a0001c0008t0001g0295 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.74+160C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570095 | ||||||
chrX:13570123 | T | C | 1 | a0001c0001t0013g0006 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.74+188T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570123 | ||||||
chrX:13570156 | TG | T | 1 | a0001c0001t0008g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.74+222delG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570156 | ||||||
chrX:13570158 | C | T | 1 | a0001c0001t0008g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.74+223C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570158 | ||||||
chrX:13570173 | A | T | 116 | a0001c0001t0001g0005a0001c0001t0001g0180a0001c0001t0001g0181others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.74+238A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570173 | ||||||
chrX:13570482 | G | A | 17 | a0001c0001t0001g0007a0001c0001t0008g0011a0001c0001t0008g0012others(14): Show | 18 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.74+547G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570482 | ||||||
chrX:13570563 | C | G | 1 | a0001c0008t0001g0295 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.74+628C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570563 | ||||||
chrX:13570642 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.74+707A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570642 | ||||||
chrX:13570739 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.74+804C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570739 | ||||||
chrX:13570749 | T | C | 1 | a0001c0001t0003g0022 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.74+814T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570749 | ||||||
chrX:13571107 | C | CCCCCCA | 150 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0059others(147): Show | 154 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.74+1175_74+1180dup others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13571107 | |||||
chrX:13571107 | C | CCCCCCCA | 2 | a0001c0001t0002g0177a0011c0023t0001g0176 | 2 | NA18994.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.74+1177_74+1178ins others(7): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13571107 | |||||
chrX:13571113 | A | ACCCCCC | 2 | a0001c0001t0001g0174a0001c0008t0001g0173 | 2 | HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.74+1180_74+1181ins others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13571113 | |||||
chrX:13571113 | A | ACCCCCCC | 1 | a0004c0022t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.74+1180_74+1181ins others(7): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13571113 | |||||
chrX:13571116 | A | C | 16 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0003g0043others(13): Show | 16 | HG01243.hp1 HG02293.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.74+1181A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13571116 | ||||||
chrX:13571522 | A | G | 3 | a0001c0001t0001g0174a0001c0008t0001g0173a0004c0022t0001g0175 | 3 | HG02647.hp1 HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.74+1587A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13571522 | ||||||
chrX:13571643 | A | T | 153 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0059others(150): Show | 157 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.74+1708A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13571643 | ||||||
chrX:13571669 | G | A | 2 | a0001c0001t0001g0056a0001c0004t0004g0055 | 2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.74+1734G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13571669 | ||||||
chrX:13571844 | T | C | 162 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0056others(159): Show | 166 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.74+1909T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13571844 | ||||||
chrX:13572165 | G | GA | 1 | a0001c0001t0009g0057 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.74+2232dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13572165 | |||||
chrX:13572386 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.74+2451T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572386 | ||||||
chrX:13572570 | G | A | 2 | a0001c0001t0002g0038a0002c0003t0006g0037 | 2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.74+2635G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572570 | ||||||
chrX:13572639 | C | A | 39 | a0001c0001t0001g0005a0001c0001t0001g0180a0001c0001t0001g0181others(36): Show | 40 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.74+2704C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572639 | ||||||
chrX:13572760 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.74+2825G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572760 | ||||||
chrX:13572837 | G | C | 15 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0003g0043others(12): Show | 15 | HG01106.hp1 HG02293.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.74+2902G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572837 | ||||||
chrX:13572868 | C | T | 9 | a0001c0001t0003g0043a0001c0001t0005g0044a0001c0001t0005g0045others(6): Show | 9 | HG02293.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+2933C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572868 | ||||||
chrX:13572960 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.74+3025T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572960 | ||||||
chrX:13573053 | T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.74+3118T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573053 | ||||||
chrX:13573056 | C | T | 3 | a0001c0005t0001g0049a0001c0008t0001g0048a0005c0012t0001g0050 | 3 | HG02293.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.74+3121C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573056 | ||||||
chrX:13573216 | C | T | 3 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288 | 3 | HG00597.hp2 HG02523.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.74+3281C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573216 | ||||||
chrX:13573507 | T | G | 17 | a0001c0001t0001g0007a0001c0001t0008g0011a0001c0001t0008g0012others(14): Show | 18 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.74+3572T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573507 | ||||||
chrX:13573510 | T | C | 1 | a0001c0004t0003g0061 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.74+3575T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573510 | ||||||
chrX:13573546 | C | T | 3 | a0001c0005t0001g0049a0001c0008t0001g0048a0005c0012t0001g0050 | 3 | HG02293.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.74+3611C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573546 | ||||||
chrX:13573656 | A | C | 1 | a0001c0001t0002g0039 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.74+3721A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573656 | ||||||
chrX:13573688 | G | A | 17 | a0001c0001t0001g0007a0001c0001t0008g0011a0001c0001t0008g0012others(14): Show | 18 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.74+3753G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573688 | ||||||
chrX:13573745 | G | T | 165 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0059others(162): Show | 169 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.74+3810G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573745 | ||||||
chrX:13573754 | TTTGATTT others(23): Show |
T | 12 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0003g0043others(9): Show | 12 | HG02293.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.74+3823_74+3852del others(30): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13573754 | |||||
chrX:13573815 | A | G | 2 | a0001c0007t0003g0171a0001c0007t0003g0172 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.74+3880A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573815 | ||||||
chrX:13574011 | T | C | 5 | a0002c0003t0004g0030a0002c0003t0004g0031a0002c0003t0004g0032others(2): Show | 5 | HG02630.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+4076T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574011 | ||||||
chrX:13574047 | G | A | 153 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0059others(150): Show | 157 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.74+4112G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574047 | ||||||
chrX:13574079 | C | T | 10 | a0001c0001t0002g0039a0001c0001t0003g0043a0001c0001t0005g0044others(7): Show | 10 | HG02293.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.74+4144C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574079 | ||||||
chrX:13574080 | G | A | 1 | a0001c0004t0003g0061 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.74+4145G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574080 | ||||||
chrX:13574327 | A | G | 1 | a0001c0005t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.74+4392A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574327 | ||||||
chrX:13574397 | TGACAAAT others(5): Show |
T | 1 | a0002c0003t0006g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.74+4469_74+4480del others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13574397 | |||||
chrX:13574590 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.74+4655T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574590 | ||||||
chrX:13574625 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.74+4690G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574625 | ||||||
chrX:13574638 | G | A | 1 | a0001c0001t0013g0006 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.74+4703G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574638 | ||||||
chrX:13574730 | C | CA | 20 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(17): Show | 21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.74+4810dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13574730 | |||||
chrX:13574730 | C | CAA | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.74+4809_74+4810dup others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13574730 | |||||
chrX:13574730 | C | CAAA | 9 | a0001c0001t0003g0043a0001c0001t0005g0044a0001c0001t0005g0045others(6): Show | 9 | HG02451.hp1 HG02622.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+4808_74+4810dup others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13574730 | |||||
chrX:13574730 | C | CAAAA | 1 | a0001c0008t0001g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.74+4807_74+4810dup others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13574730 | |||||
chrX:13574730 | CA | C | 5 | a0001c0001t0001g0170a0001c0001t0001g0217a0001c0001t0002g0169others(2): Show | 5 | HG00621.hp1 HG01433.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+4810delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13574730 | |||||
chrX:13574762 | G | A | 166 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0059others(163): Show | 170 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.74+4827G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574762 | ||||||
chrX:13574801 | T | C | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0039 | 3 | HG02280.hp1 HG03831.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.74+4866T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574801 | ||||||
chrX:13574804 | TG | T | 1 | a0001c0001t0001g0222 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.74+4871delG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13574804 | |||||
chrX:13574806 | G | A | 3 | a0001c0001t0001g0068a0001c0001t0002g0067a0001c0004t0001g0066 | 3 | HG00639.hp1 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.74+4871G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574806 | ||||||
chrX:13575004 | A | G | 5 | a0001c0008t0001g0295a0002c0003t0004g0036a0002c0003t0004g0051others(2): Show | 5 | HG01243.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.74+5069A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575004 | ||||||
chrX:13575094 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.74+5159C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575094 | ||||||
chrX:13575111 | A | AAAAC | 2 | a0001c0001t0003g0223a0001c0001t0003g0224 | 2 | HG00280.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.74+5210_74+5213dup others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13575111 | |||||
chrX:13575111 | AAAAC | A | 11 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(8): Show | 11 | HG00673.hp1 HG01175.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.74+5210_74+5213del others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13575111 | |||||
chrX:13575111 | AAAACAAA others(1): Show |
A | 18 | a0001c0001t0001g0023a0001c0001t0001g0069a0001c0001t0002g0026others(15): Show | 18 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.74+5206_74+5213del others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13575111 | |||||
chrX:13575111 | AAAACAAA others(5): Show |
A | 153 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0059others(150): Show | 157 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.74+5202_74+5213del others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13575111 | |||||
chrX:13575111 | AAAACAAA others(9): Show |
A | 13 | a0001c0001t0002g0038a0001c0001t0003g0043a0001c0001t0005g0044others(10): Show | 13 | HG02293.hp1 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.74+5198_74+5213del others(16): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13575111 | |||||
chrX:13575131 | C | A | 9 | a0001c0001t0003g0043a0001c0001t0005g0044a0001c0001t0005g0045others(6): Show | 9 | HG02293.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+5196C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575131 | ||||||
chrX:13575361 | C | T | 1 | a0001c0005t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.74+5426C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575361 | ||||||
chrX:13575362 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.74+5427G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575362 | ||||||
chrX:13575381 | G | A | 1 | a0002c0003t0005g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.74+5446G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575381 | ||||||
chrX:13575442 | C | G | 17 | a0001c0001t0001g0007a0001c0001t0008g0011a0001c0001t0008g0012others(14): Show | 18 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.74+5507C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575442 | ||||||
chrX:13575713 | G | T | 1 | a0001c0005t0001g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.74+5778G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575713 | ||||||
chrX:13575985 | G | A | 6 | a0001c0001t0003g0043a0001c0001t0005g0044a0001c0001t0005g0045others(3): Show | 6 | HG02451.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.74+6050G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575985 | ||||||
chrX:13576076 | C | A | 153 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0059others(150): Show | 157 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.74+6141C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576076 | ||||||
chrX:13576224 | C | CG | 1 | a0002c0002t0004g0213 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.74+6292dupG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13576224 | |||||
chrX:13576252 | C | G | 1 | a0001c0001t0002g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.74+6317C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576252 | ||||||
chrX:13576282 | A | G | 13 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0068others(10): Show | 13 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.74+6347A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576282 | ||||||
chrX:13576285 | C | A | 4 | a0001c0001t0001g0023a0001c0001t0002g0026a0001c0001t0004g0024others(1): Show | 4 | HG01109.hp1 HG02257.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.74+6350C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576285 | ||||||
chrX:13576308 | T | C | 174 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0056others(171): Show | 178 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.74+6373T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576308 | ||||||
chrX:13576477 | C | A | 11 | a0001c0001t0002g0038a0001c0001t0003g0043a0001c0001t0005g0044others(8): Show | 11 | HG02293.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.74+6542C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576477 | ||||||
chrX:13576575 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.74+6640C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576575 | ||||||
chrX:13576705 | G | C | 1 | a0001c0005t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.74+6770G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576705 | ||||||
chrX:13576941 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.74+7006G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576941 | ||||||
chrX:13576996 | A | T | 19 | a0001c0001t0001g0023a0001c0001t0002g0026a0001c0001t0004g0024others(16): Show | 19 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+7061A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576996 | ||||||
chrX:13577118 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.74+7183T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577118 | ||||||
chrX:13577224 | T | TA | 1 | a0001c0001t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.74+7293dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577224 | |||||
chrX:13577295 | AT | A | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.74+7364delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577295 | |||||
chrX:13577296 | T | TTA | 1 | a0001c0001t0004g0228 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.74+7362_74+7363ins others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | |||||
chrX:13577296 | TTTTATAT others(3): Show |
T | 1 | a0005c0014t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.74+7363_74+7372del others(10): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | |||||
chrX:13577296 | TTTTATAT others(5): Show |
T | 1 | a0005c0013t0004g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.74+7363_74+7374del others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | |||||
chrX:13577296 | TTTTATAT others(7): Show |
T | 1 | a0006c0009t0004g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.74+7363_74+7376del others(14): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | |||||
chrX:13577296 | TTTTATAT others(9): Show |
T | 3 | a0002c0003t0004g0052a0002c0003t0006g0037a0004c0021t0001g0041 | 3 | HG01243.hp1 HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.74+7363_74+7378del others(16): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | |||||
chrX:13577296 | TTTTATAT others(11): Show |
T | 5 | a0001c0001t0002g0038a0001c0008t0001g0295a0002c0003t0004g0051others(2): Show | 5 | HG01891.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.74+7363_74+7380del others(18): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | |||||
chrX:13577296 | TTTTATAT others(13): Show |
T | 4 | a0002c0003t0004g0030a0002c0003t0004g0031a0002c0003t0004g0032others(1): Show | 4 | HG03209.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+7363_74+7382del others(20): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | |||||
chrX:13577296 | TTTTATAT others(15): Show |
T | 6 | a0001c0001t0001g0023a0001c0001t0002g0026a0001c0001t0004g0024others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.74+7363_74+7384del others(22): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | |||||
chrX:13577296 | TTTTATAT others(21): Show |
T | 8 | a0001c0001t0001g0174a0001c0004t0001g0019a0001c0008t0001g0173others(5): Show | 9 | HG02647.hp1 HG02895.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+7363_74+7390del others(28): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | |||||
chrX:13577296 | TTTTATAT others(23): Show |
T | 182 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(179): Show | 186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.74+7363_74+7392del others(30): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | |||||
chrX:13577297 | T | A | 2 | a0001c0001t0001g0212a0001c0001t0002g0211 | 2 | NA18950.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.74+7362T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577297 | ||||||
chrX:13577298 | T | A | 11 | a0001c0001t0001g0212a0001c0001t0001g0227a0001c0001t0002g0211others(8): Show | 11 | HG01070.hp2 HG01106.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.74+7363T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577298 | ||||||
chrX:13577298 | T | TATA | 1 | a0001c0001t0004g0230 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.74+7363_74+7364ins others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577298 | ||||||
chrX:13577298 | T | TTA | 17 | a0001c0001t0001g0222a0001c0001t0001g0250a0001c0001t0001g0251others(14): Show | 17 | HG00673.hp1 HG01952.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.74+7406_74+7407dup others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | |||||
chrX:13577298 | T | TTATA | 10 | a0001c0001t0001g0218a0001c0001t0001g0266a0001c0001t0001g0267others(7): Show | 10 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.74+7404_74+7407dup others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | |||||
chrX:13577298 | T | TTATATA | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG01261.hp1 HG01934.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+7402_74+7407dup others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | |||||
chrX:13577298 | T | TTATATAT others(1): Show |
2 | a0001c0001t0001g0277a0001c0001t0001g0278 | 2 | HG00639.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.74+7400_74+7407dup others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | |||||
chrX:13577298 | TTA | T | 10 | a0001c0001t0001g0220a0001c0001t0001g0242a0001c0001t0003g0223others(7): Show | 10 | HG00735.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.74+7406_74+7407del others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | |||||
chrX:13577298 | TTATA | T | 14 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(11): Show | 14 | HG00099.hp1 HG00597.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.74+7404_74+7407del others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | |||||
chrX:13577298 | TTATATA | T | 1 | a0001c0001t0003g0034 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.74+7402_74+7407del others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | |||||
chrX:13577298 | TTATATAT others(1): Show |
T | 1 | a0001c0005t0001g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.74+7400_74+7407del others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | |||||
chrX:13577298 | TTATATAT others(3): Show |
T | 1 | a0009c0020t0001g0232 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.74+7398_74+7407del others(10): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | |||||
chrX:13577298 | TTATATAT others(5): Show |
T | 1 | a0001c0005t0001g0231 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.74+7396_74+7407del others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | |||||
chrX:13577315 | TATATATA others(25): Show |
T | 2 | a0001c0001t0001g0212a0001c0001t0002g0211 | 2 | NA18950.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.74+7382_74+7413del others(32): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577315 | |||||
chrX:13577321 | TATATATA others(19): Show |
T | 7 | a0001c0001t0001g0227a0001c0001t0003g0043a0001c0001t0005g0044others(4): Show | 7 | HG02451.hp1 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.74+7388_74+7413del others(26): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577321 | |||||
chrX:13577323 | TATATATA others(17): Show |
T | 1 | a0001c0005t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.74+7390_74+7413del others(24): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577323 | |||||
chrX:13577325 | T | A | 8 | a0001c0001t0001g0174a0001c0004t0001g0019a0001c0008t0001g0173others(5): Show | 9 | HG02647.hp1 HG02895.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+7390T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577325 | ||||||
chrX:13577327 | T | A | 182 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(179): Show | 186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.74+7392T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577327 | ||||||
chrX:13577329 | TATATATA others(7): Show |
T | 1 | a0001c0001t0002g0039 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.74+7398_74+7411del others(14): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577329 | |||||
chrX:13577333 | T | TA | 1 | a0001c0001t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.74+7399dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577333 | |||||
chrX:13577340 | A | G | 4 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0158others(1): Show | 4 | NA18954.hp1 NA18955.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+7405A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577340 | ||||||
chrX:13577343 | C | T | 209 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(206): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.74+7408C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577343 | ||||||
chrX:13577343 | CAT | C | 2 | a0002c0003t0004g0051a0002c0003t0004g0052 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.74+7410_74+7411del others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577343 | |||||
chrX:13577378 | C | G | 222 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(219): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.74+7443C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577378 | ||||||
chrX:13577438 | T | C | 190 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(187): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.74+7503T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577438 | ||||||
chrX:13577439 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.74+7504G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577439 | ||||||
chrX:13577443 | A | G | 8 | a0001c0001t0001g0227a0001c0001t0003g0043a0001c0001t0005g0044others(5): Show | 8 | HG01106.hp1 HG02451.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.74+7508A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577443 | ||||||
chrX:13577475 | A | T | 1 | a0002c0002t0005g0153 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.74+7540A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577475 | ||||||
chrX:13577603 | C | A | 200 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(197): Show | 205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.74+7668C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577603 | ||||||
chrX:13577652 | G | C | 1 | a0001c0001t0001g0214 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.74+7717G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577652 | ||||||
chrX:13577896 | G | C | 191 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(188): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.74+7961G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577896 | ||||||
chrX:13577949 | A | C | 9 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(6): Show | 9 | HG01106.hp1 HG02451.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+8014A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577949 | ||||||
chrX:13577979 | T | TA | 19 | a0001c0001t0001g0023a0001c0001t0002g0026a0001c0001t0004g0024others(16): Show | 19 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+8045dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577979 | |||||
chrX:13578089 | C | CA | 1 | a0001c0001t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.74+8158dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13578089 | |||||
chrX:13578142 | C | T | 200 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(197): Show | 205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.74+8207C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578142 | ||||||
chrX:13578256 | A | G | 1 | a0001c0005t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.74+8321A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578256 | ||||||
chrX:13578260 | A | C | 220 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(217): Show | 225 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.74+8325A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578260 | ||||||
chrX:13578300 | G | C | 192 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(189): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.74+8365G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578300 | ||||||
chrX:13578406 | A | T | 12 | a0001c0008t0001g0295a0002c0003t0004g0030a0002c0003t0004g0031others(9): Show | 12 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.74+8471A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578406 | ||||||
chrX:13578424 | A | G | 193 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(190): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.74+8489A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578424 | ||||||
chrX:13578523 | G | C | 192 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(189): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.74+8588G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578523 | ||||||
chrX:13578634 | G | A | 2 | a0001c0001t0002g0038a0002c0003t0006g0037 | 2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.74+8699G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578634 | ||||||
chrX:13578698 | A | G | 2 | a0001c0001t0002g0159a0002c0002t0004g0213 | 2 | NA18956.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.74+8763A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578698 | ||||||
chrX:13578710 | A | G | 193 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(190): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.74+8775A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578710 | ||||||
chrX:13578758 | A | G | 25 | a0001c0001t0001g0023a0001c0001t0001g0227a0001c0001t0002g0026others(22): Show | 25 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.74+8823A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578758 | ||||||
chrX:13578777 | C | T | 19 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(16): Show | 19 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+8842C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578777 | ||||||
chrX:13578784 | T | TG | 20 | a0001c0001t0001g0225a0001c0001t0001g0227a0001c0001t0002g0039others(17): Show | 20 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.74+8854dupG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13578784 | |||||
chrX:13578790 | C | G | 19 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(16): Show | 19 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+8855C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578790 | ||||||
chrX:13578793 | C | G | 19 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(16): Show | 19 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+8858C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578793 | ||||||
chrX:13578810 | G | A | 211 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.74+8875G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578810 | ||||||
chrX:13578812 | T | G | 221 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(218): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.74+8877T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578812 | ||||||
chrX:13578848 | C | T | 1 | a0002c0003t0005g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.74+8913C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578848 | ||||||
chrX:13578926 | A | AAAAT | 1 | a0002c0003t0004g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.74+9011_74+9014dup others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13578926 | |||||
chrX:13579060 | G | A | 10 | a0001c0001t0001g0023a0001c0001t0002g0026a0001c0001t0002g0038others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.74+9125G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579060 | ||||||
chrX:13579118 | A | AG | 1 | a0001c0001t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.74+9187dupG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13579118 | |||||
chrX:13579156 | C | T | 212 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(209): Show | 217 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.74+9221C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579156 | ||||||
chrX:13579247 | C | T | 19 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(16): Show | 19 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+9312C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579247 | ||||||
chrX:13579312 | C | T | 19 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(16): Show | 19 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+9377C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579312 | ||||||
chrX:13579676 | C | T | 211 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.74+9741C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579676 | ||||||
chrX:13579766 | C | G | 12 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(9): Show | 12 | HG01106.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.75-9790C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579766 | ||||||
chrX:13579820 | C | T | 8 | a0002c0003t0004g0030a0002c0003t0004g0031a0002c0003t0004g0032others(5): Show | 8 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-9736C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579820 | ||||||
chrX:13579928 | T | G | 1 | a0003c0006t0004g0289 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.75-9628T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579928 | ||||||
chrX:13579995 | C | A | 1 | a0001c0001t0002g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75-9561C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579995 | ||||||
chrX:13580060 | A | AG | 1 | a0001c0001t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.75-9492dupG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13580060 | |||||
chrX:13580072 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.75-9484C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13580072 | ||||||
chrX:13580080 | T | C | 38 | a0001c0001t0001g0069a0001c0001t0001g0080a0001c0001t0002g0094others(35): Show | 40 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.75-9476T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13580080 | ||||||
chrX:13580364 | C | T | 18 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(15): Show | 18 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.75-9192C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13580364 | ||||||
chrX:13580365 | G | T | 20 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(17): Show | 20 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.75-9191G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13580365 | ||||||
chrX:13580908 | T | A | 1 | a0002c0002t0006g0097 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.75-8648T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13580908 | ||||||
chrX:13581011 | G | A | 4 | a0001c0001t0002g0038a0002c0003t0004g0051a0002c0003t0004g0052others(1): Show | 4 | HG01243.hp1 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-8545G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581011 | ||||||
chrX:13581158 | A | G | 192 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0056others(189): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.75-8398A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581158 | ||||||
chrX:13581226 | G | A | 221 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(218): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.75-8330G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581226 | ||||||
chrX:13581286 | G | A | 2 | a0001c0008t0001g0295a0012c0011t0004g0054 | 2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75-8270G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581286 | ||||||
chrX:13581333 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.75-8223C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581333 | ||||||
chrX:13581357 | C | G | 12 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(9): Show | 12 | HG01106.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.75-8199C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581357 | ||||||
chrX:13581438 | T | TA | 12 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(9): Show | 12 | HG01106.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.75-8110dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13581438 | |||||
chrX:13581467 | G | A | 10 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(7): Show | 10 | HG01106.hp1 HG02451.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.75-8089G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581467 | ||||||
chrX:13581499 | G | A | 118 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0110others(115): Show | 120 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.75-8057G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581499 | ||||||
chrX:13581558 | A | G | 2 | a0002c0002t0004g0263a0002c0002t0004g0264 | 2 | NA18968.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.75-7998A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581558 | ||||||
chrX:13581962 | G | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0162others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-7594G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581962 | ||||||
chrX:13582061 | CT | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0110others(116): Show | 121 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.75-7482delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13582061 | |||||
chrX:13582123 | C | T | 77 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0059others(74): Show | 80 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.75-7433C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582123 | ||||||
chrX:13582136 | G | C | 218 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(215): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.75-7420G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582136 | ||||||
chrX:13582344 | G | A | 218 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(215): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.75-7212G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582344 | ||||||
chrX:13582597 | G | A | 17 | a0001c0001t0001g0007a0001c0001t0008g0011a0001c0001t0008g0012others(14): Show | 18 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.75-6959G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582597 | ||||||
chrX:13582738 | G | C | 120 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0110others(117): Show | 122 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.75-6818G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582738 | ||||||
chrX:13582746 | A | G | 121 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0110others(118): Show | 123 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.75-6810A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582746 | ||||||
chrX:13583073 | G | A | 19 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(16): Show | 19 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.75-6483G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583073 | ||||||
chrX:13583080 | C | T | 13 | a0001c0001t0008g0011a0001c0001t0008g0012a0001c0001t0008g0013others(10): Show | 14 | HG00544.hp1 HG02155.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.75-6476C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583080 | ||||||
chrX:13583207 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.75-6349A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583207 | ||||||
chrX:13583648 | A | C | 1 | a0001c0001t0001g0249 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.75-5908A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583648 | ||||||
chrX:13583695 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.75-5861C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583695 | ||||||
chrX:13583953 | GAAGGTCA | G | 1 | a0001c0019t0002g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.75-5601_75-5595del others(7): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13583953 | |||||
chrX:13583987 | A | G | 1 | a0002c0002t0006g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.75-5569A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583987 | ||||||
chrX:13583992 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75-5564G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583992 | ||||||
chrX:13584607 | A | G | 12 | a0001c0001t0008g0012a0001c0001t0008g0013a0001c0004t0001g0019others(9): Show | 13 | HG00544.hp1 HG02155.hp2 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.75-4949A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13584607 | ||||||
chrX:13584693 | C | T | 1 | a0002c0003t0007g0010 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75-4863C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13584693 | ||||||
chrX:13584822 | T | TTGAA | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75-4716_75-4713dup others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13584822 | |||||
chrX:13584852 | T | C | 12 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(9): Show | 12 | HG01106.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.75-4704T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13584852 | ||||||
chrX:13584929 | C | T | 1 | a0001c0005t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.75-4627C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13584929 | ||||||
chrX:13585027 | G | A | 1 | a0002c0003t0004g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75-4529G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585027 | ||||||
chrX:13585149 | C | A | 2 | a0002c0003t0004g0051a0002c0003t0004g0052 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.75-4407C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585149 | ||||||
chrX:13585347 | C | T | 4 | a0001c0001t0002g0038a0002c0003t0004g0051a0002c0003t0004g0052others(1): Show | 4 | HG01243.hp1 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-4209C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585347 | ||||||
chrX:13585755 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.75-3801C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585755 | ||||||
chrX:13585756 | C | CT | 142 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0109others(139): Show | 144 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.75-3800_75-3799ins others(1): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585756 | ||||||
chrX:13585867 | G | A | 10 | a0001c0001t0001g0227a0001c0001t0002g0039a0001c0001t0003g0043others(7): Show | 10 | HG01106.hp1 HG02451.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.75-3689G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585867 | ||||||
chrX:13585908 | A | G | 3 | a0001c0001t0001g0174a0001c0008t0001g0173a0004c0022t0001g0175 | 3 | HG02647.hp1 HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.75-3648A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585908 | ||||||
chrX:13585931 | C | T | 3 | a0001c0005t0001g0148a0002c0003t0004g0146a0002c0003t0004g0147 | 3 | HG01070.hp1 HG01074.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.75-3625C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585931 | ||||||
chrX:13586133 | C | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0109others(135): Show | 140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.75-3423C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13586133 | ||||||
chrX:13586166 | T | TATCATTA others(6): Show |
221 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(218): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.75-3389_75-3388ins others(13): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13586166 | |||||
chrX:13586509 | C | G | 80 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0059others(77): Show | 83 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.75-3047C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13586509 | ||||||
chrX:13586647 | A | C | 18 | a0001c0001t0001g0023a0001c0001t0001g0227a0001c0001t0002g0026others(15): Show | 18 | HG01106.hp1 HG01109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.75-2909A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13586647 | ||||||
chrX:13586768 | T | G | 13 | a0001c0001t0008g0011a0001c0001t0008g0012a0001c0001t0008g0013others(10): Show | 14 | HG00544.hp1 HG02155.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.75-2788T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13586768 | ||||||
chrX:13586992 | G | T | 221 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(218): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.75-2564G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13586992 | ||||||
chrX:13587062 | A | G | 129 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0109others(126): Show | 131 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.75-2494A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13587062 | ||||||
chrX:13587117 | T | TG | 1 | a0001c0001t0003g0184 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.75-2435dupG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13587117 | |||||
chrX:13587558 | G | A | 3 | a0001c0001t0002g0039a0001c0008t0001g0295a0012c0011t0004g0054 | 3 | HG02630.hp2 HG03195.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.75-1998G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13587558 | ||||||
chrX:13587673 | G | C | 3 | a0002c0003t0004g0051a0002c0003t0004g0052a0002c0003t0006g0037 | 3 | HG01243.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.75-1883G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13587673 | ||||||
chrX:13587682 | C | T | 3 | a0002c0003t0004g0051a0002c0003t0004g0052a0002c0003t0006g0037 | 3 | HG01243.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.75-1874C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13587682 | ||||||
chrX:13587851 | G | A | 6 | a0001c0001t0001g0023a0001c0001t0002g0026a0001c0001t0004g0024others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.75-1705G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13587851 | ||||||
chrX:13588010 | A | G | 3 | a0001c0001t0002g0039a0001c0008t0001g0295a0012c0011t0004g0054 | 3 | HG02630.hp2 HG03195.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.75-1546A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588010 | ||||||
chrX:13588192 | C | G | 221 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(218): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.75-1364C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588192 | ||||||
chrX:13588313 | G | A | 1 | a0002c0002t0006g0099 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.75-1243G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588313 | ||||||
chrX:13588465 | TA | T | 1 | a0001c0001t0003g0184 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.75-1088delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13588465 | |||||
chrX:13588616 | C | T | 6 | a0001c0001t0001g0218a0001c0001t0004g0228a0001c0001t0004g0230others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.75-940C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588616 | ||||||
chrX:13588684 | G | C | 1 | a0002c0003t0004g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75-872G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588684 | ||||||
chrX:13588687 | C | A | 3 | a0002c0003t0004g0051a0002c0003t0004g0052a0002c0003t0006g0037 | 3 | HG01243.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.75-869C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588687 | ||||||
chrX:13588704 | AT | A | 1 | a0001c0001t0003g0184 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.75-847delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13588704 | |||||
chrX:13588725 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.75-831G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588725 | ||||||
chrX:13588742 | C | T | 224 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(221): Show | 229 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.75-814C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588742 | ||||||
chrX:13588779 | TAC | T | 2 | a0001c0008t0001g0295a0012c0011t0004g0054 | 2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75-775_75-774delCA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13588779 | |||||
chrX:13588784 | T | C | 2 | a0001c0001t0008g0012a0001c0001t0008g0013 | 2 | NA18970.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.75-772T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588784 | ||||||
chrX:13588821 | G | A | 7 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(4): Show | 7 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.75-735G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588821 | ||||||
chrX:13589278 | A | G | 221 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(218): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.75-278A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13589278 | ||||||
chrX:13589303 | T | C | 221 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(218): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.75-253T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13589303 | ||||||
chrX:13589725 | T | G | 1 | a0001c0001t0003g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.187+57T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13589725 | ||||||
chrX:13589762 | C | G | 125 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0109others(122): Show | 127 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.187+94C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13589762 | ||||||
chrX:13589844 | C | T | 8 | a0001c0001t0002g0064a0001c0001t0002g0139a0001c0001t0002g0140others(5): Show | 8 | NA18944.hp1 NA18960.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.187+176C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13589844 | ||||||
chrX:13589888 | A | T | 1 | a0002c0002t0007g0018 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.187+220A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13589888 | ||||||
chrX:13589979 | G | A | 2 | a0001c0001t0003g0074a0001c0018t0003g0075 | 2 | HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.187+311G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13589979 | ||||||
chrX:13590006 | A | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(209): Show | 217 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.187+338A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13590006 | ||||||
chrX:13590383 | A | G | 10 | a0002c0003t0004g0030a0002c0003t0004g0031a0002c0003t0004g0032others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.187+715A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13590383 | ||||||
chrX:13590618 | C | T | 4 | a0001c0001t0002g0039a0002c0003t0004g0051a0002c0003t0004g0052others(1): Show | 4 | HG01243.hp1 HG03453.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+950C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13590618 | ||||||
chrX:13590656 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187+988C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13590656 | ||||||
chrX:13591147 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.187+1479G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13591147 | ||||||
chrX:13591328 | G | A | 4 | a0001c0001t0002g0039a0002c0003t0004g0051a0002c0003t0004g0052others(1): Show | 4 | HG01243.hp1 HG03453.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+1660G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13591328 | ||||||
chrX:13591368 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.187+1700G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13591368 | ||||||
chrX:13591895 | T | TC | 1 | a0001c0001t0009g0057 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.187+2229dupC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13591895 | |||||
chrX:13592103 | AG | A | 1 | a0001c0001t0009g0057 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.187+2438delG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592103 | |||||
chrX:13592215 | T | TA | 83 | a0001c0001t0001g0007a0001c0001t0001g0056a0001c0001t0001g0059others(80): Show | 86 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.187+2562dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592215 | |||||
chrX:13592215 | TA | T | 2 | a0001c0001t0001g0248a0002c0003t0004g0036 | 2 | NA18957.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.187+2562delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592215 | |||||
chrX:13592215 | TAA | T | 2 | a0002c0003t0004g0051a0002c0003t0004g0052 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.187+2561_187+2562d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592215 | |||||
chrX:13592236 | A | AT | 123 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0110others(120): Show | 125 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.187+2573dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592236 | |||||
chrX:13592306 | T | G | 3 | a0001c0005t0001g0049a0001c0008t0001g0048a0005c0012t0001g0050 | 3 | HG02293.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.188-2530T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592306 | ||||||
chrX:13592553 | G | A | 6 | a0001c0001t0001g0023a0001c0001t0002g0026a0001c0001t0004g0024others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-2283G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592553 | ||||||
chrX:13592588 | TA | T | 1 | a0001c0001t0009g0057 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.188-2246delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592588 | |||||
chrX:13592706 | G | C | 10 | a0001c0001t0001g0290a0001c0001t0002g0071a0001c0001t0002g0101others(7): Show | 10 | HG00544.hp2 HG02071.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.188-2130G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592706 | ||||||
chrX:13592720 | T | G | 11 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(8): Show | 11 | HG02135.hp1 NA18940.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-2116T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592720 | ||||||
chrX:13592723 | T | G | 7 | a0001c0001t0001g0023a0001c0001t0002g0026a0001c0001t0004g0024others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-2113T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592723 | ||||||
chrX:13592861 | C | CG | 2 | a0001c0001t0002g0159a0001c0001t0003g0078 | 2 | HG02738.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.188-1968dupG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592861 | |||||
chrX:13592870 | G | C | 16 | a0001c0001t0001g0023a0001c0001t0001g0174a0001c0001t0002g0026others(13): Show | 16 | HG01109.hp1 HG01891.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.188-1966G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592870 | ||||||
chrX:13592911 | T | A | 26 | a0001c0001t0001g0056a0001c0001t0001g0227a0001c0001t0002g0038others(23): Show | 27 | HG00544.hp1 HG02155.hp2 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.188-1925T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592911 | ||||||
chrX:13592917 | C | CT | 119 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0109others(116): Show | 121 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.188-1902dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592917 | |||||
chrX:13592917 | C | CTT | 32 | a0001c0001t0001g0056a0001c0001t0001g0174a0001c0001t0001g0214others(29): Show | 33 | HG00544.hp1 HG01891.hp1 HG02132.hp1 others(30): Show |
intron_variant | MODIFIER | c.188-1903_188-1902d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592917 | |||||
chrX:13592917 | CT | C | 1 | a0001c0001t0001g0251 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.188-1902delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592917 | |||||
chrX:13592999 | C | T | 1 | a0001c0007t0003g0297 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.188-1837C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592999 | ||||||
chrX:13593021 | TCTC | T | 98 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0110others(95): Show | 100 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.188-1812_188-1810d others(5): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13593021 | |||||
chrX:13593053 | T | TA | 7 | a0001c0001t0002g0064a0001c0001t0002g0139a0001c0001t0002g0140others(4): Show | 7 | NA18960.hp1 NA18980.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-1782dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13593053 | |||||
chrX:13593105 | T | C | 1 | a0012c0011t0004g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.188-1731T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593105 | ||||||
chrX:13593114 | T | C | 18 | a0001c0001t0001g0056a0001c0001t0001g0214a0001c0001t0002g0071others(15): Show | 19 | HG00544.hp1 HG00544.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-1722T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593114 | ||||||
chrX:13593124 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.188-1712G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593124 | ||||||
chrX:13593153 | G | A | 62 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0149others(59): Show | 64 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.188-1683G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593153 | ||||||
chrX:13593265 | G | A | 3 | a0001c0001t0001g0174a0001c0008t0001g0173a0002c0026t0004g0029 | 3 | HG02895.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.188-1571G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593265 | ||||||
chrX:13593317 | A | G | 1 | a0011c0023t0001g0176 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.188-1519A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593317 | ||||||
chrX:13593344 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.188-1492G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593344 | ||||||
chrX:13593384 | G | C | 1 | a0001c0008t0001g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.188-1452G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593384 | ||||||
chrX:13593458 | C | G | 195 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(192): Show | 200 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.188-1378C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593458 | ||||||
chrX:13593542 | T | G | 4 | a0001c0001t0002g0026a0001c0001t0004g0024a0002c0003t0007g0010others(1): Show | 4 | HG01109.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-1294T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593542 | ||||||
chrX:13593611 | G | A | 2 | a0005c0013t0004g0027a0005c0014t0001g0028 | 2 | HG02258.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.188-1225G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593611 | ||||||
chrX:13593757 | G | A | 20 | a0001c0001t0001g0023a0001c0001t0001g0218a0001c0001t0001g0278others(17): Show | 20 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.188-1079G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593757 | ||||||
chrX:13593828 | A | T | 7 | a0005c0012t0001g0050a0005c0013t0004g0027a0005c0014t0001g0028others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-1008A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593828 | ||||||
chrX:13593903 | G | A | 1 | a0002c0026t0004g0029 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-933G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593903 | ||||||
chrX:13593905 | C | T | 1 | a0006c0009t0001g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.188-931C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593905 | ||||||
chrX:13593977 | T | C | 3 | a0001c0001t0002g0026a0001c0001t0004g0024a0010c0016t0004g0025 | 3 | HG01109.hp1 HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188-859T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593977 | ||||||
chrX:13594022 | G | C | 2 | a0001c0001t0002g0100a0001c0001t0002g0115 | 2 | NA18950.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.188-814G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594022 | ||||||
chrX:13594143 | C | A | 3 | a0001c0001t0002g0156a0001c0001t0002g0157a0001c0001t0002g0159 | 3 | NA18954.hp1 NA18956.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.188-693C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594143 | ||||||
chrX:13594154 | T | C | 202 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(199): Show | 207 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.188-682T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594154 | ||||||
chrX:13594362 | A | G | 2 | a0002c0003t0004g0152a0007c0024t0001g0040 | 2 | HG02559.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.188-474A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594362 | ||||||
chrX:13594403 | C | T | 202 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(199): Show | 207 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.188-433C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594403 | ||||||
chrX:13594596 | T | C | 203 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(200): Show | 208 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.188-240T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594596 | ||||||
chrX:13594666 | T | C | 3 | a0002c0003t0004g0030a0002c0003t0004g0146a0002c0003t0004g0147 | 3 | HG01070.hp1 HG01074.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.188-170T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594666 | ||||||
chrX:13594739 | G | A | 1 | a0002c0003t0005g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.188-97G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594739 | ||||||
chrX:13594740 | G | A | 1 | a0002c0003t0005g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.188-96G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594740 | ||||||
chrX:13594761 | G | A | 1 | a0001c0008t0001g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.188-75G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594761 | ||||||
chrX:13594776 | G | A | 8 | a0001c0001t0001g0278a0001c0001t0002g0094a0001c0001t0003g0090others(5): Show | 8 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-60G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594776 | ||||||
chrX:13594942 | C | T | 5 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0003g0087others(2): Show | 5 | HG01496.hp2 HG01517.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+14C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13594942 | ||||||
chrX:13594963 | C | T | 2 | a0001c0008t0001g0295a0002c0025t0004g0265 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.280+35C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13594963 | ||||||
chrX:13595000 | G | C | 1 | a0001c0001t0002g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.280+72G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595000 | ||||||
chrX:13595216 | G | A | 1 | a0001c0008t0001g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.280+288G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595216 | ||||||
chrX:13595235 | C | G | 1 | a0001c0001t0002g0145 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.280+307C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595235 | ||||||
chrX:13595276 | C | A | 5 | a0001c0005t0001g0053a0001c0008t0001g0048a0001c0008t0001g0295others(2): Show | 5 | HG01106.hp1 HG02293.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+348C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595276 | ||||||
chrX:13595619 | C | A | 5 | a0001c0008t0001g0048a0001c0008t0001g0295a0002c0003t0004g0036others(2): Show | 5 | HG02293.hp1 HG02647.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+691C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595619 | ||||||
chrX:13595722 | C | CT | 19 | a0001c0001t0002g0026a0001c0001t0004g0024a0001c0005t0001g0053others(16): Show | 19 | HG01106.hp1 HG01109.hp1 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.280+809dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13595722 | |||||
chrX:13595722 | C | CTT | 1 | a0013c0015t0007g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.280+808_280+809dup others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13595722 | |||||
chrX:13595722 | CT | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0278 | 2 | HG02622.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.280+809delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13595722 | |||||
chrX:13595968 | C | T | 5 | a0002c0003t0004g0030a0002c0003t0004g0146a0002c0003t0004g0147others(2): Show | 5 | HG01070.hp1 HG01074.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+1040C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595968 | ||||||
chrX:13596349 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.280+1421T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13596349 | ||||||
chrX:13596366 | C | T | 1 | a0002c0003t0004g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.280+1438C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13596366 | ||||||
chrX:13596372 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.280+1444C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13596372 | ||||||
chrX:13596640 | A | G | 1 | a0001c0001t0001g0292 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.280+1712A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13596640 | ||||||
chrX:13596869 | C | G | 1 | a0003c0006t0004g0289 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.280+1941C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13596869 | ||||||
chrX:13596999 | A | G | 238 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(235): Show | 243 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.280+2071A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13596999 | ||||||
chrX:13597066 | T | C | 1 | a0001c0001t0002g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.280+2138T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597066 | ||||||
chrX:13597107 | G | A | 163 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0080others(160): Show | 167 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.280+2179G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597107 | ||||||
chrX:13597149 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.280+2221C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597149 | ||||||
chrX:13597276 | A | G | 3 | a0002c0003t0004g0031a0002c0003t0004g0032a0002c0003t0004g0160 | 3 | HG01891.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.280+2348A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597276 | ||||||
chrX:13597326 | C | G | 1 | a0001c0001t0003g0184 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.280+2398C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597326 | ||||||
chrX:13597357 | G | A | 1 | a0012c0011t0004g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.280+2429G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597357 | ||||||
chrX:13597407 | C | T | 1 | a0001c0001t0012g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.280+2479C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597407 | ||||||
chrX:13597492 | C | T | 1 | a0001c0019t0002g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.281-2483C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597492 | ||||||
chrX:13597510 | A | G | 1 | a0001c0001t0012g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.281-2465A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597510 | ||||||
chrX:13597546 | G | C | 109 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0080others(106): Show | 111 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.281-2429G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597546 | ||||||
chrX:13597548 | T | C | 226 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(223): Show | 231 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.281-2427T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597548 | ||||||
chrX:13597549 | C | T | 223 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(220): Show | 228 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.281-2426C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597549 | ||||||
chrX:13597558 | T | C | 2 | a0002c0003t0007g0010a0010c0016t0004g0025 | 2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.281-2417T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597558 | ||||||
chrX:13597612 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.281-2363C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597612 | ||||||
chrX:13597613 | A | G | 1 | a0001c0001t0002g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.281-2362A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597613 | ||||||
chrX:13597644 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.281-2331C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597644 | ||||||
chrX:13597654 | A | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | NA18946.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.281-2321A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597654 | ||||||
chrX:13597771 | G | A | 1 | a0001c0001t0001g0292 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.281-2204G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597771 | ||||||
chrX:13597783 | C | CA | 51 | a0001c0001t0001g0199a0001c0001t0002g0094a0001c0001t0002g0120others(48): Show | 53 | HG00544.hp1 HG00735.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.281-2191dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13597783 | |||||
chrX:13597784 | AG | A | 5 | a0001c0001t0002g0156a0001c0001t0002g0158a0001c0001t0002g0159others(2): Show | 5 | NA18954.hp1 NA18955.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-2190delG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597784 | ||||||
chrX:13597785 | G | A | 201 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(198): Show | 206 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.281-2190G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597785 | ||||||
chrX:13597785 | G | GA | 1 | a0001c0005t0001g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.281-2181dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13597785 | |||||
chrX:13597788 | A | G | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.281-2187A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597788 | ||||||
chrX:13597982 | T | C | 1 | a0007c0024t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.281-1993T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597982 | ||||||
chrX:13597994 | T | C | 5 | a0001c0005t0001g0053a0002c0026t0004g0029a0006c0009t0001g0283others(2): Show | 5 | HG01106.hp1 HG02280.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-1981T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597994 | ||||||
chrX:13598234 | G | C | 1 | a0002c0003t0006g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.281-1741G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598234 | ||||||
chrX:13598249 | A | G | 2 | a0001c0001t0010g0151a0007c0024t0001g0040 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.281-1726A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598249 | ||||||
chrX:13598273 | G | C | 1 | a0001c0001t0001g0258 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.281-1702G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598273 | ||||||
chrX:13598275 | G | C | 1 | a0001c0001t0003g0076 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.281-1700G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598275 | ||||||
chrX:13598558 | A | AGTT | 11 | a0001c0001t0001g0218a0001c0001t0003g0090a0001c0004t0004g0055others(8): Show | 11 | HG02280.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-1386_281-1384d others(5): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598558 | |||||
chrX:13598558 | A | AGTTGTT | 2 | a0001c0005t0001g0053a0005c0014t0001g0028 | 2 | HG01106.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.281-1389_281-1384d others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598558 | |||||
chrX:13598558 | AGTT | A | 5 | a0001c0001t0001g0281a0001c0001t0002g0229a0002c0003t0004g0032others(2): Show | 5 | HG01175.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-1386_281-1384d others(5): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598558 | |||||
chrX:13598558 | AGTTGTT | A | 128 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0059others(125): Show | 130 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.281-1389_281-1384d others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598558 | |||||
chrX:13598558 | AGTTGTTG others(2): Show |
A | 1 | a0001c0001t0002g0159 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.281-1392_281-1384d others(11): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598558 | |||||
chrX:13598558 | AGTTGTTG others(8): Show |
A | 1 | a0001c0001t0002g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.281-1398_281-1384d others(17): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598558 | |||||
chrX:13598691 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.281-1284T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598691 | ||||||
chrX:13598761 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.281-1214G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598761 | ||||||
chrX:13598784 | G | A | 7 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0204others(4): Show | 7 | HG00408.hp1 HG00609.hp1 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-1191G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598784 | ||||||
chrX:13598863 | C | CAT | 218 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(215): Show | 223 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.281-1105_281-1104d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598863 | |||||
chrX:13598863 | C | CATATATA others(75): Show |
1 | a0001c0001t0003g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.281-1104_281-1103i others(84): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598863 | |||||
chrX:13598863 | C | CATATATA others(34): Show |
3 | a0002c0003t0004g0031a0002c0003t0004g0032a0002c0003t0004g0160 | 3 | HG01891.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.281-1062_281-1022d others(43): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598863 | |||||
chrX:13598943 | C | CAT | 1 | a0001c0001t0002g0120 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.281-1017_281-1016d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598943 | |||||
chrX:13598943 | CAT | C | 1 | a0001c0001t0001g0276 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.281-1017_281-1016d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598943 | |||||
chrX:13598954 | A | AT | 1 | a0010c0016t0004g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-1020dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598954 | |||||
chrX:13598954 | A | T | 2 | a0001c0001t0003g0090a0001c0004t0004g0055 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.281-1021A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598954 | ||||||
chrX:13598956 | A | T | 5 | a0001c0001t0001g0218a0001c0001t0003g0090a0001c0004t0004g0055others(2): Show | 5 | HG02572.hp1 HG02809.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-1019A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598956 | ||||||
chrX:13598958 | A | ATATATAA others(33): Show |
1 | a0010c0016t0004g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-1016_281-1015i others(42): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598958 | |||||
chrX:13598958 | A | T | 55 | a0001c0001t0001g0218a0001c0001t0001g0267a0001c0001t0001g0268others(52): Show | 57 | HG00544.hp1 HG00621.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.281-1017A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598958 | ||||||
chrX:13598965 | T | A | 3 | a0002c0003t0004g0030a0002c0003t0004g0146a0004c0021t0001g0041 | 3 | HG01070.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.281-1010T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598965 | ||||||
chrX:13599193 | T | G | 44 | a0001c0001t0001g0193a0001c0001t0001g0218a0001c0001t0003g0090others(41): Show | 46 | HG00544.hp1 HG00735.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.281-782T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13599193 | ||||||
chrX:13599524 | G | A | 2 | a0002c0003t0004g0036a0010c0016t0004g0025 | 2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.281-451G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13599524 | ||||||
chrX:13599644 | T | C | 5 | a0001c0001t0001g0056a0001c0001t0002g0094a0002c0003t0004g0030others(2): Show | 5 | HG01070.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-331T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13599644 | ||||||
chrX:13599852 | G | A | 4 | a0001c0001t0002g0038a0002c0003t0004g0031a0002c0003t0004g0032others(1): Show | 4 | HG01891.hp1 HG03540.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-123G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13599852 | ||||||
chrX:13599866 | T | C | 3 | a0001c0004t0002g0123a0001c0004t0002g0124a0001c0004t0002g0125 | 3 | NA19057.hp1 NA19072.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.281-109T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13599866 | ||||||
chrX:13600164 | G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0201 | 2 | NA18972.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.400+70G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600164 | ||||||
chrX:13600206 | GC | G | 1 | a0001c0001t0002g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.400+117delC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600206 | |||||
chrX:13600266 | C | CTTCT | 40 | a0001c0001t0001g0056a0001c0001t0001g0193a0001c0001t0002g0062others(37): Show | 42 | HG00544.hp1 HG00735.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.400+182_400+185dup others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600266 | |||||
chrX:13600274 | T | TTTCTTTC | 7 | a0001c0001t0003g0079a0002c0003t0004g0160a0002c0026t0004g0029others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.400+185_400+186ins others(7): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600274 | |||||
chrX:13600277 | C | CT | 5 | a0002c0003t0004g0030a0002c0003t0004g0036a0002c0003t0004g0146others(2): Show | 5 | HG01070.hp1 HG01109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+185dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600277 | |||||
chrX:13600277 | C | CTTTCTTC others(1): Show |
8 | a0001c0005t0001g0049a0001c0005t0001g0231a0001c0005t0001g0246others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+185_400+186ins others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600277 | |||||
chrX:13600277 | C | CTTTCTTC others(2): Show |
3 | a0001c0005t0001g0148a0001c0005t0001g0219a0001c0005t0001g0280 | 3 | HG02145.hp1 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.400+185_400+186ins others(9): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600277 | |||||
chrX:13600277 | C | CTTTCTTC others(3): Show |
1 | a0001c0005t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.400+185_400+186ins others(10): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600277 | |||||
chrX:13600277 | CTTCT | C | 1 | a0004c0022t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.400+186_400+189del others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600277 | |||||
chrX:13600278 | T | TTTCTTC | 41 | a0001c0001t0001g0170a0001c0001t0001g0181a0001c0001t0001g0186others(38): Show | 42 | HG00639.hp2 HG00738.hp1 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.400+185_400+186ins others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600278 | |||||
chrX:13600279 | T | TTCTTC | 111 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0059others(108): Show | 113 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.400+185_400+186ins others(5): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600279 | ||||||
chrX:13600280 | C | CT | 9 | a0001c0001t0001g0060a0001c0001t0001g0163a0001c0001t0001g0183others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.400+210dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600280 | |||||
chrX:13600280 | C | CTT | 1 | a0001c0001t0001g0281 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.400+209_400+210dup others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600280 | |||||
chrX:13600280 | C | T | 171 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0059others(168): Show | 174 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.400+186C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600280 | ||||||
chrX:13600281 | T | TTC | 5 | a0002c0003t0004g0030a0002c0003t0004g0036a0002c0003t0004g0146others(2): Show | 5 | HG01070.hp1 HG01109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+188_400+189ins others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600281 | |||||
chrX:13600285 | T | C | 1 | a0004c0022t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.400+191T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600285 | ||||||
chrX:13600288 | T | C | 1 | a0004c0022t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.400+194T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600288 | ||||||
chrX:13600390 | A | G | 217 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(214): Show | 222 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.400+296A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600390 | ||||||
chrX:13600436 | G | T | 1 | a0007c0024t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.400+342G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600436 | ||||||
chrX:13600444 | G | A | 4 | a0001c0001t0001g0056a0002c0003t0004g0030a0002c0003t0004g0146others(1): Show | 4 | HG01070.hp1 HG02486.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+350G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600444 | ||||||
chrX:13600634 | A | G | 9 | a0001c0007t0001g0272a0001c0007t0003g0171a0001c0007t0003g0172others(6): Show | 9 | HG01243.hp1 HG02027.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.400+540A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600634 | ||||||
chrX:13600718 | C | T | 2 | a0002c0003t0004g0036a0010c0016t0004g0025 | 2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.400+624C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600718 | ||||||
chrX:13600735 | T | TA | 23 | a0001c0001t0001g0056a0001c0001t0001g0251a0001c0005t0001g0053others(20): Show | 23 | HG01070.hp1 HG01106.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.400+659dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600735 | |||||
chrX:13600735 | T | TAA | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.400+658_400+659dup others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600735 | |||||
chrX:13600735 | TA | T | 3 | a0001c0001t0002g0118a0001c0001t0002g0139a0002c0003t0004g0147 | 3 | HG01074.hp1 NA18969.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.400+659delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600735 | |||||
chrX:13600745 | A | G | 7 | a0001c0001t0001g0199a0001c0001t0001g0237a0001c0001t0001g0242others(4): Show | 7 | HG01975.hp2 NA18975.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+651A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600745 | ||||||
chrX:13600753 | A | AAAT | 1 | a0002c0025t0004g0265 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.400+659_400+660ins others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600753 | ||||||
chrX:13600753 | A | AAT | 44 | a0001c0001t0001g0193a0001c0001t0001g0218a0001c0001t0002g0094others(41): Show | 46 | HG00544.hp1 HG00735.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.400+659_400+660ins others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600753 | ||||||
chrX:13600780 | G | T | 4 | a0001c0001t0002g0038a0002c0003t0004g0031a0002c0003t0004g0032others(1): Show | 4 | HG01891.hp1 HG03540.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+686G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600780 | ||||||
chrX:13600795 | G | GA | 9 | a0001c0005t0001g0049a0001c0005t0001g0148a0001c0005t0001g0219others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.400+704dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600795 | |||||
chrX:13600798 | AG | A | 1 | a0013c0015t0007g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.400+705delG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600798 | ||||||
chrX:13600799 | G | A | 13 | a0001c0005t0001g0049a0001c0005t0001g0053a0001c0005t0001g0148others(10): Show | 13 | HG01106.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.400+705G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600799 | ||||||
chrX:13600799 | GA | G | 2 | a0001c0001t0002g0211a0001c0004t0001g0194 | 2 | HG00735.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.400+715delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600799 | |||||
chrX:13600822 | T | C | 12 | a0001c0001t0002g0038a0001c0007t0001g0272a0001c0007t0003g0171others(9): Show | 12 | HG01243.hp1 HG01891.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+728T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600822 | ||||||
chrX:13600909 | G | T | 1 | a0007c0024t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.400+815G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600909 | ||||||
chrX:13601081 | A | G | 1 | a0007c0024t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.400+987A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601081 | ||||||
chrX:13601186 | A | C | 22 | a0001c0005t0001g0049a0001c0005t0001g0053a0001c0005t0001g0148others(19): Show | 22 | HG01106.hp1 HG01891.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.400+1092A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601186 | ||||||
chrX:13601399 | T | C | 1 | a0001c0004t0001g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.400+1305T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601399 | ||||||
chrX:13601573 | T | G | 4 | a0001c0001t0001g0225a0001c0001t0002g0127a0001c0001t0009g0057others(1): Show | 4 | NA18967.hp1 NA18978.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+1479T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601573 | ||||||
chrX:13601634 | C | G | 1 | a0010c0016t0004g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.400+1540C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601634 | ||||||
chrX:13601645 | G | A | 5 | a0001c0001t0004g0228a0001c0001t0004g0230a0002c0003t0004g0284others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+1551G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601645 | ||||||
chrX:13601866 | T | C | 1 | a0001c0004t0001g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.401-1451T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601866 | ||||||
chrX:13601869 | T | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0174a0001c0001t0003g0150 | 3 | HG02257.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.401-1448T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601869 | ||||||
chrX:13601889 | A | G | 5 | a0001c0007t0001g0272a0001c0007t0003g0171a0001c0007t0003g0172others(2): Show | 5 | HG02027.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-1428A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601889 | ||||||
chrX:13602174 | C | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0203a0001c0001t0001g0206 | 4 | HG00323.hp2 HG01192.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-1143C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602174 | ||||||
chrX:13602257 | G | A | 14 | a0001c0005t0001g0049a0001c0005t0001g0053a0001c0005t0001g0148others(11): Show | 14 | HG01106.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.401-1060G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602257 | ||||||
chrX:13602344 | T | C | 2 | a0001c0001t0001g0212a0001c0001t0002g0130 | 2 | NA18945.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.401-973T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602344 | ||||||
chrX:13602548 | C | T | 1 | a0002c0002t0006g0126 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.401-769C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602548 | ||||||
chrX:13602820 | G | A | 4 | a0001c0001t0011g0210a0003c0006t0002g0128a0003c0006t0004g0289others(1): Show | 5 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-497G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602820 | ||||||
chrX:13602963 | C | T | 4 | a0001c0001t0011g0210a0003c0006t0002g0128a0003c0006t0004g0289others(1): Show | 5 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-354C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602963 | ||||||
chrX:13602974 | A | T | 5 | a0001c0001t0011g0210a0003c0006t0002g0121a0003c0006t0002g0128others(2): Show | 6 | HG01975.hp1 HG02004.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-343A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602974 | ||||||
chrX:13603001 | AC | A | 1 | a0001c0001t0002g0143 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.401-315delC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13603001 | ||||||
chrX:13603517 | A | G | 1 | a0001c0001t0002g0138 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.520+81A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13603517 | ||||||
chrX:13603820 | C | T | 1 | a0004c0022t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.520+384C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13603820 | ||||||
chrX:13603857 | A | G | 1 | a0002c0003t0006g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.520+421A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13603857 | ||||||
chrX:13603980 | A | G | 137 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0059others(134): Show | 139 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.520+544A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13603980 | ||||||
chrX:13604187 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.520+751A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13604187 | ||||||
chrX:13604675 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.520+1239T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13604675 | ||||||
chrX:13605047 | CT | C | 135 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0059others(132): Show | 137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.521-1327delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605047 | |||||
chrX:13605054 | G | T | 135 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0059others(132): Show | 137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.521-1325G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605054 | ||||||
chrX:13605359 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.521-1020A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605359 | ||||||
chrX:13605409 | C | CA | 3 | a0001c0001t0002g0038a0001c0001t0003g0092a0001c0001t0004g0270 | 3 | NA19030.hp1 NA19030.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.521-960dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605409 | |||||
chrX:13605409 | CA | C | 1 | a0010c0016t0004g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.521-960delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605409 | |||||
chrX:13605459 | G | C | 1 | a0004c0022t0001g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.521-920G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605459 | ||||||
chrX:13605509 | A | G | 4 | a0001c0001t0011g0210a0003c0006t0002g0128a0003c0006t0004g0289others(1): Show | 5 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.521-870A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605509 | ||||||
chrX:13605578 | C | CA | 67 | a0001c0001t0001g0005a0001c0001t0001g0056a0001c0001t0001g0059others(64): Show | 68 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.521-781dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605578 | |||||
chrX:13605578 | C | CAA | 2 | a0008c0017t0003g0296a0013c0015t0007g0009 | 2 | HG02280.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.521-782_521-781dup others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605578 | |||||
chrX:13605578 | CA | C | 11 | a0001c0001t0001g0162a0001c0001t0001g0208a0001c0001t0001g0262others(8): Show | 11 | HG01069.hp1 HG01169.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.521-781delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605578 | |||||
chrX:13605578 | CAAA | C | 46 | a0001c0001t0001g0218a0001c0001t0003g0090a0001c0001t0005g0044others(43): Show | 49 | HG00544.hp1 HG00735.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.521-783_521-781del others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605578 | |||||
chrX:13605578 | CAAAA | C | 1 | a0001c0001t0005g0045 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.521-784_521-781del others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605578 | |||||
chrX:13605599 | G | A | 1 | a0001c0001t0003g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.521-780G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605599 | ||||||
chrX:13605828 | C | T | 7 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0256others(4): Show | 7 | HG00597.hp2 HG02071.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.521-551C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605828 | ||||||
chrX:13605857 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.521-522C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605857 | ||||||
chrX:13605982 | C | T | 3 | a0001c0001t0002g0064a0001c0001t0002g0106a0001c0001t0002g0107 | 3 | NA18975.hp2 NA18998.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.521-397C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605982 | ||||||
chrX:13606159 | T | C | 3 | a0002c0003t0004g0051a0002c0003t0004g0052a0002c0003t0004g0152 | 3 | HG01243.hp1 HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.521-220T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13606159 | ||||||
chrX:13606163 | G | A | 54 | a0001c0001t0001g0056a0001c0001t0001g0218a0001c0001t0002g0094others(51): Show | 56 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.521-216G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13606163 | ||||||
chrX:13606286 | C | G | 1 | a0001c0001t0002g0211 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.521-93C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13606286 | ||||||
chrX:13606522 | C | T | 5 | a0001c0007t0001g0272a0001c0007t0003g0171a0001c0007t0003g0172others(2): Show | 5 | HG02027.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+9C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13606522 | ||||||
chrX:13606627 | G | C | 1 | a0001c0001t0002g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.655+114G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13606627 | ||||||
chrX:13606714 | TA | T | 1 | a0001c0001t0002g0134 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.655+204delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chrX | 13606714 | |||||
chrX:13606813 | A | AT | 1 | a0001c0001t0002g0134 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.655+306dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chrX | 13606813 | |||||
chrX:13606872 | AT | A | 1 | a0001c0001t0002g0134 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.655+362delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chrX | 13606872 | |||||
chrX:13607010 | GC | G | 1 | a0001c0001t0002g0134 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.655+500delC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chrX | 13607010 | |||||
chrX:13607264 | C | G | 2 | a0002c0003t0004g0240a0007c0024t0001g0040 | 2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.655+751C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607264 | ||||||
chrX:13607283 | C | T | 1 | a0013c0015t0007g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.655+770C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607283 | ||||||
chrX:13607291 | G | A | 1 | a0002c0003t0004g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.655+778G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607291 | ||||||
chrX:13607357 | C | T | 4 | a0001c0001t0011g0210a0003c0006t0002g0128a0003c0006t0004g0289others(1): Show | 5 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+844C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607357 | ||||||
chrX:13607426 | C | T | 1 | a0002c0003t0006g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.656-898C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607426 | ||||||
chrX:13607434 | C | T | 53 | a0001c0001t0001g0056a0001c0001t0001g0218a0001c0001t0002g0094others(50): Show | 55 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.656-890C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607434 | ||||||
chrX:13607653 | CA | C | 1 | a0001c0001t0002g0134 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.656-667delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chrX | 13607653 | |||||
chrX:13607928 | G | A | 6 | a0002c0003t0004g0030a0002c0003t0004g0146a0002c0026t0004g0029others(3): Show | 6 | HG01070.hp1 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-396G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607928 | ||||||
chrX:13607934 | G | A | 16 | a0001c0005t0001g0049a0001c0005t0001g0148a0001c0005t0001g0219others(13): Show | 16 | HG01070.hp1 HG01109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.656-390G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607934 | ||||||
chrX:13608033 | G | A | 89 | a0001c0001t0001g0056a0001c0001t0001g0218a0001c0001t0002g0094others(86): Show | 92 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.656-291G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13608033 | ||||||
chrX:13608051 | C | T | 1 | a0001c0004t0002g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.656-273C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13608051 | ||||||
chrX:13608196 | C | T | 1 | a0001c0001t0012g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.656-128C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13608196 | ||||||
chrX:13608284 | T | C | 87 | a0001c0001t0001g0056a0001c0001t0001g0218a0001c0001t0002g0094others(84): Show | 90 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.656-40T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13608284 | ||||||
chrX:13608480 | T | G | 5 | a0001c0007t0001g0272a0001c0007t0003g0171a0001c0007t0003g0172others(2): Show | 5 | HG02027.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.778+34T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13608480 | ||||||
chrX:13608501 | A | G | 9 | a0001c0001t0001g0226a0001c0001t0001g0234a0001c0001t0001g0252others(6): Show | 9 | HG00639.hp2 HG01168.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.778+55A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13608501 | ||||||
chrX:13608573 | C | CTG | 1 | a0007c0024t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.778+138_778+139dup others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13608573 | |||||
chrX:13608755 | T | A | 10 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0002g0141others(7): Show | 11 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.778+309T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13608755 | ||||||
chrX:13609169 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.778+723G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13609169 | ||||||
chrX:13609728 | T | C | 46 | a0001c0001t0001g0218a0001c0001t0002g0094a0001c0001t0003g0090others(43): Show | 48 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.778+1282T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13609728 | ||||||
chrX:13610055 | AC | A | 1 | a0001c0001t0001g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.778+1612delC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13610055 | |||||
chrX:13610917 | T | C | 26 | a0001c0001t0001g0185a0001c0001t0001g0190a0001c0001t0001g0191others(23): Show | 26 | HG00597.hp2 HG00642.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.778+2471T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13610917 | ||||||
chrX:13611142 | G | A | 21 | a0001c0001t0011g0210a0001c0005t0001g0049a0001c0005t0001g0053others(18): Show | 22 | HG01070.hp1 HG01106.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.778+2696G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13611142 | ||||||
chrX:13611302 | G | T | 4 | a0001c0007t0001g0272a0001c0007t0003g0171a0001c0007t0003g0172others(1): Show | 4 | HG02027.hp1 HG02723.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.778+2856G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13611302 | ||||||
chrX:13611391 | A | G | 4 | a0002c0003t0004g0031a0002c0003t0004g0032a0002c0003t0004g0160others(1): Show | 4 | HG01891.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+2945A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13611391 | ||||||
chrX:13611403 | C | T | 53 | a0001c0001t0001g0056a0001c0001t0001g0218a0001c0001t0002g0094others(50): Show | 55 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.778+2957C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13611403 | ||||||
chrX:13611860 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.778+3414T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13611860 | ||||||
chrX:13612007 | T | C | 5 | a0001c0001t0005g0044a0001c0001t0005g0045a0001c0008t0001g0048others(2): Show | 5 | HG02293.hp1 HG02895.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.778+3561T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612007 | ||||||
chrX:13612026 | T | C | 85 | a0001c0001t0001g0056a0001c0001t0001g0218a0001c0001t0002g0094others(82): Show | 88 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.778+3580T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612026 | ||||||
chrX:13612038 | C | CT | 2 | a0004c0021t0001g0041a0012c0011t0004g0054 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.778+3603dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13612038 | |||||
chrX:13612038 | CT | C | 2 | a0001c0001t0002g0127a0001c0001t0002g0143 | 2 | NA18981.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.778+3603delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13612038 | |||||
chrX:13612048 | T | A | 1 | a0001c0001t0011g0210 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.778+3602T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612048 | ||||||
chrX:13612049 | T | A | 12 | a0001c0001t0002g0098a0001c0001t0011g0210a0001c0007t0001g0272others(9): Show | 13 | HG01258.hp1 HG01975.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.778+3603T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612049 | ||||||
chrX:13612049 | TA | T | 2 | a0001c0004t0001g0243a0001c0004t0003g0061 | 2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.778+3606delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13612049 | |||||
chrX:13612050 | A | T | 35 | a0001c0001t0002g0058a0001c0001t0003g0178a0001c0004t0001g0019others(32): Show | 37 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.778+3604A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612050 | ||||||
chrX:13612323 | T | G | 2 | a0004c0021t0001g0041a0012c0011t0004g0054 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.778+3877T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612323 | ||||||
chrX:13612324 | A | G | 3 | a0001c0001t0001g0248a0001c0001t0001g0262a0001c0001t0001g0269 | 3 | NA18957.hp2 NA18980.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.778+3878A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612324 | ||||||
chrX:13612459 | A | G | 16 | a0001c0005t0001g0049a0001c0005t0001g0053a0001c0005t0001g0148others(13): Show | 16 | HG01070.hp1 HG01106.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.778+4013A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612459 | ||||||
chrX:13612540 | C | T | 1 | a0001c0001t0003g0084 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.778+4094C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612540 | ||||||
chrX:13612567 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.778+4121T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612567 | ||||||
chrX:13612574 | C | CG | 6 | a0001c0001t0001g0069a0001c0001t0001g0192a0001c0001t0001g0273others(3): Show | 6 | HG01109.hp1 HG01175.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+4132dupG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13612574 | |||||
chrX:13612583 | G | A | 47 | a0001c0001t0001g0218a0001c0001t0003g0090a0001c0001t0003g0178others(44): Show | 49 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.778+4137G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612583 | ||||||
chrX:13612586 | C | T | 6 | a0001c0007t0001g0272a0001c0007t0003g0171a0001c0007t0003g0172others(3): Show | 6 | HG02027.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+4140C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612586 | ||||||
chrX:13612620 | G | A | 6 | a0001c0007t0001g0272a0001c0007t0003g0171a0001c0007t0003g0172others(3): Show | 6 | HG02027.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+4174G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612620 | ||||||
chrX:13612670 | G | T | 15 | a0001c0005t0001g0049a0001c0005t0001g0148a0001c0005t0001g0219others(12): Show | 15 | HG01070.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.778+4224G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612670 | ||||||
chrX:13612687 | C | T | 7 | a0001c0001t0005g0044a0001c0001t0005g0045a0001c0008t0001g0048others(4): Show | 7 | HG02293.hp1 HG02895.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.778+4241C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612687 | ||||||
chrX:13612814 | C | T | 35 | a0001c0001t0003g0178a0001c0004t0001g0019a0001c0004t0001g0066others(32): Show | 37 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.778+4368C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612814 | ||||||
chrX:13612947 | C | T | 1 | a0001c0001t0002g0108 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.778+4501C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612947 | ||||||
chrX:13613018 | G | A | 1 | a0002c0003t0004g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.778+4572G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13613018 | ||||||
chrX:13613123 | C | T | 2 | a0004c0022t0001g0175a0007c0024t0001g0040 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.779-4607C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13613123 | ||||||
chrX:13613157 | C | CAT | 111 | a0001c0001t0001g0005a0001c0001t0001g0059a0001c0001t0001g0069others(108): Show | 115 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.779-4552_779-4551d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | C | CATAT | 12 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0187others(9): Show | 12 | HG00323.hp2 HG01192.hp1 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.779-4554_779-4551d others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | C | CATATAT | 13 | a0001c0005t0001g0053a0001c0005t0001g0148a0001c0005t0001g0219others(10): Show | 13 | HG01070.hp1 HG01106.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.779-4556_779-4551d others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | C | CATATATA others(1): Show |
1 | a0001c0005t0001g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.779-4558_779-4551d others(10): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | C | CATATATA others(3): Show |
3 | a0002c0003t0004g0031a0002c0003t0004g0160a0005c0014t0001g0028 | 3 | HG01891.hp1 HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.779-4560_779-4551d others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | C | CATATATA others(5): Show |
1 | a0002c0003t0006g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.779-4562_779-4551d others(14): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | C | CATATATA others(7): Show |
1 | a0002c0003t0004g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.779-4564_779-4551d others(16): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | C | CATATATA others(11): Show |
4 | a0001c0007t0001g0272a0001c0008t0001g0048a0001c0008t0001g0295others(1): Show | 4 | HG02293.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.779-4568_779-4551d others(20): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | C | CATATATA others(13): Show |
8 | a0001c0001t0004g0228a0001c0001t0004g0230a0001c0001t0005g0045others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.779-4570_779-4551d others(22): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | C | CATATATA others(15): Show |
6 | a0001c0001t0001g0056a0002c0003t0004g0036a0002c0003t0004g0240others(3): Show | 6 | HG01109.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.779-4572_779-4551d others(24): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | C | CATATATA others(25): Show |
1 | a0002c0025t0004g0265 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.779-4551_779-4550i others(34): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | CAT | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | NA18946.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.779-4552_779-4551d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613157 | CATATATA others(3): Show |
C | 6 | a0001c0001t0001g0218a0001c0001t0002g0094a0001c0001t0003g0090others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.779-4560_779-4551d others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | |||||
chrX:13613178 | A | ATATATG | 1 | a0001c0005t0001g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.779-4551_779-4550i others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613178 | |||||
chrX:13613179 | T | TATATATA others(12): Show |
1 | a0001c0001t0005g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.779-4551_779-4550i others(21): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13613179 | ||||||
chrX:13613245 | A | T | 1 | a0002c0003t0006g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.779-4485A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13613245 | ||||||
chrX:13613531 | C | T | 1 | a0001c0001t0003g0022 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.779-4199C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13613531 | ||||||
chrX:13613913 | C | CT | 1 | a0001c0001t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.779-3817_779-3816i others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13613913 | ||||||
chrX:13614161 | G | A | 2 | a0001c0001t0003g0082a0001c0001t0003g0293 | 2 | HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.779-3569G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614161 | ||||||
chrX:13614338 | T | C | 1 | a0002c0003t0006g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.779-3392T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614338 | ||||||
chrX:13614508 | G | T | 1 | a0001c0005t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.779-3222G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614508 | ||||||
chrX:13614659 | C | CA | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-3065dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13614659 | |||||
chrX:13614673 | G | A | 1 | a0001c0001t0012g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.779-3057G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614673 | ||||||
chrX:13614749 | A | AT | 61 | a0001c0001t0001g0218a0001c0001t0002g0094a0001c0001t0002g0107others(58): Show | 64 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.779-2965dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13614749 | |||||
chrX:13614749 | A | ATTT | 5 | a0002c0003t0004g0030a0002c0003t0004g0146a0002c0026t0004g0029others(2): Show | 5 | HG01070.hp1 HG02280.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.779-2967_779-2965d others(5): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13614749 | |||||
chrX:13614749 | A | ATTTT | 1 | a0006c0009t0004g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.779-2968_779-2965d others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13614749 | |||||
chrX:13614749 | A | ATTTTT | 1 | a0001c0005t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.779-2969_779-2965d others(7): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13614749 | |||||
chrX:13614749 | AT | A | 4 | a0001c0001t0001g0162a0001c0001t0001g0193a0001c0001t0001g0288others(1): Show | 4 | HG01169.hp1 HG02015.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.779-2965delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13614749 | |||||
chrX:13614749 | ATTTT | A | 9 | a0001c0005t0001g0049a0001c0005t0001g0148a0001c0005t0001g0219others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.779-2968_779-2965d others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13614749 | |||||
chrX:13614751 | T | TA | 6 | a0001c0007t0001g0272a0001c0007t0003g0171a0001c0007t0003g0172others(3): Show | 6 | HG02027.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.779-2979_779-2978i others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614751 | ||||||
chrX:13614922 | AT | A | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-2803delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13614922 | |||||
chrX:13614947 | G | T | 169 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(166): Show | 172 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.779-2783G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614947 | ||||||
chrX:13615008 | TC | T | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-2719delC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13615008 | |||||
chrX:13615124 | G | A | 2 | a0002c0003t0004g0036a0010c0016t0004g0025 | 2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.779-2606G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615124 | ||||||
chrX:13615224 | T | C | 1 | a0001c0001t0003g0043 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.779-2506T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615224 | ||||||
chrX:13615330 | G | GT | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-2397dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13615330 | |||||
chrX:13615456 | C | G | 1 | a0001c0004t0003g0061 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.779-2274C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615456 | ||||||
chrX:13615479 | C | T | 6 | a0001c0007t0001g0272a0001c0007t0003g0171a0001c0007t0003g0172others(3): Show | 6 | HG02027.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.779-2251C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615479 | ||||||
chrX:13615490 | G | A | 159 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0059others(156): Show | 162 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.779-2240G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615490 | ||||||
chrX:13615654 | T | C | 2 | a0004c0021t0001g0041a0012c0011t0004g0054 | 2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.779-2076T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615654 | ||||||
chrX:13615710 | T | C | 1 | a0001c0001t0003g0155 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.779-2020T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615710 | ||||||
chrX:13615815 | GT | G | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-1912delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13615815 | |||||
chrX:13615838 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.779-1892A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615838 | ||||||
chrX:13615998 | A | T | 2 | a0002c0003t0004g0036a0010c0016t0004g0025 | 2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.779-1732A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615998 | ||||||
chrX:13616049 | CT | C | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-1678delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616049 | |||||
chrX:13616064 | T | C | 48 | a0001c0001t0001g0218a0001c0001t0002g0094a0001c0001t0003g0090others(45): Show | 50 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.779-1666T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616064 | ||||||
chrX:13616196 | C | T | 4 | a0001c0001t0011g0210a0003c0006t0002g0128a0003c0006t0004g0289others(1): Show | 5 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.779-1534C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616196 | ||||||
chrX:13616243 | G | C | 13 | a0001c0001t0011g0210a0001c0005t0001g0049a0001c0005t0001g0148others(10): Show | 14 | HG01975.hp1 HG02132.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.779-1487G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616243 | ||||||
chrX:13616265 | CCTTAAT | C | 1 | a0001c0001t0008g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.779-1459_779-1454d others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616265 | |||||
chrX:13616373 | GC | G | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-1355delC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616373 | |||||
chrX:13616480 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.779-1250C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616480 | ||||||
chrX:13616514 | G | A | 124 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0059others(121): Show | 126 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.779-1216G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616514 | ||||||
chrX:13616529 | C | CA | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-1199dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616529 | |||||
chrX:13616574 | C | CA | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-1155dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616574 | |||||
chrX:13616610 | CA | C | 1 | a0001c0001t0002g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.779-1107delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616610 | |||||
chrX:13616662 | A | G | 1 | a0001c0005t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.779-1068A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616662 | ||||||
chrX:13616683 | C | T | 1 | a0002c0003t0006g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.779-1047C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616683 | ||||||
chrX:13616772 | T | G | 1 | a0001c0007t0001g0272 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.779-958T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616772 | ||||||
chrX:13616783 | C | G | 9 | a0001c0001t0001g0056a0001c0007t0001g0272a0001c0007t0003g0171others(6): Show | 9 | HG02027.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.779-947C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616783 | ||||||
chrX:13616790 | C | T | 1 | a0004c0021t0001g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.779-940C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616790 | ||||||
chrX:13616859 | A | AT | 61 | a0001c0001t0001g0109a0001c0001t0001g0170a0001c0001t0001g0197others(58): Show | 63 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.779-850dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616859 | |||||
chrX:13616859 | A | ATT | 19 | a0001c0001t0001g0218a0001c0001t0002g0067a0001c0001t0002g0073others(16): Show | 20 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.779-851_779-850dup others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616859 | |||||
chrX:13616859 | A | ATTT | 2 | a0002c0003t0004g0030a0002c0003t0004g0285 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.779-852_779-850dup others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616859 | |||||
chrX:13616859 | AT | A | 1 | a0001c0001t0003g0155 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.779-850delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616859 | |||||
chrX:13616890 | T | TC | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-839dupC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616890 | |||||
chrX:13616910 | CG | C | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-818delG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616910 | |||||
chrX:13616956 | G | A | 1 | a0013c0015t0007g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.779-774G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616956 | ||||||
chrX:13617024 | C | T | 64 | a0001c0001t0001g0056a0001c0001t0001g0218a0001c0001t0002g0094others(61): Show | 66 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.779-706C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13617024 | ||||||
chrX:13617027 | GC | G | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-700delC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13617027 | |||||
chrX:13617053 | TAG | T | 84 | a0001c0001t0001g0056a0001c0001t0001g0218a0001c0001t0002g0094others(81): Show | 87 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.779-671_779-670del others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13617053 | |||||
chrX:13617171 | G | C | 5 | a0001c0001t0001g0218a0001c0001t0003g0090a0001c0004t0004g0055others(2): Show | 5 | HG02572.hp1 HG02809.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.779-559G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13617171 | ||||||
chrX:13617196 | G | GA | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-528dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13617196 | |||||
chrX:13617312 | C | CA | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-416dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13617312 | |||||
chrX:13617430 | T | TG | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-298dupG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13617430 | |||||
chrX:13617448 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.779-282G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13617448 | ||||||
chrX:13617485 | AC | A | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-244delC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13617485 | ||||||
chrX:13617492 | T | TG | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-236dupG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13617492 | |||||
chrX:13617525 | TA | T | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-203delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13617525 | |||||
chrX:13617590 | TATC | T | 80 | a0001c0001t0001g0056a0001c0001t0001g0218a0001c0001t0002g0094others(77): Show | 83 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.779-135_779-133del others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13617590 | |||||
chrX:13617680 | TA | T | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.779-48delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13617680 | |||||
chrX:13618125 | C | CA | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1102+77dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chrX | 13618125 | |||||
chrX:13618185 | AT | A | 1 | a0008c0017t0003g0296 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1102+134delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chrX | 13618185 | |||||
chrX:13618227 | C | T | 5 | a0001c0004t0001g0066a0001c0004t0001g0194a0001c0004t0001g0243others(2): Show | 6 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1102+174C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618227 | ||||||
chrX:13618406 | G | T | 1 | a0005c0013t0004g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1102+353G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618406 | ||||||
chrX:13618524 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1102+471G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618524 | ||||||
chrX:13618638 | TC | T | 1 | a0002c0002t0004g0202 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1103-519delC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chrX | 13618638 | |||||
chrX:13618832 | G | T | 1 | a0001c0001t0001g0221 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1103-331G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618832 | ||||||
chrX:13618864 | T | C | 1 | a0002c0003t0004g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1103-299T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618864 | ||||||
chrX:13618881 | CA | C | 1 | a0001c0001t0002g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1103-275delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chrX | 13618881 | |||||
chrX:13618889 | GA | G | 217 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(214): Show | 222 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1103-263delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chrX | 13618889 | |||||
chrX:13618993 | G | A | 1 | a0012c0011t0004g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1103-170G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618993 | ||||||
chrX:13619000 | G | T | 1 | a0001c0001t0002g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1103-163G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13619000 | ||||||
chrX:13619308 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1183+65T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619308 | ||||||
chrX:13619463 | G | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0142 | 2 | NA18989.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1183+220G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619463 | ||||||
chrX:13619580 | T | G | 2 | a0001c0001t0005g0044a0001c0001t0005g0045 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1183+337T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619580 | ||||||
chrX:13619615 | G | A | 15 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0073others(12): Show | 16 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1183+372G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619615 | ||||||
chrX:13619666 | T | C | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1183+423T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619666 | ||||||
chrX:13619751 | G | T | 1 | a0005c0013t0004g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1183+508G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619751 | ||||||
chrX:13619759 | A | G | 10 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0002g0141others(7): Show | 11 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1183+516A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619759 | ||||||
chrX:13619815 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1183+572G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619815 | ||||||
chrX:13620017 | C | T | 79 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0276others(76): Show | 82 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.1183+774C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620017 | ||||||
chrX:13620130 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1183+887C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620130 | ||||||
chrX:13620173 | T | C | 1 | a0001c0008t0001g0173 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1183+930T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620173 | ||||||
chrX:13620324 | CACTTACC others(58): Show |
C | 1 | a0001c0001t0001g0174 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1183+1126_1183+119 others(69): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13620324 | |||||
chrX:13620434 | G | A | 1 | a0001c0001t0008g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1183+1191G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620434 | ||||||
chrX:13620475 | T | G | 2 | a0001c0001t0001g0292a0001c0001t0002g0137 | 2 | HG02293.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1183+1232T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620475 | ||||||
chrX:13620511 | C | G | 4 | a0003c0006t0002g0121a0003c0006t0002g0128a0003c0006t0004g0289others(1): Show | 5 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1183+1268C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620511 | ||||||
chrX:13620517 | C | CA | 5 | a0001c0005t0002g0119a0003c0006t0002g0121a0003c0006t0002g0128others(2): Show | 6 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1183+1283dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13620517 | |||||
chrX:13620670 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1183+1427C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620670 | ||||||
chrX:13620797 | A | G | 1 | a0009c0020t0001g0232 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1183+1554A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620797 | ||||||
chrX:13620918 | C | G | 1 | a0001c0008t0001g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1183+1675C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620918 | ||||||
chrX:13621127 | G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0217others(1): Show | 4 | HG00408.hp1 HG00544.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183+1884G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621127 | ||||||
chrX:13621201 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1183+1958C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621201 | ||||||
chrX:13621331 | T | C | 1 | a0001c0005t0001g0053 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1183+2088T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621331 | ||||||
chrX:13621717 | G | C | 1 | a0005c0013t0004g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1184-2107G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621717 | ||||||
chrX:13621791 | A | G | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1184-2033A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621791 | ||||||
chrX:13621956 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1184-1868A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621956 | ||||||
chrX:13622211 | AGAAAG | A | 48 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0073others(45): Show | 50 | HG00621.hp1 HG00735.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.1184-1607_1184-160 others(9): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13622211 | |||||
chrX:13622271 | G | A | 2 | a0004c0022t0001g0175a0007c0024t0001g0040 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1184-1553G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622271 | ||||||
chrX:13622284 | G | A | 3 | a0003c0006t0002g0128a0003c0006t0004g0289a0003c0006t0006g0004 | 4 | HG01975.hp1 HG02148.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184-1540G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622284 | ||||||
chrX:13622348 | A | C | 1 | a0001c0001t0001g0238 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1184-1476A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622348 | ||||||
chrX:13622669 | A | G | 219 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(216): Show | 224 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.1184-1155A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622669 | ||||||
chrX:13622756 | G | A | 2 | a0001c0001t0001g0133a0001c0001t0002g0026 | 2 | HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1184-1068G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622756 | ||||||
chrX:13622854 | CTT | C | 1 | a0002c0003t0004g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1184-969_1184-968d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622854 | ||||||
chrX:13622913 | G | C | 1 | a0002c0003t0004g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1184-911G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622913 | ||||||
chrX:13623188 | CA | C | 1 | a0001c0001t0001g0149 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1184-627delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623188 | |||||
chrX:13623197 | AG | A | 1 | a0001c0001t0001g0251 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1184-626delG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623197 | ||||||
chrX:13623336 | AT | A | 6 | a0001c0001t0001g0162a0001c0001t0002g0106a0001c0001t0002g0127others(3): Show | 6 | HG01169.hp1 HG01256.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184-474delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623336 | |||||
chrX:13623338 | T | TA | 1 | a0001c0001t0001g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1184-486_1184-485i others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623338 | ||||||
chrX:13623339 | T | A | 214 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(211): Show | 219 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1184-485T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623339 | ||||||
chrX:13623340 | T | A | 2 | a0001c0001t0002g0106a0001c0001t0003g0076 | 2 | NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1184-484T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623340 | ||||||
chrX:13623349 | T | A | 1 | a0005c0013t0004g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1184-475T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623349 | ||||||
chrX:13623350 | T | A | 18 | a0001c0001t0001g0196a0001c0001t0002g0140a0001c0001t0002g0141others(15): Show | 18 | HG01070.hp1 HG01074.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1184-474T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623350 | ||||||
chrX:13623350 | T | TA | 1 | a0001c0001t0001g0251 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1184-468dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623350 | |||||
chrX:13623351 | A | T | 4 | a0003c0006t0002g0121a0003c0006t0002g0128a0003c0006t0004g0289others(1): Show | 5 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184-473A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623351 | ||||||
chrX:13623376 | G | GTTTTTTT others(2): Show |
4 | a0003c0006t0002g0121a0003c0006t0002g0128a0003c0006t0004g0289others(1): Show | 5 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184-448_1184-447i others(11): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623376 | ||||||
chrX:13623377 | G | GT | 18 | a0001c0001t0001g0069a0001c0001t0001g0198a0001c0001t0001g0205others(15): Show | 18 | HG00408.hp1 HG02071.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1184-427dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTT | 3 | a0001c0001t0002g0026a0001c0005t0001g0049a0006c0009t0001g0283 | 3 | HG02622.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1184-430_1184-427d others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTT | 2 | a0001c0001t0001g0133a0001c0001t0003g0150 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1184-431_1184-427d others(7): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTT | 2 | a0001c0001t0001g0023a0004c0010t0003g0086 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1184-432_1184-427d others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT | 2 | a0004c0010t0001g0241a0004c0022t0001g0175 | 2 | HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1184-433_1184-427d others(9): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(1): Show |
5 | a0001c0001t0001g0276a0001c0001t0004g0228a0001c0001t0004g0230others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184-434_1184-427d others(10): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(2): Show |
1 | a0001c0004t0004g0055 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1184-435_1184-427d others(11): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0004g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1184-436_1184-427d others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(4): Show |
1 | a0002c0003t0004g0147 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1184-437_1184-427d others(13): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(5): Show |
1 | a0005c0013t0004g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1184-438_1184-427d others(14): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(6): Show |
22 | a0001c0001t0005g0045a0001c0008t0001g0173a0002c0002t0004g0020others(19): Show | 23 | HG01109.hp1 HG01243.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.1184-439_1184-427d others(15): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(7): Show |
20 | a0001c0001t0003g0083a0001c0001t0004g0024a0001c0001t0005g0044others(17): Show | 20 | HG00621.hp1 HG01070.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1184-440_1184-427d others(16): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(8): Show |
4 | a0002c0003t0004g0240a0002c0003t0005g0047a0002c0003t0007g0010others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184-441_1184-427d others(17): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(9): Show |
1 | a0002c0003t0005g0042 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1184-442_1184-427d others(18): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(10): Show |
3 | a0001c0001t0002g0073a0001c0001t0003g0224a0001c0007t0001g0272 | 3 | HG00280.hp1 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1184-443_1184-427d others(19): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(11): Show |
24 | a0001c0001t0001g0131a0001c0001t0001g0220a0001c0001t0001g0221others(21): Show | 24 | HG00099.hp2 HG00408.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.1184-444_1184-427d others(20): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(12): Show |
57 | a0001c0001t0001g0059a0001c0001t0001g0080a0001c0001t0001g0110others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1184-445_1184-427d others(21): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(13): Show |
42 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0111others(39): Show | 44 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1184-446_1184-427d others(22): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(14): Show |
13 | a0001c0001t0001g0056a0001c0001t0001g0174a0001c0001t0001g0179others(10): Show | 13 | HG01346.hp1 HG02074.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1184-427_1184-426i others(23): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(15): Show |
5 | a0001c0001t0001g0238a0001c0001t0001g0254a0001c0001t0002g0094others(2): Show | 5 | HG01358.hp1 HG01891.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184-427_1184-426i others(24): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | GTTTTTTT others(17): Show |
1 | a0001c0001t0002g0140 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1184-427_1184-426i others(26): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | G | T | 4 | a0003c0006t0002g0121a0003c0006t0002g0128a0003c0006t0004g0289others(1): Show | 5 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184-447G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623377 | ||||||
chrX:13623377 | GT | G | 1 | a0001c0001t0002g0239 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1184-427delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623377 | GTTTTTT | G | 1 | a0001c0001t0002g0072 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1184-432_1184-427d others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | |||||
chrX:13623379 | T | TTTTTTTG | 1 | a0007c0024t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1184-439_1184-438i others(9): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623379 | |||||
chrX:13623438 | G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0249a0001c0001t0003g0095 | 3 | HG02602.hp1 HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1184-386G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623438 | ||||||
chrX:13623467 | C | T | 29 | a0002c0002t0004g0008a0002c0002t0004g0020a0002c0002t0004g0021others(26): Show | 30 | HG00621.hp1 HG02155.hp2 HG02451.hp1 others(27): Show |
intron_variant | MODIFIER | c.1184-357C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623467 | ||||||
chrX:13623657 | C | A | 139 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(136): Show | 141 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.1184-167C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623657 | ||||||
chrX:13623712 | T | C | 1 | a0001c0001t0003g0155 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1184-112T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623712 | ||||||
chrX:13623812 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1184-12T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623812 | ||||||
chrX:13623959 | A | G | 1 | a0001c0001t0011g0210 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1285+34A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13623959 | ||||||
chrX:13624158 | C | T | 3 | a0001c0001t0001g0149a0005c0013t0004g0027a0010c0016t0004g0025 | 3 | HG01109.hp1 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1285+233C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624158 | ||||||
chrX:13624246 | A | G | 9 | a0001c0001t0001g0056a0001c0001t0008g0294a0001c0005t0001g0049others(6): Show | 9 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285+321A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624246 | ||||||
chrX:13624528 | C | T | 196 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(193): Show | 199 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1285+603C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624528 | ||||||
chrX:13624653 | T | A | 217 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(214): Show | 222 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1285+728T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624653 | ||||||
chrX:13624680 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1285+755G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624680 | ||||||
chrX:13624773 | C | T | 3 | a0001c0001t0004g0228a0001c0001t0004g0230a0001c0004t0004g0055 | 3 | HG01070.hp2 HG01071.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1285+848C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624773 | ||||||
chrX:13624924 | G | A | 2 | a0001c0001t0001g0131a0001c0001t0003g0122 | 2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1285+999G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624924 | ||||||
chrX:13624953 | A | G | 7 | a0002c0003t0004g0051a0002c0003t0004g0052a0002c0003t0004g0147others(4): Show | 7 | HG01074.hp1 HG01243.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1285+1028A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624953 | ||||||
chrX:13624963 | A | T | 2 | a0001c0001t0005g0044a0001c0001t0005g0045 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1285+1038A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624963 | ||||||
chrX:13624990 | A | T | 14 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0073others(11): Show | 15 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1285+1065A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624990 | ||||||
chrX:13625103 | G | A | 3 | a0003c0006t0002g0121a0003c0006t0004g0289a0003c0006t0006g0004 | 4 | HG02004.hp1 HG02148.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285+1178G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625103 | ||||||
chrX:13625154 | TACAA | T | 5 | a0004c0010t0001g0241a0004c0010t0003g0086a0004c0021t0001g0041others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1285+1233_1285+123 others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625154 | |||||
chrX:13625204 | T | C | 1 | a0001c0007t0003g0297 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1285+1279T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625204 | ||||||
chrX:13625227 | C | A | 139 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(136): Show | 141 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.1285+1302C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625227 | ||||||
chrX:13625352 | C | T | 149 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(146): Show | 151 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1285+1427C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625352 | ||||||
chrX:13625410 | T | A | 1 | a0001c0001t0002g0113 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1285+1485T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625410 | ||||||
chrX:13625536 | T | C | 1 | a0001c0004t0004g0055 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1286-1475T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625536 | ||||||
chrX:13625537 | A | G | 2 | a0001c0001t0001g0276a0001c0001t0004g0270 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1286-1474A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625537 | ||||||
chrX:13625641 | A | T | 3 | a0003c0006t0002g0121a0003c0006t0004g0289a0003c0006t0006g0004 | 4 | HG02004.hp1 HG02148.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286-1370A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625641 | ||||||
chrX:13625643 | T | C | 2 | a0001c0001t0002g0132a0001c0001t0002g0142 | 2 | NA18989.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1286-1368T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625643 | ||||||
chrX:13625662 | C | T | 3 | a0003c0006t0002g0121a0003c0006t0004g0289a0003c0006t0006g0004 | 4 | HG02004.hp1 HG02148.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286-1349C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625662 | ||||||
chrX:13625828 | A | G | 217 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(214): Show | 222 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1286-1183A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625828 | ||||||
chrX:13625864 | T | C | 1 | a0010c0016t0004g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1286-1147T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625864 | ||||||
chrX:13625885 | C | CA | 11 | a0001c0001t0001g0197a0001c0001t0001g0216a0001c0001t0001g0225others(8): Show | 11 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1286-1108dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | |||||
chrX:13625885 | C | CAA | 8 | a0002c0002t0004g0213a0002c0002t0005g0077a0002c0003t0004g0036others(5): Show | 9 | HG02004.hp1 HG02148.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1286-1109_1286-110 others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | |||||
chrX:13625885 | C | CAAA | 36 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0073others(33): Show | 38 | HG00621.hp1 HG00735.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1286-1110_1286-110 others(7): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | |||||
chrX:13625885 | C | CAAAA | 9 | a0001c0001t0004g0228a0001c0001t0004g0230a0001c0001t0010g0151others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1286-1111_1286-110 others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | |||||
chrX:13625885 | C | CAAAAA | 1 | a0001c0004t0004g0055 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1286-1112_1286-110 others(9): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | |||||
chrX:13625885 | C | CAAAAAA | 1 | a0001c0008t0001g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1286-1113_1286-110 others(10): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | |||||
chrX:13625885 | C | CAAAAAAA | 8 | a0001c0001t0001g0007a0001c0001t0001g0149a0001c0001t0001g0278others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286-1114_1286-110 others(11): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | |||||
chrX:13625885 | C | CAAAAAAA others(1): Show |
2 | a0001c0001t0002g0038a0002c0003t0004g0284 | 2 | HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1286-1115_1286-110 others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | |||||
chrX:13625895 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0002g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1286-1108_1286-109 others(19): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625895 | |||||
chrX:13625896 | AAAAAAAA others(7): Show |
A | 139 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(136): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1286-1102_1286-108 others(18): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625896 | |||||
chrX:13625897 | AAAAAAAG others(6): Show |
A | 8 | a0001c0001t0003g0224a0002c0003t0004g0051a0002c0003t0004g0052others(5): Show | 8 | HG00280.hp1 HG01074.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286-1107_1286-109 others(17): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625897 | |||||
chrX:13625898 | A | AAG | 5 | a0002c0003t0004g0030a0002c0003t0004g0031a0002c0003t0004g0032others(2): Show | 5 | HG01070.hp1 HG01891.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286-1112_1286-111 others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625898 | |||||
chrX:13625899 | A | AAAG | 3 | a0001c0007t0001g0272a0001c0008t0001g0295a0002c0025t0004g0265 | 3 | HG02723.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1286-1110_1286-110 others(7): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625899 | |||||
chrX:13626223 | C | G | 6 | a0001c0008t0001g0048a0002c0003t0004g0030a0002c0003t0004g0031others(3): Show | 6 | HG01070.hp1 HG01891.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286-788C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13626223 | ||||||
chrX:13626394 | G | A | 1 | a0002c0003t0006g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1286-617G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13626394 | ||||||
chrX:13626676 | A | G | 43 | a0001c0001t0001g0133a0001c0001t0002g0026a0001c0001t0004g0024others(40): Show | 45 | HG00621.hp1 HG01070.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.1286-335A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13626676 | ||||||
chrX:13626752 | T | TCTTTGTG others(4): Show |
1 | a0001c0019t0002g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1286-246_1286-236d others(13): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13626752 | |||||
chrX:13626773 | T | C | 1 | a0001c0001t0002g0064 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1286-238T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13626773 | ||||||
chrX:13626879 | G | T | 40 | a0001c0001t0001g0133a0001c0001t0002g0026a0001c0001t0004g0024others(37): Show | 41 | HG00621.hp1 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1286-132G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13626879 | ||||||
chrX:13626938 | C | CT | 1 | a0001c0001t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1286-66dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13626938 | |||||
chrX:13626990 | A | AT | 1 | a0001c0001t0001g0225 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1286-15dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13626990 | |||||
chrX:13627413 | C | T | 1 | a0001c0001t0008g0011 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1551+137C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627413 | ||||||
chrX:13627530 | C | A | 1 | a0001c0001t0003g0089 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1551+254C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627530 | ||||||
chrX:13627544 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1551+268C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627544 | ||||||
chrX:13627550 | A | G | 2 | a0004c0010t0001g0241a0004c0010t0003g0086 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1551+274A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627550 | ||||||
chrX:13627663 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1551+387C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627663 | ||||||
chrX:13627781 | T | C | 6 | a0001c0008t0001g0048a0002c0003t0004g0284a0002c0003t0004g0285others(3): Show | 7 | HG02004.hp1 HG02109.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1551+505T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627781 | ||||||
chrX:13627923 | A | C | 2 | a0005c0013t0004g0027a0010c0016t0004g0025 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1551+647A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627923 | ||||||
chrX:13628060 | A | G | 6 | a0001c0001t0001g0276a0004c0010t0001g0241a0004c0010t0003g0086others(3): Show | 6 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1551+784A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628060 | ||||||
chrX:13628135 | C | G | 2 | a0003c0006t0004g0289a0003c0006t0006g0004 | 3 | HG02148.hp2 NA18959.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1551+859C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628135 | ||||||
chrX:13628475 | A | G | 40 | a0001c0001t0001g0133a0001c0001t0002g0026a0001c0001t0004g0024others(37): Show | 41 | HG00621.hp1 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1551+1199A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628475 | ||||||
chrX:13628552 | G | A | 8 | a0002c0002t0004g0008a0002c0002t0004g0020a0002c0002t0004g0021others(5): Show | 9 | NA18939.hp2 NA18944.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.1551+1276G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628552 | ||||||
chrX:13628607 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1551+1331A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628607 | ||||||
chrX:13628641 | C | A | 4 | a0001c0005t0001g0231a0001c0005t0001g0246a0001c0005t0001g0271others(1): Show | 4 | HG03041.hp1 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1551+1365C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628641 | ||||||
chrX:13628731 | C | T | 1 | a0001c0001t0003g0096 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1551+1455C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628731 | ||||||
chrX:13628761 | C | T | 2 | a0005c0013t0004g0027a0010c0016t0004g0025 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1551+1485C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628761 | ||||||
chrX:13628807 | C | CA | 5 | a0001c0001t0001g0080a0001c0001t0001g0188a0001c0001t0002g0038others(2): Show | 5 | HG01928.hp1 HG02738.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1551+1539dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13628807 | |||||
chrX:13628815 | AC | A | 80 | a0001c0001t0001g0133a0001c0001t0001g0220a0001c0001t0001g0221others(77): Show | 83 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(80): Show |
intron_variant | MODIFIER | c.1551+1543delC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13628815 | |||||
chrX:13628816 | C | A | 208 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0023others(205): Show | 210 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.1551+1540C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628816 | ||||||
chrX:13628851 | G | T | 12 | a0002c0003t0004g0030a0002c0003t0004g0031a0002c0003t0004g0032others(9): Show | 12 | HG01070.hp1 HG01074.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1551+1575G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628851 | ||||||
chrX:13628893 | A | G | 2 | a0001c0001t0001g0133a0001c0001t0002g0026 | 2 | HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1551+1617A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628893 | ||||||
chrX:13629114 | T | C | 1 | a0001c0001t0003g0083 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1551+1838T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629114 | ||||||
chrX:13629387 | T | C | 74 | a0001c0001t0001g0005a0001c0001t0001g0059a0001c0001t0001g0080others(71): Show | 75 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1551+2111T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629387 | ||||||
chrX:13629417 | A | AT | 1 | a0001c0001t0003g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1551+2151dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13629417 | |||||
chrX:13629417 | AT | A | 1 | a0001c0001t0001g0149 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1551+2151delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13629417 | |||||
chrX:13629501 | T | C | 35 | a0001c0001t0005g0044a0001c0001t0005g0045a0002c0002t0004g0008others(32): Show | 37 | HG00621.hp1 HG01109.hp1 HG02148.hp2 others(34): Show |
intron_variant | MODIFIER | c.1551+2225T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629501 | ||||||
chrX:13629571 | G | A | 3 | a0001c0001t0002g0156a0001c0001t0002g0159a0001c0001t0003g0022 | 3 | NA18954.hp1 NA18956.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1551+2295G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629571 | ||||||
chrX:13629695 | T | G | 71 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0073others(68): Show | 74 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.1551+2419T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629695 | ||||||
chrX:13629801 | G | T | 2 | a0001c0001t0002g0072a0001c0001t0003g0083 | 2 | HG02683.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1551+2525G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629801 | ||||||
chrX:13629810 | G | GC | 1 | a0001c0001t0001g0251 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1551+2539dupC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13629810 | |||||
chrX:13629930 | C | T | 3 | a0002c0003t0004g0284a0002c0003t0004g0285a0010c0016t0004g0025 | 3 | HG01109.hp1 HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1551+2654C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629930 | ||||||
chrX:13629950 | A | G | 5 | a0001c0001t0004g0024a0001c0001t0004g0228a0001c0001t0004g0230others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1551+2674A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629950 | ||||||
chrX:13630077 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1551+2801A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630077 | ||||||
chrX:13630118 | T | TC | 1 | a0001c0001t0001g0251 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1551+2846dupC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13630118 | |||||
chrX:13630291 | G | A | 58 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0073others(55): Show | 60 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1552-2694G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630291 | ||||||
chrX:13630296 | A | G | 58 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0073others(55): Show | 60 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1552-2689A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630296 | ||||||
chrX:13630429 | T | C | 1 | a0001c0001t0002g0136 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1552-2556T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630429 | ||||||
chrX:13630442 | C | G | 3 | a0002c0003t0004g0031a0002c0003t0004g0032a0002c0003t0004g0160 | 3 | HG01891.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1552-2543C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630442 | ||||||
chrX:13630611 | G | A | 1 | a0001c0001t0004g0270 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1552-2374G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630611 | ||||||
chrX:13630736 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1552-2249C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630736 | ||||||
chrX:13630737 | T | C | 77 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0276others(74): Show | 80 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.1552-2248T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630737 | ||||||
chrX:13631029 | CAT | C | 46 | a0002c0002t0004g0008a0002c0002t0004g0020a0002c0002t0004g0021others(43): Show | 47 | HG00621.hp1 HG01070.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.1552-1955_1552-195 others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13631029 | ||||||
chrX:13631217 | T | A | 71 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0073others(68): Show | 74 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.1552-1768T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13631217 | ||||||
chrX:13631441 | TA | T | 1 | a0001c0001t0013g0006 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1552-1540delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13631441 | |||||
chrX:13631458 | AT | A | 2 | a0001c0001t0001g0220a0001c0019t0002g0065 | 2 | HG02280.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1552-1516delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13631458 | |||||
chrX:13631470 | A | T | 6 | a0002c0003t0004g0030a0002c0003t0004g0146a0002c0003t0004g0152others(3): Show | 7 | HG01070.hp1 HG02004.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1552-1515A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13631470 | ||||||
chrX:13631503 | C | T | 41 | a0002c0002t0004g0008a0002c0002t0004g0020a0002c0002t0004g0021others(38): Show | 42 | HG00621.hp1 HG01070.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1552-1482C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13631503 | ||||||
chrX:13631504 | G | A | 9 | a0001c0001t0004g0024a0001c0001t0004g0228a0001c0001t0004g0230others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1552-1481G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13631504 | ||||||
chrX:13631815 | TAAAAC | T | 4 | a0002c0003t0004g0284a0002c0003t0004g0285a0002c0003t0006g0037others(1): Show | 4 | HG01109.hp1 HG02109.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1552-1165_1552-116 others(9): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13631815 | |||||
chrX:13632019 | G | T | 1 | a0002c0002t0006g0168 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1552-966G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632019 | ||||||
chrX:13632162 | C | G | 139 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0056others(136): Show | 141 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1552-823C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632162 | ||||||
chrX:13632169 | C | T | 1 | a0002c0002t0006g0168 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1552-816C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632169 | ||||||
chrX:13632215 | C | CA | 11 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0073others(8): Show | 12 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1552-759dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13632215 | |||||
chrX:13632215 | C | CAA | 1 | a0001c0001t0010g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1552-760_1552-759d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13632215 | |||||
chrX:13632297 | G | GT | 72 | a0001c0001t0001g0023a0001c0001t0001g0069a0001c0001t0001g0080others(69): Show | 72 | HG00544.hp1 HG00621.hp1 HG01175.hp2 others(69): Show |
intron_variant | MODIFIER | c.1552-666dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13632297 | |||||
chrX:13632297 | G | GTT | 4 | a0001c0001t0001g0186a0001c0001t0001g0199a0001c0001t0001g0257others(1): Show | 4 | HG00597.hp2 NA18961.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1552-667_1552-666d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13632297 | |||||
chrX:13632297 | GT | G | 25 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0276others(22): Show | 26 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1552-666delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13632297 | |||||
chrX:13632333 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1552-652A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632333 | ||||||
chrX:13632341 | G | A | 6 | a0002c0003t0004g0240a0002c0003t0005g0042a0002c0003t0005g0046others(3): Show | 6 | HG02451.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1552-644G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632341 | ||||||
chrX:13632403 | G | A | 1 | a0009c0020t0001g0232 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1552-582G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632403 | ||||||
chrX:13632549 | C | T | 1 | a0001c0001t0010g0151 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1552-436C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632549 | ||||||
chrX:13632644 | CA | C | 1 | a0001c0001t0013g0006 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1552-338delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13632644 | |||||
chrX:13632824 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1552-161C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632824 | ||||||
chrX:13632901 | C | T | 4 | a0002c0003t0004g0284a0002c0003t0004g0285a0002c0003t0006g0037others(1): Show | 4 | HG01109.hp1 HG02109.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1552-84C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632901 |