geneid | 129804 |
---|---|
ensemblid | ENSG00000144152.13 |
hgncid | 26740 |
symbol | FBLN7 |
name | fibulin 7 |
refseq_nuc | NM_153214.3 |
refseq_prot | NP_694946.2 |
ensembl_nuc | ENST00000331203.7 |
ensembl_prot | ENSP00000331411.2 |
mane_status | MANE Select |
chr | chr2 |
start | 112138385 |
end | 112188218 |
strand | + |
ver | v1.2 |
region | chr2:112138385-112188218 |
region5000 | chr2:112133385-112193218 |
regionname0 | FBLN7_chr2_112138385_112188218 |
regionname5000 | FBLN7_chr2_112133385_112193218 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 439 | 329 | 82 | 67 | 125 | 17 | 36 | 91 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0002 | 0/0 | 439 | 6 | 5 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0003 | 0/0 | 438 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0004 | 0/0 | 439 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0005 | 0/0 | 439 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0006 | 0/0 | 439 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0007 | 0/0 | 439 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0008 | 0/0 | 439 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0009 | 0/0 | 439 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0010 | 0/0 | 439 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1320 | 325 | 81 | 67 | 125 | 17 | 33 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0002 | 0/0 | 1320 | 6 | 5 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0003 | 0/0 | 1317 | 3 | 3 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0004 | 0/0 | 1320 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0005 | 0/0 | 1320 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0006 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0007 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0008 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0009 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0010 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0011 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0012 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
c0013 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 984 | 268 | 54 | 60 | 118 | 10 | 25 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0002 | 0/0 | 984 | 25 | 10 | 6 | 2 | 4 | 3 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0003 | 1/0 | 984 | 23 | 17 | 1 | 0 | 1 | 3 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0004 | 0/0 | 984 | 9 | 0 | 3 | 5 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0005 | 0/0 | 983 | 6 | 5 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0006 | 0/0 | 984 | 6 | 0 | 1 | 0 | 2 | 3 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0007 | 0/0 | 984 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0008 | 0/0 | 984 | 2 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0009 | 0/0 | 984 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0010 | 0/0 | 984 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0011 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0012 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
t0013 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0009 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0310 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1320 | 325 | 81 | 67 | 125 | 17 | 33 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0005 | 0/0 | 1320 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0007 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0012 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0002c0002 | 0/0 | 1320 | 6 | 5 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0003c0003 | 0/0 | 1317 | 3 | 3 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0004c0004 | 0/0 | 1320 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0005c0009 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0006c0010 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0007c0011 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0008c0008 | 0/0 | 1320 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0009c0013 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0010c0006 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2303 | 256 | 48 | 57 | 117 | 10 | 23 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0001t0002 | 0/0 | 2303 | 21 | 8 | 4 | 2 | 4 | 3 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0001t0003 | 1/0 | 2303 | 21 | 16 | 1 | 0 | 0 | 3 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0001t0004 | 0/0 | 2303 | 9 | 0 | 3 | 5 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0001t0005 | 0/0 | 2302 | 6 | 5 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0001t0006 | 0/0 | 2303 | 6 | 0 | 1 | 0 | 2 | 3 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0001t0008 | 0/0 | 2303 | 2 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0001t0010 | 0/0 | 2303 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0001t0011 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0001t0012 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0001t0013 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0005t0007 | 0/0 | 2303 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0007t0001 | 0/0 | 2303 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0001c0012t0001 | 0/0 | 2303 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0002c0002t0001 | 0/0 | 2303 | 2 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0002c0002t0002 | 0/0 | 2303 | 2 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0002c0002t0003 | 0/0 | 2303 | 2 | 1 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0003c0003t0001 | 0/0 | 2300 | 3 | 3 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0004c0004t0002 | 0/0 | 2303 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0005c0009t0001 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0006c0010t0001 | 0/0 | 2303 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0007c0011t0001 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0008c0008t0001 | 0/0 | 2303 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0009c0013t0001 | 0/0 | 2303 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
a0010c0006t0009 | 0/0 | 2303 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | copy fasta | chr2 | 112133385 | 112193218 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0009 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0003g0310 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0010g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0012g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0001t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0005t0007g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0007t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0001c0012t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0002c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0003c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0003c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0003c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0004c0004t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0005c0009t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0006c0010t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0007c0011t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0008c0008t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0009c0013t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
a0010c0006t0009g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0293 | EUR | GBR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | GBR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00140 | hp1 | a0001 | c0001 | t0006 | g0058 | EUR | GBR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | GBR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0066 | EUR | FIN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00280 | hp2 | a0001 | c0001 | t0010 | g0163 | EUR | FIN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | FIN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01169 | hp1 | a0007 | c0011 | t0001 | g0205 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01257 | hp1 | a0004 | c0004 | t0002 | g0020 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01258 | hp1 | a0004 | c0004 | t0002 | g0020 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0269 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0045 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01891 | hp2 | a0002 | c0002 | t0003 | g0084 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0062 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01934 | hp2 | a0008 | c0008 | t0001 | g0300 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0061 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01975 | hp1 | a0005 | c0009 | t0001 | g0266 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CDX | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0060 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0063 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0244 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0119 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0065 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0191 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0094 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0080 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0196 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03225 | hp2 | a0001 | c0001 | t0013 | g0248 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03239 | hp1 | a0001 | c0007 | t0001 | g0264 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0153 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03490 | hp2 | a0001 | c0005 | t0007 | g0011 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03491 | hp1 | a0006 | c0010 | t0001 | g0223 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03492 | hp1 | a0001 | c0005 | t0007 | g0011 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03516 | hp1 | a0001 | c0012 | t0001 | g0106 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0187 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03704 | hp1 | a0010 | c0006 | t0009 | g0247 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0274 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0074 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0067 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0262 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0278 | SAS | STU | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | YRI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0095 | AFR | YRI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0186 | AFR | YRI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18969 | hp1 | a0009 | c0013 | t0001 | g0174 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0056 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19043 | hp1 | a0001 | c0001 | t0012 | g0255 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19065 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | TSI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA20805 | hp1 | a0002 | c0002 | t0003 | g0075 | EUR | TSI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | TSI | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | USA | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | USA | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0259 | REF | REF | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0310 | REF | REF | FBLN7_chr2_112133385_112193218 | FBLN7 | chr2 | 112133385 | 112193218 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112159787
|
G | A | 1 | a0010 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.187G>A | p.Ala63Thr | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/8 | 458/2303 | 187/1320 | 63/439 | chr2 | 112159787 | ||
chr2:112165061
|
T | A | 1 | a0004 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.296T>A | p.Val99Glu | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/8 | 567/2303 | 296/1320 | 99/439 | chr2 | 112165061 | ||
chr2:112165120
|
G | A | 1 | a0002 | 6 | HG01891.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
missense_variant | MODERATE | c.355G>A | p.Val119Met | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/8 | 626/2303 | 355/1320 | 119/439 | chr2 | 112165120 | ||
chr2:112175762
|
TAGA | T | 1 | a0003 | 3 | HG01884.hp2 HG03041.hp2 NA18522.hp2 |
disruptive_inframe_deletion | MODERATE | c.458_460delAAG | p.Glu153del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/8 | 729/2303 | 458/1320 | 153/439 | INFO_REALIGN_3_PRIME | chr2 | 112175762 | |
chr2:112181760
|
C | G | 1 | a0009 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.554C>G | p.Ala185Gly | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/8 | 825/2303 | 554/1320 | 185/439 | chr2 | 112181760 | ||
chr2:112181861
|
G | A | 1 | a0008 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.655G>A | p.Asp219Asn | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/8 | 926/2303 | 655/1320 | 219/439 | chr2 | 112181861 | ||
chr2:112182833
|
G | A | 1 | a0005 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.713G>A | p.Arg238Gln | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/8 | 984/2303 | 713/1320 | 238/439 | chr2 | 112182833 | ||
chr2:112182853
|
G | A | 1 | a0006 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.733G>A | p.Val245Met | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/8 | 1004/2303 | 733/1320 | 245/439 | chr2 | 112182853 | ||
chr2:112187330
|
G | A | 1 | a0007 | 1 | HG01169.hp1 | missense_variant | MODERATE | c.1144G>A | p.Gly382Ser | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 1415/2303 | 1144/1320 | 382/439 | chr2 | 112187330 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112165119
|
C | T | 1 | a0001c0005 | 2 | HG03490.hp2 HG03492.hp1 |
synonymous_variant | LOW | c.354C>T | p.Ser118Ser | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/8 | 625/2303 | 354/1320 | 118/439 | chr2 | 112165119 | ||
chr2:112181770
|
C | A | 1 | a0001c0007 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.564C>A | p.Ser188Ser | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/8 | 835/2303 | 564/1320 | 188/439 | chr2 | 112181770 | ||
chr2:112185262
|
C | T | 1 | a0001c0012 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.870C>T | p.Thr290Thr | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/8 | 1141/2303 | 870/1320 | 290/439 | chr2 | 112185262 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112138525
|
C | T | 2 | a0001c0001t0008a0001c0001t0013 | 3 | HG03225.hp2 HG03540.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-131C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/8 | 131 | chr2 | 112138525 | |||||
chr2:112138535
|
C | T | 4 | a0001c0001t0004a0001c0001t0006a0001c0001t0012others(1): Show | 18 | HG00140.hp1 HG00280.hp1 HG01928.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-121C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/8 | 121 | chr2 | 112138535 | |||||
chr2:112138615
|
A | C | 1 | a0001c0001t0011 | 1 | NA19065.hp1 | 5_prime_UTR_variant | MODIFIER | c.-41A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/8 | 41 | chr2 | 112138615 | |||||
chr2:112187611
|
T | A | 15 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(12): Show | 282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*105T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 105 | chr2 | 112187611 | |||||
chr2:112187643
|
G | A | 6 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(3): Show | 38 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*137G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 137 | chr2 | 112187643 | |||||
chr2:112187649
|
C | T | 1 | a0001c0001t0010 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*143C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 143 | chr2 | 112187649 | |||||
chr2:112187801
|
C | T | 1 | a0001c0005t0007 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*295C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 295 | chr2 | 112187801 | |||||
chr2:112187874
|
GC | G | 1 | a0001c0001t0005 | 6 | HG01109.hp1 HG01884.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*371delC | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 371 | INFO_REALIGN_3_PRIME | chr2 | 112187874 | ||||
chr2:112188213
|
C | T | 1 | a0010c0006t0009 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*707C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 8/8 | 707 | chr2 | 112188213 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:112138732
|
TCAGTGTC others(20): Show |
T | 3 | a0001c0001t0001g0004a0001c0001t0002g0009a0001c0001t0002g0031 | 4 | HG01516.hp1 HG01517.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+60_75+86delTGTC others(23): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138732 | |||||
chr2:112138789
|
GTGTCCCT others(42): Show |
G | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0027others(28): Show | 35 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.75+80_75+128delAGG others(46): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138789 | |||||
chr2:112138817
|
CGTCCCTC others(15): Show |
C | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(218): Show | 242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.75+129_75+150delCC others(20): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138817 | |||||
chr2:112138817
|
CGTCCCTC others(37): Show |
C | 1 | a0001c0001t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.75+107_75+150delCC others(42): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138817 | |||||
chr2:112138835
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.75+105C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112138835 | ||||||
chr2:112138839
|
T | C | 31 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0027others(28): Show | 35 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.75+109T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112138839 | ||||||
chr2:112138842
|
CCCTCCCG others(14): Show |
C | 1 | a0001c0001t0001g0054 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.75+115_75+135delTC others(19): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138842 | |||||
chr2:112138860
|
CTGTCCCT others(856): Show |
C | 1 | a0001c0001t0001g0256 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.75+174_75+1036del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138860 | |||||
chr2:112138909
|
CTGTCCCG others(20): Show |
C | 1 | a0001c0001t0012g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75+186_75+212delGC others(25): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138909 | |||||
chr2:112138918
|
GCGCCTCT others(915): Show |
G | 1 | a0001c0001t0002g0254 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.75+234_75+1155del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112138918 | |||||
chr2:112138964
|
C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(216): Show | 244 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.75+234C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112138964 | ||||||
chr2:112139014
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+284T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139014 | ||||||
chr2:112139041
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+311C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139041 | ||||||
chr2:112139050
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.75+320C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139050 | ||||||
chr2:112139068
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+338T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139068 | ||||||
chr2:112139095
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0257 | 2 | NA18961.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.75+365C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139095 | ||||||
chr2:112139099
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0257 | 2 | NA18961.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.75+369T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139099 | ||||||
chr2:112139115
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.75+385C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139115 | ||||||
chr2:112139120
|
G | C | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+390G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139120 | ||||||
chr2:112139120
|
GGCCA | G | 10 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(7): Show | 10 | HG00323.hp1 HG01243.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+396_75+399delCC others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139120 | |||||
chr2:112139124
|
A | AGTGTCCC others(43): Show |
1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+395_75+396insTG others(48): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139124 | |||||
chr2:112139124
|
A | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0251 | 2 | NA18946.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.75+394A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139124 | ||||||
chr2:112139151
|
C | G | 3 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0005g0055 | 3 | HG01884.hp1 NA18961.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.75+421C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139151 | ||||||
chr2:112139153
|
C | T | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+423C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139153 | ||||||
chr2:112139155
|
AGTGTCCC others(16): Show |
A | 1 | a0001c0001t0001g0257 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+427_75+449delTG others(21): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139155 | |||||
chr2:112139155
|
AGTGTCCC others(178): Show |
A | 1 | a0001c0001t0001g0253 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.75+427_75+611del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139155 | |||||
chr2:112139184
|
T | C | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+454T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139184 | ||||||
chr2:112139192
|
C | A | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+462C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139192 | ||||||
chr2:112139205
|
G | C | 1 | a0001c0001t0001g0257 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+475G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139205 | ||||||
chr2:112139207
|
C | T | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+477C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139207 | ||||||
chr2:112139216
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(223): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.75+486T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139216 | ||||||
chr2:112139219
|
A | C | 10 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(7): Show | 10 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+489A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139219 | ||||||
chr2:112139234
|
T | C | 2 | a0001c0001t0001g0257a0001c0001t0005g0055 | 2 | HG01884.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.75+504T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139234 | ||||||
chr2:112139238
|
T | C | 13 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0089others(10): Show | 13 | HG00597.hp2 HG01167.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+508T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139238 | ||||||
chr2:112139238
|
T | TGTCCCTC others(20): Show |
1 | a0001c0001t0003g0262 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+531_75+557dupCC others(25): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139238 | |||||
chr2:112139238
|
TGTCCCTC others(344): Show |
T | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG01243.hp2 HG02486.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+532_75+882del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139238 | |||||
chr2:112139259
|
GGCCAGCG others(317): Show |
G | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0043others(6): Show | 11 | HG00639.hp2 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+535_75+858del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139259 | |||||
chr2:112139261
|
CCAGCGTC others(20): Show |
C | 1 | a0002c0002t0002g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+558_75+584delTC others(25): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139261 | |||||
chr2:112139262
|
CAGCGTCC others(344): Show |
C | 7 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0040others(4): Show | 7 | HG01070.hp2 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+535_75+885del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139262 | |||||
chr2:112139265
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+535C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139265 | ||||||
chr2:112139265
|
CGTCCCTC others(344): Show |
C | 9 | a0001c0001t0001g0036a0001c0001t0001g0089a0001c0001t0001g0096others(6): Show | 9 | HG01255.hp2 HG02258.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+558_75+908del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139265 | |||||
chr2:112139265
|
CGTCCCTC others(533): Show |
C | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.75+558_75+1097del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139265 | |||||
chr2:112139270
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+540C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139270 | ||||||
chr2:112139273
|
C | A | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+543C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139273 | ||||||
chr2:112139288
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.75+558T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139288 | ||||||
chr2:112139292
|
C | T | 8 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(5): Show | 8 | HG00323.hp1 HG01243.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+562C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139292 | ||||||
chr2:112139292
|
CGTCCCTC others(452): Show |
C | 1 | a0002c0002t0003g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.75+583_75+1041del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139292 | |||||
chr2:112139313
|
G | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+583G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139313 | ||||||
chr2:112139315
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.75+585C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139315 | ||||||
chr2:112139316
|
CAGCGTCC others(290): Show |
C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+589_75+885del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139316 | |||||
chr2:112139319
|
CGTCCCTC others(263): Show |
C | 1 | a0002c0002t0002g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+610_75+879del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139319 | |||||
chr2:112139319
|
CGTCCCTC others(398): Show |
C | 175 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(172): Show | 196 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.75+610_75+1014del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139319 | |||||
chr2:112139319
|
CGTCCCTC others(425): Show |
C | 1 | a0001c0001t0013g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.75+639_75+1070del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139319 | |||||
chr2:112139340
|
C | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(95): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.75+610C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139340 | ||||||
chr2:112139342
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+612C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139342 | ||||||
chr2:112139346
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(95): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.75+616T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139346 | ||||||
chr2:112139367
|
G | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(86): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.75+637G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139367 | ||||||
chr2:112139369
|
T | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(87): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.75+639T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139369 | ||||||
chr2:112139373
|
T | C | 10 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(7): Show | 10 | HG00323.hp1 HG01243.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+643T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139373 | ||||||
chr2:112139394
|
G | C | 2 | a0001c0001t0001g0258a0001c0001t0005g0055 | 2 | HG01433.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.75+664G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139394 | ||||||
chr2:112139396
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(81): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.75+666C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139396 | ||||||
chr2:112139400
|
T | C | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+670T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139400 | ||||||
chr2:112139421
|
G | C | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+691G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139421 | ||||||
chr2:112139421
|
GGCCAGTG others(501): Show |
G | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.75+705_75+1212del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139421 | |||||
chr2:112139423
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+693C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139423 | ||||||
chr2:112139427
|
TGTCCCTC others(101): Show |
T | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(74): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.75+705_75+812del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139427 | |||||
chr2:112139427
|
TGTCCCTC others(128): Show |
T | 1 | a0001c0001t0003g0024 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.75+705_75+839del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139427 | |||||
chr2:112139435
|
A | C | 19 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(16): Show | 19 | HG00323.hp1 HG01243.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.75+705A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139435 | ||||||
chr2:112139448
|
G | C | 2 | a0003c0003t0001g0094a0003c0003t0001g0095 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.75+718G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139448 | ||||||
chr2:112139450
|
T | C | 9 | a0001c0001t0001g0258a0001c0001t0001g0309a0001c0001t0003g0240others(6): Show | 9 | HG01433.hp2 HG01884.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+720T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139450 | ||||||
chr2:112139450
|
TCAGTGTC others(128): Show |
T | 2 | a0001c0001t0001g0311a0001c0001t0003g0026 | 2 | HG02602.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.75+882_75+1016del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139450 | |||||
chr2:112139454
|
T | C | 1 | a0001c0001t0003g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.75+724T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139454 | ||||||
chr2:112139462
|
C | A | 5 | a0001c0001t0001g0309a0001c0001t0003g0240a0001c0001t0003g0241others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+732C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139462 | ||||||
chr2:112139475
|
G | C | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+745G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139475 | ||||||
chr2:112139477
|
C | T | 5 | a0001c0001t0001g0309a0001c0001t0003g0240a0001c0001t0003g0241others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+747C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139477 | ||||||
chr2:112139478
|
T | C | 19 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(16): Show | 19 | HG00323.hp1 HG01243.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.75+748T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139478 | ||||||
chr2:112139481
|
T | C | 2 | a0001c0001t0001g0253a0001c0001t0003g0240 | 2 | HG02818.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.75+751T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139481 | ||||||
chr2:112139485
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+755C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139485 | ||||||
chr2:112139489
|
C | A | 1 | a0001c0001t0001g0258 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+759C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139489 | ||||||
chr2:112139502
|
G | C | 2 | a0003c0003t0001g0094a0003c0003t0001g0095 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.75+772G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139502 | ||||||
chr2:112139502
|
GGCCAGCG others(74): Show |
G | 1 | a0001c0001t0001g0258 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+778_75+858delCG others(79): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139502 | |||||
chr2:112139505
|
C | T | 5 | a0001c0001t0001g0309a0001c0001t0003g0240a0001c0001t0003g0241others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+775C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139505 | ||||||
chr2:112139508
|
C | T | 16 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(13): Show | 16 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+778C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139508 | ||||||
chr2:112139508
|
CGTCCCTC others(101): Show |
C | 1 | a0001c0001t0003g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.75+801_75+908del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139508 | |||||
chr2:112139516
|
C | A | 1 | a0001c0001t0001g0257 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+786C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139516 | ||||||
chr2:112139516
|
C | CCGCCTCT others(15): Show |
1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+797_75+798insCC others(20): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139516 | |||||
chr2:112139529
|
G | GGCCAGTG others(42): Show |
1 | a0003c0003t0001g0095 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+800_75+801insCC others(47): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139529 | |||||
chr2:112139529
|
G | T | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+799G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139529 | ||||||
chr2:112139531
|
T | C | 15 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(12): Show | 15 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+801T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139531 | ||||||
chr2:112139531
|
TCAGCGTC others(47): Show |
T | 1 | a0001c0001t0001g0257 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.75+805_75+858delCG others(52): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139531 | |||||
chr2:112139535
|
C | T | 11 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(8): Show | 11 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+805C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139535 | ||||||
chr2:112139543
|
C | CCGCCTCT others(69): Show |
1 | a0001c0001t0001g0076 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.75+825_75+826insCG others(74): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139543 | |||||
chr2:112139543
|
C | CCGCCTCT others(15): Show |
1 | a0003c0003t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75+824_75+825insCC others(20): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139543 | |||||
chr2:112139556
|
G | C | 11 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(8): Show | 11 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+826G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139556 | ||||||
chr2:112139558
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+828C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139558 | ||||||
chr2:112139558
|
CCAGCGTC others(101): Show |
C | 3 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0005g0244 | 3 | HG02451.hp2 HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.75+853_75+960del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139558 | |||||
chr2:112139562
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(84): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.75+832C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139562 | ||||||
chr2:112139562
|
CGTCCCTC others(182): Show |
C | 1 | a0001c0001t0001g0253 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.75+883_75+1071del | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139562 | |||||
chr2:112139570
|
C | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(74): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.75+840C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139570 | ||||||
chr2:112139570
|
C | CCGCCTCT others(42): Show |
4 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0002g0078others(1): Show | 4 | HG03098.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+852_75+853insGG others(47): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139570 | |||||
chr2:112139583
|
C | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(81): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.75+853C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139583 | ||||||
chr2:112139583
|
C | T | 1 | a0001c0001t0005g0080 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.75+853C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139583 | ||||||
chr2:112139585
|
C | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(75): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.75+855C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139585 | ||||||
chr2:112139586
|
CAGTGTCC others(20): Show |
C | 9 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0043others(6): Show | 11 | HG00639.hp2 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+883_75+909delTA others(25): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139586 | |||||
chr2:112139589
|
T | C | 3 | a0001c0001t0001g0076a0001c0001t0001g0309a0001c0001t0005g0055 | 3 | HG01243.hp1 HG01884.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.75+859T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139589 | ||||||
chr2:112139597
|
C | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01192.hp1 HG01255.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+867C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139597 | ||||||
chr2:112139608
|
CAGGCT | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+881_75+885delGC others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139608 | |||||
chr2:112139610
|
G | C | 5 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0309others(2): Show | 5 | HG03017.hp2 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+880G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139610 | ||||||
chr2:112139612
|
C | T | 1 | a0001c0001t0003g0262 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+882C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139612 | ||||||
chr2:112139613
|
T | C | 14 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 14 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+883T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139613 | ||||||
chr2:112139614
|
A | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+884A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139614 | ||||||
chr2:112139615
|
G | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+885G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139615 | ||||||
chr2:112139616
|
T | C | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+886T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139616 | ||||||
chr2:112139622
|
T | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+892T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139622 | ||||||
chr2:112139624
|
C | A | 1 | a0003c0003t0001g0095 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+894C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139624 | ||||||
chr2:112139624
|
C | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+894C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139624 | ||||||
chr2:112139637
|
G | C | 2 | a0001c0001t0003g0262a0001c0001t0005g0055 | 2 | HG01884.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.75+907G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139637 | ||||||
chr2:112139637
|
G | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+907G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139637 | ||||||
chr2:112139639
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0309others(1): Show | 4 | HG02896.hp2 HG03017.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+909C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139639 | ||||||
chr2:112139643
|
C | T | 10 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0092others(7): Show | 10 | HG00323.hp1 HG01884.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+913C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139643 | ||||||
chr2:112139651
|
C | A | 1 | a0003c0003t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75+921C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139651 | ||||||
chr2:112139664
|
G | C | 6 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(3): Show | 6 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+934G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139664 | ||||||
chr2:112139666
|
T | C | 15 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(12): Show | 15 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+936T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139666 | ||||||
chr2:112139670
|
C | T | 9 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+940C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139670 | ||||||
chr2:112139673
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.75+943C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139673 | ||||||
chr2:112139691
|
G | C | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(2): Show | 5 | HG01243.hp1 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+961G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139691 | ||||||
chr2:112139693
|
C | T | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0005g0055others(1): Show | 4 | HG00323.hp1 HG01884.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+963C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139693 | ||||||
chr2:112139697
|
C | T | 11 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(8): Show | 11 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+967C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139697 | ||||||
chr2:112139697
|
CGTCCCTC others(47): Show |
C | 6 | a0001c0001t0001g0089a0001c0001t0001g0178a0001c0001t0001g0199others(3): Show | 6 | HG01255.hp2 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1017_75+1070del others(54): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139697 | |||||
chr2:112139718
|
C | G | 8 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(5): Show | 8 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+988C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139718 | ||||||
chr2:112139720
|
C | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0082others(4): Show | 7 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+990C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139720 | ||||||
chr2:112139724
|
T | C | 2 | a0003c0003t0001g0094a0003c0003t0001g0095 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.75+994T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139724 | ||||||
chr2:112139727
|
C | T | 1 | a0010c0006t0009g0247 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.75+997C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139727 | ||||||
chr2:112139745
|
G | C | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1015G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139745 | ||||||
chr2:112139747
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(182): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.75+1017T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139747 | ||||||
chr2:112139751
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(174): Show | 198 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.75+1021T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139751 | ||||||
chr2:112139771
|
A | C | 1 | a0001c0001t0003g0262 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1041A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139771 | ||||||
chr2:112139772
|
C | G | 12 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(9): Show | 12 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+1042C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139772 | ||||||
chr2:112139774
|
C | T | 9 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0081others(6): Show | 9 | HG00323.hp1 HG01884.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1044C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139774 | ||||||
chr2:112139784
|
T | G | 1 | a0001c0001t0003g0262 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1054T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139784 | ||||||
chr2:112139786
|
C | G | 1 | a0001c0001t0003g0262 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1056C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139786 | ||||||
chr2:112139788
|
G | A | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+1058G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139788 | ||||||
chr2:112139788
|
G | GCCTCTCT others(20): Show |
1 | a0001c0001t0001g0076 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.75+1070_75+1071ins others(27): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139788 | |||||
chr2:112139799
|
G | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1069G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139799 | ||||||
chr2:112139799
|
G | T | 1 | a0001c0001t0003g0262 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1069G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139799 | ||||||
chr2:112139801
|
C | CCAGTGTC others(47): Show |
4 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0002g0078others(1): Show | 4 | HG03098.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1097_75+1098ins others(54): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139801 | |||||
chr2:112139801
|
C | T | 4 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0005g0055others(1): Show | 4 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1071C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139801 | ||||||
chr2:112139811
|
T | G | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1081T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139811 | ||||||
chr2:112139813
|
C | G | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1083C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139813 | ||||||
chr2:112139826
|
G | C | 1 | a0001c0001t0003g0262 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1096G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139826 | ||||||
chr2:112139826
|
G | T | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1096G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139826 | ||||||
chr2:112139832
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.75+1102T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139832 | ||||||
chr2:112139852
|
A | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1122A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139852 | ||||||
chr2:112139853
|
C | G | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1123C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139853 | ||||||
chr2:112139853
|
CGCCAGTG others(69): Show |
C | 1 | a0001c0001t0003g0262 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+1150_75+1225del others(76): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139853 | |||||
chr2:112139855
|
C | T | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1125C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139855 | ||||||
chr2:112139865
|
T | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1135T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139865 | ||||||
chr2:112139867
|
C | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1137C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139867 | ||||||
chr2:112139880
|
G | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1150G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139880 | ||||||
chr2:112139880
|
GGCCAGTG others(42): Show |
G | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1176_75+1224del others(49): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139880 | |||||
chr2:112139894
|
CCGCCTCT others(15): Show |
C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1176_75+1197del others(22): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139894 | |||||
chr2:112139901
|
T | G | 1 | a0001c0001t0001g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.75+1171T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139901 | ||||||
chr2:112139905
|
C | CAGG | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1175_75+1176ins others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139905 | ||||||
chr2:112139906
|
C | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1176C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139906 | ||||||
chr2:112139907
|
C | CAG | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1177_75+1178ins others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139907 | ||||||
chr2:112139907
|
C | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1177C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139907 | ||||||
chr2:112139914
|
G | T | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1184G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139914 | ||||||
chr2:112139916
|
G | C | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1186G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139916 | ||||||
chr2:112139916
|
GCGCCTCT others(20): Show |
G | 1 | a0001c0001t0001g0098 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.75+1199_75+1225del others(27): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139916 | |||||
chr2:112139918
|
G | A | 1 | a0001c0001t0005g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.75+1188G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139918 | ||||||
chr2:112139929
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(112): Show | 128 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.75+1199T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139929 | ||||||
chr2:112139929
|
T | G | 8 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+1199T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139929 | ||||||
chr2:112139935
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0309 | 3 | HG03017.hp2 NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1205T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139935 | ||||||
chr2:112139938
|
C | G | 5 | a0001c0001t0001g0086a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | HG00597.hp2 NA18950.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+1208C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139938 | ||||||
chr2:112139956
|
C | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(113): Show | 129 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.75+1226C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139956 | ||||||
chr2:112139958
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1228C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139958 | ||||||
chr2:112139962
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(111): Show | 127 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.75+1232T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139962 | ||||||
chr2:112139962
|
TGTCCCTC others(47): Show |
T | 1 | a0001c0001t0001g0263 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.75+1280_75+1333del others(54): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112139962 | |||||
chr2:112139980
|
C | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.75+1250C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139980 | ||||||
chr2:112139983
|
G | C | 1 | a0001c0001t0001g0098 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.75+1253G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139983 | ||||||
chr2:112139985
|
C | T | 5 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0096others(2): Show | 5 | HG00323.hp1 HG02723.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+1255C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139985 | ||||||
chr2:112139989
|
C | T | 12 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(9): Show | 12 | HG00323.hp1 HG00741.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+1259C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112139989 | ||||||
chr2:112140010
|
G | C | 1 | a0001c0001t0001g0309 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+1280G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140010 | ||||||
chr2:112140012
|
T | C | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0099others(1): Show | 4 | HG03017.hp2 NA18990.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1282T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140012 | ||||||
chr2:112140016
|
C | T | 10 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(7): Show | 10 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+1286C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140016 | ||||||
chr2:112140037
|
G | C | 5 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0096others(2): Show | 5 | HG00323.hp1 HG02723.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+1307G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140037 | ||||||
chr2:112140037
|
G | GGCCAGCG others(20): Show |
1 | a0001c0007t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.75+1367_75+1393dup others(27): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112140037 | |||||
chr2:112140039
|
C | T | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1309C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140039 | ||||||
chr2:112140043
|
C | T | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1313C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140043 | ||||||
chr2:112140070
|
C | T | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1340C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140070 | ||||||
chr2:112140097
|
C | T | 11 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(8): Show | 11 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+1367C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140097 | ||||||
chr2:112140097
|
CGTCCCTC others(20): Show |
C | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0250others(1): Show | 4 | HG00408.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1415_75+1441del others(27): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112140097 | |||||
chr2:112140118
|
C | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1388C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140118 | ||||||
chr2:112140124
|
T | C | 4 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0265others(1): Show | 4 | HG02300.hp1 NA18989.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1394T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140124 | ||||||
chr2:112140144
|
A | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1414A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140144 | ||||||
chr2:112140145
|
C | G | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1415C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140145 | ||||||
chr2:112140145
|
CGCCAG | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1416_75+1420del others(5): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140145 | ||||||
chr2:112140151
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0178 | 3 | NA18939.hp1 NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.75+1421T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140151 | ||||||
chr2:112140157
|
T | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1427T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140157 | ||||||
chr2:112140159
|
C | CCGCCTCT others(15): Show |
6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+1440_75+1441ins others(22): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112140159 | |||||
chr2:112140159
|
C | G | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1429C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140159 | ||||||
chr2:112140172
|
G | C | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1442G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140172 | ||||||
chr2:112140178
|
C | T | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1448C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140178 | ||||||
chr2:112140215
|
G | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.75+1485G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140215 | ||||||
chr2:112140233
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.75+1503G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140233 | ||||||
chr2:112140336
|
A | G | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1606A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140336 | ||||||
chr2:112140342
|
CCTT | C | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG02615.hp2 HG02647.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1614_75+1616del others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112140342 | |||||
chr2:112140392
|
G | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02723.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+1662G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140392 | ||||||
chr2:112140514
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.75+1784G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140514 | ||||||
chr2:112140551
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.75+1821G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140551 | ||||||
chr2:112140604
|
A | G | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+1874A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140604 | ||||||
chr2:112140746
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.75+2016G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140746 | ||||||
chr2:112140927
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.75+2197G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112140927 | ||||||
chr2:112141053
|
A | T | 2 | a0001c0001t0004g0074a0001c0005t0007g0011 | 3 | HG03490.hp2 HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.75+2323A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141053 | ||||||
chr2:112141271
|
T | C | 9 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+2541T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141271 | ||||||
chr2:112141356
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(188): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.75+2626C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141356 | ||||||
chr2:112141412
|
A | G | 1 | a0001c0001t0003g0052 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.75+2682A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141412 | ||||||
chr2:112141495
|
G | A | 1 | a0002c0002t0003g0075 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.75+2765G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141495 | ||||||
chr2:112141704
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.75+2974G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141704 | ||||||
chr2:112141861
|
C | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 210 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.75+3131C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141861 | ||||||
chr2:112141872
|
G | A | 1 | a0001c0001t0003g0242 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.75+3142G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141872 | ||||||
chr2:112141932
|
G | A | 1 | a0001c0001t0006g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.75+3202G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141932 | ||||||
chr2:112141932
|
G | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 210 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.75+3202G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112141932 | ||||||
chr2:112142136
|
G | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+3406G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142136 | ||||||
chr2:112142277
|
T | G | 1 | a0001c0001t0001g0185 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.75+3547T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142277 | ||||||
chr2:112142338
|
G | A | 12 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(9): Show | 12 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+3608G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142338 | ||||||
chr2:112142405
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(114): Show | 131 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.75+3675T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142405 | ||||||
chr2:112142444
|
C | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.75+3714C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142444 | ||||||
chr2:112142531
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.75+3801C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142531 | ||||||
chr2:112142622
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.75+3892A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142622 | ||||||
chr2:112142720
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 165 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.75+3990C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142720 | ||||||
chr2:112142736
|
G | A | 14 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(11): Show | 15 | HG02109.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+4006G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142736 | ||||||
chr2:112142741
|
A | G | 12 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(9): Show | 12 | HG00323.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+4011A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142741 | ||||||
chr2:112142768
|
T | TTGTGTG | 33 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(30): Show | 37 | HG00323.hp1 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.75+4048_75+4053dup others(6): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112142768 | |||||
chr2:112142768
|
T | TTGTGTGT others(1): Show |
116 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(113): Show | 129 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.75+4046_75+4053dup others(8): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112142768 | |||||
chr2:112142768
|
T | TTGTGTGT others(3): Show |
4 | a0001c0001t0001g0019a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 5 | HG02602.hp1 HG03688.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+4044_75+4053dup others(10): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112142768 | |||||
chr2:112142772
|
G | T | 1 | a0001c0001t0001g0308 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.75+4042G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142772 | ||||||
chr2:112142788
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.75+4058A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142788 | ||||||
chr2:112142848
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+4118G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142848 | ||||||
chr2:112142897
|
G | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0251 | 2 | NA18946.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.75+4167G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142897 | ||||||
chr2:112142926
|
G | A | 3 | a0001c0001t0008g0186a0001c0001t0008g0187a0001c0001t0013g0248 | 3 | HG03225.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.75+4196G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142926 | ||||||
chr2:112142947
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.75+4217T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112142947 | ||||||
chr2:112143232
|
C | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079 | 3 | HG01243.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.75+4502C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143232 | ||||||
chr2:112143311
|
T | C | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+4581T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143311 | ||||||
chr2:112143338
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.75+4608G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143338 | ||||||
chr2:112143442
|
T | C | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(112): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.75+4712T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143442 | ||||||
chr2:112143468
|
G | T | 1 | a0001c0001t0012g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75+4738G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143468 | ||||||
chr2:112143628
|
G | A | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(21): Show | 28 | HG00323.hp1 HG00639.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.75+4898G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143628 | ||||||
chr2:112143683
|
C | G | 1 | a0001c0001t0003g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.75+4953C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143683 | ||||||
chr2:112143720
|
T | C | 4 | a0001c0001t0001g0082a0001c0001t0001g0188a0002c0002t0003g0075others(1): Show | 5 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+4990T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143720 | ||||||
chr2:112143760
|
TG | T | 5 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0070others(2): Show | 5 | HG02056.hp1 HG02129.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+5031delG | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143760 | ||||||
chr2:112143825
|
C | T | 106 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(103): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.75+5095C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143825 | ||||||
chr2:112143914
|
A | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+5184A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112143914 | ||||||
chr2:112144013
|
C | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0026 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.75+5283C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144013 | ||||||
chr2:112144101
|
T | C | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+5371T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144101 | ||||||
chr2:112144170
|
C | G | 2 | a0001c0001t0003g0024a0001c0001t0003g0026 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.75+5440C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144170 | ||||||
chr2:112144181
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.75+5451G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144181 | ||||||
chr2:112144426
|
T | C | 1 | a0001c0001t0001g0312 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.75+5696T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144426 | ||||||
chr2:112144479
|
G | T | 1 | a0001c0001t0001g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.75+5749G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144479 | ||||||
chr2:112144494
|
T | C | 13 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0188others(10): Show | 14 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+5764T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144494 | ||||||
chr2:112144523
|
C | CT | 6 | a0001c0001t0001g0114a0001c0001t0001g0175a0001c0001t0001g0177others(3): Show | 6 | HG01496.hp2 HG01952.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+5812dupT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112144523 | |||||
chr2:112144523
|
CTTT | C | 111 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(108): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.75+5810_75+5812del others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112144523 | |||||
chr2:112144623
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.75+5893C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144623 | ||||||
chr2:112144650
|
G | A | 13 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0188others(10): Show | 14 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+5920G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112144650 | ||||||
chr2:112145140
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.75+6410G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145140 | ||||||
chr2:112145144
|
G | A | 105 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(102): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.75+6414G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145144 | ||||||
chr2:112145165
|
C | T | 1 | a0009c0013t0001g0174 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.75+6435C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145165 | ||||||
chr2:112145166
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.75+6436G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145166 | ||||||
chr2:112145225
|
T | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.75+6495T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145225 | ||||||
chr2:112145244
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0227 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.75+6514G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145244 | ||||||
chr2:112145316
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.75+6586T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145316 | ||||||
chr2:112145327
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.75+6597G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145327 | ||||||
chr2:112145447
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0267a0001c0001t0001g0299others(8): Show | 14 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+6717C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145447 | ||||||
chr2:112145662
|
A | G | 105 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(102): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.75+6932A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145662 | ||||||
chr2:112145744
|
A | G | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0173others(2): Show | 5 | HG01167.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+7014A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145744 | ||||||
chr2:112145891
|
C | T | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(308): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.75+7161C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145891 | ||||||
chr2:112145948
|
C | T | 1 | a0001c0001t0005g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.75+7218C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112145948 | ||||||
chr2:112146132
|
C | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+7402C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112146132 | ||||||
chr2:112146260
|
C | A | 1 | a0001c0001t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.75+7530C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112146260 | ||||||
chr2:112146352
|
C | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG02027.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.75+7622C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112146352 | ||||||
chr2:112146568
|
C | CT | 12 | a0001c0001t0001g0036a0001c0001t0001g0170a0001c0001t0001g0188others(9): Show | 13 | HG01175.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+7856dupT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112146568 | |||||
chr2:112146568
|
CT | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0041others(18): Show | 22 | HG01099.hp2 HG01167.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.75+7856delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112146568 | |||||
chr2:112147109
|
G | C | 1 | a0001c0001t0001g0298 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.75+8379G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147109 | ||||||
chr2:112147192
|
G | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0170 | 2 | NA18960.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.75+8462G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147192 | ||||||
chr2:112147290
|
T | C | 4 | a0001c0001t0001g0059a0001c0001t0008g0186a0001c0001t0008g0187others(1): Show | 4 | HG03225.hp2 HG03540.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+8560T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147290 | ||||||
chr2:112147409
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.75+8679A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147409 | ||||||
chr2:112147480
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.75+8750C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147480 | ||||||
chr2:112147584
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.75+8854C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147584 | ||||||
chr2:112147642
|
C | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0193others(3): Show | 8 | NA18941.hp2 NA18957.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+8912C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147642 | ||||||
chr2:112147681
|
C | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0251 | 2 | NA18946.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.75+8951C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147681 | ||||||
chr2:112147727
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.75+8997T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147727 | ||||||
chr2:112147975
|
T | G | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.75+9245T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147975 | ||||||
chr2:112147983
|
G | A | 5 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+9253G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147983 | ||||||
chr2:112147992
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+9262G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112147992 | ||||||
chr2:112148004
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.75+9274G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148004 | ||||||
chr2:112148048
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.75+9318C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148048 | ||||||
chr2:112148068
|
G | A | 2 | a0001c0001t0001g0082a0002c0002t0003g0075 | 2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+9338G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148068 | ||||||
chr2:112148602
|
C | G | 1 | a0001c0001t0001g0051 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.75+9872C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148602 | ||||||
chr2:112148634
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.75+9904G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148634 | ||||||
chr2:112148738
|
G | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0257a0001c0001t0001g0259others(23): Show | 29 | HG00408.hp1 HG00558.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.75+10008G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148738 | ||||||
chr2:112148992
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.75+10262G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112148992 | ||||||
chr2:112149022
|
C | T | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.75+10292C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149022 | ||||||
chr2:112149178
|
GC | G | 15 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0092others(12): Show | 16 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+10449delC | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149178 | ||||||
chr2:112149314
|
G | A | 1 | a0001c0001t0002g0195 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.76-10362G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149314 | ||||||
chr2:112149596
|
G | A | 16 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0092others(13): Show | 18 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-10080G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149596 | ||||||
chr2:112149629
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-10047G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149629 | ||||||
chr2:112149645
|
G | C | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-10031G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149645 | ||||||
chr2:112149687
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.76-9989T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149687 | ||||||
chr2:112149976
|
G | C | 1 | a0001c0001t0001g0178 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.76-9700G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149976 | ||||||
chr2:112149997
|
A | C | 1 | a0001c0001t0001g0167 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.76-9679A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112149997 | ||||||
chr2:112150036
|
G | A | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.76-9640G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150036 | ||||||
chr2:112150037
|
T | C | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.76-9639T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150037 | ||||||
chr2:112150145
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.76-9531C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150145 | ||||||
chr2:112150161
|
G | A | 1 | a0002c0002t0003g0084 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.76-9515G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150161 | ||||||
chr2:112150255
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.76-9421T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150255 | ||||||
chr2:112150382
|
G | GA | 20 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0038others(17): Show | 20 | HG01175.hp2 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.76-9284dupA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112150382 | |||||
chr2:112150543
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-9133C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150543 | ||||||
chr2:112150556
|
T | C | 16 | a0001c0001t0001g0059a0001c0001t0001g0082a0001c0001t0001g0092others(13): Show | 18 | HG00323.hp1 HG01257.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-9120T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150556 | ||||||
chr2:112150939
|
G | T | 1 | a0001c0001t0001g0305 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.76-8737G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112150939 | ||||||
chr2:112151111
|
G | C | 1 | a0001c0001t0001g0312 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.76-8565G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151111 | ||||||
chr2:112151127
|
G | A | 1 | a0004c0004t0002g0020 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.76-8549G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151127 | ||||||
chr2:112151181
|
G | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0298 | 2 | NA19009.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.76-8495G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151181 | ||||||
chr2:112151190
|
C | T | 2 | a0003c0003t0001g0094a0003c0003t0001g0095 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.76-8486C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151190 | ||||||
chr2:112151215
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.76-8461C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151215 | ||||||
chr2:112151231
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.76-8445A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151231 | ||||||
chr2:112151243
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-8433C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151243 | ||||||
chr2:112151335
|
C | G | 1 | a0001c0001t0006g0066 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.76-8341C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151335 | ||||||
chr2:112151513
|
C | G | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-8163C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151513 | ||||||
chr2:112151566
|
T | C | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(100): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.76-8110T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151566 | ||||||
chr2:112151627
|
A | G | 5 | a0001c0001t0001g0185a0001c0001t0001g0198a0001c0001t0001g0225others(2): Show | 5 | HG01175.hp2 HG02559.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-8049A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151627 | ||||||
chr2:112151898
|
G | T | 1 | a0002c0002t0003g0075 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.76-7778G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112151898 | ||||||
chr2:112152002
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-7674C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152002 | ||||||
chr2:112152079
|
T | A | 4 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(1): Show | 4 | NA18942.hp1 NA18999.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-7597T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152079 | ||||||
chr2:112152171
|
C | T | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76-7505C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152171 | ||||||
chr2:112152282
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-7394G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152282 | ||||||
chr2:112152318
|
G | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0251 | 2 | NA18946.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.76-7358G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152318 | ||||||
chr2:112152465
|
G | T | 1 | a0001c0001t0001g0304 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.76-7211G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152465 | ||||||
chr2:112152467
|
C | A | 1 | a0002c0002t0003g0075 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.76-7209C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152467 | ||||||
chr2:112152467
|
C | T | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(99): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.76-7209C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152467 | ||||||
chr2:112152482
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0114 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.76-7194C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152482 | ||||||
chr2:112152523
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.76-7153G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152523 | ||||||
chr2:112152813
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-6863G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152813 | ||||||
chr2:112152887
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-6789T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152887 | ||||||
chr2:112152911
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0183 | 2 | NA18954.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.76-6765T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152911 | ||||||
chr2:112152927
|
A | G | 2 | a0001c0001t0001g0082a0002c0002t0003g0075 | 2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.76-6749A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112152927 | ||||||
chr2:112153079
|
T | C | 1 | a0002c0002t0002g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-6597T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153079 | ||||||
chr2:112153089
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.76-6587T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153089 | ||||||
chr2:112153133
|
G | A | 2 | a0001c0001t0001g0082a0002c0002t0003g0075 | 2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.76-6543G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153133 | ||||||
chr2:112153147
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0114 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.76-6529C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153147 | ||||||
chr2:112153199
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.76-6477C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153199 | ||||||
chr2:112153254
|
A | G | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-6422A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153254 | ||||||
chr2:112153328
|
C | T | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76-6348C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153328 | ||||||
chr2:112153540
|
G | A | 1 | a0001c0001t0004g0068 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.76-6136G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153540 | ||||||
chr2:112153732
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.76-5944G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153732 | ||||||
chr2:112153771
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.76-5905T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153771 | ||||||
chr2:112153900
|
G | A | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76-5776G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153900 | ||||||
chr2:112153924
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.76-5752T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153924 | ||||||
chr2:112153955
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.76-5721C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153955 | ||||||
chr2:112153957
|
C | G | 3 | a0001c0001t0001g0057a0001c0001t0001g0073a0001c0001t0005g0025 | 3 | HG01109.hp1 HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.76-5719C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112153957 | ||||||
chr2:112154346
|
G | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(111): Show | 122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.76-5330G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154346 | ||||||
chr2:112154423
|
C | T | 5 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0188others(2): Show | 5 | HG00323.hp1 HG02145.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-5253C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154423 | ||||||
chr2:112154441
|
C | G | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-5235C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154441 | ||||||
chr2:112154455
|
G | A | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-5221G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154455 | ||||||
chr2:112154541
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-5135G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154541 | ||||||
chr2:112154676
|
T | C | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(117): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.76-5000T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154676 | ||||||
chr2:112154812
|
T | C | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-4864T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154812 | ||||||
chr2:112154850
|
T | C | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-4826T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154850 | ||||||
chr2:112154945
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.76-4731C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112154945 | ||||||
chr2:112155065
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.76-4611G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155065 | ||||||
chr2:112155122
|
T | G | 18 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(15): Show | 22 | HG00639.hp2 HG01070.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.76-4554T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155122 | ||||||
chr2:112155292
|
G | A | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(112): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.76-4384G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155292 | ||||||
chr2:112155315
|
C | T | 1 | a0001c0001t0010g0163 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.76-4361C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155315 | ||||||
chr2:112155401
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.76-4275C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155401 | ||||||
chr2:112155440
|
C | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0003g0240others(8): Show | 12 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-4236C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155440 | ||||||
chr2:112155449
|
G | A | 3 | a0001c0001t0008g0186a0001c0001t0008g0187a0001c0001t0013g0248 | 3 | HG03225.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.76-4227G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155449 | ||||||
chr2:112155709
|
C | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0297 | 3 | HG02132.hp1 NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.76-3967C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155709 | ||||||
chr2:112155745
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.76-3931G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155745 | ||||||
chr2:112155753
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0188 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.76-3923A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155753 | ||||||
chr2:112155809
|
C | T | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-3867C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155809 | ||||||
chr2:112155853
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-3823C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155853 | ||||||
chr2:112155877
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-3799C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155877 | ||||||
chr2:112155924
|
G | A | 113 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(110): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-3752G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112155924 | ||||||
chr2:112156077
|
C | T | 14 | a0001c0001t0001g0018a0001c0001t0001g0099a0001c0001t0001g0115others(11): Show | 15 | HG00558.hp2 HG01978.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-3599C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156077 | ||||||
chr2:112156099
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.76-3577C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156099 | ||||||
chr2:112156160
|
C | G | 4 | a0001c0001t0001g0032a0001c0001t0002g0009a0001c0001t0002g0031others(1): Show | 5 | HG01192.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-3516C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156160 | ||||||
chr2:112156332
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-3344T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156332 | ||||||
chr2:112156362
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.76-3314A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156362 | ||||||
chr2:112156385
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.76-3291A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156385 | ||||||
chr2:112156390
|
C | T | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(53): Show | 63 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.76-3286C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156390 | ||||||
chr2:112156426
|
T | C | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76-3250T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156426 | ||||||
chr2:112156528
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.76-3148T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156528 | ||||||
chr2:112156602
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0155 | 2 | HG02027.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.76-3074G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156602 | ||||||
chr2:112156681
|
C | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0188 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.76-2995C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156681 | ||||||
chr2:112156752
|
G | A | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(53): Show | 63 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.76-2924G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156752 | ||||||
chr2:112156784
|
C | G | 1 | a0001c0001t0001g0271 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.76-2892C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156784 | ||||||
chr2:112156901
|
ATTCCCAC others(12): Show |
A | 1 | a0001c0001t0001g0199 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.76-2774_76-2756del others(19): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156901 | ||||||
chr2:112156962
|
C | T | 2 | a0001c0001t0001g0082a0002c0002t0003g0075 | 2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.76-2714C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112156962 | ||||||
chr2:112157032
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-2644G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157032 | ||||||
chr2:112157107
|
C | T | 6 | a0001c0001t0001g0190a0001c0001t0001g0224a0001c0001t0001g0227others(3): Show | 6 | HG00099.hp2 HG00741.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-2569C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157107 | ||||||
chr2:112157108
|
A | G | 6 | a0001c0001t0001g0190a0001c0001t0001g0224a0001c0001t0001g0227others(3): Show | 6 | HG00099.hp2 HG00741.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-2568A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157108 | ||||||
chr2:112157114
|
A | T | 6 | a0001c0001t0001g0190a0001c0001t0001g0224a0001c0001t0001g0227others(3): Show | 6 | HG00099.hp2 HG00741.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-2562A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157114 | ||||||
chr2:112157190
|
C | T | 1 | a0002c0002t0002g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-2486C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157190 | ||||||
chr2:112157235
|
C | T | 3 | a0002c0002t0001g0153a0002c0002t0001g0154a0002c0002t0002g0119 | 3 | HG02922.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.76-2441C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157235 | ||||||
chr2:112157246
|
T | G | 1 | a0001c0001t0010g0163 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.76-2430T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157246 | ||||||
chr2:112157553
|
C | T | 44 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(41): Show | 50 | HG00099.hp2 HG00140.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.76-2123C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157553 | ||||||
chr2:112157673
|
G | C | 1 | a0001c0001t0001g0204 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.76-2003G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157673 | ||||||
chr2:112157718
|
G | C | 113 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(110): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-1958G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157718 | ||||||
chr2:112157746
|
G | A | 113 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(110): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-1930G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157746 | ||||||
chr2:112157747
|
A | C | 113 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(110): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-1929A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157747 | ||||||
chr2:112157864
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-1812G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157864 | ||||||
chr2:112157902
|
C | CT | 20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(17): Show | 24 | HG00639.hp2 HG01070.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.76-1760dupT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112157902 | |||||
chr2:112157957
|
C | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0003g0240others(8): Show | 12 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-1719C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112157957 | ||||||
chr2:112158151
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.76-1525C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158151 | ||||||
chr2:112158177
|
G | T | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(48): Show | 58 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.76-1499G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158177 | ||||||
chr2:112158187
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-1489G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158187 | ||||||
chr2:112158232
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0245 | 3 | HG00741.hp2 NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.76-1444A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158232 | ||||||
chr2:112158244
|
TTTG | T | 12 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0295others(9): Show | 13 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.76-1417_76-1415del others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112158244 | |||||
chr2:112158500
|
G | A | 4 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0188others(1): Show | 4 | HG00323.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-1176G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158500 | ||||||
chr2:112158560
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0114 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.76-1116C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158560 | ||||||
chr2:112158596
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.76-1080C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158596 | ||||||
chr2:112158597
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.76-1079G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158597 | ||||||
chr2:112158719
|
A | G | 284 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.76-957A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158719 | ||||||
chr2:112158920
|
C | T | 1 | a0001c0001t0004g0068 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.76-756C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112158920 | ||||||
chr2:112159039
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.76-637A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159039 | ||||||
chr2:112159191
|
G | GT | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(106): Show | 116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.76-474dupT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112159191 | |||||
chr2:112159254
|
T | G | 2 | a0001c0001t0001g0082a0002c0002t0003g0075 | 2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.76-422T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159254 | ||||||
chr2:112159282
|
G | GC | 99 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(96): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.76-391dupC | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 112159282 | |||||
chr2:112159292
|
T | C | 2 | a0001c0001t0001g0204a0007c0011t0001g0205 | 2 | HG00140.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.76-384T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159292 | ||||||
chr2:112159390
|
A | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0155 | 2 | HG02027.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.76-286A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159390 | ||||||
chr2:112159525
|
G | C | 113 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(110): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.76-151G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159525 | ||||||
chr2:112159647
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.76-29G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 1/7 | chr2 | 112159647 | ||||||
chr2:112159845
|
C | T | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.235+10C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112159845 | ||||||
chr2:112159852
|
G | A | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.235+17G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112159852 | ||||||
chr2:112159940
|
A | G | 2 | a0001c0001t0006g0058a0001c0001t0006g0066 | 2 | HG00140.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.235+105A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112159940 | ||||||
chr2:112159997
|
A | T | 2 | a0001c0001t0001g0082a0002c0002t0003g0075 | 2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.235+162A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112159997 | ||||||
chr2:112160001
|
A | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0188a0002c0002t0003g0075 | 3 | HG00323.hp1 HG02970.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.235+166A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160001 | ||||||
chr2:112160030
|
G | A | 10 | a0001c0001t0001g0092a0001c0001t0001g0311a0001c0001t0003g0240others(7): Show | 10 | HG02451.hp2 HG02602.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+195G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160030 | ||||||
chr2:112160043
|
T | C | 9 | a0001c0001t0001g0092a0001c0001t0003g0240a0001c0001t0003g0241others(6): Show | 9 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+208T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160043 | ||||||
chr2:112160043
|
T | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0189 | 3 | HG02145.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.235+208T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160043 | ||||||
chr2:112160048
|
T | G | 1 | a0001c0001t0001g0311 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.235+213T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160048 | ||||||
chr2:112160051
|
C | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0311others(8): Show | 11 | HG02451.hp2 HG02602.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.235+216C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160051 | ||||||
chr2:112160053
|
C | G | 1 | a0001c0001t0005g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.235+218C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160053 | ||||||
chr2:112160092
|
G | A | 5 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+257G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160092 | ||||||
chr2:112160117
|
C | A | 2 | a0001c0001t0001g0082a0002c0002t0003g0075 | 2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.235+282C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160117 | ||||||
chr2:112160136
|
G | A | 6 | a0001c0001t0001g0057a0001c0001t0001g0073a0001c0001t0001g0164others(3): Show | 6 | HG01109.hp1 HG02083.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+301G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160136 | ||||||
chr2:112160139
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0073a0001c0001t0001g0185others(1): Show | 4 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+304C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160139 | ||||||
chr2:112160145
|
C | A | 2 | a0003c0003t0001g0094a0003c0003t0001g0095 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.235+310C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160145 | ||||||
chr2:112160145
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0001g0222a0006c0010t0001g0223 | 3 | HG03239.hp2 HG03491.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.235+310C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160145 | ||||||
chr2:112160158
|
T | C | 20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(17): Show | 24 | HG00639.hp2 HG01070.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.235+323T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160158 | ||||||
chr2:112160181
|
G | T | 1 | a0006c0010t0001g0223 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.235+346G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160181 | ||||||
chr2:112160192
|
T | G | 17 | a0001c0001t0001g0017a0001c0001t0001g0076a0001c0001t0001g0077others(14): Show | 18 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+357T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160192 | ||||||
chr2:112160211
|
C | G | 8 | a0001c0001t0001g0082a0001c0001t0001g0110a0001c0001t0001g0111others(5): Show | 8 | HG00323.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+376C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160211 | ||||||
chr2:112160225
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.235+390C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160225 | ||||||
chr2:112160263
|
G | T | 1 | a0001c0001t0001g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.235+428G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160263 | ||||||
chr2:112160273
|
G | A | 4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0297others(1): Show | 4 | HG00558.hp1 HG02132.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+438G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160273 | ||||||
chr2:112160285
|
G | C | 3 | a0001c0001t0001g0057a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | NA18994.hp1 NA19030.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.235+450G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160285 | ||||||
chr2:112160640
|
ACACACGC others(5): Show |
A | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.235+825_235+836del others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160640 | |||||
chr2:112160642
|
ACACGCGC others(11): Show |
A | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.235+813_235+830del others(18): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160642 | |||||
chr2:112160648
|
GCACGCAC others(11): Show |
G | 4 | a0001c0001t0001g0188a0001c0005t0007g0011a0002c0002t0002g0056others(1): Show | 5 | HG02970.hp1 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+825_235+842del others(18): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160648 | |||||
chr2:112160679
|
G | C | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.235+844G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160679 | ||||||
chr2:112160688
|
ACACGCAC others(5): Show |
A | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+865_235+876del others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160688 | |||||
chr2:112160704
|
GCA | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(119): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.235+878_235+879del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160704 | |||||
chr2:112160718
|
A | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0185others(9): Show | 13 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.235+883A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160718 | ||||||
chr2:112160720
|
G | A | 19 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(16): Show | 20 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.235+885G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160720 | ||||||
chr2:112160720
|
GCGCACAC others(9): Show |
G | 3 | a0001c0001t0001g0132a0001c0001t0001g0233a0001c0001t0001g0271 | 3 | HG02083.hp1 NA18968.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.235+893_235+908del others(16): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160720 | |||||
chr2:112160726
|
A | G | 11 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(8): Show | 11 | HG01070.hp2 HG01346.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.235+891A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160726 | ||||||
chr2:112160728
|
G | A | 11 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(8): Show | 11 | HG01070.hp2 HG01346.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.235+893G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160728 | ||||||
chr2:112160732
|
G | A | 1 | a0001c0001t0004g0068 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.235+897G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160732 | ||||||
chr2:112160734
|
A | G | 1 | a0001c0001t0004g0068 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.235+899A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160734 | ||||||
chr2:112160736
|
A | ACGCACAC others(1): Show |
17 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(14): Show | 19 | HG01243.hp1 HG01257.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.235+908_235+909ins others(8): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160736 | |||||
chr2:112160738
|
GCA | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(95): Show | 108 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.235+909_235+910del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160738 | |||||
chr2:112160740
|
A | G | 10 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 10 | HG01070.hp2 HG01346.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+905A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160740 | ||||||
chr2:112160744
|
A | G | 15 | a0001c0001t0001g0059a0001c0001t0001g0207a0001c0001t0001g0224others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.235+909A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160744 | ||||||
chr2:112160744
|
ACG | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 5 | HG01070.hp2 HG01346.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+913_235+914del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160744 | |||||
chr2:112160746
|
G | A | 23 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(20): Show | 25 | HG00408.hp1 HG01243.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.235+911G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160746 | ||||||
chr2:112160746
|
GCGCACGC others(5): Show |
G | 1 | a0001c0001t0001g0306 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.235+923_235+934del others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160746 | |||||
chr2:112160747
|
C | A | 1 | a0001c0001t0001g0308 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.235+912C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160747 | ||||||
chr2:112160747
|
CGCACGCA others(19): Show |
C | 7 | a0001c0001t0001g0207a0001c0001t0001g0224a0001c0001t0004g0069others(4): Show | 7 | HG00099.hp2 HG01884.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+913_235+938del others(26): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160747 | ||||||
chr2:112160748
|
G | A | 13 | a0001c0001t0001g0059a0001c0001t0004g0062a0001c0001t0004g0064others(10): Show | 13 | HG00140.hp1 HG00280.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.235+913G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160748 | ||||||
chr2:112160750
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0188 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.235+915A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160750 | ||||||
chr2:112160750
|
ACG | A | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(92): Show | 105 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.235+917_235+918del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160750 | |||||
chr2:112160752
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.235+917G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160752 | ||||||
chr2:112160753
|
CACACACG others(13): Show |
C | 12 | a0001c0001t0001g0059a0001c0001t0004g0062a0001c0001t0004g0064others(9): Show | 12 | HG00140.hp1 HG00280.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+921_235+940del others(20): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160753 | |||||
chr2:112160754
|
A | G | 3 | a0001c0001t0001g0188a0001c0001t0002g0269a0001c0001t0004g0068 | 3 | HG01516.hp2 HG02970.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.235+919A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160754 | ||||||
chr2:112160754
|
ACACACGC others(15): Show |
A | 1 | a0001c0001t0010g0163 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.235+938_235+959del others(22): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160754 | |||||
chr2:112160758
|
A | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0118others(9): Show | 15 | HG01433.hp1 HG01496.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.235+923A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160758 | ||||||
chr2:112160760
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0118others(8): Show | 14 | HG01433.hp1 HG01496.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.235+925G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160760 | ||||||
chr2:112160760
|
GCACGCA | G | 5 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 5 | HG01070.hp2 HG01346.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+932_235+937del others(6): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160760 | |||||
chr2:112160761
|
C | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0118others(8): Show | 14 | HG01433.hp1 HG01496.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.235+926C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160761 | ||||||
chr2:112160761
|
CACGCACA others(5): Show |
C | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(96): Show | 109 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.235+938_235+949del others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160761 | |||||
chr2:112160764
|
GCA | G | 11 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0003g0240others(8): Show | 12 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+933_235+934del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160764 | |||||
chr2:112160776
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0224a0001c0001t0005g0055 | 3 | HG00099.hp2 HG01884.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.235+941G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160776 | ||||||
chr2:112160782
|
GCACGCAC others(21): Show |
G | 1 | a0001c0001t0001g0252 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.235+957_235+984del others(28): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160782 | |||||
chr2:112160792
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+957G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160792 | ||||||
chr2:112160792
|
G | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.235+957G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160792 | ||||||
chr2:112160794
|
ACACACGC others(3): Show |
A | 1 | a0001c0001t0003g0109 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.235+965_235+974del others(10): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160794 | |||||
chr2:112160796
|
ACACG | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0185others(9): Show | 13 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.235+969_235+972del others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160796 | |||||
chr2:112160800
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+965G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160800 | ||||||
chr2:112160800
|
GCACGCAC others(3): Show |
G | 1 | a0001c0001t0001g0125 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.235+978_235+987del others(10): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160800 | |||||
chr2:112160803
|
C | A | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+968C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160803 | ||||||
chr2:112160808
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.235+973A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160808 | ||||||
chr2:112160813
|
CGCACACA others(3): Show |
C | 1 | a0001c0001t0001g0220 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.235+983_235+992del others(10): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160813 | |||||
chr2:112160818
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+983A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160818 | ||||||
chr2:112160823
|
A | C | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+988A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160823 | ||||||
chr2:112160823
|
AGCACGCA others(5): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.235+996_235+1007de others(13): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160823 | |||||
chr2:112160826
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+991A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160826 | ||||||
chr2:112160828
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+993G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160828 | ||||||
chr2:112160831
|
T | C | 22 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(19): Show | 24 | HG01070.hp2 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.235+996T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160831 | ||||||
chr2:112160836
|
G | A | 2 | a0002c0002t0002g0056a0002c0002t0003g0075 | 2 | NA19030.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.235+1001G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160836 | ||||||
chr2:112160842
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+1007A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160842 | ||||||
chr2:112160846
|
G | A | 6 | a0001c0001t0001g0188a0001c0001t0003g0240a0001c0001t0003g0241others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+1011G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160846 | ||||||
chr2:112160846
|
G | GCGCGCAC others(17): Show |
2 | a0002c0002t0002g0056a0002c0002t0003g0075 | 2 | NA19030.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.235+1014_235+1015i others(26): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160846 | |||||
chr2:112160848
|
G | A | 5 | a0001c0001t0001g0093a0001c0001t0008g0186a0001c0001t0008g0187others(2): Show | 6 | HG01257.hp1 HG01258.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+1013G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160848 | ||||||
chr2:112160848
|
G | GCACACAC others(1): Show |
3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0297 | 3 | HG02132.hp1 NA18990.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.235+1025_235+1032d others(10): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160848 | |||||
chr2:112160848
|
GCA | G | 111 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(108): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.235+1031_235+1032d others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160848 | |||||
chr2:112160848
|
GCACA | G | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+1029_235+1032d others(6): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160848 | |||||
chr2:112160850
|
A | ACG | 5 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+1016_235+1017i others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112160850 | |||||
chr2:112160850
|
A | G | 1 | a0001c0001t0001g0304 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.235+1015A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160850 | ||||||
chr2:112160852
|
A | G | 3 | a0001c0001t0001g0188a0002c0002t0002g0056a0002c0002t0003g0075 | 3 | HG02970.hp1 NA19030.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.235+1017A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160852 | ||||||
chr2:112160881
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.235+1046G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160881 | ||||||
chr2:112160968
|
A | C | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.235+1133A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112160968 | ||||||
chr2:112161216
|
G | A | 1 | a0001c0001t0003g0109 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.235+1381G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161216 | ||||||
chr2:112161288
|
T | G | 1 | a0001c0001t0003g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.235+1453T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161288 | ||||||
chr2:112161397
|
A | G | 7 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(4): Show | 7 | HG01070.hp2 HG01346.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+1562A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161397 | ||||||
chr2:112161495
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0002g0269 | 2 | HG01257.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.235+1660G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161495 | ||||||
chr2:112161548
|
C | T | 12 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0103others(9): Show | 13 | HG01257.hp1 HG01258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.235+1713C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161548 | ||||||
chr2:112161669
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.235+1834G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161669 | ||||||
chr2:112161736
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.235+1901C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161736 | ||||||
chr2:112161993
|
T | A | 1 | a0001c0001t0001g0053 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.235+2158T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112161993 | ||||||
chr2:112162042
|
A | G | 8 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(5): Show | 9 | HG01070.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.235+2207A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162042 | ||||||
chr2:112162102
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.235+2267C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162102 | ||||||
chr2:112162290
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.235+2455G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162290 | ||||||
chr2:112162308
|
C | A | 1 | a0001c0001t0001g0294 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.235+2473C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162308 | ||||||
chr2:112162318
|
CT | C | 19 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(16): Show | 19 | HG00733.hp1 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.235+2499delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 112162318 | |||||
chr2:112162487
|
C | T | 1 | a0001c0001t0005g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236-2514C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162487 | ||||||
chr2:112162502
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.236-2499A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162502 | ||||||
chr2:112162558
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.236-2443G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162558 | ||||||
chr2:112162642
|
C | T | 151 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(148): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.236-2359C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162642 | ||||||
chr2:112162647
|
C | T | 8 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(5): Show | 8 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-2354C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162647 | ||||||
chr2:112162754
|
A | G | 2 | a0002c0002t0002g0056a0002c0002t0003g0075 | 2 | NA19030.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.236-2247A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162754 | ||||||
chr2:112162766
|
A | T | 119 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(116): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.236-2235A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162766 | ||||||
chr2:112162849
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.236-2152C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162849 | ||||||
chr2:112162891
|
T | C | 2 | a0003c0003t0001g0094a0003c0003t0001g0095 | 2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.236-2110T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112162891 | ||||||
chr2:112163070
|
C | T | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.236-1931C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163070 | ||||||
chr2:112163140
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.236-1861C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163140 | ||||||
chr2:112163189
|
G | A | 10 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0003g0240others(7): Show | 10 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-1812G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163189 | ||||||
chr2:112163272
|
A | G | 3 | a0001c0001t0001g0188a0002c0002t0002g0056a0002c0002t0003g0075 | 3 | HG02970.hp1 NA19030.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.236-1729A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163272 | ||||||
chr2:112163337
|
A | C | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.236-1664A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163337 | ||||||
chr2:112163485
|
C | T | 3 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG01192.hp1 HG01255.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.236-1516C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163485 | ||||||
chr2:112163723
|
G | GTCAGGCT others(17): Show |
4 | a0001c0001t0001g0188a0002c0002t0002g0056a0002c0002t0003g0075others(1): Show | 4 | HG01891.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-1278_236-1277i others(26): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163723 | ||||||
chr2:112163725
|
G | A | 4 | a0001c0001t0001g0188a0002c0002t0002g0056a0002c0002t0003g0075others(1): Show | 4 | HG01891.hp2 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-1276G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163725 | ||||||
chr2:112163990
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.236-1011G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112163990 | ||||||
chr2:112164036
|
C | T | 1 | a0001c0001t0001g0282 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.236-965C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164036 | ||||||
chr2:112164210
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.236-791A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164210 | ||||||
chr2:112164213
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(83): Show | 99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.236-788G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164213 | ||||||
chr2:112164345
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 6 | NA18941.hp2 NA18957.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-656G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164345 | ||||||
chr2:112164379
|
T | C | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(65): Show | 75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.236-622T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164379 | ||||||
chr2:112164915
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.236-86C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164915 | ||||||
chr2:112164951
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.236-50G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 2/7 | chr2 | 112164951 | ||||||
chr2:112165529
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.406+358C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112165529 | ||||||
chr2:112165751
|
G | T | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.406+580G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112165751 | ||||||
chr2:112166024
|
A | AG | 24 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(21): Show | 24 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.406+853_406+854ins others(1): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166024 | ||||||
chr2:112166074
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.406+903G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166074 | ||||||
chr2:112166094
|
A | G | 1 | a0001c0001t0012g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.406+923A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166094 | ||||||
chr2:112166153
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.406+982C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166153 | ||||||
chr2:112166276
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220 | 3 | HG01109.hp2 HG01515.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.406+1105C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166276 | ||||||
chr2:112166406
|
T | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(115): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.406+1235T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166406 | ||||||
chr2:112166532
|
T | C | 24 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(21): Show | 24 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.406+1361T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166532 | ||||||
chr2:112166569
|
A | C | 146 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(143): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.406+1398A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166569 | ||||||
chr2:112166592
|
A | AAC | 6 | a0002c0002t0001g0153a0002c0002t0001g0154a0002c0002t0002g0056others(3): Show | 6 | HG01891.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+1423_406+1424d others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112166592 | |||||
chr2:112166631
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.406+1460C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166631 | ||||||
chr2:112166672
|
T | C | 1 | a0004c0004t0002g0020 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.406+1501T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166672 | ||||||
chr2:112166832
|
C | T | 6 | a0002c0002t0001g0153a0002c0002t0001g0154a0002c0002t0002g0056others(3): Show | 6 | HG01891.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+1661C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166832 | ||||||
chr2:112166931
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.406+1760G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112166931 | ||||||
chr2:112167092
|
G | A | 1 | a0004c0004t0002g0020 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.406+1921G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167092 | ||||||
chr2:112167103
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.406+1932C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167103 | ||||||
chr2:112167192
|
A | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(22): Show | 29 | HG00639.hp2 HG01243.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.406+2021A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167192 | ||||||
chr2:112167330
|
T | C | 146 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(143): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.406+2159T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167330 | ||||||
chr2:112167387
|
TA | T | 18 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(15): Show | 18 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.406+2217delA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167387 | ||||||
chr2:112167396
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(69): Show | 79 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.406+2225G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167396 | ||||||
chr2:112167456
|
T | G | 24 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(21): Show | 24 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.406+2285T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167456 | ||||||
chr2:112167486
|
G | A | 7 | a0001c0001t0001g0085a0002c0002t0001g0153a0002c0002t0001g0154others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.406+2315G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167486 | ||||||
chr2:112167584
|
C | T | 6 | a0002c0002t0001g0153a0002c0002t0001g0154a0002c0002t0002g0056others(3): Show | 6 | HG01891.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+2413C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167584 | ||||||
chr2:112167618
|
C | T | 1 | a0002c0002t0002g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.406+2447C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167618 | ||||||
chr2:112167869
|
C | CGTTAT | 23 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0096others(20): Show | 25 | HG00099.hp1 HG00597.hp2 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.406+2747_406+2751d others(7): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(3): Show |
23 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(20): Show | 27 | HG00323.hp2 HG00735.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.406+2742_406+2751d others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(8): Show |
28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0102others(25): Show | 34 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.406+2737_406+2751d others(17): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(13): Show |
33 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0053others(30): Show | 36 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.406+2732_406+2751d others(22): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(18): Show |
15 | a0001c0001t0001g0017a0001c0001t0001g0101a0001c0001t0001g0120others(12): Show | 16 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.406+2727_406+2751d others(27): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(23): Show |
8 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0122others(5): Show | 10 | HG01175.hp1 HG01256.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.406+2722_406+2751d others(32): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(28): Show |
6 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(3): Show | 6 | HG01346.hp1 HG02083.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+2717_406+2751d others(37): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(33): Show |
1 | a0001c0001t0001g0271 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.406+2712_406+2751d others(42): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(48): Show |
1 | a0001c0001t0001g0233 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.406+2751_406+2752i others(57): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(12): Show |
30 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(27): Show | 34 | HG00140.hp2 HG00733.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.406+2713_406+2714i others(21): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(17): Show |
47 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0027others(44): Show | 52 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.406+2713_406+2714i others(26): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(22): Show |
39 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0054others(36): Show | 42 | HG00280.hp1 HG00741.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.406+2713_406+2714i others(31): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(27): Show |
13 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0048others(10): Show | 13 | HG00140.hp1 HG00323.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.406+2713_406+2714i others(36): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(32): Show |
4 | a0001c0001t0001g0166a0001c0001t0001g0172a0001c0001t0001g0245others(1): Show | 4 | HG00673.hp2 HG02074.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.406+2713_406+2714i others(41): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
C | CGTTATGT others(42): Show |
1 | a0001c0001t0001g0171 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.406+2713_406+2714i others(51): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167869
|
CGTTATGT others(3): Show |
C | 1 | a0001c0001t0001g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.406+2742_406+2751d others(12): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167869 | |||||
chr2:112167870
|
G | GTTATGTT others(7): Show |
9 | a0001c0001t0001g0035a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 10 | HG00639.hp1 HG00738.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.406+2700_406+2713d others(16): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112167870 | |||||
chr2:112167890
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.406+2719G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167890 | ||||||
chr2:112167895
|
G | C | 16 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(13): Show | 16 | HG01175.hp2 HG01243.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.406+2724G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112167895 | ||||||
chr2:112168129
|
G | A | 9 | a0001c0001t0001g0103a0001c0001t0003g0024a0001c0001t0003g0026others(6): Show | 9 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+2958G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112168129 | ||||||
chr2:112168284
|
C | G | 1 | a0001c0001t0001g0304 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.406+3113C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112168284 | ||||||
chr2:112168892
|
C | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0225others(4): Show | 7 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.406+3721C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112168892 | ||||||
chr2:112168969
|
G | A | 1 | a0004c0004t0002g0020 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.406+3798G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112168969 | ||||||
chr2:112169045
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0188 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.406+3874C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169045 | ||||||
chr2:112169133
|
G | A | 1 | a0001c0001t0010g0163 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.406+3962G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169133 | ||||||
chr2:112169213
|
C | T | 18 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(15): Show | 18 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.406+4042C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169213 | ||||||
chr2:112169240
|
T | G | 6 | a0002c0002t0001g0153a0002c0002t0001g0154a0002c0002t0002g0056others(3): Show | 6 | HG01891.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+4069T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169240 | ||||||
chr2:112169454
|
G | A | 1 | a0001c0001t0003g0243 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.406+4283G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169454 | ||||||
chr2:112169489
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.406+4318C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169489 | ||||||
chr2:112169508
|
G | A | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0220 | 3 | HG01109.hp2 HG01515.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.406+4337G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169508 | ||||||
chr2:112169616
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.406+4445C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169616 | ||||||
chr2:112169771
|
A | G | 20 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(17): Show | 20 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.406+4600A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169771 | ||||||
chr2:112169820
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.406+4649G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169820 | ||||||
chr2:112169990
|
T | C | 146 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(143): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.406+4819T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112169990 | ||||||
chr2:112170157
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.406+4986G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170157 | ||||||
chr2:112170267
|
C | CAGAAA | 2 | a0001c0005t0007g0011a0004c0004t0002g0020 | 4 | HG01257.hp1 HG01258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.406+5113_406+5117d others(7): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112170267 | |||||
chr2:112170267
|
CAGAAA | C | 7 | a0001c0001t0001g0092a0001c0001t0001g0093a0002c0002t0001g0153others(4): Show | 7 | HG02896.hp2 HG02922.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.406+5113_406+5117d others(7): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112170267 | |||||
chr2:112170324
|
C | T | 5 | a0002c0002t0001g0153a0002c0002t0001g0154a0002c0002t0002g0056others(2): Show | 5 | HG02922.hp2 HG03486.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.406+5153C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170324 | ||||||
chr2:112170404
|
G | A | 117 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(114): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.406+5233G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170404 | ||||||
chr2:112170424
|
G | A | 1 | a0004c0004t0002g0020 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.406+5253G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170424 | ||||||
chr2:112170476
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.407-5238G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170476 | ||||||
chr2:112170544
|
AAAAAG | A | 17 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(14): Show | 17 | HG01070.hp2 HG01243.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.407-5159_407-5155d others(7): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112170544 | |||||
chr2:112170605
|
C | A | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.407-5109C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170605 | ||||||
chr2:112170692
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.407-5022C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170692 | ||||||
chr2:112170736
|
T | C | 1 | a0001c0001t0003g0197 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.407-4978T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170736 | ||||||
chr2:112170795
|
T | C | 19 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049others(16): Show | 19 | HG01070.hp2 HG01175.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.407-4919T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112170795 | ||||||
chr2:112171066
|
A | T | 6 | a0001c0001t0001g0092a0002c0002t0001g0153a0002c0002t0001g0154others(3): Show | 6 | HG02896.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-4648A>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171066 | ||||||
chr2:112171238
|
A | G | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(123): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.407-4476A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171238 | ||||||
chr2:112171359
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.407-4355C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171359 | ||||||
chr2:112171416
|
GT | G | 6 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-4294delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112171416 | |||||
chr2:112171470
|
C | G | 1 | a0001c0001t0002g0232 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.407-4244C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171470 | ||||||
chr2:112171542
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.407-4172T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171542 | ||||||
chr2:112171663
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.407-4051A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171663 | ||||||
chr2:112171904
|
A | G | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(140): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.407-3810A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171904 | ||||||
chr2:112171907
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.407-3807C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171907 | ||||||
chr2:112171908
|
G | A | 142 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(139): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.407-3806G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171908 | ||||||
chr2:112171933
|
A | G | 1 | a0001c0001t0005g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.407-3781A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171933 | ||||||
chr2:112171937
|
C | T | 1 | a0001c0001t0005g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.407-3777C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171937 | ||||||
chr2:112171938
|
A | G | 1 | a0001c0001t0005g0025 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.407-3776A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171938 | ||||||
chr2:112171949
|
G | A | 1 | a0001c0001t0006g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.407-3765G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171949 | ||||||
chr2:112171962
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.407-3752T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112171962 | ||||||
chr2:112172057
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.407-3657A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172057 | ||||||
chr2:112172219
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.407-3495T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172219 | ||||||
chr2:112172400
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.407-3314A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172400 | ||||||
chr2:112172487
|
C | T | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.407-3227C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172487 | ||||||
chr2:112172627
|
C | CT | 28 | a0001c0001t0001g0051a0001c0001t0001g0085a0001c0001t0001g0101others(25): Show | 28 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.407-3063dupT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112172627 | |||||
chr2:112172627
|
CT | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(79): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.407-3063delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112172627 | |||||
chr2:112172914
|
G | A | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(33): Show | 42 | HG00639.hp2 HG01074.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.407-2800G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172914 | ||||||
chr2:112172942
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.407-2772G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112172942 | ||||||
chr2:112173058
|
G | C | 5 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.407-2656G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173058 | ||||||
chr2:112173415
|
A | G | 1 | a0001c0001t0004g0074 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.407-2299A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173415 | ||||||
chr2:112173613
|
G | A | 5 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.407-2101G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173613 | ||||||
chr2:112173614
|
C | G | 5 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.407-2100C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173614 | ||||||
chr2:112173830
|
G | C | 1 | a0001c0001t0001g0214 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.407-1884G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173830 | ||||||
chr2:112173968
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.407-1746C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112173968 | ||||||
chr2:112174170
|
C | G | 1 | a0001c0001t0001g0294 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.407-1544C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174170 | ||||||
chr2:112174177
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.407-1537C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174177 | ||||||
chr2:112174359
|
T | C | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(58): Show | 67 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.407-1355T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174359 | ||||||
chr2:112174379
|
A | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(34): Show | 43 | HG00639.hp2 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.407-1335A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174379 | ||||||
chr2:112174473
|
G | A | 1 | a0001c0001t0001g0017 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.407-1241G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174473 | ||||||
chr2:112174703
|
T | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0210 | 2 | HG01081.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.407-1011T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174703 | ||||||
chr2:112174780
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.407-934G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174780 | ||||||
chr2:112174858
|
T | A | 2 | a0001c0001t0003g0200a0001c0001t0003g0231 | 2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.407-856T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174858 | ||||||
chr2:112174919
|
T | TA | 5 | a0001c0001t0001g0083a0001c0001t0001g0102a0001c0001t0001g0135others(2): Show | 5 | HG02135.hp1 HG02135.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.407-787dupA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112174919 | |||||
chr2:112174932
|
T | C | 2 | a0001c0001t0001g0291a0001c0001t0004g0064 | 2 | HG00735.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.407-782T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112174932 | ||||||
chr2:112175015
|
G | GA | 101 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0021others(98): Show | 108 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.407-692dupA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 112175015 | |||||
chr2:112175314
|
A | G | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 119 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.407-400A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112175314 | ||||||
chr2:112175548
|
T | C | 10 | a0001c0001t0004g0069a0001c0001t0004g0070a0001c0001t0004g0071others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.407-166T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 3/7 | chr2 | 112175548 | ||||||
chr2:112175944
|
C | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(58): Show | 67 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.532+105C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112175944 | ||||||
chr2:112176075
|
C | T | 6 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(3): Show | 6 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.532+236C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176075 | ||||||
chr2:112176172
|
C | A | 1 | a0001c0001t0001g0289 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.532+333C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176172 | ||||||
chr2:112176346
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.532+507C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176346 | ||||||
chr2:112176418
|
C | T | 4 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.532+579C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176418 | ||||||
chr2:112176681
|
G | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0183 | 2 | NA18954.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.532+842G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176681 | ||||||
chr2:112176856
|
C | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(113): Show | 130 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.532+1017C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176856 | ||||||
chr2:112176934
|
AT | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.532+1111delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112176934 | |||||
chr2:112176934
|
ATT | A | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0034others(42): Show | 52 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.532+1110_532+1111d others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112176934 | |||||
chr2:112176951
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 254 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.532+1112A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112176951 | ||||||
chr2:112177134
|
C | T | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.532+1295C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112177134 | ||||||
chr2:112177474
|
G | T | 60 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(57): Show | 66 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.532+1635G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112177474 | ||||||
chr2:112177535
|
A | G | 15 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0203others(12): Show | 17 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.532+1696A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112177535 | ||||||
chr2:112177595
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.532+1756A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112177595 | ||||||
chr2:112177950
|
G | A | 60 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(57): Show | 66 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.532+2111G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112177950 | ||||||
chr2:112178008
|
CA | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 229 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.532+2181delA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112178008 | |||||
chr2:112178147
|
G | A | 4 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0113others(1): Show | 4 | HG02258.hp2 HG02723.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+2308G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178147 | ||||||
chr2:112178257
|
C | CA | 21 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0076others(18): Show | 22 | HG01074.hp2 HG01081.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.532+2429dupA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112178257 | |||||
chr2:112178257
|
C | CAA | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.532+2428_532+2429d others(4): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112178257 | |||||
chr2:112178265
|
A | C | 1 | a0001c0001t0001g0181 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.532+2426A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178265 | ||||||
chr2:112178269
|
C | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 255 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.532+2430C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178269 | ||||||
chr2:112178274
|
A | G | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0034others(41): Show | 51 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.532+2435A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178274 | ||||||
chr2:112178327
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG01346.hp2 HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.532+2488C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178327 | ||||||
chr2:112178373
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.532+2534C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178373 | ||||||
chr2:112178512
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.532+2673G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178512 | ||||||
chr2:112178583
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.532+2744C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178583 | ||||||
chr2:112178685
|
A | C | 14 | a0001c0001t0001g0040a0001c0001t0001g0073a0001c0001t0001g0076others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.532+2846A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178685 | ||||||
chr2:112178799
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.533-2940A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112178799 | ||||||
chr2:112178904
|
G | GGCAAAAG others(6): Show |
228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 255 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.533-2832_533-2831i others(15): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112178904 | |||||
chr2:112179084
|
A | C | 1 | a0001c0001t0001g0117 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.533-2655A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179084 | ||||||
chr2:112179425
|
C | T | 1 | a0001c0001t0001g0282 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.533-2314C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179425 | ||||||
chr2:112179488
|
ATTACT | A | 6 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(3): Show | 6 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.533-2247_533-2243d others(7): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112179488 | |||||
chr2:112179569
|
A | G | 1 | a0001c0001t0012g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.533-2170A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179569 | ||||||
chr2:112179647
|
G | A | 1 | a0001c0001t0005g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.533-2092G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179647 | ||||||
chr2:112179661
|
C | T | 1 | a0002c0002t0002g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.533-2078C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179661 | ||||||
chr2:112179709
|
C | A | 1 | a0006c0010t0001g0223 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.533-2030C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179709 | ||||||
chr2:112179729
|
A | G | 1 | a0002c0002t0002g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.533-2010A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179729 | ||||||
chr2:112179890
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.533-1849G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179890 | ||||||
chr2:112179893
|
G | A | 60 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(57): Show | 66 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.533-1846G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112179893 | ||||||
chr2:112180120
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.533-1619A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180120 | ||||||
chr2:112180174
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.533-1565C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180174 | ||||||
chr2:112180187
|
A | C | 7 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0203others(4): Show | 8 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.533-1552A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180187 | ||||||
chr2:112180387
|
G | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0036others(11): Show | 18 | HG00639.hp2 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.533-1352G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180387 | ||||||
chr2:112180432
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.533-1307G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180432 | ||||||
chr2:112180534
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.533-1205C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180534 | ||||||
chr2:112180562
|
G | C | 1 | a0001c0001t0001g0181 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.533-1177G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180562 | ||||||
chr2:112180646
|
C | T | 3 | a0001c0001t0002g0087a0001c0001t0002g0195a0001c0001t0013g0248 | 3 | HG03225.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.533-1093C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180646 | ||||||
chr2:112180649
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.533-1090G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180649 | ||||||
chr2:112180731
|
T | C | 1 | a0001c0001t0006g0067 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.533-1008T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180731 | ||||||
chr2:112180763
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.533-976A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180763 | ||||||
chr2:112180774
|
T | A | 11 | a0001c0001t0002g0124a0001c0001t0004g0069a0001c0001t0004g0070others(8): Show | 11 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.533-965T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180774 | ||||||
chr2:112180795
|
C | T | 3 | a0001c0001t0001g0192a0001c0001t0001g0210a0001c0001t0001g0213 | 3 | HG01074.hp2 HG01081.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.533-944C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180795 | ||||||
chr2:112180871
|
G | A | 1 | a0001c0001t0005g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.533-868G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180871 | ||||||
chr2:112180877
|
C | T | 1 | a0001c0001t0005g0244 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.533-862C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180877 | ||||||
chr2:112180892
|
CAGCCTGG others(34): Show |
C | 4 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(1): Show | 4 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-845_533-805del others(41): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112180892 | |||||
chr2:112180901
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.533-838C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180901 | ||||||
chr2:112180902
|
G | A | 2 | a0001c0001t0003g0262a0001c0001t0003g0274 | 2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.533-837G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180902 | ||||||
chr2:112180922
|
C | CA | 14 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0048others(11): Show | 14 | HG00642.hp2 HG01884.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.533-794dupA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112180922 | |||||
chr2:112180922
|
CA | C | 63 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(60): Show | 69 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.533-794delA | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112180922 | |||||
chr2:112180922
|
CAA | C | 27 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0092others(24): Show | 28 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.533-795_533-794del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112180922 | |||||
chr2:112180922
|
CAAA | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.533-796_533-794del others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 112180922 | |||||
chr2:112180998
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.533-741C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112180998 | ||||||
chr2:112181040
|
A | G | 9 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(6): Show | 9 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.533-699A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181040 | ||||||
chr2:112181131
|
T | C | 1 | a0001c0001t0005g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.533-608T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181131 | ||||||
chr2:112181138
|
C | T | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0035others(40): Show | 50 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.533-601C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181138 | ||||||
chr2:112181159
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.533-580G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181159 | ||||||
chr2:112181288
|
A | C | 1 | a0002c0002t0002g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.533-451A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181288 | ||||||
chr2:112181415
|
G | T | 1 | a0001c0001t0001g0301 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.533-324G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181415 | ||||||
chr2:112181465
|
C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(175): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.533-274C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181465 | ||||||
chr2:112181538
|
T | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 255 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.533-201T>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181538 | ||||||
chr2:112181626
|
C | T | 54 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(51): Show | 60 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.533-113C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181626 | ||||||
chr2:112181632
|
G | A | 25 | a0001c0001t0001g0035a0001c0001t0001g0192a0001c0001t0001g0210others(22): Show | 28 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.533-107G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181632 | ||||||
chr2:112181680
|
A | C | 1 | a0001c0001t0004g0068 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.533-59A>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 4/7 | chr2 | 112181680 | ||||||
chr2:112181971
|
T | C | 72 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(69): Show | 79 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.670+95T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112181971 | ||||||
chr2:112182034
|
G | C | 1 | a0001c0001t0006g0063 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.670+158G>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182034 | ||||||
chr2:112182315
|
A | G | 1 | a0001c0001t0005g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.670+439A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182315 | ||||||
chr2:112182422
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.671-369A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182422 | ||||||
chr2:112182483
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0227 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.671-308G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182483 | ||||||
chr2:112182566
|
ACTC | A | 72 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(69): Show | 79 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.671-219_671-217del others(3): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 112182566 | |||||
chr2:112182594
|
G | A | 70 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(67): Show | 76 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.671-197G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182594 | ||||||
chr2:112182729
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.671-62G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 5/7 | chr2 | 112182729 | ||||||
chr2:112183001
|
C | T | 71 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0016others(68): Show | 78 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.808+73C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183001 | ||||||
chr2:112183152
|
C | T | 1 | a0001c0001t0008g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.808+224C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183152 | ||||||
chr2:112183215
|
A | G | 8 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0085others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.808+287A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183215 | ||||||
chr2:112183216
|
C | T | 1 | a0001c0001t0005g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.808+288C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183216 | ||||||
chr2:112183409
|
A | G | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.808+481A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183409 | ||||||
chr2:112183507
|
T | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0035others(37): Show | 47 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.808+579T>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183507 | ||||||
chr2:112183610
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.808+682C>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183610 | ||||||
chr2:112183696
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG01346.hp2 HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.808+768C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183696 | ||||||
chr2:112183795
|
A | G | 46 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0035others(43): Show | 53 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.808+867A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183795 | ||||||
chr2:112183807
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.808+879A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112183807 | ||||||
chr2:112184073
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 259 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.809-1128T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184073 | ||||||
chr2:112184074
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.809-1127G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184074 | ||||||
chr2:112184082
|
C | G | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.809-1119C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184082 | ||||||
chr2:112184107
|
A | G | 6 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(3): Show | 6 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-1094A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184107 | ||||||
chr2:112184146
|
G | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0112a0001c0001t0001g0173others(2): Show | 5 | HG01167.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-1055G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184146 | ||||||
chr2:112184245
|
T | C | 6 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(3): Show | 6 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-956T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184245 | ||||||
chr2:112184272
|
C | T | 6 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(3): Show | 6 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-929C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184272 | ||||||
chr2:112184353
|
T | C | 11 | a0001c0001t0001g0092a0001c0001t0003g0024a0001c0001t0003g0026others(8): Show | 11 | HG02451.hp1 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.809-848T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184353 | ||||||
chr2:112184363
|
G | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0035others(36): Show | 46 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.809-838G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184363 | ||||||
chr2:112184455
|
C | T | 1 | a0002c0002t0002g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.809-746C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184455 | ||||||
chr2:112184576
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.809-625C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184576 | ||||||
chr2:112184685
|
G | A | 1 | a0009c0013t0001g0174 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.809-516G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184685 | ||||||
chr2:112184685
|
G | GTATATAT others(95): Show |
1 | a0001c0001t0001g0117 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.809-458_809-457ins others(102): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184685 | |||||
chr2:112184685
|
G | GTATATAT others(19): Show |
1 | a0001c0001t0001g0267 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.809-497_809-496ins others(26): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184685 | |||||
chr2:112184685
|
G | GTATATAT others(21): Show |
153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 174 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.809-497_809-496ins others(28): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184685 | |||||
chr2:112184722
|
T | C | 5 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.809-479T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184722 | ||||||
chr2:112184734
|
G | T | 1 | a0001c0001t0001g0178 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.809-467G>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184734 | ||||||
chr2:112184745
|
T | C | 5 | a0001c0001t0003g0024a0001c0001t0003g0026a0001c0001t0003g0200others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.809-456T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184745 | ||||||
chr2:112184807
|
CAT | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.809-382_809-381del others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184807 | |||||
chr2:112184836
|
T | TAC | 6 | a0001c0001t0001g0188a0001c0001t0005g0025a0001c0001t0005g0080others(3): Show | 6 | HG01109.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-355_809-354dup others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184836 | |||||
chr2:112184846
|
C | CAT | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0035others(31): Show | 41 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.809-344_809-343dup others(2): Show |
FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 112184846 | |||||
chr2:112184869
|
A | G | 1 | a0002c0002t0003g0075 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.809-332A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 6/7 | chr2 | 112184869 | ||||||
chr2:112185493
|
C | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 281 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.947+154C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112185493 | ||||||
chr2:112185698
|
G | A | 1 | a0001c0001t0005g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.947+359G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112185698 | ||||||
chr2:112185868
|
CT | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0141a0001c0001t0001g0228others(3): Show | 6 | HG00140.hp1 HG01516.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+545delT | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 112185868 | |||||
chr2:112185961
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.947+622T>C | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112185961 | ||||||
chr2:112186006
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 282 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.947+667G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186006 | ||||||
chr2:112186136
|
C | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0001g0126others(2): Show | 5 | NA18960.hp1 NA18962.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.947+797C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186136 | ||||||
chr2:112186295
|
A | G | 47 | a0001c0001t0001g0093a0001c0001t0002g0009a0001c0001t0002g0010others(44): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.948-839A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186295 | ||||||
chr2:112186339
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0114 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.948-795C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186339 | ||||||
chr2:112186340
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.948-794G>A | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186340 | ||||||
chr2:112186404
|
C | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0176a0001c0001t0001g0177others(1): Show | 5 | HG03239.hp1 HG03688.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-730C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186404 | ||||||
chr2:112186414
|
C | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0089a0001c0001t0001g0188 | 3 | HG02970.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.948-720C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186414 | ||||||
chr2:112186446
|
C | G | 1 | a0001c0001t0005g0080 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.948-688C>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186446 | ||||||
chr2:112186468
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0005g0191 | 2 | HG00673.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.948-666C>T | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186468 | ||||||
chr2:112186519
|
A | G | 1 | a0001c0005t0007g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.948-615A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186519 | ||||||
chr2:112186747
|
A | G | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0245others(1): Show | 4 | HG00741.hp2 HG01981.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.948-387A>G | FBLN7 | ENSG00000144152.13 | transcript | ENST00000331203.7 | protein_coding | 7/7 | chr2 | 112186747 |