geneid | 2155 |
---|---|
ensemblid | ENSG00000057593.14 |
hgncid | 3544 |
symbol | F7 |
name | coagulation factor VII |
refseq_nuc | NM_019616.4 |
refseq_prot | NP_062562.1 |
ensembl_nuc | ENST00000346342.8 |
ensembl_prot | ENSP00000329546.4 |
mane_status | MANE Select |
chr | chr13 |
start | 113105791 |
end | 113120685 |
strand | + |
ver | v1.2 |
region | chr13:113105791-113120685 |
region5000 | chr13:113100791-113125685 |
regionname0 | F7_chr13_113105791_113120685 |
regionname5000 | F7_chr13_113100791_113125685 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 444 | 359 | 70 | 71 | 166 | 18 | 32 | 119 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002 | 0/0 | 444 | 37 | 12 | 4 | 7 | 0 | 14 | 6 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0003 | 0/0 | 444 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0004 | 0/0 | 444 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0005 | 0/0 | 444 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0006 | 0/0 | 253 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1335 | 351 | 66 | 70 | 165 | 16 | 32 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
c0002 | 0/0 | 1335 | 35 | 12 | 3 | 6 | 0 | 14 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
c0003 | 0/0 | 1335 | 6 | 4 | 0 | 0 | 2 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
c0004 | 0/0 | 1335 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
c0005 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
c0006 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
c0007 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
c0008 | 0/0 | 1324 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
c0009 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
c0010 | 0/0 | 1335 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
c0011 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1729 | 297 | 49 | 59 | 144 | 14 | 30 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0002 | 0/0 | 1729 | 29 | 0 | 10 | 19 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0003 | 0/0 | 1731 | 28 | 10 | 3 | 6 | 0 | 9 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0004 | 0/0 | 1731 | 8 | 7 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0005 | 0/0 | 1731 | 5 | 5 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0006 | 0/1 | 1725 | 5 | 0 | 1 | 0 | 2 | 1 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0007 | 0/0 | 1729 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0008 | 0/0 | 1731 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0009 | 0/0 | 1727 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0010 | 0/0 | 1731 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0011 | 0/0 | 1731 | 2 | 1 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0012 | 0/0 | 1731 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0013 | 0/0 | 1729 | 2 | 1 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0014 | 0/0 | 1729 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0015 | 0/0 | 1731 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0016 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0017 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0018 | 0/0 | 1729 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0019 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0020 | 0/0 | 1717 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0021 | 0/0 | 1729 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0022 | 0/0 | 1729 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0023 | 0/0 | 1725 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0024 | 0/0 | 1729 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
t0025 | 0/0 | 1729 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 19 | 1 | 4 | 10 | 2 | 2 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0002 | 0/0 | 17 | 1 | 5 | 11 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0003 | 0/0 | 17 | 2 | 7 | 3 | 1 | 4 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0004 | 0/0 | 11 | 0 | 5 | 6 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0007 | 0/0 | 7 | 0 | 3 | 0 | 1 | 3 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0008 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0009 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0022 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0026 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0030 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0056 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1335 | 351 | 66 | 70 | 165 | 16 | 32 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0003 | 0/0 | 1335 | 6 | 4 | 0 | 0 | 2 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0004 | 0/0 | 1335 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0009 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002c0002 | 0/0 | 1335 | 35 | 12 | 3 | 6 | 0 | 14 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002c0007 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002c0010 | 0/0 | 1335 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0003c0011 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0004c0006 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0005c0005 | 0/0 | 1335 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0006c0008 | 0/0 | 1324 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3063 | 289 | 46 | 58 | 142 | 12 | 30 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0002 | 0/0 | 3063 | 28 | 0 | 9 | 19 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0004 | 0/0 | 3065 | 8 | 7 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0005 | 0/0 | 3065 | 5 | 5 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0006 | 0/1 | 3059 | 5 | 0 | 1 | 0 | 2 | 1 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0007 | 0/0 | 3063 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0012 | 0/0 | 3065 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0013 | 0/0 | 3063 | 2 | 1 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0016 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0017 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0018 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0019 | 0/0 | 3047 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0020 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0022 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0023 | 0/0 | 3059 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0024 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0001t0025 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0003t0001 | 0/0 | 3063 | 2 | 0 | 0 | 0 | 2 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0003t0010 | 0/0 | 3065 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0003t0014 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0004t0001 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0001c0009t0001 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002c0002t0001 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002c0002t0003 | 0/0 | 3065 | 28 | 10 | 3 | 6 | 0 | 9 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002c0002t0008 | 0/0 | 3065 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002c0002t0009 | 0/0 | 3061 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002c0002t0011 | 0/0 | 3065 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002c0002t0021 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002c0007t0011 | 0/0 | 3065 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0002c0010t0015 | 0/0 | 3065 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0003c0011t0001 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0004c0006t0001 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0005c0005t0001 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
a0006c0008t0002 | 0/0 | 3052 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | copy fasta | chr13 | 113100791 | 113125685 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 18 | 1 | 4 | 9 | 2 | 2 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0002 | 0/0 | 16 | 0 | 5 | 11 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0003 | 0/0 | 16 | 2 | 6 | 3 | 1 | 4 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 3 | 0 | 0 | 3 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0009 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0004 | 0/0 | 11 | 0 | 5 | 6 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0004g0026 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0005g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0006g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0006g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0006g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0007g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0012g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0012g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0013g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0016g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0017g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0018g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0019g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0020g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0022g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0023g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0024g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0001t0025g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0003t0010g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0003t0014g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0003t0014g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0004t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0001c0009t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0008g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0008g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0009g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0011g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0002t0021g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0007t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0002c0010t0015g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0003c0011t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0004c0006t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0005c0005t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
a0006c0008t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0034 | EUR | GBR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00323 | hp2 | a0001 | c0001 | t0006 | g0034 | EUR | FIN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00609 | hp1 | a0001 | c0009 | t0001 | g0001 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00673 | hp1 | a0002 | c0002 | t0003 | g0078 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0094 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0037 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01243 | hp2 | a0002 | c0002 | t0003 | g0195 | AMR | PUR | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01346 | hp1 | a0001 | c0004 | t0001 | g0003 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01496 | hp2 | a0002 | c0010 | t0015 | g0097 | AMR | CLM | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01515 | hp2 | a0001 | c0003 | t0001 | g0060 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0070 | EUR | IBS | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01952 | hp2 | a0002 | c0002 | t0003 | g0068 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01975 | hp1 | a0006 | c0008 | t0002 | g0170 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01981 | hp1 | a0001 | c0001 | t0020 | g0011 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02135 | hp1 | a0001 | c0001 | t0025 | g0165 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02145 | hp1 | a0002 | c0002 | t0003 | g0081 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CDX | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02257 | hp2 | a0002 | c0002 | t0003 | g0030 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02258 | hp1 | a0002 | c0002 | t0003 | g0073 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0082 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02300 | hp1 | a0002 | c0002 | t0003 | g0071 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02602 | hp1 | a0002 | c0002 | t0021 | g0061 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02630 | hp1 | a0001 | c0003 | t0010 | g0050 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02698 | hp2 | a0001 | c0001 | t0023 | g0200 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02717 | hp2 | a0002 | c0002 | t0003 | g0029 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02723 | hp1 | a0001 | c0001 | t0012 | g0080 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02723 | hp2 | a0001 | c0003 | t0010 | g0050 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02735 | hp2 | a0002 | c0002 | t0003 | g0075 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02738 | hp1 | a0002 | c0002 | t0003 | g0074 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02809 | hp1 | a0005 | c0005 | t0001 | g0140 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02818 | hp2 | a0001 | c0001 | t0017 | g0233 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02976 | hp2 | a0002 | c0002 | t0003 | g0198 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03209 | hp1 | a0001 | c0001 | t0016 | g0242 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03209 | hp2 | a0001 | c0003 | t0014 | g0090 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03239 | hp2 | a0002 | c0002 | t0003 | g0072 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03453 | hp2 | a0004 | c0006 | t0001 | g0002 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0065 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03491 | hp2 | a0002 | c0002 | t0009 | g0027 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03492 | hp2 | a0002 | c0002 | t0009 | g0027 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03516 | hp1 | a0001 | c0003 | t0014 | g0112 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03540 | hp2 | a0002 | c0002 | t0003 | g0067 | AFR | GWD | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03579 | hp1 | a0002 | c0002 | t0003 | g0066 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03654 | hp2 | a0002 | c0002 | t0003 | g0063 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03688 | hp1 | a0001 | c0001 | t0006 | g0093 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0028 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03704 | hp2 | a0002 | c0002 | t0003 | g0028 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG04115 | hp2 | a0002 | c0002 | t0003 | g0059 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG04184 | hp2 | a0002 | c0002 | t0003 | g0084 | SAS | BEB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG04204 | hp1 | a0002 | c0002 | t0003 | g0058 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG04228 | hp1 | a0002 | c0002 | t0008 | g0030 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG04228 | hp2 | a0002 | c0002 | t0008 | g0069 | SAS | STU | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18747 | hp2 | a0001 | c0001 | t0019 | g0214 | EAS | CHB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18940 | hp1 | a0002 | c0002 | t0003 | g0239 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18947 | hp2 | a0001 | c0001 | t0018 | g0192 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18950 | hp2 | a0002 | c0002 | t0003 | g0076 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18956 | hp2 | a0001 | c0001 | t0024 | g0023 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18964 | hp1 | a0002 | c0002 | t0003 | g0144 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18970 | hp1 | a0002 | c0007 | t0011 | g0077 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0238 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19030 | hp1 | a0002 | c0002 | t0003 | g0029 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19030 | hp2 | a0002 | c0002 | t0003 | g0134 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19063 | hp1 | a0003 | c0011 | t0001 | g0105 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19068 | hp1 | a0002 | c0002 | t0003 | g0240 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19240 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ASW | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0026 | EUR | TSI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA20805 | hp2 | a0001 | c0001 | t0022 | g0007 | EUR | TSI | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | GIH | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG02559 | hp2 | a0001 | c0001 | t0012 | g0079 | AFR | ACB | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG03471 | hp2 | a0002 | c0002 | t0011 | g0164 | AFR | MSL | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | USA | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | USA | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0095 | REF | REF | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0241 | REF | REF | F7_chr13_113100791_113125685 | F7 | chr13 | 113100791 | 113125685 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:113113773
|
A | C | 1 | a0003 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.247A>C | p.Ser83Arg | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 3/8 | 298/3063 | 247/1335 | 83/444 | chr13 | 113113773 | ||
chr13:113115761
|
T | G | 1 | a0003 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.466T>G | p.Tyr156Asp | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/8 | 517/3063 | 466/1335 | 156/444 | chr13 | 113115761 | ||
chr13:113118436
|
G | C | 1 | a0005 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.763G>C | p.Asp255His | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 814/3063 | 763/1335 | 255/444 | chr13 | 113118436 | ||
chr13:113118458
|
G | A | 1 | a0004 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.785G>A | p.Arg262Gln | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 836/3063 | 785/1335 | 262/444 | chr13 | 113118458 | ||
chr13:113118845
|
G | A | 1 | a0002 | 37 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(34): Show |
missense_variant | MODERATE | c.1172G>A | p.Arg391Gln | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1223/3063 | 1172/1335 | 391/444 | chr13 | 113118845 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:113110844
|
G | A | 1 | a0001c0004 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.219G>A | p.Glu73Glu | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/8 | 270/3063 | 219/1335 | 73/444 | chr13 | 113110844 | ||
chr13:113115754
|
C | T | 3 | a0001c0003a0002c0002a0002c0010 | 42 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
synonymous_variant | LOW | c.459C>T | p.His153His | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/8 | 510/3063 | 459/1335 | 153/444 | chr13 | 113115754 | ||
chr13:113115778
|
C | T | 2 | a0001c0009a0002c0010 | 2 | HG00609.hp1 HG01496.hp2 |
synonymous_variant | LOW | c.483C>T | p.Asp161Asp | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/8 | 534/3063 | 483/1335 | 161/444 | chr13 | 113115778 | ||
chr13:113118975
|
C | T | 1 | a0006c0008 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.1302C>T | p.Arg434Arg | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1353/3063 | 1302/1335 | 434/444 | chr13 | 113118975 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:113119090
|
T | C | 1 | a0002c0002t0008 | 2 | HG04228.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*82T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 82 | chr13 | 113119090 | |||||
chr13:113119162
|
C | CAA | 12 | a0001c0001t0004a0001c0001t0005a0001c0001t0012others(9): Show | 54 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*155_*156insAA | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 156 | INFO_REALIGN_3_PRIME | chr13 | 113119162 | ||||
chr13:113119166
|
G | A | 1 | a0001c0001t0007 | 3 | HG01884.hp2 HG02280.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*158G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 158 | chr13 | 113119166 | |||||
chr13:113119176
|
G | A | 1 | a0001c0001t0018 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 168 | chr13 | 113119176 | |||||
chr13:113119365
|
C | T | 1 | a0001c0001t0025 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*357C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 357 | chr13 | 113119365 | |||||
chr13:113119541
|
A | C | 1 | a0001c0001t0005 | 5 | HG01891.hp2 HG02280.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*533A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 533 | chr13 | 113119541 | |||||
chr13:113119606
|
GATGCACG others(9): Show |
G | 1 | a0001c0001t0019 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*610_*625delTGCCAA others(10): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 610 | INFO_REALIGN_3_PRIME | chr13 | 113119606 | ||||
chr13:113119628
|
C | T | 1 | a0001c0001t0012 | 2 | HG02559.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*620C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 620 | chr13 | 113119628 | |||||
chr13:113119646
|
C | T | 1 | a0001c0001t0024 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*638C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 638 | chr13 | 113119646 | |||||
chr13:113119647
|
G | A | 1 | a0001c0001t0004 | 8 | HG02145.hp2 HG02451.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*639G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 639 | chr13 | 113119647 | |||||
chr13:113119681
|
A | G | 3 | a0001c0001t0004a0001c0001t0005a0001c0001t0017 | 14 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*673A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 673 | chr13 | 113119681 | |||||
chr13:113119743
|
ACACACAC others(5): Show |
A | 1 | a0001c0001t0020 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*756_*767delGATGCA others(6): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 756 | INFO_REALIGN_3_PRIME | chr13 | 113119743 | ||||
chr13:113119778
|
G | A | 5 | a0002c0002t0003a0002c0002t0008a0002c0002t0009others(2): Show | 34 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*770G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 770 | chr13 | 113119778 | |||||
chr13:113119896
|
G | A | 3 | a0001c0001t0002a0001c0001t0024a0006c0008t0002 | 30 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*888G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 888 | chr13 | 113119896 | |||||
chr13:113119951
|
G | A | 1 | a0001c0001t0013 | 2 | HG01243.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*943G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 943 | chr13 | 113119951 | |||||
chr13:113120132
|
T | C | 1 | a0001c0003t0010 | 2 | HG02630.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1124T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1124 | chr13 | 113120132 | |||||
chr13:113120154
|
A | G | 4 | a0001c0001t0004a0001c0001t0005a0001c0001t0017others(1): Show | 16 | HG01891.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1146A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1146 | chr13 | 113120154 | |||||
chr13:113120248
|
C | G | 1 | a0001c0001t0016 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1240C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1240 | chr13 | 113120248 | |||||
chr13:113120283
|
A | G | 2 | a0001c0001t0004a0001c0003t0014 | 10 | HG02145.hp2 HG02451.hp2 HG02886.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1275A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1275 | chr13 | 113120283 | |||||
chr13:113120450
|
G | A | 1 | a0001c0001t0022 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1442G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1442 | chr13 | 113120450 | |||||
chr13:113120484
|
G | A | 1 | a0002c0010t0015 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1476G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1476 | chr13 | 113120484 | |||||
chr13:113120504
|
GCACT | G | 2 | a0001c0001t0023a0002c0002t0009 | 3 | HG02698.hp2 HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1500_*1503delTCAC | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1500 | INFO_REALIGN_3_PRIME | chr13 | 113120504 | ||||
chr13:113120534
|
GCACT | G | 1 | a0001c0001t0006 | 5 | HG00140.hp2 HG00323.hp2 HG01192.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1530_*1533delTCAC | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1530 | INFO_REALIGN_3_PRIME | chr13 | 113120534 | ||||
chr13:113120657
|
G | A | 1 | a0001c0001t0016 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1649G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 8/8 | 1649 | chr13 | 113120657 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:113105909
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02809.hp2 NA20300.hp2 |
splice_region_variant&intron_variant | LOW | c.64+4C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113105909 | ||||||
chr13:113105914
|
G | A | 39 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0064others(36): Show | 53 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.64+9G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113105914 | ||||||
chr13:113106022
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.64+117G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106022 | ||||||
chr13:113106101
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(146): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.64+196G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106101 | ||||||
chr13:113106189
|
G | A | 1 | a0001c0001t0004g0025 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64+284G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106189 | ||||||
chr13:113106210
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0087a0001c0001t0001g0088 | 4 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+305G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106210 | ||||||
chr13:113106273
|
C | T | 1 | a0001c0001t0018g0192 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.64+368C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106273 | ||||||
chr13:113106305
|
G | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0089 | 3 | HG02451.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.64+400G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106305 | ||||||
chr13:113106335
|
G | A | 1 | a0001c0003t0010g0050 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+430G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106335 | ||||||
chr13:113106388
|
G | A | 1 | a0001c0003t0014g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.64+483G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106388 | ||||||
chr13:113106396
|
C | T | 1 | a0002c0002t0003g0084 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64+491C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106396 | ||||||
chr13:113106516
|
G | C | 1 | a0001c0001t0002g0091 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.64+611G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106516 | ||||||
chr13:113106541
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(62): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.64+636T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106541 | ||||||
chr13:113106548
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(58): Show | 103 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.64+643G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106548 | ||||||
chr13:113106553
|
C | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(58): Show | 103 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.64+648C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106553 | ||||||
chr13:113106565
|
A | ATGGAAAG others(4): Show |
1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+662_64+663insGA others(9): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106565 | |||||
chr13:113106565
|
A | G | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+660A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106565 | ||||||
chr13:113106583
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+678G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106583 | ||||||
chr13:113106587
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+682C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106587 | ||||||
chr13:113106588
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+683A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106588 | ||||||
chr13:113106589
|
T | A | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+684T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106589 | ||||||
chr13:113106592
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+687A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106592 | ||||||
chr13:113106593
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+688A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106593 | ||||||
chr13:113106595
|
G | T | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+690G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106595 | ||||||
chr13:113106598
|
C | T | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+693C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106598 | ||||||
chr13:113106602
|
T | G | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+697T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106602 | ||||||
chr13:113106607
|
T | TGTGGGGA others(49): Show |
1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+703_64+704insTG others(54): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106607 | |||||
chr13:113106612
|
A | G | 3 | a0001c0001t0001g0243a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02630.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+707A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106612 | ||||||
chr13:113106622
|
A | ATGGAGGT others(129): Show |
5 | a0001c0001t0001g0087a0001c0001t0001g0101a0001c0001t0001g0103others(2): Show | 5 | HG01433.hp2 HG03098.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+720_64+721insAG others(134): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106622 | |||||
chr13:113106623
|
T | G | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+718T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106623 | ||||||
chr13:113106624
|
G | GGAGGTGT others(130): Show |
1 | a0001c0001t0002g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+720_64+721insAG others(135): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | |||||
chr13:113106624
|
G | GGAGGTGT others(127): Show |
1 | a0001c0001t0001g0193 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.64+720_64+721insAG others(132): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | |||||
chr13:113106624
|
G | GGAGGTGT others(128): Show |
34 | a0001c0001t0001g0064a0001c0001t0004g0026a0001c0001t0012g0079others(31): Show | 38 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(35): Show |
intron_variant | MODIFIER | c.64+720_64+721insAG others(133): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | |||||
chr13:113106624
|
G | GGAGGTGT others(127): Show |
1 | a0001c0001t0001g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+720_64+721insAG others(132): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | |||||
chr13:113106624
|
G | GGAGGTGT others(128): Show |
66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(63): Show | 119 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.64+720_64+721insAG others(133): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | |||||
chr13:113106624
|
G | GGAGGTGT others(129): Show |
2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | NA18955.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.64+720_64+721insAG others(134): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | |||||
chr13:113106624
|
G | GGAGGTGT others(129): Show |
1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.64+720_64+721insAG others(134): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | |||||
chr13:113106624
|
G | GGAGGTGT others(128): Show |
138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(135): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.64+720_64+721insAG others(133): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | |||||
chr13:113106624
|
G | GGGGATGG others(5): Show |
1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+722_64+723insAT others(10): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106624 | |||||
chr13:113106624
|
G | T | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+719G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106624 | ||||||
chr13:113106625
|
G | GAGGTGTG others(129): Show |
1 | a0001c0001t0001g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.64+720_64+721insAG others(134): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106625 | ||||||
chr13:113106640
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.64+735C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106640 | ||||||
chr13:113106723
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+818G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106723 | ||||||
chr13:113106750
|
T | TG | 8 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 8 | HG01243.hp2 HG01261.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+851dupG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113106750 | |||||
chr13:113106842
|
C | T | 1 | a0001c0001t0004g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64+937C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106842 | ||||||
chr13:113106846
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.64+941C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106846 | ||||||
chr13:113106888
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0106a0001c0001t0001g0107 | 5 | HG01109.hp1 HG02717.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+983G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113106888 | ||||||
chr13:113107199
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(63): Show | 116 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.64+1294C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107199 | ||||||
chr13:113107245
|
GGGTGTCC others(128): Show |
G | 1 | a0001c0001t0023g0200 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64+1343_64+1477del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107245 | |||||
chr13:113107249
|
G | T | 1 | a0001c0001t0002g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1344G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107249 | ||||||
chr13:113107250
|
T | G | 1 | a0001c0001t0002g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1345T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107250 | ||||||
chr13:113107251
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1346C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107251 | ||||||
chr13:113107254
|
GGGAGTGT others(27): Show |
G | 9 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(6): Show | 19 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.64+1383_64+1416del others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107254 | |||||
chr13:113107257
|
A | AGTGTGGG others(10): Show |
1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1365_64+1366ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107257 | |||||
chr13:113107271
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.64+1366G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107271 | ||||||
chr13:113107271
|
GGGGGCGT others(10): Show |
G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.64+1369_64+1385del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107271 | |||||
chr13:113107276
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 96 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.64+1371C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107276 | ||||||
chr13:113107278
|
TGGGTGTC others(163): Show |
T | 1 | a0001c0001t0001g0203 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.64+1383_64+1552del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107278 | |||||
chr13:113107287
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+1382C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107287 | ||||||
chr13:113107288
|
A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.64+1383A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107288 | ||||||
chr13:113107291
|
A | G | 2 | a0001c0001t0001g0235a0001c0001t0016g0242 | 2 | HG03209.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.64+1386A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107291 | ||||||
chr13:113107293
|
T | C | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1388T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107293 | ||||||
chr13:113107304
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.64+1399C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107304 | ||||||
chr13:113107308
|
G | A | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1403G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107308 | ||||||
chr13:113107309
|
G | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.64+1404G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107309 | ||||||
chr13:113107310
|
C | A | 3 | a0001c0001t0004g0025a0001c0001t0004g0026a0002c0010t0015g0097 | 5 | HG01496.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+1405C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107310 | ||||||
chr13:113107310
|
C | T | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0016g0242 | 3 | HG03098.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64+1405C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107310 | ||||||
chr13:113107310
|
CGTGGGTG others(146): Show |
C | 2 | a0001c0001t0004g0234a0001c0001t0017g0233 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.64+1420_64+1572del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107310 | |||||
chr13:113107312
|
TGGGTGTC others(129): Show |
T | 46 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(43): Show | 87 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.64+1470_64+1605del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107312 | |||||
chr13:113107325
|
A | G | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1420A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107325 | ||||||
chr13:113107327
|
T | C | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1422T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107327 | ||||||
chr13:113107336
|
C | T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1431C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107336 | ||||||
chr13:113107339
|
G | A | 1 | a0001c0001t0004g0026 | 2 | HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.64+1434G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107339 | ||||||
chr13:113107341
|
G | A | 2 | a0001c0001t0004g0025a0002c0010t0015g0097 | 3 | HG01496.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64+1436G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107341 | ||||||
chr13:113107344
|
C | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.64+1439C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107344 | ||||||
chr13:113107345
|
G | A | 30 | a0001c0001t0001g0064a0001c0003t0001g0060a0001c0003t0001g0070others(27): Show | 33 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(30): Show |
intron_variant | MODIFIER | c.64+1440G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107345 | ||||||
chr13:113107346
|
T | A | 2 | a0001c0001t0004g0025a0002c0010t0015g0097 | 3 | HG01496.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64+1441T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107346 | ||||||
chr13:113107346
|
TGGGTGTC others(27): Show |
T | 6 | a0001c0001t0001g0051a0001c0001t0001g0189a0001c0001t0001g0194others(3): Show | 7 | HG02129.hp2 HG02132.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+1470_64+1503del others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107346 | |||||
chr13:113107356
|
G | A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1451G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107356 | ||||||
chr13:113107369
|
TCCCGGAG others(23): Show |
T | 1 | a0001c0001t0001g0199 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.64+1465_64+1494del others(30): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107369 | ||||||
chr13:113107370
|
C | T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1465C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107370 | ||||||
chr13:113107373
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(74): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.64+1468G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107373 | ||||||
chr13:113107375
|
A | G | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(181): Show | 279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.64+1470A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107375 | ||||||
chr13:113107379
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.64+1474G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107379 | ||||||
chr13:113107380
|
A | T | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(181): Show | 279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.64+1475A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107380 | ||||||
chr13:113107390
|
G | A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1485G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107390 | ||||||
chr13:113107404
|
C | T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1499C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107404 | ||||||
chr13:113107407
|
G | A | 1 | a0001c0003t0010g0050 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1502G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107407 | ||||||
chr13:113107409
|
G | A | 5 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(2): Show | 6 | HG01496.hp2 HG01516.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+1504G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107409 | ||||||
chr13:113107412
|
A | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(190): Show | 298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.64+1507A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107412 | ||||||
chr13:113107412
|
A | T | 1 | a0001c0001t0023g0200 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64+1507A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107412 | ||||||
chr13:113107414
|
T | A | 5 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(2): Show | 6 | HG01496.hp2 HG01516.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+1509T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107414 | ||||||
chr13:113107414
|
T | TGGGTGTC others(10): Show |
1 | a0001c0001t0001g0043 | 2 | NA18960.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.64+1525_64+1526ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107414 | |||||
chr13:113107438
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1533C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107438 | ||||||
chr13:113107441
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1536G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107441 | ||||||
chr13:113107443
|
A | G | 20 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0043others(17): Show | 33 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.64+1538A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107443 | ||||||
chr13:113107446
|
C | A | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1541C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107446 | ||||||
chr13:113107448
|
A | AG | 6 | a0001c0001t0001g0101a0001c0001t0002g0091a0001c0001t0002g0096others(3): Show | 6 | HG01928.hp2 HG04115.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+1546dupG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107448 | |||||
chr13:113107448
|
A | AGGGTGTC others(96): Show |
1 | a0001c0001t0001g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(103): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107448 | |||||
chr13:113107448
|
A | AGGGTGTC others(200): Show |
1 | a0001c0001t0001g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(207): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107448 | |||||
chr13:113107448
|
A | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0043others(14): Show | 30 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.64+1543A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107448 | ||||||
chr13:113107453
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1548G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107453 | ||||||
chr13:113107458
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1553G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107458 | ||||||
chr13:113107460
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1555G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107460 | ||||||
chr13:113107461
|
A | G | 2 | a0001c0001t0002g0108a0001c0001t0006g0095 | 2 | NA18964.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.64+1556A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107461 | ||||||
chr13:113107467
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1562G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107467 | ||||||
chr13:113107475
|
G | A | 10 | a0001c0001t0001g0051a0001c0001t0001g0189a0001c0001t0001g0194others(7): Show | 11 | HG02129.hp2 HG02132.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+1570G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107475 | ||||||
chr13:113107479
|
G | GAGTGGGT others(78): Show |
1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1574_64+1575ins others(85): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107479 | ||||||
chr13:113107479
|
G | GCGTGGGT others(62): Show |
1 | a0001c0001t0001g0113 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(69): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107479 | |||||
chr13:113107479
|
G | T | 2 | a0001c0001t0002g0108a0001c0001t0006g0095 | 2 | NA18964.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.64+1574G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107479 | ||||||
chr13:113107480
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1575C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107480 | ||||||
chr13:113107482
|
T | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 5 | HG01516.hp1 HG02602.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1577T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107482 | ||||||
chr13:113107495
|
A | G | 6 | a0001c0001t0001g0043a0001c0001t0001g0145a0001c0001t0001g0184others(3): Show | 7 | HG01516.hp1 HG02602.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.64+1590A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107495 | ||||||
chr13:113107497
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.64+1592T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107497 | ||||||
chr13:113107497
|
TGTGGGTG others(485): Show |
T | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64+1593_64+2084del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107497 | ||||||
chr13:113107499
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.64+1594T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107499 | ||||||
chr13:113107506
|
C | T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1601C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107506 | ||||||
chr13:113107508
|
C | CA | 4 | a0001c0001t0001g0043a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 5 | HG01516.hp1 HG02602.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1603_64+1604ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107508 | ||||||
chr13:113107511
|
G | A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1606G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107511 | ||||||
chr13:113107513
|
G | GCGAGGGG others(29): Show |
1 | a0001c0001t0001g0147 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(36): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | ||||||
chr13:113107513
|
G | GCGAGGGT others(29): Show |
1 | a0001c0001t0002g0102 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(36): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | ||||||
chr13:113107513
|
G | GCGAGGGT others(29): Show |
1 | a0001c0001t0001g0148 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(36): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | ||||||
chr13:113107513
|
G | GCGAGGGT others(28): Show |
3 | a0001c0001t0001g0139a0001c0001t0004g0172a0003c0011t0001g0105 | 3 | HG00544.hp2 HG03195.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.64+1608_64+1609ins others(35): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | ||||||
chr13:113107513
|
G | GCGAGGGT others(27): Show |
1 | a0001c0001t0001g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | ||||||
chr13:113107513
|
G | GCGAGGGT others(28): Show |
1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(35): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | ||||||
chr13:113107513
|
G | GCGAGGGT others(29): Show |
1 | a0002c0002t0003g0144 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(36): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | ||||||
chr13:113107513
|
G | GTGTGGGT others(11): Show |
1 | a0001c0001t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.64+1608_64+1609ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | ||||||
chr13:113107513
|
G | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 5 | HG01516.hp1 HG02602.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1608G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107513 | ||||||
chr13:113107514
|
A | AGGGTGTC others(26): Show |
1 | a0001c0001t0001g0110 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.64+1610_64+1611ins others(33): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107514 | |||||
chr13:113107514
|
A | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(197): Show | 306 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.64+1609A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107514 | ||||||
chr13:113107516
|
T | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(125): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.64+1611T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107516 | ||||||
chr13:113107522
|
T | TCCCGGGG others(28): Show |
1 | a0001c0001t0002g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1623_64+1624ins others(35): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107522 | |||||
chr13:113107525
|
C | G | 1 | a0001c0003t0010g0050 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1620C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107525 | ||||||
chr13:113107529
|
A | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(123): Show | 215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.64+1624A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107529 | ||||||
chr13:113107540
|
C | CCCGGGGG others(27): Show |
1 | a0001c0001t0001g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+1639_64+1640ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107540 | |||||
chr13:113107540
|
C | T | 2 | a0001c0003t0010g0050a0002c0010t0015g0097 | 3 | HG01496.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1635C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107540 | ||||||
chr13:113107542
|
C | CA | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(122): Show | 214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.64+1637_64+1638ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107542 | ||||||
chr13:113107543
|
G | A | 9 | a0001c0001t0001g0051a0001c0001t0001g0189a0001c0001t0001g0194others(6): Show | 10 | HG01496.hp2 HG02129.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+1638G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107543 | ||||||
chr13:113107545
|
A | G | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.64+1640A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107545 | ||||||
chr13:113107547
|
G | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(122): Show | 214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.64+1642G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107547 | ||||||
chr13:113107550
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.64+1645A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107550 | ||||||
chr13:113107550
|
A | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.64+1645A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107550 | ||||||
chr13:113107565
|
T | C | 1 | a0001c0003t0014g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.64+1660T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107565 | ||||||
chr13:113107577
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(43): Show | 87 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.64+1672G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107577 | ||||||
chr13:113107582
|
A | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.64+1677A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107582 | ||||||
chr13:113107589
|
G | T | 1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+1684G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107589 | ||||||
chr13:113107590
|
T | G | 1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+1685T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107590 | ||||||
chr13:113107591
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+1686C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107591 | ||||||
chr13:113107593
|
C | G | 9 | a0001c0001t0001g0113a0001c0001t0002g0108a0001c0001t0004g0026others(6): Show | 10 | HG00673.hp1 HG02735.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+1688C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107593 | ||||||
chr13:113107608
|
C | CCCGGGGG others(27): Show |
1 | a0001c0001t0001g0064 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.64+1707_64+1708ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107608 | |||||
chr13:113107608
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(15): Show | 29 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.64+1703C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107608 | ||||||
chr13:113107613
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.64+1708A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107613 | ||||||
chr13:113107618
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.64+1713A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107618 | ||||||
chr13:113107618
|
A | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.64+1713A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107618 | ||||||
chr13:113107627
|
C | G | 43 | a0001c0001t0001g0043a0001c0001t0001g0099a0001c0001t0001g0110others(40): Show | 47 | HG00544.hp2 HG01515.hp2 HG01516.hp1 others(44): Show |
intron_variant | MODIFIER | c.64+1722C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107627 | ||||||
chr13:113107631
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64+1726A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107631 | ||||||
chr13:113107633
|
T | C | 1 | a0001c0001t0001g0044 | 2 | HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.64+1728T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107633 | ||||||
chr13:113107633
|
TGTGGGTG others(27): Show |
T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1762_64+1795del others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107633 | |||||
chr13:113107642
|
C | T | 43 | a0001c0001t0001g0043a0001c0001t0001g0099a0001c0001t0001g0110others(40): Show | 47 | HG00544.hp2 HG01515.hp2 HG01516.hp1 others(44): Show |
intron_variant | MODIFIER | c.64+1737C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107642 | ||||||
chr13:113107645
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 90 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.64+1740G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107645 | ||||||
chr13:113107647
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(90): Show | 138 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.64+1742G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107647 | ||||||
chr13:113107647
|
GGGCGTGG others(113): Show |
G | 1 | a0001c0001t0001g0199 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.64+1744_64+1863del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107647 | |||||
chr13:113107649
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64+1744G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107649 | ||||||
chr13:113107650
|
C | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0064others(15): Show | 29 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.64+1745C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107650 | ||||||
chr13:113107650
|
CGTGGGTG others(112): Show |
C | 3 | a0001c0001t0001g0189a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG03098.hp2 HG03471.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.64+1762_64+1880del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107650 | |||||
chr13:113107652
|
T | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(89): Show | 137 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.64+1747T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107652 | ||||||
chr13:113107652
|
T | G | 1 | a0002c0002t0003g0240 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.64+1747T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107652 | ||||||
chr13:113107654
|
G | GGTGTCCG others(27): Show |
1 | a0001c0001t0001g0142 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.64+1755_64+1756ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107654 | |||||
chr13:113107655
|
G | GTGTCCGG others(28): Show |
1 | a0001c0001t0001g0101 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.64+1755_64+1756ins others(35): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107655 | |||||
chr13:113107661
|
C | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(121): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.64+1756C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107661 | ||||||
chr13:113107667
|
C | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(243): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.64+1762C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107667 | ||||||
chr13:113107676
|
C | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(119): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.64+1771C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107676 | ||||||
chr13:113107681
|
G | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(144): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.64+1776G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107681 | ||||||
chr13:113107684
|
C | A | 49 | a0001c0001t0001g0043a0001c0001t0001g0099a0001c0001t0001g0101others(46): Show | 54 | HG00544.hp2 HG01496.hp2 HG01515.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+1779C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107684 | ||||||
chr13:113107686
|
T | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(143): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.64+1781T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107686 | ||||||
chr13:113107686
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.64+1781T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107686 | ||||||
chr13:113107695
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.64+1790C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107695 | ||||||
chr13:113107710
|
C | T | 3 | a0001c0001t0001g0125a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1805C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107710 | ||||||
chr13:113107713
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.64+1808G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107713 | ||||||
chr13:113107715
|
G | A | 49 | a0001c0001t0001g0043a0001c0001t0001g0099a0001c0001t0001g0101others(46): Show | 54 | HG00544.hp2 HG01496.hp2 HG01515.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+1810G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107715 | ||||||
chr13:113107716
|
GGCGTGGG others(44): Show |
G | 2 | a0001c0001t0001g0005a0001c0001t0001g0031 | 9 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+1813_64+1863del others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107716 | |||||
chr13:113107718
|
C | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(121): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.64+1813C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107718 | ||||||
chr13:113107720
|
T | A | 49 | a0001c0001t0001g0043a0001c0001t0001g0099a0001c0001t0001g0101others(46): Show | 54 | HG00544.hp2 HG01496.hp2 HG01515.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+1815T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107720 | ||||||
chr13:113107720
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.64+1815T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107720 | ||||||
chr13:113107720
|
TGGGTGTC others(469): Show |
T | 1 | a0001c0001t0004g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64+1839_64+2314del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107720 | |||||
chr13:113107735
|
TGTGGGTG others(129): Show |
T | 4 | a0001c0001t0001g0051a0001c0001t0001g0194a0001c0001t0001g0209others(1): Show | 5 | HG02129.hp2 HG02132.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1839_64+1974del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107735 | |||||
chr13:113107739
|
G | C | 3 | a0001c0001t0001g0125a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1834G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107739 | ||||||
chr13:113107749
|
G | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(121): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.64+1844G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107749 | ||||||
chr13:113107750
|
GGCGTGGG others(10): Show |
G | 15 | a0001c0001t0001g0064a0001c0001t0001g0083a0001c0001t0001g0243others(12): Show | 19 | HG00673.hp1 HG02280.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+1847_64+1863del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107750 | |||||
chr13:113107752
|
C | CGAGGGGT others(45): Show |
1 | a0001c0001t0001g0151 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.64+1848_64+1849ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107752 | |||||
chr13:113107752
|
C | CGAGGGTG others(46): Show |
1 | a0001c0001t0001g0181 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64+1848_64+1849ins others(53): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107752 | |||||
chr13:113107754
|
T | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(118): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.64+1849T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107754 | ||||||
chr13:113107754
|
T | G | 1 | a0005c0005t0001g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64+1849T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107754 | ||||||
chr13:113107763
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64+1858C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107763 | ||||||
chr13:113107763
|
C | T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1858C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107763 | ||||||
chr13:113107767
|
A | G | 5 | a0001c0001t0001g0125a0001c0001t0001g0151a0001c0001t0001g0181others(2): Show | 6 | HG00733.hp2 HG02080.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+1862A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107767 | ||||||
chr13:113107769
|
T | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0064others(16): Show | 30 | HG00673.hp1 HG00733.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.64+1864T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107769 | ||||||
chr13:113107769
|
T | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0199a0001c0001t0016g0242others(1): Show | 5 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+1864T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107769 | ||||||
chr13:113107769
|
T | TGTGGGGT others(11): Show |
1 | a0001c0003t0001g0060 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.64+1869_64+1870ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | |||||
chr13:113107769
|
T | TGTGGGTG others(10): Show |
40 | a0001c0001t0001g0043a0001c0001t0001g0099a0001c0001t0001g0110others(37): Show | 44 | HG01496.hp2 HG01516.hp1 HG01517.hp2 others(41): Show |
intron_variant | MODIFIER | c.64+1878_64+1879ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | |||||
chr13:113107769
|
T | TGTGGGTG others(10): Show |
1 | a0001c0001t0001g0111 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | |||||
chr13:113107769
|
T | TGTGGGTG others(45): Show |
1 | a0001c0001t0001g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | |||||
chr13:113107769
|
T | TGTGGGTG others(45): Show |
1 | a0001c0001t0001g0114 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | |||||
chr13:113107769
|
T | TGTGGGTG others(44): Show |
116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.64+1878_64+1879ins others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | |||||
chr13:113107769
|
T | TGTGGGTG others(45): Show |
1 | a0005c0005t0001g0140 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | |||||
chr13:113107769
|
T | TGTGGGTG others(44): Show |
1 | a0001c0001t0001g0180 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | |||||
chr13:113107769
|
T | TGTGGGTG others(45): Show |
1 | a0001c0001t0001g0098 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | |||||
chr13:113107769
|
T | TGTGGGTG others(146): Show |
1 | a0001c0001t0001g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64+1872_64+1873ins others(153): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107769 | |||||
chr13:113107771
|
T | TGGGTGTC others(11): Show |
2 | a0001c0001t0001g0101a0002c0002t0003g0240 | 2 | NA19054.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.64+1878_64+1879ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107771 | |||||
chr13:113107771
|
T | TGGGTGTC others(249): Show |
1 | a0001c0001t0001g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(256): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107771 | |||||
chr13:113107776
|
G | GTCCCGGG others(11): Show |
1 | a0001c0001t0002g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107776 | |||||
chr13:113107778
|
C | CCCGGGGG others(9): Show |
1 | a0001c0001t0001g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.64+1878_64+1879ins others(16): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107778 | |||||
chr13:113107778
|
CCCGGGAG others(10): Show |
C | 50 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(47): Show | 91 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.64+1878_64+1894del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107778 | |||||
chr13:113107780
|
C | T | 1 | a0001c0003t0010g0050 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1875C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107780 | ||||||
chr13:113107784
|
A | G | 4 | a0001c0001t0001g0139a0001c0001t0016g0242a0001c0003t0010g0050others(1): Show | 5 | HG00544.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+1879A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107784 | ||||||
chr13:113107786
|
T | A | 2 | a0001c0001t0001g0139a0003c0011t0001g0105 | 2 | HG00544.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.64+1881T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107786 | ||||||
chr13:113107786
|
T | C | 2 | a0001c0001t0016g0242a0001c0003t0010g0050 | 3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1881T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107786 | ||||||
chr13:113107795
|
T | C | 4 | a0001c0001t0001g0189a0001c0001t0001g0199a0001c0001t0001g0201others(1): Show | 4 | HG03098.hp2 HG03471.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1890T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107795 | ||||||
chr13:113107805
|
A | AG | 4 | a0001c0001t0001g0115a0001c0001t0001g0139a0001c0001t0001g0143others(1): Show | 4 | HG00544.hp2 HG03710.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+1903dupG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107805 | |||||
chr13:113107808
|
GTGTCCCG others(9): Show |
G | 1 | a0001c0001t0001g0207 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.64+1904_64+1919del others(16): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107808 | ||||||
chr13:113107810
|
G | A | 2 | a0001c0001t0016g0242a0001c0003t0010g0050 | 3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1905G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107810 | ||||||
chr13:113107815
|
G | A | 2 | a0001c0001t0016g0242a0001c0003t0010g0050 | 3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1910G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107815 | ||||||
chr13:113107817
|
G | A | 2 | a0001c0001t0016g0242a0001c0003t0010g0050 | 3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1912G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107817 | ||||||
chr13:113107820
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.64+1915T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107820 | ||||||
chr13:113107820
|
T | TGTGAGTG others(10): Show |
1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.64+1918_64+1919ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107820 | |||||
chr13:113107820
|
TGTGCGTG others(10): Show |
T | 52 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(49): Show | 93 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.64+1919_64+1935del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107820 | |||||
chr13:113107824
|
C | A | 1 | a0001c0003t0010g0050 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1919C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107824 | ||||||
chr13:113107824
|
C | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0189a0001c0001t0016g0242 | 3 | HG02080.hp2 HG03209.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.64+1919C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107824 | ||||||
chr13:113107832
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0022g0007a0001c0003t0010g0050 | 9 | HG01069.hp2 HG01106.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+1927G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107832 | ||||||
chr13:113107835
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.64+1930G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107835 | ||||||
chr13:113107837
|
C | CGTGGGTG others(10): Show |
1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+1946_64+1947ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107837 | |||||
chr13:113107837
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0016g0242 | 2 | HG03209.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.64+1932C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107837 | ||||||
chr13:113107839
|
TGGGTGTC others(350): Show |
T | 1 | a0001c0001t0001g0189 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.64+1947_64+2303del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107839 | |||||
chr13:113107854
|
C | T | 1 | a0001c0003t0010g0050 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1949C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107854 | ||||||
chr13:113107857
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.64+1952G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107857 | ||||||
chr13:113107859
|
G | T | 1 | a0001c0001t0002g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+1954G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107859 | ||||||
chr13:113107866
|
G | A | 1 | a0002c0002t0021g0061 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.64+1961G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107866 | ||||||
chr13:113107869
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 96 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.64+1964G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107869 | ||||||
chr13:113107871
|
C | CGTGGGTG others(10): Show |
1 | a0001c0003t0010g0050 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.64+1974_64+1975ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107871 | |||||
chr13:113107871
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 96 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.64+1966C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107871 | ||||||
chr13:113107883
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 99 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.64+1978G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107883 | ||||||
chr13:113107888
|
C | T | 2 | a0001c0001t0016g0242a0001c0003t0010g0050 | 3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1983C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107888 | ||||||
chr13:113107890
|
A | AGGGTGTC others(727): Show |
1 | a0001c0001t0001g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+1989_64+1990ins others(734): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107890 | |||||
chr13:113107895
|
A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0125others(2): Show | 13 | HG01069.hp1 HG01071.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+1990A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107895 | ||||||
chr13:113107900
|
A | G | 2 | a0001c0001t0016g0242a0001c0003t0010g0050 | 3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+1995A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107900 | ||||||
chr13:113107902
|
A | G | 3 | a0001c0001t0001g0125a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1997A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107902 | ||||||
chr13:113107903
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+1998A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107903 | ||||||
chr13:113107909
|
A | G | 3 | a0001c0001t0001g0125a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2004A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107909 | ||||||
chr13:113107914
|
C | T | 2 | a0001c0001t0016g0242a0001c0003t0010g0050 | 3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+2009C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107914 | ||||||
chr13:113107917
|
A | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.64+2012A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107917 | ||||||
chr13:113107919
|
G | A | 2 | a0001c0001t0016g0242a0001c0003t0010g0050 | 3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+2014G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107919 | ||||||
chr13:113107922
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 99 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.64+2017C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107922 | ||||||
chr13:113107924
|
T | A | 2 | a0001c0001t0016g0242a0001c0003t0010g0050 | 3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+2019T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107924 | ||||||
chr13:113107933
|
C | A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2028C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107933 | ||||||
chr13:113107937
|
G | A | 3 | a0001c0001t0001g0125a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02080.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2032G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107937 | ||||||
chr13:113107939
|
T | C | 4 | a0001c0001t0001g0117a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | HG01099.hp1 HG01496.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2034T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107939 | ||||||
chr13:113107939
|
TGTGGGTG others(9): Show |
T | 1 | a0001c0001t0001g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+2035_64+2050del others(16): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107939 | ||||||
chr13:113107939
|
TGTGGGTG others(43): Show |
T | 6 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 6 | HG01261.hp1 HG01261.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+2035_64+2084del others(50): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107939 | ||||||
chr13:113107939
|
TGTGGGTG others(247): Show |
T | 49 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 90 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.64+2035_64+2288del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107939 | ||||||
chr13:113107939
|
TGTGGGTG others(367): Show |
T | 1 | a0001c0001t0001g0057 | 2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.64+2035_65-2377del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107939 | ||||||
chr13:113107955
|
G | GCGTGGGT others(11): Show |
2 | a0001c0001t0016g0242a0001c0003t0010g0050 | 3 | HG02630.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64+2065_64+2066ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113107955 | |||||
chr13:113107956
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+2051C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107956 | ||||||
chr13:113107956
|
C | T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2051C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107956 | ||||||
chr13:113107971
|
A | G | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2066A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107971 | ||||||
chr13:113107972
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.64+2067G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107972 | ||||||
chr13:113107973
|
TGTGGGTG others(9): Show |
T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2069_64+2084del others(16): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107973 | ||||||
chr13:113107982
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+2077T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107982 | ||||||
chr13:113107985
|
G | A | 1 | a0001c0001t0001g0045 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.64+2080G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107985 | ||||||
chr13:113107987
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0179 | 2 | HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.64+2082A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107987 | ||||||
chr13:113107990
|
T | C | 18 | a0001c0001t0001g0035a0001c0001t0001g0119a0001c0001t0001g0125others(15): Show | 20 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.64+2085T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107990 | ||||||
chr13:113107992
|
A | T | 8 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0201others(5): Show | 8 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+2087A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113107992 | ||||||
chr13:113108001
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.64+2096C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108001 | ||||||
chr13:113108016
|
T | C | 9 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0199others(6): Show | 9 | HG01261.hp1 HG01261.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+2111T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108016 | ||||||
chr13:113108019
|
G | A | 4 | a0001c0001t0001g0036a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 5 | HG01358.hp1 HG01361.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+2114G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108019 | ||||||
chr13:113108021
|
A | G | 3 | a0001c0001t0001g0150a0001c0001t0001g0179a0001c0001t0001g0194 | 3 | HG01934.hp1 HG02293.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.64+2116A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108021 | ||||||
chr13:113108026
|
A | AGGGTGTC others(27): Show |
2 | a0001c0001t0001g0150a0001c0001t0001g0179 | 2 | HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.64+2133_64+2134ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108026 | |||||
chr13:113108026
|
A | T | 1 | a0001c0001t0001g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+2121A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108026 | ||||||
chr13:113108032
|
TCCCGGGA others(11): Show |
T | 1 | a0001c0001t0001g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+2130_64+2147del others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108032 | |||||
chr13:113108041
|
T | TGTGGGGT others(11): Show |
1 | a0001c0001t0001g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.64+2141_64+2142ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108041 | |||||
chr13:113108041
|
T | TGTGGGTT others(12): Show |
1 | a0001c0001t0002g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+2142_64+2143ins others(19): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108041 | |||||
chr13:113108050
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0179a0002c0010t0015g0097 | 3 | HG01496.hp2 HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.64+2145C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108050 | ||||||
chr13:113108052
|
C | G | 1 | a0002c0002t0003g0144 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.64+2147C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108052 | ||||||
chr13:113108053
|
G | A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2148G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108053 | ||||||
chr13:113108055
|
G | A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2150G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108055 | ||||||
chr13:113108057
|
G | GCGTGGGT others(11): Show |
170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(167): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.64+2167_64+2168ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108057 | |||||
chr13:113108057
|
G | GCGTGGGT others(45): Show |
1 | a0001c0001t0001g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+2167_64+2168ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108057 | |||||
chr13:113108057
|
G | GCGTGGGT others(12): Show |
1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.64+2159_64+2160ins others(19): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108057 | |||||
chr13:113108058
|
C | T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2153C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108058 | ||||||
chr13:113108058
|
CGTGGGTG others(300): Show |
C | 2 | a0001c0001t0001g0204a0001c0001t0001g0210 | 2 | NA18612.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.64+2168_65-2311del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108058 | |||||
chr13:113108060
|
T | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0179a0002c0010t0015g0097 | 3 | HG01496.hp2 HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.64+2155T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108060 | ||||||
chr13:113108061
|
G | GGGTGTCC others(10): Show |
1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+2167_64+2168ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108061 | |||||
chr13:113108069
|
C | CGGGGGTC others(11): Show |
1 | a0001c0001t0002g0178 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.64+2167_64+2168ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108069 | |||||
chr13:113108070
|
GGGAGTGT others(316): Show |
G | 1 | a0001c0001t0001g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+2168_65-2295del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108070 | |||||
chr13:113108071
|
GGAGTGTG others(77): Show |
G | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0002c0002t0003g0063 | 3 | HG01978.hp1 HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.64+2168_64+2251del others(84): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108071 | |||||
chr13:113108073
|
A | G | 6 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 6 | HG01261.hp1 HG01261.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+2168A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108073 | ||||||
chr13:113108075
|
T | C | 6 | a0001c0001t0001g0125a0001c0001t0001g0197a0001c0001t0001g0199others(3): Show | 6 | HG01261.hp1 HG01261.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+2170T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108075 | ||||||
chr13:113108077
|
TGGGTGTT others(10): Show |
T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2179_64+2195del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108077 | |||||
chr13:113108084
|
T | C | 6 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 6 | HG01261.hp1 HG01261.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+2179T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108084 | ||||||
chr13:113108086
|
C | T | 1 | a0002c0002t0003g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2181C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108086 | ||||||
chr13:113108087
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0179 | 2 | HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.64+2182G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108087 | ||||||
chr13:113108089
|
A | G | 6 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 6 | HG01261.hp1 HG01261.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+2184A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108089 | ||||||
chr13:113108090
|
G | A | 1 | a0002c0002t0003g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2185G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108090 | ||||||
chr13:113108092
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(173): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.64+2187T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108092 | ||||||
chr13:113108092
|
T | TC | 5 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0201others(2): Show | 5 | HG01261.hp1 HG01261.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2187_64+2188ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108092 | ||||||
chr13:113108094
|
A | T | 6 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 6 | HG01261.hp1 HG01261.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+2189A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108094 | ||||||
chr13:113108101
|
C | T | 1 | a0002c0002t0003g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2196C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108101 | ||||||
chr13:113108104
|
G | A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.64+2199G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108104 | ||||||
chr13:113108106
|
G | A | 1 | a0002c0002t0003g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2201G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108106 | ||||||
chr13:113108107
|
A | G | 2 | a0002c0002t0003g0073a0002c0010t0015g0097 | 2 | HG01496.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.64+2202A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108107 | ||||||
chr13:113108109
|
T | C | 1 | a0002c0002t0003g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2204T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108109 | ||||||
chr13:113108111
|
T | A | 1 | a0002c0002t0003g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2206T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108111 | ||||||
chr13:113108118
|
T | C | 8 | a0001c0001t0001g0123a0001c0001t0001g0197a0001c0001t0001g0199others(5): Show | 8 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+2213T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108118 | ||||||
chr13:113108123
|
A | G | 7 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 7 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+2218A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108123 | ||||||
chr13:113108124
|
G | A | 1 | a0002c0002t0003g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2219G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108124 | ||||||
chr13:113108126
|
C | A | 6 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0201others(3): Show | 6 | HG01261.hp1 HG01261.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+2221C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108126 | ||||||
chr13:113108126
|
C | T | 1 | a0002c0002t0003g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2221C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108126 | ||||||
chr13:113108128
|
A | AG | 5 | a0001c0001t0001g0103a0001c0001t0001g0155a0001c0001t0002g0091others(2): Show | 5 | HG03098.hp1 HG03942.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+2226dupG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108128 | |||||
chr13:113108128
|
A | AGGGTGTC others(44): Show |
1 | a0002c0002t0003g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2249_64+2250ins others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108128 | |||||
chr13:113108128
|
A | T | 7 | a0001c0001t0001g0197a0001c0001t0001g0199a0001c0001t0001g0201others(4): Show | 7 | HG01261.hp1 HG01261.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+2223A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108128 | ||||||
chr13:113108141
|
A | AGTGTGGG others(10): Show |
3 | a0001c0001t0001g0180a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2249_64+2250ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108141 | |||||
chr13:113108141
|
A | G | 1 | a0002c0002t0003g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2236A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108141 | ||||||
chr13:113108143
|
T | C | 1 | a0002c0002t0003g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2238T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108143 | ||||||
chr13:113108143
|
T | TGTGGGTG others(44): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0031 | 9 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+2246_64+2247ins others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108143 | |||||
chr13:113108152
|
CCCAGGGG others(350): Show |
C | 1 | a0001c0001t0001g0199 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.64+2250_65-2179del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108152 | |||||
chr13:113108155
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.64+2250A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108155 | ||||||
chr13:113108155
|
A | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(185): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.64+2250A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108155 | ||||||
chr13:113108158
|
GGCGTGGG others(351): Show |
G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.64+2270_65-2158del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108158 | |||||
chr13:113108159
|
G | GCGTGGGT others(11): Show |
175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(172): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.64+2269_64+2270ins others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108159 | |||||
chr13:113108159
|
G | GCGTGGGT others(13): Show |
1 | a0001c0001t0002g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64+2261_64+2262ins others(20): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108159 | |||||
chr13:113108159
|
G | GGCGTGGG others(12): Show |
2 | a0001c0001t0001g0124a0001c0001t0001g0139 | 2 | HG00544.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.64+2254_64+2255ins others(19): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108159 | ||||||
chr13:113108159
|
G | GT | 3 | a0001c0001t0001g0005a0001c0001t0001g0031a0002c0002t0003g0073 | 10 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+2254_64+2255ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108159 | ||||||
chr13:113108159
|
G | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0002c0002t0003g0063 | 3 | HG01978.hp1 HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.64+2254G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108159 | ||||||
chr13:113108160
|
C | A | 1 | a0002c0002t0003g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2255C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108160 | ||||||
chr13:113108160
|
C | T | 3 | a0001c0001t0001g0180a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2255C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108160 | ||||||
chr13:113108162
|
T | TGGGTGTT others(10): Show |
1 | a0001c0001t0001g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+2263_64+2264ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108162 | |||||
chr13:113108168
|
T | TCCCGGGG others(12): Show |
1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.64+2269_64+2270ins others(19): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108168 | |||||
chr13:113108171
|
C | G | 2 | a0001c0001t0001g0197a0001c0001t0001g0229 | 2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.64+2266C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108171 | ||||||
chr13:113108172
|
GGGAGTGT others(350): Show |
G | 2 | a0001c0001t0001g0197a0001c0001t0001g0229 | 2 | HG01261.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.64+2270_65-2159del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108172 | |||||
chr13:113108175
|
A | G | 1 | a0001c0001t0004g0025 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64+2270A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108175 | ||||||
chr13:113108177
|
TGTGGGTG others(9): Show |
T | 1 | a0001c0001t0004g0025 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.64+2273_64+2288del others(16): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108177 | ||||||
chr13:113108186
|
T | C | 3 | a0001c0001t0001g0180a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2281T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108186 | ||||||
chr13:113108188
|
C | T | 32 | a0001c0001t0001g0064a0001c0001t0012g0079a0001c0001t0012g0080others(29): Show | 35 | HG00673.hp1 HG01496.hp2 HG01515.hp2 others(32): Show |
intron_variant | MODIFIER | c.64+2283C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108188 | ||||||
chr13:113108191
|
A | G | 3 | a0001c0001t0001g0180a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2286A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108191 | ||||||
chr13:113108194
|
C | A | 3 | a0001c0001t0001g0180a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2289C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108194 | ||||||
chr13:113108196
|
A | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(50): Show | 96 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.64+2291A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108196 | ||||||
chr13:113108206
|
G | A | 1 | a0002c0002t0003g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2301G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108206 | ||||||
chr13:113108220
|
T | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(47): Show | 91 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.64+2315T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108220 | ||||||
chr13:113108223
|
G | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0189a0001c0001t0001g0209others(1): Show | 5 | HG02129.hp2 HG02132.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2318G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108223 | ||||||
chr13:113108225
|
A | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0104a0001c0001t0001g0209 | 4 | HG02129.hp2 HG02132.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2320A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108225 | ||||||
chr13:113108228
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+2323C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108228 | ||||||
chr13:113108230
|
A | AG | 4 | a0001c0001t0001g0106a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG03927.hp1 HG03927.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2328dupG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108230 | |||||
chr13:113108230
|
A | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0104a0001c0001t0001g0209 | 4 | HG02129.hp2 HG02132.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2325A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108230 | ||||||
chr13:113108235
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0004g0236 | 2 | HG02145.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.64+2330G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108235 | ||||||
chr13:113108239
|
C | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0209 | 3 | HG02129.hp2 HG02132.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.64+2334C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108239 | ||||||
chr13:113108240
|
G | A | 6 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0004g0236others(3): Show | 7 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+2335G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108240 | ||||||
chr13:113108242
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0004g0236 | 2 | HG02145.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.64+2337G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108242 | ||||||
chr13:113108243
|
A | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0104a0001c0001t0001g0209 | 4 | HG02129.hp2 HG02132.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2338A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108243 | ||||||
chr13:113108244
|
G | A | 1 | a0002c0002t0009g0027 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.64+2339G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108244 | ||||||
chr13:113108245
|
T | C | 4 | a0001c0001t0001g0051a0001c0001t0001g0180a0001c0001t0001g0209others(1): Show | 5 | HG02129.hp2 HG02132.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2340T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108245 | ||||||
chr13:113108247
|
T | TGGGTGTT others(10): Show |
3 | a0001c0001t0001g0180a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2348_64+2349ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108247 | |||||
chr13:113108249
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0004g0236 | 2 | HG02145.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.64+2344G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108249 | ||||||
chr13:113108257
|
G | A | 3 | a0001c0001t0001g0180a0001c0001t0016g0242a0001c0003t0010g0050 | 4 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2352G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108257 | ||||||
chr13:113108260
|
G | A | 4 | a0001c0001t0001g0104a0001c0001t0001g0180a0001c0001t0016g0242others(1): Show | 5 | HG02630.hp1 HG02723.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+2355G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108260 | ||||||
chr13:113108260
|
G | GGTGTGGG others(129): Show |
1 | a0001c0001t0001g0175 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64+2356_64+2357ins others(136): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108260 | |||||
chr13:113108261
|
GCGTGGGT others(95): Show |
G | 1 | a0001c0001t0001g0230 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.64+2357_65-2327del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108261 | ||||||
chr13:113108262
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(173): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.64+2357C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108262 | ||||||
chr13:113108262
|
CGTGGGTG others(96): Show |
C | 46 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(43): Show | 86 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.64+2375_65-2308del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108262 | |||||
chr13:113108274
|
G | GGGAGTGT others(111): Show |
1 | a0001c0001t0001g0126 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.64+2371_64+2372ins others(118): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108274 | |||||
chr13:113108277
|
G | A | 1 | a0002c0002t0003g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2372G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108277 | ||||||
chr13:113108278
|
GT | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(153): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.64+2375delT | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108278 | |||||
chr13:113108279
|
T | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0175 | 2 | HG00544.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.64+2374T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | ||||||
chr13:113108279
|
T | TGTGGGGT others(130): Show |
1 | a0001c0001t0001g0143 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.64+2374_64+2375ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | ||||||
chr13:113108279
|
T | TGTGGGTG others(26): Show |
14 | a0001c0001t0001g0020a0001c0003t0001g0060a0001c0003t0001g0070others(11): Show | 17 | HG01515.hp2 HG01517.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.64+2374_64+2375ins others(33): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | ||||||
chr13:113108279
|
T | TGTGGGTG others(130): Show |
1 | a0001c0001t0001g0156 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.64+2374_64+2375ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | ||||||
chr13:113108279
|
T | TGTGGGTG others(129): Show |
1 | a0002c0002t0003g0144 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.64+2374_64+2375ins others(136): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | ||||||
chr13:113108279
|
T | TGTGGGTG others(129): Show |
1 | a0001c0001t0002g0091 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.64+2374_64+2375ins others(136): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108279 | ||||||
chr13:113108280
|
T | A | 15 | a0001c0001t0001g0020a0001c0001t0001g0104a0001c0003t0001g0060others(12): Show | 18 | HG01515.hp2 HG01517.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.64+2375T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108280 | ||||||
chr13:113108280
|
T | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0051others(25): Show | 40 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.64+2375T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108280 | ||||||
chr13:113108280
|
T | G | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.64+2375T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108280 | ||||||
chr13:113108281
|
G | T | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.64+2376G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108281 | ||||||
chr13:113108282
|
T | G | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.64+2377T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108282 | ||||||
chr13:113108295
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0002c0002t0003g0072 | 3 | HG03239.hp2 HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.64+2390A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108295 | ||||||
chr13:113108297
|
T | A | 1 | a0002c0002t0003g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64+2392T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108297 | ||||||
chr13:113108297
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+2392T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108297 | ||||||
chr13:113108299
|
T | TGGGTGTT others(10): Show |
1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-2377_65-2376ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108299 | |||||
chr13:113108306
|
T | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(163): Show | 259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.65-2384T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108306 | ||||||
chr13:113108308
|
C | T | 1 | a0002c0002t0003g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.65-2382C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108308 | ||||||
chr13:113108311
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(159): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.65-2379A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108311 | ||||||
chr13:113108314
|
C | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(159): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.65-2376C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108314 | ||||||
chr13:113108316
|
A | AGGGTGTC others(95): Show |
1 | a0001c0001t0001g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.65-2365_65-2364ins others(102): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108316 | |||||
chr13:113108316
|
A | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(160): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.65-2374A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108316 | ||||||
chr13:113108326
|
G | A | 14 | a0001c0001t0001g0020a0001c0003t0001g0060a0001c0003t0001g0070others(11): Show | 17 | HG01515.hp2 HG01517.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.65-2364G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108326 | ||||||
chr13:113108331
|
T | C | 8 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0006g0034others(5): Show | 13 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-2359T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108331 | ||||||
chr13:113108333
|
TGGGTGTT others(10): Show |
T | 3 | a0001c0001t0001g0051a0001c0001t0001g0189a0001c0001t0001g0209 | 4 | HG02129.hp2 HG02132.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2350_65-2334del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108333 | |||||
chr13:113108340
|
T | C | 13 | a0001c0001t0001g0057a0001c0001t0001g0104a0001c0001t0001g0126others(10): Show | 15 | HG00544.hp1 HG01934.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.65-2350T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108340 | ||||||
chr13:113108340
|
T | TCCGGAGG others(128): Show |
1 | a0001c0001t0001g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(135): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108340 | |||||
chr13:113108340
|
T | TCCGGAGG others(130): Show |
1 | a0001c0001t0001g0127 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108340 | |||||
chr13:113108345
|
A | C | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-2345A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108345 | ||||||
chr13:113108345
|
A | G | 1 | a0001c0001t0004g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-2345A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108345 | ||||||
chr13:113108350
|
A | AGGGTGTC others(95): Show |
1 | a0001c0001t0018g0192 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(102): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108350 | |||||
chr13:113108350
|
A | AGGGTGTC others(131): Show |
1 | a0001c0001t0001g0152 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(138): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108350 | |||||
chr13:113108350
|
A | AGGGTGTC others(96): Show |
1 | a0001c0001t0002g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(103): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108350 | |||||
chr13:113108350
|
A | AGGGTGTC others(59): Show |
1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-2329_65-2328ins others(66): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108350 | |||||
chr13:113108350
|
A | T | 1 | a0001c0001t0004g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-2340A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108350 | ||||||
chr13:113108352
|
G | A | 1 | a0001c0003t0010g0050 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.65-2338G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108352 | ||||||
chr13:113108353
|
G | T | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65-2337G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108353 | ||||||
chr13:113108356
|
T | TCCCAGGA others(130): Show |
1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.65-2331_65-2330ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108356 | |||||
chr13:113108360
|
G | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(147): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.65-2330G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108360 | ||||||
chr13:113108363
|
A | G | 4 | a0001c0001t0001g0051a0001c0001t0001g0189a0001c0001t0001g0209others(1): Show | 5 | HG02129.hp2 HG02132.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-2327A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108363 | ||||||
chr13:113108365
|
T | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(143): Show | 238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.65-2325T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108365 | ||||||
chr13:113108367
|
T | TGGGTGTT others(10): Show |
1 | a0001c0001t0004g0136 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-2317_65-2316ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108367 | |||||
chr13:113108367
|
T | TGGGTGTT others(10): Show |
1 | a0001c0001t0001g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.65-2317_65-2316ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108367 | |||||
chr13:113108374
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(140): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.65-2316C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108374 | ||||||
chr13:113108377
|
G | A | 3 | a0001c0001t0001g0186a0001c0001t0004g0136a0002c0010t0015g0097 | 3 | HG01496.hp2 HG02451.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.65-2313G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108377 | ||||||
chr13:113108378
|
G | GAGGCGA | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(139): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.65-2312_65-2311ins others(6): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108378 | ||||||
chr13:113108379
|
G | A | 2 | a0001c0001t0002g0096a0001c0001t0018g0192 | 2 | NA18947.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.65-2311G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108379 | ||||||
chr13:113108380
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0004g0136 | 2 | HG02451.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.65-2310G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108380 | ||||||
chr13:113108382
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-2308T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108382 | ||||||
chr13:113108382
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.65-2308T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108382 | ||||||
chr13:113108382
|
T | TGTCCCAG others(4): Show |
142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(139): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.65-2306_65-2305ins others(11): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108382 | |||||
chr13:113108384
|
T | A | 2 | a0001c0001t0002g0096a0001c0001t0018g0192 | 2 | NA18947.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.65-2306T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108384 | ||||||
chr13:113108384
|
T | TCCCAGGA others(5): Show |
1 | a0001c0001t0001g0043 | 2 | NA18960.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.65-2306_65-2305ins others(12): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108384 | ||||||
chr13:113108397
|
G | A | 17 | a0001c0001t0001g0099a0001c0001t0002g0096a0001c0001t0004g0236others(14): Show | 18 | HG01515.hp2 HG01517.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.65-2293G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108397 | ||||||
chr13:113108398
|
G | T | 1 | a0001c0001t0001g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.65-2292G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108398 | ||||||
chr13:113108399
|
T | A | 1 | a0001c0001t0001g0020 | 3 | HG02257.hp1 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-2291T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108399 | ||||||
chr13:113108399
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(144): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.65-2291T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108399 | ||||||
chr13:113108399
|
T | TC | 67 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 109 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.65-2291_65-2290ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108399 | ||||||
chr13:113108408
|
C | CCCGGAGG others(27): Show |
1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-2278_65-2277ins others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108408 | |||||
chr13:113108410
|
C | T | 1 | a0002c0002t0003g0198 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.65-2280C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108410 | ||||||
chr13:113108411
|
G | A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-2279G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108411 | ||||||
chr13:113108414
|
A | G | 18 | a0001c0001t0001g0057a0001c0001t0001g0099a0001c0001t0002g0096others(15): Show | 20 | HG01496.hp2 HG01515.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.65-2276A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108414 | ||||||
chr13:113108416
|
T | A | 13 | a0001c0003t0001g0060a0001c0003t0001g0070a0002c0002t0003g0030others(10): Show | 14 | HG01515.hp2 HG01517.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-2274T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108416 | ||||||
chr13:113108416
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0002g0096a0001c0001t0018g0192 | 3 | NA18947.hp2 NA18955.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.65-2274T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108416 | ||||||
chr13:113108425
|
C | T | 15 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0126others(12): Show | 16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2265C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108425 | ||||||
chr13:113108427
|
C | CGGAGGCG others(45): Show |
1 | a0001c0001t0001g0020 | 3 | HG02257.hp1 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-2261_65-2260ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108427 | |||||
chr13:113108428
|
G | A | 1 | a0001c0001t0004g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-2262G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108428 | ||||||
chr13:113108430
|
G | A | 15 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0126others(12): Show | 16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2260G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108430 | ||||||
chr13:113108431
|
GGAGTGGG others(78): Show |
G | 1 | a0001c0001t0004g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-2257_65-2173del others(85): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108431 | |||||
chr13:113108432
|
G | GT | 3 | a0001c0001t0001g0099a0001c0001t0002g0096a0001c0001t0018g0192 | 3 | NA18947.hp2 NA18955.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.65-2258_65-2257ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108432 | ||||||
chr13:113108432
|
G | T | 1 | a0001c0001t0001g0020 | 3 | HG02257.hp1 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-2258G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108432 | ||||||
chr13:113108433
|
A | AGTGGGTG others(96): Show |
1 | a0002c0002t0003g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.65-2243_65-2242ins others(103): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108433 | |||||
chr13:113108433
|
A | C | 19 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0001g0100others(16): Show | 22 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.65-2257A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108433 | ||||||
chr13:113108435
|
T | A | 15 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0126others(12): Show | 16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2255T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108435 | ||||||
chr13:113108452
|
TGGGTGTT others(44): Show |
T | 54 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 96 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.65-2231_65-2181del others(51): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108452 | |||||
chr13:113108459
|
T | C | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(154): Show | 249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.65-2231T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108459 | ||||||
chr13:113108462
|
G | A | 15 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0126others(12): Show | 16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2228G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108462 | ||||||
chr13:113108479
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(174): Show | 272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.65-2211A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108479 | ||||||
chr13:113108484
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(171): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.65-2206C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108484 | ||||||
chr13:113108493
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0031others(17): Show | 32 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.65-2197C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108493 | ||||||
chr13:113108496
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0002g0096others(2): Show | 7 | HG02257.hp1 HG02258.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-2194G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108496 | ||||||
chr13:113108498
|
A | G | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(169): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.65-2192A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108498 | ||||||
chr13:113108501
|
C | A | 15 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0126others(12): Show | 16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2189C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108501 | ||||||
chr13:113108501
|
C | CGTGGGTG others(96): Show |
2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.65-2188_65-2187ins others(103): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108501 | |||||
chr13:113108503
|
A | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(169): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.65-2187A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108503 | ||||||
chr13:113108513
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(58): Show | 103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.65-2177G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108513 | ||||||
chr13:113108513
|
G | GGGGGTCG others(131): Show |
1 | a0002c0002t0003g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.65-2175_65-2174ins others(138): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108513 | |||||
chr13:113108513
|
G | GGGGGTCG others(131): Show |
1 | a0001c0001t0001g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.65-2175_65-2174ins others(138): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108513 | |||||
chr13:113108513
|
G | GGGGGTCG others(130): Show |
147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(144): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.65-2175_65-2174ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108513 | |||||
chr13:113108513
|
G | GGGGGTCG others(131): Show |
1 | a0002c0002t0003g0239 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.65-2175_65-2174ins others(138): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108513 | |||||
chr13:113108513
|
G | GGGGGTCG others(148): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0106a0001c0001t0001g0107 | 5 | HG01109.hp1 HG02717.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-2175_65-2174ins others(155): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108513 | |||||
chr13:113108516
|
A | AGTGTGGG others(10): Show |
15 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0126others(12): Show | 16 | HG00544.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-2173_65-2172ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108516 | |||||
chr13:113108516
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.65-2174A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108516 | ||||||
chr13:113108518
|
C | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0002g0096others(3): Show | 8 | HG01496.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-2172C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108518 | ||||||
chr13:113108519
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0189 | 3 | NA18945.hp2 NA19070.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.65-2171G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108519 | ||||||
chr13:113108529
|
C | CGGGAGTG others(130): Show |
2 | a0001c0001t0001g0157a0005c0005t0001g0140 | 2 | HG02809.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.65-2158_65-2157ins others(137): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108529 | |||||
chr13:113108529
|
C | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.65-2161C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108529 | ||||||
chr13:113108535
|
C | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0002g0096others(2): Show | 7 | HG02257.hp1 HG02258.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-2155C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108535 | ||||||
chr13:113108550
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.65-2140A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108550 | ||||||
chr13:113108563
|
C | CAGGGGCG others(45): Show |
2 | a0001c0001t0001g0020a0002c0002t0003g0073 | 4 | HG02257.hp1 HG02258.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-2127_65-2126ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108563 | ||||||
chr13:113108563
|
C | CAGGGGCG others(46): Show |
1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-2127_65-2126ins others(53): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108563 | ||||||
chr13:113108563
|
C | CAGGGGCG others(46): Show |
1 | a0001c0001t0018g0192 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.65-2127_65-2126ins others(53): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108563 | ||||||
chr13:113108563
|
C | CAGGGGCG others(47): Show |
1 | a0001c0001t0002g0096 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.65-2127_65-2126ins others(54): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108563 | ||||||
chr13:113108568
|
G | GT | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.65-2122_65-2121ins others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108568 | ||||||
chr13:113108568
|
G | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0099a0001c0001t0002g0096others(2): Show | 7 | HG02257.hp1 HG02258.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-2122G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108568 | ||||||
chr13:113108569
|
A | AGTGGGTG others(267): Show |
3 | a0001c0001t0004g0025a0001c0001t0005g0014a0001c0001t0005g0082 | 6 | HG02280.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-2076_65-2075ins others(274): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108569 | |||||
chr13:113108569
|
A | AGTGGGTG others(267): Show |
3 | a0001c0001t0001g0125a0001c0001t0001g0150a0001c0001t0001g0179 | 3 | HG01934.hp1 HG02080.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.65-2076_65-2075ins others(274): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108569 | |||||
chr13:113108569
|
A | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.65-2121A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108569 | ||||||
chr13:113108569
|
A | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0174a0001c0001t0001g0181 | 4 | HG02698.hp1 NA18951.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2121A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108569 | ||||||
chr13:113108584
|
A | AGTGTGGG others(267): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(2): Show | 12 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-2076_65-2075ins others(274): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108584 | |||||
chr13:113108615
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(63): Show | 108 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.65-2075A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108615 | ||||||
chr13:113108624
|
G | T | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65-2066G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108624 | ||||||
chr13:113108637
|
C | CGTGGGTG others(10): Show |
5 | a0001c0001t0001g0021a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 7 | HG02451.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-2044_65-2028dup others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108637 | |||||
chr13:113108649
|
GGGAGTGT others(180): Show |
G | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-2038_65-1852del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108649 | |||||
chr13:113108652
|
A | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.65-2038A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108652 | ||||||
chr13:113108654
|
TGTGGGTG others(214): Show |
T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.65-2035_65-1815del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108654 | ||||||
chr13:113108752
|
A | G | 2 | a0001c0001t0012g0079a0001c0001t0012g0080 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.65-1938A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108752 | ||||||
chr13:113108759
|
AGGGTGTC others(78): Show |
A | 58 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 100 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.65-1907_65-1823del others(85): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108759 | |||||
chr13:113108768
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.65-1922C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108768 | ||||||
chr13:113108768
|
CGGGAGTG others(11): Show |
C | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1918_65-1901del others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108768 | |||||
chr13:113108769
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.65-1921G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108769 | ||||||
chr13:113108776
|
T | TGGGTGTT others(10): Show |
1 | a0001c0001t0004g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-1908_65-1907ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108776 | |||||
chr13:113108786
|
A | G | 1 | a0001c0001t0004g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-1904A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108786 | ||||||
chr13:113108789
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0004g0236 | 2 | HG02145.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.65-1901G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108789 | ||||||
chr13:113108790
|
G | T | 1 | a0001c0001t0001g0031 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.65-1900G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108790 | ||||||
chr13:113108796
|
G | T | 1 | a0002c0002t0003g0068 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.65-1894G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108796 | ||||||
chr13:113108800
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0004g0236 | 2 | HG02145.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.65-1890C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108800 | ||||||
chr13:113108805
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0004g0236 | 2 | HG02145.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.65-1885G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108805 | ||||||
chr13:113108810
|
T | A | 2 | a0001c0001t0001g0210a0001c0001t0004g0236 | 2 | HG02145.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.65-1880T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108810 | ||||||
chr13:113108825
|
TGTGGGTG others(10): Show |
T | 1 | a0001c0001t0004g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-1850_65-1834del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108825 | |||||
chr13:113108834
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1856C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108834 | ||||||
chr13:113108839
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1851G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108839 | ||||||
chr13:113108841
|
G | T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-1849G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108841 | ||||||
chr13:113108842
|
A | C | 2 | a0001c0001t0001g0210a0002c0010t0015g0097 | 2 | HG01496.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.65-1848A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108842 | ||||||
chr13:113108844
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1846T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108844 | ||||||
chr13:113108861
|
TGGGTGTT others(197): Show |
T | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1822_65-1619del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108861 | |||||
chr13:113108878
|
A | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.65-1812A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108878 | ||||||
chr13:113108895
|
TGGGTGTT others(163): Show |
T | 9 | a0001c0001t0001g0012a0001c0001t0001g0053a0001c0001t0001g0057others(6): Show | 14 | HG01975.hp2 HG02015.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-1788_65-1619del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108895 | |||||
chr13:113108902
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0087a0001c0001t0001g0088 | 4 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-1788T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108902 | ||||||
chr13:113108905
|
G | A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-1785G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108905 | ||||||
chr13:113108912
|
AGGGTGTC others(78): Show |
A | 1 | a0001c0001t0004g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.65-1763_65-1679del others(85): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108912 | |||||
chr13:113108925
|
A | AGTGTGGG others(10): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(2): Show | 12 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-1764_65-1763ins others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108925 | |||||
chr13:113108927
|
C | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(233): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.65-1763C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108927 | ||||||
chr13:113108929
|
TGGGTGTC others(129): Show |
T | 48 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(45): Show | 85 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.65-1748_65-1613del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108929 | |||||
chr13:113108936
|
CCCGGGGG others(128): Show |
C | 1 | a0001c0001t0001g0207 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.65-1751_65-1617del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108936 | |||||
chr13:113108939
|
G | A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-1751G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108939 | ||||||
chr13:113108944
|
C | T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-1746C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108944 | ||||||
chr13:113108959
|
AGCGTGGG others(10): Show |
A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-1729_65-1713del others(17): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108959 | |||||
chr13:113108964
|
G | A | 32 | a0001c0001t0001g0064a0001c0001t0012g0079a0001c0001t0012g0080others(29): Show | 35 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(32): Show |
intron_variant | MODIFIER | c.65-1726G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108964 | ||||||
chr13:113108964
|
G | GGGTGTCC others(214): Show |
1 | a0001c0001t0005g0149 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.65-1657_65-1656ins others(221): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113108964 | |||||
chr13:113108973
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0118a0001c0001t0016g0242others(1): Show | 6 | HG00140.hp1 HG00738.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-1717A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108973 | ||||||
chr13:113108978
|
T | C | 6 | a0001c0001t0001g0016a0001c0001t0001g0110a0001c0001t0001g0115others(3): Show | 8 | HG00558.hp2 NA18612.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-1712T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113108978 | ||||||
chr13:113109034
|
A | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(186): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.65-1656A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109034 | ||||||
chr13:113109034
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.65-1656A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109034 | ||||||
chr13:113109123
|
C | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 100 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.65-1567C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109123 | ||||||
chr13:113109124
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.65-1566C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109124 | ||||||
chr13:113109128
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(56): Show | 101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.65-1562G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109128 | ||||||
chr13:113109133
|
T | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(56): Show | 101 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.65-1557T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109133 | ||||||
chr13:113109236
|
G | T | 1 | a0001c0003t0010g0050 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.65-1454G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109236 | ||||||
chr13:113109269
|
G | A | 1 | a0001c0001t0019g0214 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.65-1421G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109269 | ||||||
chr13:113109416
|
A | T | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.65-1274A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109416 | ||||||
chr13:113109474
|
A | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.65-1216A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109474 | ||||||
chr13:113109519
|
C | G | 2 | a0001c0001t0001g0043a0001c0001t0004g0026 | 4 | HG02886.hp1 NA18960.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-1171C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109519 | ||||||
chr13:113109612
|
G | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(100): Show | 171 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.65-1078G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109612 | ||||||
chr13:113109652
|
G | T | 1 | a0001c0001t0001g0135 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.65-1038G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109652 | ||||||
chr13:113109771
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.65-919A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109771 | ||||||
chr13:113109833
|
G | C | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-857G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109833 | ||||||
chr13:113109943
|
G | C | 1 | a0001c0001t0004g0025 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.65-747G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113109943 | ||||||
chr13:113110081
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.65-609G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110081 | ||||||
chr13:113110154
|
C | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0119a0001c0001t0004g0236 | 4 | HG02145.hp2 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-536C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110154 | ||||||
chr13:113110275
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.65-415T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110275 | ||||||
chr13:113110296
|
T | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(183): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.65-394T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110296 | ||||||
chr13:113110335
|
T | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.65-355T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110335 | ||||||
chr13:113110347
|
CG | C | 2 | a0001c0001t0005g0014a0001c0001t0005g0082 | 4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-339delG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 113110347 | |||||
chr13:113110435
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.65-255C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110435 | ||||||
chr13:113110510
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.65-180G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 1/7 | chr13 | 113110510 | ||||||
chr13:113110871
|
C | T | 11 | a0001c0001t0001g0012a0001c0001t0001g0053a0001c0001t0001g0057others(8): Show | 16 | HG01975.hp2 HG02015.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.225+21C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113110871 | ||||||
chr13:113110921
|
G | A | 29 | a0001c0001t0001g0064a0001c0001t0001g0163a0001c0001t0012g0079others(26): Show | 32 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.225+71G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113110921 | ||||||
chr13:113111039
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.225+189A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111039 | ||||||
chr13:113111061
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.225+211C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111061 | ||||||
chr13:113111321
|
G | GCTCACGG others(97): Show |
3 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083 | 10 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.225+563_225+564ins others(104): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111321 | |||||
chr13:113111321
|
G | GCTCACGG others(167): Show |
1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.225+542_225+543ins others(174): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111321 | |||||
chr13:113111321
|
GCTCACGG others(115): Show |
G | 5 | a0001c0001t0001g0188a0001c0001t0016g0242a0001c0001t0025g0165others(2): Show | 6 | HG00280.hp2 HG02135.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+665_225+786del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111321 | |||||
chr13:113111373
|
A | AGGGCACA others(181): Show |
1 | a0001c0001t0001g0044 | 2 | HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.225+664_225+665ins others(188): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111373 | |||||
chr13:113111393
|
A | G | 6 | a0001c0001t0001g0196a0001c0001t0001g0243a0001c0001t0001g0244others(3): Show | 8 | HG01496.hp2 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+543A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111393 | ||||||
chr13:113111396
|
TCACCTCA others(11): Show |
T | 44 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(41): Show | 70 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.225+564_225+581del others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111396 | |||||
chr13:113111403
|
ACACTCAC others(119): Show |
A | 1 | a0001c0001t0004g0025 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+557_225+682del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111403 | |||||
chr13:113111425
|
TCACAGGG others(417): Show |
T | 1 | a0001c0001t0001g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.225+615_225+1038de others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111425 | |||||
chr13:113111459
|
A | G | 1 | a0001c0001t0006g0095 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.225+609A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111459 | ||||||
chr13:113111480
|
GAGGACAC others(233): Show |
G | 56 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(53): Show | 99 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.225+665_225+904del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111480 | |||||
chr13:113111513
|
A | ACGGGTCA others(57): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(3): Show | 13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+664_225+665ins others(64): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111513 | |||||
chr13:113111515
|
A | G | 2 | a0001c0001t0005g0014a0001c0001t0005g0082 | 4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+665A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111515 | ||||||
chr13:113111529
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(3): Show | 13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+679T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111529 | ||||||
chr13:113111539
|
C | A | 1 | a0001c0001t0001g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225+689C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111539 | ||||||
chr13:113111547
|
T | TCACAGGG others(45): Show |
1 | a0001c0001t0005g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.225+736_225+737ins others(52): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111547 | |||||
chr13:113111547
|
T | TCACAGGG others(43): Show |
1 | a0001c0001t0005g0014 | 3 | HG02572.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.225+736_225+737ins others(50): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111547 | |||||
chr13:113111602
|
G | GAGGACAC others(111): Show |
2 | a0001c0001t0001g0045a0001c0001t0001g0166 | 3 | HG01256.hp2 HG01258.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.225+937_225+1054du others(119): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111602 | |||||
chr13:113111602
|
GAGGACAC others(111): Show |
G | 1 | a0001c0001t0002g0173 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.225+937_225+1054de others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111602 | |||||
chr13:113111667
|
ACAAGACA others(1): Show |
A | 2 | a0001c0001t0005g0014a0001c0001t0005g0082 | 4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+819_225+826del others(8): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111667 | |||||
chr13:113111681
|
ACG | A | 2 | a0001c0001t0005g0014a0001c0001t0005g0082 | 4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+832_225+833del others(2): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111681 | ||||||
chr13:113111682
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(3): Show | 13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+832C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111682 | ||||||
chr13:113111703
|
A | G | 2 | a0001c0001t0005g0014a0001c0001t0005g0082 | 4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+853A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111703 | ||||||
chr13:113111717
|
C | T | 2 | a0001c0001t0005g0014a0001c0001t0005g0082 | 4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+867C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111717 | ||||||
chr13:113111718
|
C | CCAAGATC others(7): Show |
2 | a0001c0001t0005g0014a0001c0001t0005g0082 | 4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+868_225+869ins others(14): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111718 | ||||||
chr13:113111720
|
C | G | 2 | a0001c0001t0005g0014a0001c0001t0005g0082 | 4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+870C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111720 | ||||||
chr13:113111731
|
A | ACACT | 6 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(3): Show | 13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+884_225+885ins others(4): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111731 | |||||
chr13:113111733
|
ACAGGGCA others(107): Show |
A | 2 | a0001c0001t0001g0231a0001c0001t0004g0025 | 3 | HG01975.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+886_225+999del | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111733 | |||||
chr13:113111751
|
T | TCACGGGT others(56): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(3): Show | 13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+920_225+921ins others(63): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111751 | |||||
chr13:113111765
|
ACACT | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0089 | 3 | HG02451.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.225+919_225+922del others(4): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111765 | |||||
chr13:113111800
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(3): Show | 13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+950C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111800 | ||||||
chr13:113111838
|
C | CAGGACAC others(63): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(3): Show | 13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+1002_225+1003i others(72): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111838 | |||||
chr13:113111838
|
C | CAGGACAC others(247): Show |
1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.225+1002_225+1003i others(256): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111838 | |||||
chr13:113111849
|
A | ACACT | 58 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.225+1002_225+1003i others(6): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113111849 | |||||
chr13:113111849
|
A | T | 2 | a0001c0001t0001g0231a0001c0001t0004g0025 | 3 | HG01975.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.225+999A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111849 | ||||||
chr13:113111869
|
T | G | 1 | a0001c0001t0004g0026 | 2 | HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.225+1019T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111869 | ||||||
chr13:113111872
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(3): Show | 13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+1022C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111872 | ||||||
chr13:113111912
|
G | A | 3 | a0001c0001t0006g0034a0001c0001t0006g0093a0001c0001t0006g0095 | 4 | HG00140.hp2 HG00323.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+1062G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113111912 | ||||||
chr13:113112039
|
C | T | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.225+1189C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112039 | ||||||
chr13:113112079
|
G | A | 3 | a0001c0001t0001g0168a0001c0001t0004g0025a0001c0001t0004g0026 | 5 | HG02886.hp1 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+1229G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112079 | ||||||
chr13:113112136
|
ACACT | A | 2 | a0001c0001t0005g0014a0001c0001t0005g0082 | 4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+1290_225+1293d others(6): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112136 | |||||
chr13:113112205
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(3): Show | 13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+1355C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112205 | ||||||
chr13:113112281
|
A | C | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.225+1431A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112281 | ||||||
chr13:113112318
|
CCT | C | 2 | a0001c0001t0005g0014a0001c0001t0005g0082 | 4 | HG02280.hp2 HG02572.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-1432_226-1431d others(4): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112318 | |||||
chr13:113112339
|
TACTCTCA others(11): Show |
T | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.226-1392_226-1375d others(20): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112339 | |||||
chr13:113112357
|
C | CACTCTCA others(484): Show |
1 | a0001c0001t0001g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.226-1200_226-710du others(492): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112357 | |||||
chr13:113112357
|
CACTCTCA others(484): Show |
C | 2 | a0001c0001t0004g0172a0002c0002t0003g0066 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.226-1200_226-710de others(1): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112357 | |||||
chr13:113112458
|
A | C | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-1294A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112458 | ||||||
chr13:113112505
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(4): Show | 14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.226-1247A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112505 | ||||||
chr13:113112574
|
GAGGTCAC others(57): Show |
G | 1 | a0001c0001t0001g0064 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.226-1131_226-1068d others(66): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112574 | |||||
chr13:113112710
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.226-1042C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112710 | ||||||
chr13:113112713
|
A | ACACT | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(74): Show | 131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.226-1036_226-1035i others(6): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112713 | |||||
chr13:113112749
|
A | G | 1 | a0001c0001t0004g0026 | 2 | HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.226-1003A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112749 | ||||||
chr13:113112828
|
C | A | 4 | a0001c0001t0006g0034a0001c0001t0006g0093a0001c0001t0006g0094others(1): Show | 5 | HG00140.hp2 HG00323.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-924C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112828 | ||||||
chr13:113112848
|
T | TACTCTCA others(11): Show |
8 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(5): Show | 15 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.226-901_226-884dup others(18): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113112848 | |||||
chr13:113112922
|
A | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(4): Show | 14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.226-830A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112922 | ||||||
chr13:113112984
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.226-768G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113112984 | ||||||
chr13:113113022
|
C | T | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.226-730C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113022 | ||||||
chr13:113113049
|
C | CATT | 7 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(4): Show | 14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.226-701_226-700ins others(3): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 113113049 | |||||
chr13:113113068
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.226-684G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113068 | ||||||
chr13:113113080
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 103 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.226-672A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113080 | ||||||
chr13:113113114
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(4): Show | 14 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.226-638C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113114 | ||||||
chr13:113113130
|
A | T | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-622A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113130 | ||||||
chr13:113113209
|
T | G | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-543T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113209 | ||||||
chr13:113113348
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.226-404C>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113348 | ||||||
chr13:113113392
|
T | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(3): Show | 13 | HG01069.hp1 HG01071.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.226-360T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113392 | ||||||
chr13:113113518
|
T | G | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-234T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113518 | ||||||
chr13:113113519
|
G | T | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-233G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113519 | ||||||
chr13:113113520
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.226-232T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113520 | ||||||
chr13:113113520
|
T | G | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.226-232T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113520 | ||||||
chr13:113113584
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.226-168G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113584 | ||||||
chr13:113113641
|
G | A | 1 | a0001c0001t0001g0039 | 2 | NA18960.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.226-111G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 2/7 | chr13 | 113113641 | ||||||
chr13:113114173
|
C | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.364+213C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114173 | ||||||
chr13:113114217
|
G | A | 1 | a0002c0002t0003g0068 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.364+257G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114217 | ||||||
chr13:113114271
|
C | T | 2 | a0001c0001t0005g0014a0001c0001t0016g0242 | 4 | HG02572.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+311C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114271 | ||||||
chr13:113114279
|
C | T | 1 | a0001c0001t0006g0093 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.364+319C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114279 | ||||||
chr13:113114324
|
AG | A | 35 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0035others(32): Show | 43 | HG01515.hp2 HG01517.hp2 HG02040.hp1 others(40): Show |
intron_variant | MODIFIER | c.364+368delG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 113114324 | |||||
chr13:113114327
|
GGT | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0042others(26): Show | 39 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.364+368_364+369del others(2): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114327 | ||||||
chr13:113114328
|
G | T | 9 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0004g0234others(6): Show | 12 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.364+368G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114328 | ||||||
chr13:113114331
|
TG | T | 57 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0013others(54): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.364+372delG | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114331 | ||||||
chr13:113114332
|
G | GT | 14 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0049others(11): Show | 21 | HG00423.hp2 HG01975.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.364+382dupT | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 113114332 | |||||
chr13:113114332
|
G | T | 72 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(69): Show | 93 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.364+372G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114332 | ||||||
chr13:113114445
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.364+485C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114445 | ||||||
chr13:113114457
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.364+497G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114457 | ||||||
chr13:113114577
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.364+617G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114577 | ||||||
chr13:113114888
|
T | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0193a0001c0001t0001g0212others(1): Show | 7 | NA18944.hp1 NA18956.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.365-772T>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114888 | ||||||
chr13:113114912
|
A | C | 7 | a0001c0001t0001g0216a0001c0001t0001g0221a0001c0001t0004g0026others(4): Show | 9 | HG00140.hp2 HG00323.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.365-748A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113114912 | ||||||
chr13:113115032
|
G | C | 37 | a0001c0003t0001g0060a0001c0003t0001g0070a0001c0003t0014g0090others(34): Show | 40 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.365-628G>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115032 | ||||||
chr13:113115114
|
C | T | 1 | a0002c0002t0003g0029 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.365-546C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115114 | ||||||
chr13:113115159
|
G | A | 1 | a0002c0002t0003g0066 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.365-501G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115159 | ||||||
chr13:113115219
|
C | T | 2 | a0001c0001t0012g0079a0001c0001t0012g0080 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.365-441C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115219 | ||||||
chr13:113115325
|
T | G | 48 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0083others(45): Show | 60 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.365-335T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115325 | ||||||
chr13:113115362
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.365-298C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115362 | ||||||
chr13:113115599
|
G | A | 1 | a0001c0001t0012g0079 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.365-61G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115599 | ||||||
chr13:113115603
|
G | A | 33 | a0001c0003t0001g0060a0001c0003t0001g0070a0001c0003t0014g0090others(30): Show | 36 | HG00673.hp1 HG01515.hp2 HG01517.hp2 others(33): Show |
intron_variant | MODIFIER | c.365-57G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115603 | ||||||
chr13:113115613
|
G | A | 1 | a0002c0002t0008g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.365-47G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 4/7 | chr13 | 113115613 | ||||||
chr13:113115849
|
A | C | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.505+49A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113115849 | ||||||
chr13:113115971
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.505+171G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113115971 | ||||||
chr13:113116038
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.505+238G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116038 | ||||||
chr13:113116046
|
G | A | 1 | a0001c0001t0017g0233 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.505+246G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116046 | ||||||
chr13:113116173
|
G | A | 1 | a0002c0010t0015g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.505+373G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116173 | ||||||
chr13:113116207
|
A | C | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.505+407A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116207 | ||||||
chr13:113116316
|
C | T | 1 | a0001c0001t0001g0054 | 2 | NA18993.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.506-450C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116316 | ||||||
chr13:113116337
|
C | T | 1 | a0001c0001t0016g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.506-429C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116337 | ||||||
chr13:113116348
|
A | G | 1 | a0002c0002t0003g0078 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.506-418A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116348 | ||||||
chr13:113116355
|
T | C | 3 | a0001c0001t0012g0079a0001c0001t0012g0080a0001c0001t0017g0233 | 3 | HG02559.hp2 HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.506-411T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116355 | ||||||
chr13:113116358
|
T | C | 1 | a0006c0008t0002g0170 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.506-408T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116358 | ||||||
chr13:113116389
|
A | C | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.506-377A>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116389 | ||||||
chr13:113116562
|
G | A | 35 | a0001c0001t0004g0026a0001c0001t0016g0242a0001c0001t0023g0200others(32): Show | 40 | HG00673.hp1 HG01243.hp2 HG01952.hp2 others(37): Show |
intron_variant | MODIFIER | c.506-204G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116562 | ||||||
chr13:113116592
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.506-174C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116592 | ||||||
chr13:113116683
|
A | T | 1 | a0002c0002t0003g0239 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.506-83A>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116683 | ||||||
chr13:113116716
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.506-50C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116716 | ||||||
chr13:113116754
|
T | G | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.506-12T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116754 | ||||||
chr13:113116755
|
G | T | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.506-11G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116755 | ||||||
chr13:113116756
|
T | G | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.506-10T>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 5/7 | chr13 | 113116756 | ||||||
chr13:113116956
|
A | G | 1 | a0003c0011t0001g0105 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.615+81A>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 6/7 | chr13 | 113116956 | ||||||
chr13:113117132
|
C | T | 2 | a0001c0001t0012g0079a0001c0001t0012g0080 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.615+257C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 6/7 | chr13 | 113117132 | ||||||
chr13:113117365
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.616-108G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 6/7 | chr13 | 113117365 | ||||||
chr13:113117585
|
TCGCGGTG others(30): Show |
T | 1 | a0006c0008t0002g0170 | 1 | HG01975.hp1 | splice_region_variant&intron_variant | LOW | c.739+7_739+43delACC others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117585 | |||||
chr13:113117603
|
A | ACCACTCT others(30): Show |
87 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(84): Show | 130 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.739+15_739+51dupCC others(35): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117603 | |||||
chr13:113117603
|
A | ACCACTCT others(67): Show |
4 | a0001c0001t0005g0014a0001c0001t0005g0082a0001c0001t0005g0149others(1): Show | 6 | HG01891.hp2 HG01952.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.739+51_739+52insCC others(72): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117603 | |||||
chr13:113117603
|
A | ACCACTCT others(29): Show |
1 | a0001c0001t0001g0224 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.739+30_739+31insTG others(34): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117603 | |||||
chr13:113117648
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(100): Show | 157 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.739+52T>C | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113117648 | ||||||
chr13:113117648
|
TCCCTGTC others(30): Show |
T | 2 | a0001c0001t0001g0046a0001c0001t0002g0091 | 3 | HG00323.hp1 HG01070.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.739+128_739+164del others(37): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117648 | |||||
chr13:113117694
|
G | GACCGCGG others(30): Show |
1 | a0002c0002t0009g0027 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.739+134_739+135ins others(37): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117694 | |||||
chr13:113117724
|
C | CCTGTCCG others(67): Show |
1 | a0001c0001t0017g0233 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.739+164_739+165ins others(74): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117724 | |||||
chr13:113117724
|
C | CCTGTCCG others(30): Show |
2 | a0001c0001t0012g0079a0001c0001t0012g0080 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.739+155_739+191dup others(37): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117724 | |||||
chr13:113117734
|
C | CGCGGTGC others(30): Show |
1 | a0001c0003t0010g0050 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.739+164_739+165ins others(37): Show |
F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr13 | 113117734 | |||||
chr13:113117761
|
G | A | 4 | a0001c0001t0002g0023a0001c0001t0002g0096a0001c0001t0002g0102others(1): Show | 5 | NA18952.hp2 NA18956.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.739+165G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113117761 | ||||||
chr13:113117773
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.739+177C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113117773 | ||||||
chr13:113117996
|
C | G | 1 | a0001c0001t0013g0037 | 2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.739+400C>G | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113117996 | ||||||
chr13:113117999
|
G | A | 1 | a0001c0001t0017g0233 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.739+403G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113117999 | ||||||
chr13:113118028
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.740-385C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118028 | ||||||
chr13:113118086
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.740-327G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118086 | ||||||
chr13:113118136
|
G | A | 1 | a0001c0001t0004g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.740-277G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118136 | ||||||
chr13:113118253
|
G | T | 1 | a0002c0002t0003g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.740-160G>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118253 | ||||||
chr13:113118326
|
C | T | 1 | a0001c0001t0001g0057 | 2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.740-87C>T | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118326 | ||||||
chr13:113118393
|
G | A | 34 | a0002c0002t0001g0062a0002c0002t0003g0028a0002c0002t0003g0029others(31): Show | 37 | HG00673.hp1 HG01243.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.740-20G>A | F7 | ENSG00000057593.14 | transcript | ENST00000346342.8 | protein_coding | 7/7 | chr13 | 113118393 |