geneid | 130540 |
---|---|
ensemblid | ENSG00000155749.13 |
hgncid | 14439 |
symbol | FLACC1 |
name | flagellum associated containing coiled-coil domains 1 |
refseq_nuc | NM_001127391.3 |
refseq_prot | NP_001120863.1 |
ensembl_nuc | ENST00000392257.8 |
ensembl_prot | ENSP00000376086.3 |
mane_status | MANE Select |
chr | chr2 |
start | 201288271 |
end | 201357345 |
strand | - |
ver | v1.2 |
region | chr2:201288271-201357345 |
region5000 | chr2:201283271-201362345 |
regionname0 | FLACC1_chr2_201288271_201357345 |
regionname5000 | FLACC1_chr2_201283271_201362345 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 422 | 255 | 68 | 33 | 119 | 5 | 29 | 93 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0002 | 1/0 | 422 | 110 | 19 | 35 | 41 | 5 | 9 | 29 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0003 | 0/0 | 422 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0004 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0005 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0006 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1269 | 251 | 67 | 32 | 118 | 5 | 28 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
c0002 | 1/0 | 1269 | 97 | 15 | 30 | 40 | 2 | 9 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
c0003 | 0/0 | 1269 | 12 | 3 | 5 | 1 | 3 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
c0004 | 0/0 | 1269 | 2 | 2 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
c0005 | 0/0 | 1269 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
c0006 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
c0007 | 0/0 | 1269 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
c0008 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
c0009 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
c0010 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
c0011 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
c0012 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 796 | 100 | 5 | 25 | 55 | 4 | 10 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0002 | 1/0 | 796 | 90 | 13 | 25 | 40 | 2 | 9 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0003 | 0/0 | 796 | 61 | 10 | 0 | 42 | 0 | 9 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0004 | 0/0 | 796 | 41 | 35 | 6 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0005 | 0/0 | 796 | 31 | 6 | 8 | 14 | 2 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0006 | 0/0 | 796 | 23 | 11 | 3 | 4 | 0 | 5 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0007 | 0/0 | 796 | 13 | 8 | 1 | 0 | 0 | 4 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0008 | 0/0 | 796 | 6 | 2 | 0 | 4 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0009 | 0/0 | 796 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0010 | 0/0 | 796 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0011 | 0/0 | 796 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0012 | 0/0 | 796 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
t0013 | 0/0 | 796 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0002 | 1/0 | 6 | 5 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1269 | 251 | 67 | 32 | 118 | 5 | 28 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0005 | 0/0 | 1269 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0007 | 0/0 | 1269 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0009 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0012 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0002c0002 | 1/0 | 1269 | 97 | 15 | 30 | 40 | 2 | 9 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0002c0003 | 0/0 | 1269 | 12 | 3 | 5 | 1 | 3 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0002c0011 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0003c0004 | 0/0 | 1269 | 2 | 2 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0004c0008 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0005c0006 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0006c0010 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2064 | 97 | 4 | 25 | 54 | 4 | 9 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0001t0002 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0001t0003 | 0/0 | 2064 | 59 | 8 | 0 | 42 | 0 | 9 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0001t0004 | 0/0 | 2064 | 36 | 32 | 4 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0001t0005 | 0/0 | 2064 | 14 | 0 | 0 | 13 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0001t0006 | 0/0 | 2064 | 22 | 11 | 2 | 4 | 0 | 5 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0001t0007 | 0/0 | 2064 | 12 | 7 | 1 | 0 | 0 | 4 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0001t0008 | 0/0 | 2064 | 6 | 2 | 0 | 4 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0001t0009 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0001t0011 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0001t0012 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0001t0013 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0005t0006 | 0/0 | 2064 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0007t0001 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0009t0001 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0001c0012t0001 | 0/0 | 2064 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0002c0002t0002 | 1/0 | 2064 | 89 | 12 | 25 | 40 | 2 | 9 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0002c0002t0003 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0002c0002t0004 | 0/0 | 2064 | 4 | 2 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0002c0002t0005 | 0/0 | 2064 | 3 | 0 | 3 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0002c0003t0005 | 0/0 | 2064 | 11 | 3 | 5 | 1 | 2 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0002c0003t0010 | 0/0 | 2064 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0002c0011t0005 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0003c0004t0005 | 0/0 | 2064 | 2 | 2 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0004c0008t0007 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0005c0006t0003 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
a0006c0010t0004 | 0/0 | 2064 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | copy fasta | chr2 | 201283271 | 201362345 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0008g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0008g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0009g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0011g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0012g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0001t0013g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0005t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0007t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0009t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0001c0012t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0002 | 1/0 | 6 | 5 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0002t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0005g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0003t0010g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0002c0011t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0003c0004t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0003c0004t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0004c0008t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0005c0006t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
a0006c0010t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00140 | hp2 | a0002 | c0003 | t0005 | g0222 | EUR | GBR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0164 | EUR | FIN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0193 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0209 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00738 | hp1 | a0002 | c0003 | t0005 | g0223 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG00738 | hp2 | a0002 | c0002 | t0005 | g0206 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01069 | hp1 | a0002 | c0003 | t0005 | g0226 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0155 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01074 | hp2 | a0002 | c0003 | t0005 | g0219 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0186 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01109 | hp1 | a0001 | c0005 | t0006 | g0039 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0201 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01167 | hp1 | a0002 | c0002 | t0005 | g0158 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01168 | hp1 | a0002 | c0002 | t0004 | g0216 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0113 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01169 | hp1 | a0002 | c0002 | t0004 | g0217 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01169 | hp2 | a0002 | c0002 | t0005 | g0159 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0174 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01192 | hp1 | a0002 | c0003 | t0005 | g0227 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0203 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0166 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01261 | hp1 | a0002 | c0003 | t0005 | g0225 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0284 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0160 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0187 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0167 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0125 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0023 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01515 | hp2 | a0001 | c0001 | t0012 | g0314 | EUR | IBS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01517 | hp1 | a0002 | c0003 | t0005 | g0224 | EUR | IBS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01884 | hp2 | a0005 | c0006 | t0003 | g0304 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01891 | hp1 | a0002 | c0002 | t0002 | g0202 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0027 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0022 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0208 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0170 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02027 | hp1 | a0002 | c0003 | t0005 | g0221 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02027 | hp2 | a0001 | c0001 | t0006 | g0058 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0309 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0240 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02080 | hp1 | a0001 | c0001 | t0009 | g0148 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0072 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0283 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0171 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02155 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | CDX | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | CDX | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02165 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | CDX | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0048 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0269 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0307 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0207 | AMR | PEL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0147 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | KHV | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0301 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0049 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02622 | hp1 | a0002 | c0003 | t0005 | g0215 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0296 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02630 | hp1 | a0003 | c0004 | t0005 | g0312 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0299 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0285 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02647 | hp2 | a0001 | c0001 | t0011 | g0313 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0124 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02717 | hp2 | a0006 | c0010 | t0004 | g0156 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0067 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0018 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0169 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02738 | hp2 | a0001 | c0007 | t0001 | g0126 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0300 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02809 | hp2 | a0002 | c0002 | t0002 | g0191 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0288 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02818 | hp2 | a0003 | c0004 | t0005 | g0311 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02886 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02895 | hp1 | a0001 | c0009 | t0001 | g0051 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0306 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0068 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02965 | hp2 | a0002 | c0002 | t0004 | g0210 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0129 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0263 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0071 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0070 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0291 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0145 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0303 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0308 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0212 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03225 | hp1 | a0002 | c0003 | t0005 | g0214 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0168 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0192 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0110 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03491 | hp2 | a0001 | c0001 | t0007 | g0121 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0294 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0241 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0026 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0018 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0177 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0251 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0024 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0248 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0264 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | BEB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03927 | hp2 | a0001 | c0001 | t0007 | g0116 | SAS | BEB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0270 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG04115 | hp2 | a0001 | c0001 | t0006 | g0120 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG04204 | hp1 | a0001 | c0001 | t0007 | g0149 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG04228 | hp1 | a0001 | c0001 | t0007 | g0041 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0026 | SAS | STU | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | YRI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | YRI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18747 | hp2 | a0001 | c0001 | t0008 | g0013 | EAS | CHB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18906 | hp1 | a0002 | c0002 | t0002 | g0162 | AFR | YRI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0196 | AFR | YRI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18959 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18962 | hp2 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18971 | hp2 | a0001 | c0001 | t0006 | g0112 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18974 | hp1 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18995 | hp1 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19000 | hp2 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19001 | hp1 | a0001 | c0012 | t0001 | g0146 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19010 | hp2 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0305 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19030 | hp2 | a0004 | c0008 | t0007 | g0076 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19043 | hp1 | a0002 | c0011 | t0005 | g0205 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19074 | hp2 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19083 | hp1 | a0001 | c0001 | t0008 | g0139 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0277 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19086 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0172 | EUR | TSI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA20752 | hp2 | a0002 | c0003 | t0010 | g0218 | EUR | TSI | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0178 | SAS | GIH | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0111 | SAS | GIH | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | CLM | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02109 | hp2 | a0002 | c0002 | t0003 | g0157 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0165 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0292 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0295 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | ACB | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | MSL | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | USA | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
HG06807 | hp2 | a0002 | c0002 | t0004 | g0211 | AFR | USA | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | USA | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0290 | AFR | USA | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA21309 | hp1 | a0002 | c0003 | t0005 | g0220 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
NA21309 | hp2 | a0001 | c0001 | t0013 | g0315 | AFR | LWK | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0045 | REF | REF | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0002 | REF | REF | FLACC1_chr2_201283271_201362345 | FLACC1 | chr2 | 201283271 | 201362345 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:201299292
|
C | G | 1 | a0004 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.888G>C | p.Leu296Phe | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/15 | 1299/2064 | 888/1269 | 296/422 | chr2 | 201299292 | ||
chr2:201330765
|
G | T | 1 | a0005 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.593C>A | p.Ala198Glu | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 8/15 | 1004/2064 | 593/1269 | 198/422 | chr2 | 201330765 | ||
chr2:201346672
|
C | G | 1 | a0006 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.238G>C | p.Val80Leu | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/15 | 649/2064 | 238/1269 | 80/422 | chr2 | 201346672 | ||
chr2:201348272
|
C | G | 1 | a0003 | 2 | HG02630.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.216G>C | p.Glu72Asp | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/15 | 627/2064 | 216/1269 | 72/422 | chr2 | 201348272 | ||
chr2:201350769
|
C | G | 4 | a0001a0003a0004others(1): Show | 259 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
missense_variant | MODERATE | c.127G>C | p.Val43Leu | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/15 | 538/2064 | 127/1269 | 43/422 | chr2 | 201350769 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:201289477
|
C | T | 4 | a0001c0009a0002c0003a0002c0011others(1): Show | 16 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
synonymous_variant | LOW | c.1122G>A | p.Thr374Thr | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/15 | 1533/2064 | 1122/1269 | 374/422 | chr2 | 201289477 | ||
chr2:201309203
|
C | T | 1 | a0001c0007 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.723G>A | p.Ala241Ala | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/15 | 1134/2064 | 723/1269 | 241/422 | chr2 | 201309203 | ||
chr2:201346661
|
C | T | 1 | a0002c0011 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.249G>A | p.Val83Val | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/15 | 660/2064 | 249/1269 | 83/422 | chr2 | 201346661 | ||
chr2:201350761
|
A | G | 1 | a0001c0005 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.135T>C | p.Ala45Ala | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/15 | 546/2064 | 135/1269 | 45/422 | chr2 | 201350761 | ||
chr2:201351381
|
G | A | 1 | a0001c0012 | 1 | NA19001.hp1 | synonymous_variant | LOW | c.24C>T | p.Tyr8Tyr | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/15 | 435/2064 | 24/1269 | 8/422 | chr2 | 201351381 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:201288355
|
T | G | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(15): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*300A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 15/15 | 300 | chr2 | 201288355 | |||||
chr2:201288429
|
G | A | 1 | a0001c0001t0009 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*226C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 15/15 | 226 | chr2 | 201288429 | |||||
chr2:201288502
|
C | A | 24 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(21): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*153G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 15/15 | 153 | chr2 | 201288502 | |||||
chr2:201288529
|
A | C | 12 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(9): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*126T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 15/15 | 126 | chr2 | 201288529 | |||||
chr2:201288653
|
G | A | 1 | a0002c0003t0010 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 15/15 | 2 | chr2 | 201288653 | |||||
chr2:201357198
|
C | T | 10 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(7): Show | 143 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(140): Show |
5_prime_UTR_variant | MODIFIER | c.-264G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/15 | 5794 | chr2 | 201357198 | |||||
chr2:201357208
|
T | C | 1 | a0001c0001t0011 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-274A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/15 | 5804 | chr2 | 201357208 | |||||
chr2:201357243
|
T | C | 1 | a0001c0001t0012 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-309A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/15 | 5839 | chr2 | 201357243 | |||||
chr2:201357337
|
C | A | 1 | a0001c0001t0013 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-403G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/15 | 5933 | chr2 | 201357337 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:201288873
|
G | A | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1143-92C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201288873 | ||||||
chr2:201288961
|
C | T | 246 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(243): Show | 275 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.1143-180G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201288961 | ||||||
chr2:201288974
|
A | G | 2 | a0002c0002t0004g0210a0002c0002t0004g0211 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1143-193T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201288974 | ||||||
chr2:201289066
|
C | T | 10 | a0002c0002t0002g0021a0002c0002t0002g0024a0002c0002t0002g0025others(7): Show | 14 | HG00639.hp1 HG01071.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1143-285G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201289066 | ||||||
chr2:201289123
|
G | A | 107 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(104): Show | 118 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.1142+334C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201289123 | ||||||
chr2:201289157
|
A | AC | 107 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(104): Show | 118 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.1142+299dupG | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201289157 | ||||||
chr2:201289197
|
A | G | 246 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(243): Show | 275 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.1142+260T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201289197 | ||||||
chr2:201289247
|
GGGAGAAG others(4): Show |
G | 1 | a0001c0001t0001g0134 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1142+199_1142+209d others(13): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 14/14 | chr2 | 201289247 | ||||||
chr2:201289674
|
C | G | 47 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0033others(44): Show | 55 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(52): Show |
intron_variant | MODIFIER | c.1032+22G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 13/14 | chr2 | 201289674 | ||||||
chr2:201289810
|
G | A | 1 | a0002c0002t0002g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.943-25C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201289810 | ||||||
chr2:201289875
|
G | A | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.943-90C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201289875 | ||||||
chr2:201289960
|
C | A | 2 | a0002c0003t0005g0220a0002c0003t0005g0223 | 2 | HG00738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.943-175G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201289960 | ||||||
chr2:201290027
|
G | A | 5 | a0002c0002t0002g0026a0002c0002t0002g0155a0002c0002t0002g0177others(2): Show | 6 | HG00639.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-242C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290027 | ||||||
chr2:201290182
|
T | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0084others(11): Show | 17 | HG00323.hp2 HG00639.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.943-397A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290182 | ||||||
chr2:201290218
|
T | C | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.943-433A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290218 | ||||||
chr2:201290425
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00323.hp2 HG01243.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.943-640G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290425 | ||||||
chr2:201290510
|
G | A | 1 | a0001c0001t0008g0046 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.943-725C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290510 | ||||||
chr2:201290603
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.943-818G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290603 | ||||||
chr2:201290711
|
T | C | 1 | a0002c0003t0005g0222 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.943-926A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290711 | ||||||
chr2:201290716
|
C | T | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.943-931G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290716 | ||||||
chr2:201290743
|
C | T | 1 | a0001c0001t0003g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.943-958G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290743 | ||||||
chr2:201290744
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.943-959C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290744 | ||||||
chr2:201290839
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.943-1054G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290839 | ||||||
chr2:201290855
|
T | C | 1 | a0006c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.943-1070A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290855 | ||||||
chr2:201290863
|
G | A | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.943-1078C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290863 | ||||||
chr2:201290918
|
G | A | 1 | a0001c0001t0004g0295 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.943-1133C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290918 | ||||||
chr2:201290923
|
G | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0098 | 2 | NA19062.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.943-1138C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290923 | ||||||
chr2:201290959
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.943-1174C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290959 | ||||||
chr2:201290963
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.943-1178A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290963 | ||||||
chr2:201290973
|
G | A | 1 | a0006c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.943-1188C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201290973 | ||||||
chr2:201291078
|
C | T | 1 | a0002c0002t0002g0204 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.943-1293G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291078 | ||||||
chr2:201291098
|
G | A | 14 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(11): Show | 15 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.943-1313C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291098 | ||||||
chr2:201291331
|
T | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(195): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.943-1546A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291331 | ||||||
chr2:201291331
|
T | G | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.943-1546A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291331 | ||||||
chr2:201291502
|
T | C | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.943-1717A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291502 | ||||||
chr2:201291601
|
T | G | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.943-1816A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291601 | ||||||
chr2:201291649
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.943-1864C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291649 | ||||||
chr2:201291672
|
T | A | 76 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(73): Show | 86 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.943-1887A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291672 | ||||||
chr2:201291688
|
C | T | 1 | a0002c0002t0002g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.943-1903G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291688 | ||||||
chr2:201291727
|
C | T | 4 | a0001c0001t0005g0242a0001c0001t0005g0243a0001c0001t0005g0244others(1): Show | 4 | HG02300.hp2 NA18939.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.943-1942G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291727 | ||||||
chr2:201291822
|
A | G | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.943-2037T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201291822 | ||||||
chr2:201292069
|
CAGGG | C | 19 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0033others(16): Show | 26 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.943-2288_943-2285d others(6): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292069 | ||||||
chr2:201292134
|
G | T | 1 | a0002c0002t0002g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.943-2349C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292134 | ||||||
chr2:201292144
|
G | A | 1 | a0002c0002t0002g0181 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.943-2359C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292144 | ||||||
chr2:201292202
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.943-2417C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292202 | ||||||
chr2:201292281
|
C | G | 1 | a0002c0002t0002g0182 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.943-2496G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292281 | ||||||
chr2:201292283
|
C | T | 1 | a0002c0002t0002g0182 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.943-2498G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292283 | ||||||
chr2:201292367
|
A | G | 1 | a0001c0001t0001g0006 | 3 | HG00140.hp1 HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.943-2582T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292367 | ||||||
chr2:201292525
|
A | G | 1 | a0002c0002t0002g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.943-2740T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292525 | ||||||
chr2:201292546
|
A | G | 1 | a0001c0001t0005g0280 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.943-2761T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292546 | ||||||
chr2:201292579
|
T | C | 1 | a0001c0001t0005g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.943-2794A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292579 | ||||||
chr2:201292800
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0140 | 2 | NA18962.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.943-3015T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201292800 | ||||||
chr2:201293001
|
G | A | 1 | a0002c0003t0010g0218 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.943-3216C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293001 | ||||||
chr2:201293108
|
C | T | 1 | a0001c0001t0003g0251 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.943-3323G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293108 | ||||||
chr2:201293133
|
G | T | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.943-3348C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293133 | ||||||
chr2:201293206
|
G | C | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.943-3421C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293206 | ||||||
chr2:201293238
|
C | T | 9 | a0001c0001t0001g0040a0002c0002t0002g0022a0002c0002t0002g0166others(6): Show | 10 | HG00438.hp1 HG00673.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.943-3453G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293238 | ||||||
chr2:201293279
|
A | T | 1 | a0001c0001t0006g0115 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.943-3494T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293279 | ||||||
chr2:201293309
|
C | T | 1 | a0001c0001t0003g0028 | 2 | NA19005.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.943-3524G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293309 | ||||||
chr2:201293320
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.943-3535C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293320 | ||||||
chr2:201293373
|
C | T | 1 | a0001c0001t0003g0247 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.943-3588G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293373 | ||||||
chr2:201293390
|
A | C | 2 | a0001c0001t0007g0116a0001c0001t0007g0149 | 2 | HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.943-3605T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293390 | ||||||
chr2:201293404
|
A | T | 13 | a0002c0003t0005g0214a0002c0003t0005g0215a0002c0003t0005g0219others(10): Show | 13 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.943-3619T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293404 | ||||||
chr2:201293602
|
A | G | 5 | a0001c0001t0003g0010a0001c0001t0003g0030a0001c0001t0003g0252others(2): Show | 8 | NA18940.hp2 NA18943.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.943-3817T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293602 | ||||||
chr2:201293617
|
G | C | 1 | a0002c0002t0004g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.943-3832C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293617 | ||||||
chr2:201293625
|
A | G | 1 | a0002c0002t0004g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.943-3840T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293625 | ||||||
chr2:201293816
|
G | A | 75 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(72): Show | 85 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.943-4031C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293816 | ||||||
chr2:201293817
|
C | CA | 122 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(119): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.943-4033dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293817 | ||||||
chr2:201293827
|
C | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(195): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.943-4042G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293827 | ||||||
chr2:201293881
|
G | A | 1 | a0002c0003t0005g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.943-4096C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293881 | ||||||
chr2:201293909
|
C | G | 92 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(89): Show | 102 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.943-4124G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293909 | ||||||
chr2:201293953
|
A | C | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.943-4168T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201293953 | ||||||
chr2:201294048
|
A | C | 3 | a0001c0001t0003g0310a0001c0001t0011g0313a0002c0002t0003g0157 | 3 | HG02109.hp2 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.943-4263T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294048 | ||||||
chr2:201294291
|
A | C | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.943-4506T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294291 | ||||||
chr2:201294328
|
C | A | 1 | a0002c0002t0002g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.943-4543G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294328 | ||||||
chr2:201294403
|
C | T | 1 | a0002c0002t0002g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.943-4618G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294403 | ||||||
chr2:201294473
|
C | T | 1 | a0002c0002t0002g0195 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.943-4688G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294473 | ||||||
chr2:201294474
|
G | A | 1 | a0002c0002t0002g0183 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.943-4689C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294474 | ||||||
chr2:201294568
|
C | T | 1 | a0002c0003t0005g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.942+4670G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294568 | ||||||
chr2:201294618
|
G | T | 1 | a0001c0001t0004g0284 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.942+4620C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294618 | ||||||
chr2:201294678
|
G | T | 5 | a0001c0001t0003g0236a0001c0001t0003g0246a0001c0001t0003g0266others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+4560C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294678 | ||||||
chr2:201294734
|
C | T | 67 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(64): Show | 76 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.942+4504G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294734 | ||||||
chr2:201294775
|
A | G | 1 | a0001c0001t0007g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.942+4463T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294775 | ||||||
chr2:201294803
|
T | C | 1 | a0002c0002t0002g0169 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.942+4435A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201294803 | ||||||
chr2:201295085
|
G | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.942+4153C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295085 | ||||||
chr2:201295376
|
T | C | 1 | a0001c0001t0007g0072 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.942+3862A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295376 | ||||||
chr2:201295393
|
A | C | 69 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(66): Show | 78 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.942+3845T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295393 | ||||||
chr2:201295595
|
G | T | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.942+3643C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295595 | ||||||
chr2:201295655
|
G | A | 3 | a0001c0001t0006g0110a0001c0001t0006g0111a0001c0001t0006g0113 | 3 | HG01168.hp2 HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.942+3583C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295655 | ||||||
chr2:201295933
|
C | A | 1 | a0002c0003t0005g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.942+3305G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295933 | ||||||
chr2:201295945
|
A | G | 1 | a0001c0001t0003g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.942+3293T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295945 | ||||||
chr2:201295948
|
C | CA | 4 | a0001c0001t0001g0066a0001c0001t0001g0092a0001c0001t0001g0153others(1): Show | 4 | HG03017.hp2 HG03453.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+3289dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201295948 | ||||||
chr2:201296039
|
C | T | 245 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(242): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.942+3199G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296039 | ||||||
chr2:201296225
|
C | T | 87 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0054others(84): Show | 97 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.942+3013G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296225 | ||||||
chr2:201296259
|
A | C | 1 | a0001c0001t0005g0235 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.942+2979T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296259 | ||||||
chr2:201296269
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.942+2969G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296269 | ||||||
chr2:201296310
|
T | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(223): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.942+2928A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296310 | ||||||
chr2:201296331
|
C | T | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.942+2907G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296331 | ||||||
chr2:201296344
|
G | T | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.942+2894C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296344 | ||||||
chr2:201296420
|
C | A | 1 | a0001c0001t0004g0299 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.942+2818G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296420 | ||||||
chr2:201296500
|
C | T | 7 | a0001c0001t0007g0070a0001c0001t0007g0071a0001c0001t0007g0072others(4): Show | 7 | HG02145.hp1 HG02559.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.942+2738G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296500 | ||||||
chr2:201296564
|
A | G | 93 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(90): Show | 103 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.942+2674T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296564 | ||||||
chr2:201296663
|
A | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0140 | 2 | NA18962.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.942+2575T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296663 | ||||||
chr2:201296913
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.942+2325C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201296913 | ||||||
chr2:201297170
|
T | C | 1 | a0001c0001t0005g0279 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.942+2068A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297170 | ||||||
chr2:201297309
|
G | C | 1 | a0001c0007t0001g0126 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.942+1929C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297309 | ||||||
chr2:201297310
|
T | TGTACTGA others(47): Show |
1 | a0001c0007t0001g0126 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.942+1927_942+1928i others(56): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297310 | ||||||
chr2:201297419
|
T | TG | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.942+1818dupC | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297419 | ||||||
chr2:201297497
|
G | A | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.942+1741C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297497 | ||||||
chr2:201297615
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.942+1623G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297615 | ||||||
chr2:201297679
|
TGAGGTGT others(6): Show |
T | 1 | a0001c0001t0003g0250 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.942+1546_942+1558d others(15): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297679 | ||||||
chr2:201297683
|
G | C | 66 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(63): Show | 75 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.942+1555C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297683 | ||||||
chr2:201297852
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0151others(1): Show | 4 | HG01074.hp1 HG01081.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+1386G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297852 | ||||||
chr2:201297934
|
G | A | 67 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(64): Show | 76 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.942+1304C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201297934 | ||||||
chr2:201298070
|
G | A | 2 | a0002c0002t0002g0186a0002c0002t0002g0193 | 2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.942+1168C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298070 | ||||||
chr2:201298088
|
A | G | 226 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(223): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.942+1150T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298088 | ||||||
chr2:201298182
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.942+1056C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298182 | ||||||
chr2:201298320
|
T | C | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.942+918A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298320 | ||||||
chr2:201298379
|
C | T | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.942+859G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298379 | ||||||
chr2:201298421
|
C | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.942+817G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298421 | ||||||
chr2:201298510
|
C | T | 1 | a0001c0001t0004g0291 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.942+728G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298510 | ||||||
chr2:201298542
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.942+696A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298542 | ||||||
chr2:201298744
|
C | A | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.942+494G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298744 | ||||||
chr2:201298760
|
G | A | 199 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(196): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.942+478C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201298760 | ||||||
chr2:201299127
|
T | G | 1 | a0002c0003t0005g0222 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.942+111A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 12/14 | chr2 | 201299127 | ||||||
chr2:201299703
|
G | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.880-403C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201299703 | ||||||
chr2:201299828
|
C | T | 1 | a0006c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.880-528G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201299828 | ||||||
chr2:201299832
|
G | A | 1 | a0001c0001t0003g0261 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.880-532C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201299832 | ||||||
chr2:201299932
|
G | A | 1 | a0002c0002t0002g0209 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.880-632C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201299932 | ||||||
chr2:201300082
|
C | G | 10 | a0002c0003t0005g0219a0002c0003t0005g0220a0002c0003t0005g0221others(7): Show | 10 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-782G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300082 | ||||||
chr2:201300103
|
C | T | 1 | a0002c0002t0002g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.880-803G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300103 | ||||||
chr2:201300114
|
A | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(196): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.880-814T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300114 | ||||||
chr2:201300129
|
G | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.880-829C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300129 | ||||||
chr2:201300194
|
C | T | 1 | a0006c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.880-894G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300194 | ||||||
chr2:201300241
|
C | T | 1 | a0001c0001t0004g0005 | 4 | HG02886.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-941G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300241 | ||||||
chr2:201300303
|
C | T | 1 | a0001c0001t0006g0019 | 2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.880-1003G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300303 | ||||||
chr2:201300315
|
T | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.880-1015A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300315 | ||||||
chr2:201300358
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.880-1058G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300358 | ||||||
chr2:201300483
|
T | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(242): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.880-1183A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300483 | ||||||
chr2:201300524
|
A | C | 2 | a0001c0001t0004g0298a0001c0001t0004g0302 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.880-1224T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300524 | ||||||
chr2:201300784
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.880-1484C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300784 | ||||||
chr2:201300960
|
A | G | 1 | a0001c0007t0001g0126 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.880-1660T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201300960 | ||||||
chr2:201301021
|
C | T | 1 | a0002c0002t0002g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.880-1721G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301021 | ||||||
chr2:201301207
|
T | C | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-1907A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301207 | ||||||
chr2:201301228
|
GT | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0081others(2): Show | 6 | HG02523.hp1 NA18945.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-1929delA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301228 | ||||||
chr2:201301692
|
T | A | 3 | a0002c0002t0002g0207a0002c0002t0002g0208a0002c0002t0002g0209 | 3 | HG00642.hp2 HG01993.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.880-2392A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301692 | ||||||
chr2:201301744
|
T | C | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-2444A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301744 | ||||||
chr2:201301868
|
T | C | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.880-2568A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301868 | ||||||
chr2:201301869
|
A | T | 72 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(69): Show | 81 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.880-2569T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201301869 | ||||||
chr2:201302208
|
G | T | 1 | a0002c0002t0002g0178 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.880-2908C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302208 | ||||||
chr2:201302232
|
T | G | 21 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0054others(18): Show | 22 | HG00544.hp1 HG00738.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.880-2932A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302232 | ||||||
chr2:201302280
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.880-2980G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302280 | ||||||
chr2:201302360
|
C | T | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.880-3060G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302360 | ||||||
chr2:201302383
|
A | G | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.880-3083T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302383 | ||||||
chr2:201302487
|
C | A | 7 | a0001c0001t0003g0310a0001c0001t0006g0014a0001c0001t0006g0047others(4): Show | 8 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-3187G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302487 | ||||||
chr2:201302810
|
A | C | 2 | a0001c0001t0001g0134a0002c0002t0002g0021 | 3 | HG01256.hp2 HG01258.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.880-3510T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302810 | ||||||
chr2:201302928
|
G | T | 199 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(196): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.880-3628C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201302928 | ||||||
chr2:201303013
|
T | G | 1 | a0002c0002t0002g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.880-3713A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303013 | ||||||
chr2:201303046
|
C | CA | 17 | a0001c0001t0013g0315a0001c0009t0001g0051a0002c0003t0005g0214others(14): Show | 17 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.880-3747dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303046 | ||||||
chr2:201303054
|
A | G | 1 | a0001c0001t0003g0031 | 2 | NA18986.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.880-3754T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303054 | ||||||
chr2:201303108
|
C | CA | 227 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(224): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.880-3809dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303108 | ||||||
chr2:201303127
|
C | G | 1 | a0002c0002t0002g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.880-3827G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303127 | ||||||
chr2:201303177
|
C | T | 1 | a0002c0002t0002g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.880-3877G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303177 | ||||||
chr2:201303317
|
C | G | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-4017G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303317 | ||||||
chr2:201303361
|
C | A | 3 | a0001c0009t0001g0051a0003c0004t0005g0311a0003c0004t0005g0312 | 3 | HG02630.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.880-4061G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303361 | ||||||
chr2:201303373
|
T | A | 1 | a0001c0001t0004g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.880-4073A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303373 | ||||||
chr2:201303473
|
G | A | 1 | a0001c0001t0004g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.879+4046C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303473 | ||||||
chr2:201303492
|
A | G | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.879+4027T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303492 | ||||||
chr2:201303519
|
C | T | 1 | a0001c0001t0005g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.879+4000G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303519 | ||||||
chr2:201303562
|
T | C | 1 | a0001c0001t0005g0243 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.879+3957A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303562 | ||||||
chr2:201303924
|
G | A | 1 | a0001c0001t0004g0292 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.879+3595C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303924 | ||||||
chr2:201303929
|
T | A | 1 | a0001c0001t0003g0255 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.879+3590A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303929 | ||||||
chr2:201303941
|
G | A | 1 | a0001c0001t0006g0019 | 2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.879+3578C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303941 | ||||||
chr2:201303982
|
G | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.879+3537C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303982 | ||||||
chr2:201303983
|
G | C | 2 | a0001c0001t0007g0116a0001c0001t0007g0149 | 2 | HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.879+3536C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201303983 | ||||||
chr2:201304026
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.879+3493A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304026 | ||||||
chr2:201304041
|
A | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.879+3478T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304041 | ||||||
chr2:201304060
|
G | C | 94 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(91): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.879+3459C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304060 | ||||||
chr2:201304270
|
A | G | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.879+3249T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304270 | ||||||
chr2:201304369
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.879+3150A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304369 | ||||||
chr2:201304384
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.879+3135C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304384 | ||||||
chr2:201304409
|
T | C | 227 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(224): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.879+3110A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304409 | ||||||
chr2:201304432
|
G | A | 68 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(65): Show | 77 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.879+3087C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304432 | ||||||
chr2:201304708
|
C | T | 1 | a0002c0002t0004g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879+2811G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304708 | ||||||
chr2:201304760
|
G | A | 2 | a0002c0002t0004g0210a0002c0002t0004g0211 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.879+2759C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304760 | ||||||
chr2:201304761
|
C | G | 2 | a0002c0002t0004g0210a0002c0002t0004g0211 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.879+2758G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304761 | ||||||
chr2:201304899
|
G | A | 3 | a0001c0001t0005g0242a0001c0001t0005g0243a0001c0001t0005g0244 | 3 | NA18939.hp1 NA18974.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.879+2620C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304899 | ||||||
chr2:201304997
|
C | T | 18 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0033others(15): Show | 25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.879+2522G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201304997 | ||||||
chr2:201305068
|
C | T | 1 | a0001c0001t0004g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.879+2451G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305068 | ||||||
chr2:201305217
|
G | T | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.879+2302C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305217 | ||||||
chr2:201305270
|
G | A | 20 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0036others(17): Show | 21 | HG02056.hp2 HG02071.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.879+2249C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305270 | ||||||
chr2:201305390
|
T | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.879+2129A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305390 | ||||||
chr2:201305411
|
G | C | 1 | a0002c0002t0002g0179 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.879+2108C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305411 | ||||||
chr2:201305526
|
C | T | 2 | a0002c0002t0005g0158a0002c0002t0005g0159 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.879+1993G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305526 | ||||||
chr2:201305655
|
T | C | 5 | a0001c0001t0006g0124a0001c0001t0006g0127a0001c0001t0006g0128others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+1864A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305655 | ||||||
chr2:201305684
|
A | C | 5 | a0001c0001t0006g0124a0001c0001t0006g0127a0001c0001t0006g0128others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+1835T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305684 | ||||||
chr2:201305691
|
C | A | 1 | a0001c0001t0001g0065 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.879+1828G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305691 | ||||||
chr2:201305692
|
C | G | 5 | a0001c0001t0006g0124a0001c0001t0006g0127a0001c0001t0006g0128others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+1827G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305692 | ||||||
chr2:201305694
|
T | A | 5 | a0001c0001t0006g0124a0001c0001t0006g0127a0001c0001t0006g0128others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+1825A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305694 | ||||||
chr2:201305866
|
T | C | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.879+1653A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305866 | ||||||
chr2:201305932
|
T | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(242): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.879+1587A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305932 | ||||||
chr2:201305935
|
G | T | 77 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(74): Show | 87 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.879+1584C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201305935 | ||||||
chr2:201306089
|
A | T | 3 | a0001c0001t0004g0005a0001c0001t0004g0306a0001c0001t0004g0308 | 6 | HG02886.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.879+1430T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306089 | ||||||
chr2:201306099
|
T | TA | 20 | a0001c0001t0003g0249a0001c0001t0004g0004a0001c0001t0004g0005others(17): Show | 27 | HG01167.hp2 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+1419dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306099 | ||||||
chr2:201306099
|
TA | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(111): Show | 125 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.879+1419delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306099 | ||||||
chr2:201306249
|
G | A | 1 | a0001c0001t0009g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.879+1270C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306249 | ||||||
chr2:201306269
|
T | A | 1 | a0001c0001t0007g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.879+1250A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306269 | ||||||
chr2:201306373
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.879+1146T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306373 | ||||||
chr2:201306679
|
T | C | 12 | a0002c0003t0005g0214a0002c0003t0005g0215a0002c0003t0005g0219others(9): Show | 12 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.879+840A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306679 | ||||||
chr2:201306786
|
C | CA | 26 | a0001c0001t0003g0310a0001c0001t0006g0014a0001c0001t0006g0047others(23): Show | 27 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.879+732dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306786 | ||||||
chr2:201306850
|
C | G | 46 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0033others(43): Show | 54 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(51): Show |
intron_variant | MODIFIER | c.879+669G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201306850 | ||||||
chr2:201307127
|
T | C | 1 | a0001c0001t0004g0307 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.879+392A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201307127 | ||||||
chr2:201307468
|
G | A | 1 | a0002c0002t0004g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879+51C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 11/14 | chr2 | 201307468 | ||||||
chr2:201307677
|
A | G | 1 | a0001c0001t0003g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.776-55T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201307677 | ||||||
chr2:201307972
|
A | G | 1 | a0002c0002t0002g0009 | 3 | NA18986.hp2 NA19009.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.776-350T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201307972 | ||||||
chr2:201308409
|
C | T | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.775+742G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201308409 | ||||||
chr2:201308415
|
T | C | 3 | a0001c0009t0001g0051a0003c0004t0005g0311a0003c0004t0005g0312 | 3 | HG02630.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.775+736A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201308415 | ||||||
chr2:201309089
|
C | A | 18 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0033others(15): Show | 25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.775+62G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201309089 | ||||||
chr2:201309100
|
G | A | 2 | a0001c0001t0003g0310a0005c0006t0003g0304 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.775+51C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 10/14 | chr2 | 201309100 | ||||||
chr2:201309794
|
C | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | NA18948.hp1 NA18959.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-544G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309794 | ||||||
chr2:201309855
|
C | T | 1 | a0001c0001t0005g0277 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.676-605G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309855 | ||||||
chr2:201309905
|
C | CA | 12 | a0001c0001t0004g0285a0001c0001t0004g0305a0001c0001t0004g0307others(9): Show | 14 | HG01123.hp2 HG01256.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.676-656dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309905 | ||||||
chr2:201309905
|
C | CAAAAA | 7 | a0001c0001t0013g0315a0002c0003t0005g0219a0002c0003t0005g0220others(4): Show | 7 | HG00140.hp2 HG00738.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-660_676-656dup others(5): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309905 | ||||||
chr2:201309905
|
C | CAAAAAA | 8 | a0001c0009t0001g0051a0002c0003t0005g0215a0002c0003t0005g0221others(5): Show | 8 | HG01069.hp1 HG01192.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-661_676-656dup others(6): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309905 | ||||||
chr2:201309922
|
A | G | 1 | a0001c0001t0003g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.676-672T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309922 | ||||||
chr2:201309925
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0053 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.676-676_676-675ins others(28): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | ||||||
chr2:201309925
|
A | AAAAAAAA others(19): Show |
3 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0117 | 3 | HG01978.hp2 HG03471.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.676-676_676-675ins others(26): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | ||||||
chr2:201309925
|
A | AAAAAAAA others(18): Show |
4 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0091others(1): Show | 4 | HG02071.hp1 HG02129.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(25): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | ||||||
chr2:201309925
|
A | AAAAAAAA others(17): Show |
15 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0073others(12): Show | 19 | HG00738.hp2 HG01258.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(24): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | ||||||
chr2:201309925
|
A | AAAAAAAA others(16): Show |
40 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0040others(37): Show | 41 | HG00673.hp2 HG01243.hp2 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(23): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | ||||||
chr2:201309925
|
A | AAAAAAAA others(15): Show |
27 | a0001c0001t0001g0017a0001c0001t0001g0042a0001c0001t0001g0043others(24): Show | 28 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(22): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | ||||||
chr2:201309925
|
A | AAAAAAAA others(14): Show |
6 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0038others(3): Show | 9 | HG00140.hp1 HG01106.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(21): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | ||||||
chr2:201309925
|
A | AAAAG | 6 | a0001c0001t0003g0310a0001c0001t0006g0014a0001c0001t0006g0047others(3): Show | 7 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | ||||||
chr2:201309925
|
A | AG | 3 | a0001c0001t0001g0087a0002c0002t0005g0158a0002c0002t0005g0159 | 3 | HG01123.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.676-676_676-675ins others(1): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | ||||||
chr2:201309925
|
A | AGAAG | 64 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(61): Show | 73 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.676-676_676-675ins others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | ||||||
chr2:201309925
|
A | G | 3 | a0001c0001t0001g0102a0001c0001t0003g0231a0001c0001t0003g0264 | 3 | HG00621.hp1 HG00621.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.676-675T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201309925 | ||||||
chr2:201310246
|
T | TC | 96 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0003g0010others(93): Show | 106 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.676-997_676-996ins others(1): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310246 | ||||||
chr2:201310248
|
T | A | 96 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0003g0010others(93): Show | 106 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.676-998A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310248 | ||||||
chr2:201310249
|
C | T | 96 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0003g0010others(93): Show | 106 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.676-999G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310249 | ||||||
chr2:201310250
|
C | G | 96 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0003g0010others(93): Show | 106 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.676-1000G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310250 | ||||||
chr2:201310251
|
C | A | 96 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0003g0010others(93): Show | 106 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.676-1001G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310251 | ||||||
chr2:201310258
|
T | A | 1 | a0002c0002t0002g0184 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.676-1008A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310258 | ||||||
chr2:201310267
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(100): Show | 114 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.676-1017C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310267 | ||||||
chr2:201310406
|
C | T | 1 | a0001c0001t0006g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.676-1156G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310406 | ||||||
chr2:201310473
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.676-1223T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310473 | ||||||
chr2:201310920
|
C | T | 1 | a0001c0001t0005g0279 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.676-1670G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310920 | ||||||
chr2:201310933
|
C | T | 60 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(57): Show | 68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.676-1683G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201310933 | ||||||
chr2:201311046
|
T | C | 94 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(91): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.676-1796A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311046 | ||||||
chr2:201311158
|
T | TA | 20 | a0001c0001t0003g0249a0001c0001t0003g0310a0001c0001t0004g0288others(17): Show | 20 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.676-1909dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311158 | ||||||
chr2:201311158
|
TA | T | 7 | a0001c0001t0001g0081a0001c0001t0001g0100a0001c0001t0001g0107others(4): Show | 7 | HG00323.hp2 HG00673.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-1909delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311158 | ||||||
chr2:201311179
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.676-1929C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311179 | ||||||
chr2:201311301
|
T | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(242): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.676-2051A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311301 | ||||||
chr2:201311315
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.676-2065A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311315 | ||||||
chr2:201311571
|
A | G | 245 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(242): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.676-2321T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311571 | ||||||
chr2:201311672
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.676-2422C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311672 | ||||||
chr2:201311688
|
G | A | 2 | a0002c0003t0005g0221a0002c0003t0010g0218 | 2 | HG02027.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.676-2438C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311688 | ||||||
chr2:201311700
|
C | CA | 143 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(140): Show | 156 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.676-2451dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311700 | ||||||
chr2:201311700
|
C | CAA | 85 | a0001c0001t0001g0100a0001c0001t0003g0010a0001c0001t0003g0028others(82): Show | 101 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.676-2452_676-2451d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311700 | ||||||
chr2:201311804
|
A | G | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.676-2554T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311804 | ||||||
chr2:201311927
|
C | A | 1 | a0001c0001t0003g0250 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.676-2677G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311927 | ||||||
chr2:201311934
|
A | G | 13 | a0002c0003t0005g0214a0002c0003t0005g0215a0002c0003t0005g0219others(10): Show | 13 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.676-2684T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201311934 | ||||||
chr2:201312314
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.676-3064G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201312314 | ||||||
chr2:201312734
|
CG | C | 19 | a0001c0001t0001g0100a0001c0001t0004g0004a0001c0001t0004g0005others(16): Show | 26 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.676-3485delC | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201312734 | ||||||
chr2:201312816
|
G | A | 24 | a0001c0001t0003g0310a0001c0001t0006g0014a0001c0001t0006g0047others(21): Show | 25 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.676-3566C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201312816 | ||||||
chr2:201312863
|
C | T | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.676-3613G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201312863 | ||||||
chr2:201312915
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.676-3665C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201312915 | ||||||
chr2:201313038
|
G | T | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.676-3788C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313038 | ||||||
chr2:201313059
|
G | C | 1 | a0002c0002t0002g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.676-3809C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313059 | ||||||
chr2:201313149
|
C | A | 2 | a0002c0002t0002g0186a0002c0002t0002g0193 | 2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.676-3899G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313149 | ||||||
chr2:201313149
|
C | G | 1 | a0001c0001t0003g0303 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.676-3899G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313149 | ||||||
chr2:201313235
|
A | C | 2 | a0002c0002t0004g0210a0002c0002t0004g0211 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.676-3985T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313235 | ||||||
chr2:201313363
|
C | G | 1 | a0001c0001t0003g0251 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.676-4113G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313363 | ||||||
chr2:201313366
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.676-4116C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313366 | ||||||
chr2:201313407
|
C | T | 18 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0033others(15): Show | 25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.676-4157G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313407 | ||||||
chr2:201313408
|
G | A | 1 | a0001c0001t0006g0120 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.676-4158C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313408 | ||||||
chr2:201313514
|
T | C | 5 | a0001c0001t0003g0239a0001c0001t0003g0256a0001c0001t0003g0257others(2): Show | 5 | NA18957.hp2 NA18971.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.676-4264A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313514 | ||||||
chr2:201313576
|
G | A | 1 | a0002c0002t0002g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.676-4326C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313576 | ||||||
chr2:201313642
|
A | G | 3 | a0001c0009t0001g0051a0003c0004t0005g0311a0003c0004t0005g0312 | 3 | HG02630.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.676-4392T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313642 | ||||||
chr2:201313674
|
C | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.676-4424G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313674 | ||||||
chr2:201313684
|
C | T | 1 | a0001c0001t0003g0239 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.676-4434G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313684 | ||||||
chr2:201313845
|
G | T | 3 | a0002c0002t0004g0210a0002c0002t0004g0211a0006c0010t0004g0156 | 3 | HG02717.hp2 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.676-4595C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313845 | ||||||
chr2:201313898
|
A | G | 6 | a0001c0001t0003g0273a0001c0001t0003g0274a0001c0001t0003g0275others(3): Show | 6 | HG00438.hp2 HG02027.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.676-4648T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313898 | ||||||
chr2:201313949
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.676-4699G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313949 | ||||||
chr2:201313952
|
A | G | 70 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(67): Show | 79 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.676-4702T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201313952 | ||||||
chr2:201314035
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.676-4785G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314035 | ||||||
chr2:201314287
|
T | TA | 77 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(74): Show | 87 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.676-5038_676-5037i others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314287 | ||||||
chr2:201314288
|
T | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(223): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.676-5038A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314288 | ||||||
chr2:201314298
|
T | A | 16 | a0001c0009t0001g0051a0002c0003t0005g0214a0002c0003t0005g0215others(13): Show | 16 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.676-5048A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314298 | ||||||
chr2:201314375
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0005g0235 | 2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.676-5125T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314375 | ||||||
chr2:201314420
|
T | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0016others(39): Show | 48 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.676-5170A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314420 | ||||||
chr2:201314461
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.676-5211A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314461 | ||||||
chr2:201314633
|
C | T | 1 | a0002c0002t0002g0167 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.676-5383G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314633 | ||||||
chr2:201314695
|
A | AC | 13 | a0002c0003t0005g0214a0002c0003t0005g0215a0002c0003t0005g0219others(10): Show | 13 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.676-5446_676-5445i others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314695 | ||||||
chr2:201314925
|
C | G | 1 | a0001c0001t0003g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.676-5675G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201314925 | ||||||
chr2:201315047
|
T | G | 3 | a0002c0002t0002g0023a0002c0002t0002g0170a0002c0002t0002g0171 | 4 | HG01081.hp2 HG01496.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-5797A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315047 | ||||||
chr2:201315062
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.676-5812T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315062 | ||||||
chr2:201315254
|
A | G | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.676-6004T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315254 | ||||||
chr2:201315319
|
A | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.676-6069T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315319 | ||||||
chr2:201315511
|
C | T | 7 | a0002c0002t0002g0160a0002c0002t0002g0164a0002c0002t0002g0167others(4): Show | 7 | HG00323.hp1 HG01099.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-6261G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315511 | ||||||
chr2:201315522
|
T | G | 28 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(25): Show | 29 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.676-6272A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315522 | ||||||
chr2:201315539
|
C | T | 10 | a0002c0003t0005g0219a0002c0003t0005g0220a0002c0003t0005g0221others(7): Show | 10 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.676-6289G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315539 | ||||||
chr2:201315543
|
C | T | 1 | a0002c0002t0002g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.676-6293G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315543 | ||||||
chr2:201315768
|
T | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(196): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.676-6518A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315768 | ||||||
chr2:201315994
|
C | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.676-6744G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201315994 | ||||||
chr2:201316012
|
C | A | 1 | a0001c0001t0003g0251 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.676-6762G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316012 | ||||||
chr2:201316092
|
T | C | 6 | a0001c0001t0003g0010a0001c0001t0003g0030a0001c0001t0003g0252others(3): Show | 9 | NA18940.hp2 NA18943.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.676-6842A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316092 | ||||||
chr2:201316117
|
A | C | 1 | a0001c0001t0004g0309 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.676-6867T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316117 | ||||||
chr2:201316435
|
C | T | 68 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(65): Show | 77 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.676-7185G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316435 | ||||||
chr2:201316524
|
C | T | 245 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(242): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.676-7274G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316524 | ||||||
chr2:201316561
|
A | G | 3 | a0001c0009t0001g0051a0003c0004t0005g0311a0003c0004t0005g0312 | 3 | HG02630.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.676-7311T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316561 | ||||||
chr2:201316580
|
C | T | 1 | a0002c0002t0002g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.676-7330G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316580 | ||||||
chr2:201316637
|
G | A | 2 | a0002c0002t0002g0027a0002c0002t0002g0187 | 3 | HG01358.hp1 HG01361.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.676-7387C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316637 | ||||||
chr2:201316975
|
A | C | 3 | a0001c0001t0003g0310a0001c0001t0011g0313a0002c0002t0003g0157 | 3 | HG02109.hp2 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.676-7725T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201316975 | ||||||
chr2:201317030
|
G | T | 1 | a0002c0002t0002g0188 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.676-7780C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201317030 | ||||||
chr2:201317047
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.676-7797G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201317047 | ||||||
chr2:201317092
|
A | T | 1 | a0001c0001t0003g0228 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.676-7842T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201317092 | ||||||
chr2:201317338
|
G | T | 29 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(26): Show | 30 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(27): Show |
intron_variant | MODIFIER | c.676-8088C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201317338 | ||||||
chr2:201317975
|
A | G | 1 | a0002c0002t0002g0166 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.676-8725T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201317975 | ||||||
chr2:201318479
|
C | T | 2 | a0001c0001t0008g0067a0001c0001t0008g0068 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.676-9229G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318479 | ||||||
chr2:201318509
|
A | C | 1 | a0002c0003t0005g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.676-9259T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318509 | ||||||
chr2:201318584
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.676-9334T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318584 | ||||||
chr2:201318585
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.676-9335A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318585 | ||||||
chr2:201318595
|
A | G | 1 | a0001c0001t0004g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.676-9345T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318595 | ||||||
chr2:201318808
|
G | A | 2 | a0001c0001t0003g0266a0001c0001t0003g0267 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.676-9558C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318808 | ||||||
chr2:201318931
|
G | C | 1 | a0002c0003t0005g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.676-9681C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318931 | ||||||
chr2:201318938
|
CAG | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.676-9690_676-9689d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201318938 | ||||||
chr2:201319285
|
T | G | 2 | a0001c0001t0002g0271a0002c0002t0002g0165 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.676-10035A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201319285 | ||||||
chr2:201319409
|
TA | T | 13 | a0002c0003t0005g0214a0002c0003t0005g0215a0002c0003t0005g0219others(10): Show | 13 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.676-10160delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201319409 | ||||||
chr2:201319442
|
C | T | 199 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(196): Show | 220 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.676-10192G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201319442 | ||||||
chr2:201319492
|
A | G | 25 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(22): Show | 26 | HG02145.hp1 HG02258.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.676-10242T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201319492 | ||||||
chr2:201319608
|
C | T | 245 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(242): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.676-10358G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201319608 | ||||||
chr2:201320188
|
G | A | 1 | a0001c0001t0003g0258 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.675+10282C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320188 | ||||||
chr2:201320216
|
G | A | 10 | a0002c0003t0005g0219a0002c0003t0005g0220a0002c0003t0005g0221others(7): Show | 10 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.675+10254C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320216 | ||||||
chr2:201320298
|
G | A | 1 | a0001c0001t0003g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.675+10172C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320298 | ||||||
chr2:201320336
|
C | T | 1 | a0001c0001t0004g0295 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.675+10134G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320336 | ||||||
chr2:201320351
|
C | T | 7 | a0001c0001t0003g0310a0001c0001t0006g0014a0001c0001t0006g0047others(4): Show | 8 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.675+10119G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320351 | ||||||
chr2:201320381
|
G | A | 1 | a0001c0001t0004g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.675+10089C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320381 | ||||||
chr2:201320409
|
A | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(172): Show | 195 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.675+10061T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320409 | ||||||
chr2:201320434
|
C | T | 1 | a0001c0001t0003g0247 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.675+10036G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320434 | ||||||
chr2:201320439
|
C | G | 1 | a0001c0001t0003g0303 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.675+10031G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320439 | ||||||
chr2:201320439
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.675+10031G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320439 | ||||||
chr2:201320566
|
T | C | 308 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(305): Show | 358 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(355): Show |
intron_variant | MODIFIER | c.675+9904A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320566 | ||||||
chr2:201320649
|
C | G | 1 | a0001c0001t0006g0047 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.675+9821G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320649 | ||||||
chr2:201320703
|
C | T | 1 | a0001c0001t0003g0283 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.675+9767G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320703 | ||||||
chr2:201320709
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.675+9761G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320709 | ||||||
chr2:201320881
|
G | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.675+9589C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201320881 | ||||||
chr2:201321081
|
C | T | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0303 | 3 | HG02896.hp2 HG02897.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.675+9389G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321081 | ||||||
chr2:201321105
|
A | G | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.675+9365T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321105 | ||||||
chr2:201321238
|
C | T | 1 | a0001c0001t0003g0259 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.675+9232G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321238 | ||||||
chr2:201321644
|
G | A | 1 | a0001c0001t0003g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.675+8826C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321644 | ||||||
chr2:201321699
|
G | C | 226 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(223): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.675+8771C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321699 | ||||||
chr2:201321860
|
C | T | 1 | a0004c0008t0007g0076 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.675+8610G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201321860 | ||||||
chr2:201322001
|
G | C | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+8469C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322001 | ||||||
chr2:201322039
|
C | T | 1 | a0001c0001t0003g0269 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.675+8431G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322039 | ||||||
chr2:201322042
|
G | A | 72 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(69): Show | 81 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.675+8428C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322042 | ||||||
chr2:201322066
|
C | T | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+8404G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322066 | ||||||
chr2:201322072
|
C | T | 1 | a0001c0001t0004g0287 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.675+8398G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322072 | ||||||
chr2:201322124
|
T | C | 1 | a0001c0001t0004g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.675+8346A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322124 | ||||||
chr2:201322262
|
T | TA | 3 | a0001c0009t0001g0051a0003c0004t0005g0311a0003c0004t0005g0312 | 3 | HG02630.hp1 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.675+8207_675+8208i others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322262 | ||||||
chr2:201322263
|
C | A | 245 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(242): Show | 274 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.675+8207G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322263 | ||||||
chr2:201322301
|
G | A | 3 | a0002c0002t0004g0210a0002c0002t0004g0211a0006c0010t0004g0156 | 3 | HG02717.hp2 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.675+8169C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322301 | ||||||
chr2:201322318
|
T | G | 1 | a0002c0002t0002g0195 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.675+8152A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322318 | ||||||
chr2:201322439
|
T | TA | 3 | a0002c0002t0002g0020a0002c0002t0002g0163a0002c0002t0002g0213 | 4 | HG00423.hp2 HG02071.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+8030dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322439 | ||||||
chr2:201322802
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.675+7668C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322802 | ||||||
chr2:201322900
|
A | G | 1 | a0002c0002t0002g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.675+7570T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201322900 | ||||||
chr2:201323055
|
A | C | 94 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(91): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.675+7415T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323055 | ||||||
chr2:201323135
|
A | G | 70 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(67): Show | 79 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.675+7335T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323135 | ||||||
chr2:201323464
|
G | A | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+7006C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323464 | ||||||
chr2:201323593
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.675+6877G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323593 | ||||||
chr2:201323784
|
C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0043others(7): Show | 12 | HG00642.hp1 HG00738.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.675+6678_675+6685d others(10): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(2): Show |
86 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(83): Show | 95 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.675+6677_675+6685d others(11): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(3): Show |
13 | a0001c0001t0001g0017a0001c0001t0001g0054a0001c0001t0001g0101others(10): Show | 14 | HG00544.hp1 HG00621.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.675+6676_675+6685d others(12): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(4): Show |
5 | a0001c0001t0004g0294a0001c0001t0007g0071a0001c0001t0007g0077others(2): Show | 5 | HG02886.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.675+6675_675+6685d others(13): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(5): Show |
17 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(14): Show | 18 | HG02145.hp1 HG02559.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.675+6674_675+6685d others(14): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(6): Show |
6 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0298others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.675+6673_675+6685d others(15): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0003g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.675+6671_675+6685d others(17): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0003g0266 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.675+6669_675+6685d others(19): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(11): Show |
7 | a0001c0001t0003g0246a0001c0001t0003g0267a0001c0001t0003g0303others(4): Show | 7 | HG01884.hp1 HG02451.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.675+6668_675+6685d others(20): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(12): Show |
17 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0228others(14): Show | 19 | HG02717.hp1 HG03239.hp2 HG03490.hp2 others(16): Show |
intron_variant | MODIFIER | c.675+6667_675+6685d others(21): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(13): Show |
21 | a0001c0001t0003g0030a0001c0001t0003g0230a0001c0001t0003g0237others(18): Show | 23 | HG00438.hp2 HG00558.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.675+6685_675+6686i others(22): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(14): Show |
21 | a0001c0001t0003g0010a0001c0001t0003g0031a0001c0001t0003g0032others(18): Show | 26 | HG00140.hp2 HG00423.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.675+6685_675+6686i others(23): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(15): Show |
6 | a0001c0001t0003g0262a0001c0001t0003g0264a0001c0001t0003g0265others(3): Show | 6 | HG02027.hp1 HG03710.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.675+6685_675+6686i others(24): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0011g0313a0002c0003t0005g0215 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.675+6685_675+6686i others(25): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(18): Show |
2 | a0001c0009t0001g0051a0002c0003t0005g0227 | 2 | HG01192.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.675+6685_675+6686i others(27): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(21): Show |
1 | a0003c0004t0005g0311 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.675+6685_675+6686i others(30): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
C | CAAAAAAA others(22): Show |
1 | a0003c0004t0005g0312 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.675+6685_675+6686i others(31): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323784
|
CA | C | 64 | a0001c0001t0002g0271a0001c0001t0004g0033a0001c0001t0008g0067others(61): Show | 85 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.675+6685delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323784 | ||||||
chr2:201323804
|
G | A | 91 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(88): Show | 101 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.675+6666C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323804 | ||||||
chr2:201323805
|
T | A | 93 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(90): Show | 103 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.675+6665A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323805 | ||||||
chr2:201323809
|
G | T | 93 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(90): Show | 102 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.675+6661C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323809 | ||||||
chr2:201323882
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.675+6588G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201323882 | ||||||
chr2:201324016
|
G | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.675+6454C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324016 | ||||||
chr2:201324022
|
T | G | 1 | a0002c0003t0005g0222 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.675+6448A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324022 | ||||||
chr2:201324037
|
C | T | 1 | a0001c0001t0007g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.675+6433G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324037 | ||||||
chr2:201324046
|
T | TAAAAAAG others(164): Show |
1 | a0001c0001t0005g0281 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.675+6423_675+6424i others(173): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324046 | ||||||
chr2:201324080
|
A | G | 70 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(67): Show | 79 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.675+6390T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324080 | ||||||
chr2:201324119
|
T | G | 1 | a0002c0002t0002g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.675+6351A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324119 | ||||||
chr2:201324193
|
C | T | 1 | a0001c0001t0003g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.675+6277G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324193 | ||||||
chr2:201324206
|
C | T | 1 | a0002c0002t0002g0172 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.675+6264G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324206 | ||||||
chr2:201324251
|
G | A | 312 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(309): Show | 362 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.675+6219C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324251 | ||||||
chr2:201324288
|
C | A | 1 | a0002c0002t0002g0188 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.675+6182G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324288 | ||||||
chr2:201324383
|
G | C | 1 | a0002c0003t0005g0222 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.675+6087C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324383 | ||||||
chr2:201324546
|
T | C | 1 | a0002c0002t0002g0189 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.675+5924A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324546 | ||||||
chr2:201324593
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.675+5877C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324593 | ||||||
chr2:201324651
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG00323.hp2 HG01243.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.675+5819C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324651 | ||||||
chr2:201324702
|
G | C | 5 | a0001c0001t0004g0289a0001c0001t0004g0290a0001c0001t0004g0291others(2): Show | 5 | HG02809.hp1 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.675+5768C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324702 | ||||||
chr2:201324728
|
T | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(101): Show | 115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.675+5742A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324728 | ||||||
chr2:201324936
|
T | C | 68 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(65): Show | 77 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.675+5534A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201324936 | ||||||
chr2:201325001
|
G | A | 26 | a0001c0001t0003g0310a0001c0001t0006g0014a0001c0001t0006g0047others(23): Show | 27 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.675+5469C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325001 | ||||||
chr2:201325004
|
T | C | 26 | a0001c0001t0003g0310a0001c0001t0006g0014a0001c0001t0006g0047others(23): Show | 27 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.675+5466A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325004 | ||||||
chr2:201325098
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | NA18948.hp1 NA18959.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+5372G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325098 | ||||||
chr2:201325141
|
A | G | 16 | a0001c0009t0001g0051a0002c0003t0005g0214a0002c0003t0005g0215others(13): Show | 16 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.675+5329T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325141 | ||||||
chr2:201325241
|
T | G | 1 | a0001c0001t0012g0314 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.675+5229A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325241 | ||||||
chr2:201325242
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.675+5228C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325242 | ||||||
chr2:201325275
|
A | C | 94 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(91): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.675+5195T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325275 | ||||||
chr2:201325539
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.675+4931C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325539 | ||||||
chr2:201325731
|
ATTCCACC others(5): Show |
A | 1 | a0001c0001t0006g0120 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.675+4727_675+4738d others(14): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325731 | ||||||
chr2:201325748
|
A | C | 1 | a0001c0001t0006g0120 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.675+4722T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325748 | ||||||
chr2:201325749
|
T | A | 1 | a0001c0001t0006g0120 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.675+4721A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325749 | ||||||
chr2:201325887
|
C | T | 18 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0033others(15): Show | 25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.675+4583G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325887 | ||||||
chr2:201325945
|
G | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(102): Show | 116 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.675+4525C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325945 | ||||||
chr2:201325948
|
C | T | 1 | a0001c0001t0005g0235 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.675+4522G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201325948 | ||||||
chr2:201326227
|
TG | T | 18 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0033others(15): Show | 25 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.675+4242delC | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201326227 | ||||||
chr2:201326526
|
C | T | 2 | a0001c0001t0008g0067a0001c0001t0008g0068 | 2 | HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.675+3944G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201326526 | ||||||
chr2:201326720
|
C | T | 1 | a0001c0001t0001g0012 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.675+3750G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201326720 | ||||||
chr2:201326913
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0053a0001c0001t0001g0081others(5): Show | 9 | HG02074.hp1 HG02523.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.675+3557T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201326913 | ||||||
chr2:201326916
|
T | A | 1 | a0002c0002t0002g0164 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.675+3554A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201326916 | ||||||
chr2:201327046
|
C | T | 1 | a0001c0001t0004g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.675+3424G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327046 | ||||||
chr2:201327067
|
T | C | 1 | a0001c0001t0004g0285 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.675+3403A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327067 | ||||||
chr2:201327123
|
T | C | 1 | a0002c0002t0002g0172 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.675+3347A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327123 | ||||||
chr2:201327290
|
CA | C | 3 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0145 | 3 | HG02559.hp2 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.675+3179delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327290 | ||||||
chr2:201327351
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.675+3119T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327351 | ||||||
chr2:201327382
|
G | A | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.675+3088C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327382 | ||||||
chr2:201327465
|
G | GA | 77 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(74): Show | 87 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.675+3004dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327465 | ||||||
chr2:201327648
|
A | G | 17 | a0001c0001t0013g0315a0001c0009t0001g0051a0002c0003t0005g0214others(14): Show | 17 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.675+2822T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327648 | ||||||
chr2:201327649
|
G | GT | 3 | a0001c0001t0003g0228a0001c0001t0003g0229a0001c0001t0003g0230 | 3 | NA18950.hp1 NA18970.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.675+2820dupA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327649 | ||||||
chr2:201327699
|
T | G | 94 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(91): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.675+2771A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327699 | ||||||
chr2:201327842
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.675+2628T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327842 | ||||||
chr2:201327920
|
GACTAA | G | 3 | a0001c0001t0004g0284a0001c0001t0004g0285a0001c0001t0004g0301 | 3 | HG01261.hp2 HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.675+2545_675+2549d others(7): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327920 | ||||||
chr2:201327971
|
C | T | 1 | a0001c0001t0003g0239 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.675+2499G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201327971 | ||||||
chr2:201328012
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.675+2458C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328012 | ||||||
chr2:201328023
|
G | A | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.675+2447C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328023 | ||||||
chr2:201328081
|
C | CACTTAAA others(13): Show |
1 | a0001c0001t0001g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.675+2369_675+2388d others(22): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328081 | ||||||
chr2:201328167
|
T | A | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.675+2303A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328167 | ||||||
chr2:201328347
|
T | A | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.675+2123A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328347 | ||||||
chr2:201328478
|
T | A | 2 | a0002c0002t0004g0210a0002c0002t0004g0211 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.675+1992A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328478 | ||||||
chr2:201328538
|
G | A | 1 | a0002c0002t0002g0174 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.675+1932C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328538 | ||||||
chr2:201328598
|
G | A | 3 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0145 | 3 | HG02559.hp2 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.675+1872C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328598 | ||||||
chr2:201328628
|
G | A | 1 | a0006c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.675+1842C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328628 | ||||||
chr2:201328727
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.675+1743A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328727 | ||||||
chr2:201328728
|
G | A | 1 | a0006c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.675+1742C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328728 | ||||||
chr2:201328740
|
A | G | 46 | a0001c0001t0004g0004a0001c0001t0004g0005a0001c0001t0004g0033others(43): Show | 54 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(51): Show |
intron_variant | MODIFIER | c.675+1730T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201328740 | ||||||
chr2:201329474
|
C | T | 1 | a0002c0002t0002g0166 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.675+996G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201329474 | ||||||
chr2:201329502
|
A | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03927.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.675+968T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201329502 | ||||||
chr2:201329529
|
C | T | 1 | a0001c0001t0004g0307 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.675+941G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201329529 | ||||||
chr2:201329736
|
T | C | 6 | a0001c0001t0003g0273a0001c0001t0003g0274a0001c0001t0003g0275others(3): Show | 6 | HG00438.hp2 HG02027.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+734A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201329736 | ||||||
chr2:201329986
|
C | T | 2 | a0002c0002t0002g0176a0002c0002t0002g0195 | 2 | HG02155.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.675+484G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201329986 | ||||||
chr2:201330047
|
G | A | 1 | a0002c0002t0002g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.675+423C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330047 | ||||||
chr2:201330156
|
T | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | NA18948.hp1 NA18959.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+314A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330156 | ||||||
chr2:201330174
|
T | C | 1 | a0001c0001t0006g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.675+296A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330174 | ||||||
chr2:201330209
|
T | C | 6 | a0002c0002t0002g0007a0002c0002t0002g0190a0002c0002t0002g0197others(3): Show | 8 | NA18939.hp2 NA18956.hp2 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.675+261A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330209 | ||||||
chr2:201330213
|
A | G | 3 | a0002c0002t0004g0210a0002c0002t0004g0211a0006c0010t0004g0156 | 3 | HG02717.hp2 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.675+257T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330213 | ||||||
chr2:201330307
|
T | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(120): Show | 134 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.675+163A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 9/14 | chr2 | 201330307 | ||||||
chr2:201330588
|
G | A | 9 | a0001c0001t0004g0004a0001c0001t0004g0033a0001c0001t0004g0284others(6): Show | 13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.623-66C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 8/14 | chr2 | 201330588 | ||||||
chr2:201330723
|
G | A | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.622+13C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 8/14 | chr2 | 201330723 | ||||||
chr2:201330971
|
C | CT | 10 | a0001c0001t0001g0036a0001c0001t0001g0073a0001c0001t0001g0074others(7): Show | 10 | HG00673.hp2 HG02055.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.525-139dupA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201330971 | ||||||
chr2:201331340
|
C | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(223): Show | 255 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.525-507G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331340 | ||||||
chr2:201331561
|
G | A | 2 | a0001c0001t0006g0128a0001c0001t0007g0129 | 2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.525-728C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331561 | ||||||
chr2:201331567
|
C | T | 1 | a0002c0002t0002g0009 | 3 | NA18986.hp2 NA19009.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.525-734G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331567 | ||||||
chr2:201331672
|
A | G | 1 | a0001c0001t0003g0237 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.525-839T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331672 | ||||||
chr2:201331811
|
T | C | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.525-978A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331811 | ||||||
chr2:201331829
|
G | C | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | NA18966.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.525-996C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331829 | ||||||
chr2:201331994
|
A | G | 66 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(63): Show | 75 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.525-1161T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201331994 | ||||||
chr2:201332166
|
G | C | 4 | a0001c0001t0003g0310a0001c0001t0013g0315a0003c0004t0005g0311others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-1333C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332166 | ||||||
chr2:201332291
|
C | T | 5 | a0001c0001t0004g0005a0001c0001t0004g0306a0001c0001t0004g0307others(2): Show | 8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.525-1458G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332291 | ||||||
chr2:201332726
|
C | T | 1 | a0002c0002t0002g0167 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.525-1893G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332726 | ||||||
chr2:201332826
|
CG | C | 3 | a0001c0001t0004g0005a0001c0001t0004g0306a0001c0001t0004g0308 | 6 | HG02886.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.525-1994delC | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332826 | ||||||
chr2:201332954
|
A | T | 4 | a0001c0001t0003g0310a0001c0001t0013g0315a0003c0004t0005g0311others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-2121T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332954 | ||||||
chr2:201332959
|
C | A | 1 | a0002c0002t0002g0023 | 2 | HG01081.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.525-2126G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201332959 | ||||||
chr2:201333065
|
A | G | 1 | a0001c0001t0004g0005 | 4 | HG02886.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-2232T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333065 | ||||||
chr2:201333225
|
G | A | 2 | a0001c0001t0007g0116a0001c0001t0007g0149 | 2 | HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.525-2392C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333225 | ||||||
chr2:201333541
|
C | T | 4 | a0001c0001t0003g0310a0001c0001t0013g0315a0003c0004t0005g0311others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-2708G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333541 | ||||||
chr2:201333617
|
G | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(188): Show | 212 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.525-2784C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333617 | ||||||
chr2:201333805
|
A | T | 5 | a0001c0001t0004g0005a0001c0001t0004g0306a0001c0001t0004g0307others(2): Show | 8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.525-2972T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333805 | ||||||
chr2:201333866
|
C | T | 4 | a0001c0001t0004g0305a0002c0002t0002g0021a0002c0002t0002g0024others(1): Show | 6 | HG01123.hp2 HG01175.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.525-3033G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333866 | ||||||
chr2:201333890
|
C | A | 2 | a0001c0001t0004g0284a0001c0001t0004g0285 | 2 | HG01261.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.525-3057G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201333890 | ||||||
chr2:201334040
|
C | T | 15 | a0002c0002t0002g0023a0002c0002t0002g0160a0002c0002t0002g0164others(12): Show | 16 | HG00323.hp1 HG01081.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.525-3207G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334040 | ||||||
chr2:201334072
|
C | G | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.525-3239G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334072 | ||||||
chr2:201334114
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.525-3281C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334114 | ||||||
chr2:201334122
|
G | C | 1 | a0001c0001t0004g0307 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.525-3289C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334122 | ||||||
chr2:201334185
|
G | GT | 312 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(309): Show | 362 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(359): Show |
intron_variant | MODIFIER | c.525-3353_525-3352i others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334185 | ||||||
chr2:201334233
|
C | T | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.525-3400G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334233 | ||||||
chr2:201334550
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.525-3717C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334550 | ||||||
chr2:201334601
|
T | C | 191 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(188): Show | 212 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.525-3768A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334601 | ||||||
chr2:201334732
|
A | G | 225 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(222): Show | 254 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.525-3899T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334732 | ||||||
chr2:201334782
|
TA | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(180): Show | 203 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.525-3950delT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334782 | ||||||
chr2:201334853
|
T | C | 1 | a0001c0001t0006g0120 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.525-4020A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334853 | ||||||
chr2:201334939
|
G | A | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.525-4106C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334939 | ||||||
chr2:201334955
|
T | G | 3 | a0001c0001t0003g0236a0001c0001t0003g0266a0001c0001t0003g0267 | 3 | HG02896.hp2 HG02897.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.525-4122A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334955 | ||||||
chr2:201334965
|
T | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(183): Show | 206 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.525-4132A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334965 | ||||||
chr2:201334976
|
G | A | 5 | a0001c0001t0004g0005a0001c0001t0004g0306a0001c0001t0004g0307others(2): Show | 8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.525-4143C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201334976 | ||||||
chr2:201335056
|
G | A | 1 | a0001c0001t0007g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.525-4223C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335056 | ||||||
chr2:201335101
|
C | T | 221 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(218): Show | 250 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.525-4268G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335101 | ||||||
chr2:201335269
|
CTA | C | 12 | a0002c0002t0004g0216a0002c0002t0004g0217a0002c0003t0005g0219others(9): Show | 12 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.525-4438_525-4437d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335269 | ||||||
chr2:201335360
|
T | C | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.525-4527A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335360 | ||||||
chr2:201335457
|
T | C | 15 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(12): Show | 16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.525-4624A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335457 | ||||||
chr2:201335540
|
T | C | 9 | a0001c0001t0004g0004a0001c0001t0004g0033a0001c0001t0004g0284others(6): Show | 13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.525-4707A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335540 | ||||||
chr2:201335600
|
T | C | 1 | a0001c0001t0008g0068 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.525-4767A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335600 | ||||||
chr2:201335608
|
C | A | 1 | a0002c0003t0005g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.525-4775G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335608 | ||||||
chr2:201335608
|
C | G | 225 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(222): Show | 254 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.525-4775G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335608 | ||||||
chr2:201335699
|
T | A | 4 | a0001c0001t0003g0310a0001c0001t0013g0315a0003c0004t0005g0311others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-4866A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335699 | ||||||
chr2:201335727
|
A | G | 260 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(257): Show | 290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.525-4894T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335727 | ||||||
chr2:201335852
|
C | T | 216 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(213): Show | 241 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.525-5019G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335852 | ||||||
chr2:201335945
|
T | A | 4 | a0001c0001t0003g0310a0001c0001t0013g0315a0003c0004t0005g0311others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-5112A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201335945 | ||||||
chr2:201336007
|
G | A | 4 | a0001c0001t0003g0310a0001c0001t0013g0315a0003c0004t0005g0311others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-5174C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336007 | ||||||
chr2:201336064
|
T | C | 15 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(12): Show | 16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.525-5231A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336064 | ||||||
chr2:201336112
|
GTGAGCAT others(6): Show |
G | 191 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(188): Show | 212 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.525-5292_525-5280d others(15): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336112 | ||||||
chr2:201336119
|
T | C | 7 | a0001c0001t0004g0004a0001c0001t0004g0033a0001c0001t0004g0286others(4): Show | 11 | HG01167.hp2 HG01175.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.525-5286A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336119 | ||||||
chr2:201336180
|
C | T | 2 | a0001c0001t0006g0052a0001c0009t0001g0051 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.525-5347G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336180 | ||||||
chr2:201336466
|
C | T | 15 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(12): Show | 16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.525-5633G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336466 | ||||||
chr2:201336622
|
C | T | 1 | a0002c0002t0002g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.524+5748G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336622 | ||||||
chr2:201336729
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.524+5641A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336729 | ||||||
chr2:201336757
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.524+5613A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336757 | ||||||
chr2:201336818
|
T | C | 1 | a0002c0003t0005g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.524+5552A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201336818 | ||||||
chr2:201337028
|
ATTGT | A | 190 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(187): Show | 211 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.524+5338_524+5341d others(6): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337028 | ||||||
chr2:201337119
|
G | A | 15 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(12): Show | 16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.524+5251C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337119 | ||||||
chr2:201337356
|
G | C | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.524+5014C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337356 | ||||||
chr2:201337696
|
A | G | 1 | a0001c0001t0003g0237 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.524+4674T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337696 | ||||||
chr2:201337711
|
C | T | 8 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(5): Show | 10 | HG00738.hp2 HG01109.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.524+4659G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337711 | ||||||
chr2:201337840
|
G | A | 190 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(187): Show | 211 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.524+4530C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337840 | ||||||
chr2:201337880
|
G | A | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.524+4490C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337880 | ||||||
chr2:201337891
|
C | T | 4 | a0001c0001t0003g0310a0001c0001t0013g0315a0003c0004t0005g0311others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+4479G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201337891 | ||||||
chr2:201338068
|
A | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(187): Show | 211 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.524+4302T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338068 | ||||||
chr2:201338340
|
C | T | 65 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(62): Show | 74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.524+4030G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338340 | ||||||
chr2:201338341
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.524+4029C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338341 | ||||||
chr2:201338512
|
G | A | 221 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(218): Show | 250 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(247): Show |
intron_variant | MODIFIER | c.524+3858C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338512 | ||||||
chr2:201338544
|
A | C | 1 | a0002c0002t0002g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.524+3826T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338544 | ||||||
chr2:201338667
|
C | T | 10 | a0001c0001t0004g0004a0001c0001t0004g0033a0001c0001t0004g0284others(7): Show | 14 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.524+3703G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338667 | ||||||
chr2:201338864
|
G | T | 10 | a0001c0001t0004g0004a0001c0001t0004g0033a0001c0001t0004g0284others(7): Show | 14 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.524+3506C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201338864 | ||||||
chr2:201339032
|
T | A | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.524+3338A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339032 | ||||||
chr2:201339055
|
T | TTGTTGGG others(119): Show |
1 | a0001c0001t0006g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.524+3314_524+3315i others(128): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339055 | ||||||
chr2:201339055
|
T | TTGTTGGG others(120): Show |
4 | a0001c0001t0006g0124a0001c0001t0006g0127a0001c0001t0006g0128others(1): Show | 4 | HG02717.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+3314_524+3315i others(129): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339055 | ||||||
chr2:201339065
|
A | G | 1 | a0001c0001t0007g0072 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.524+3305T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339065 | ||||||
chr2:201339100
|
T | C | 10 | a0001c0001t0004g0004a0001c0001t0004g0033a0001c0001t0004g0284others(7): Show | 14 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.524+3270A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339100 | ||||||
chr2:201339378
|
C | A | 15 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(12): Show | 16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.524+2992G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339378 | ||||||
chr2:201339400
|
T | C | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.524+2970A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339400 | ||||||
chr2:201339473
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.524+2897A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339473 | ||||||
chr2:201339490
|
T | C | 5 | a0001c0001t0004g0005a0001c0001t0004g0306a0001c0001t0004g0307others(2): Show | 8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.524+2880A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339490 | ||||||
chr2:201339692
|
T | G | 1 | a0001c0001t0003g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.524+2678A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339692 | ||||||
chr2:201339730
|
T | C | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.524+2640A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339730 | ||||||
chr2:201339794
|
C | G | 1 | a0001c0001t0011g0313 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.524+2576G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339794 | ||||||
chr2:201339909
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.524+2461A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201339909 | ||||||
chr2:201340018
|
T | C | 244 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(241): Show | 273 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.524+2352A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340018 | ||||||
chr2:201340026
|
A | G | 9 | a0001c0001t0004g0004a0001c0001t0004g0033a0001c0001t0004g0284others(6): Show | 13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.524+2344T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340026 | ||||||
chr2:201340035
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.524+2335C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340035 | ||||||
chr2:201340188
|
C | T | 1 | a0002c0002t0002g0021 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.524+2182G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340188 | ||||||
chr2:201340276
|
G | T | 15 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(12): Show | 16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.524+2094C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340276 | ||||||
chr2:201340278
|
T | A | 15 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(12): Show | 16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.524+2092A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340278 | ||||||
chr2:201340287
|
T | C | 65 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(62): Show | 74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.524+2083A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340287 | ||||||
chr2:201340399
|
A | G | 1 | a0001c0001t0003g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.524+1971T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340399 | ||||||
chr2:201340474
|
C | T | 95 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(92): Show | 112 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.524+1896G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340474 | ||||||
chr2:201340493
|
C | A | 1 | a0001c0001t0007g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.524+1877G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340493 | ||||||
chr2:201340626
|
C | T | 2 | a0001c0001t0007g0070a0001c0001t0007g0071 | 2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.524+1744G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340626 | ||||||
chr2:201340717
|
G | T | 65 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(62): Show | 74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.524+1653C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340717 | ||||||
chr2:201340797
|
C | T | 2 | a0001c0001t0003g0310a0001c0001t0013g0315 | 2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.524+1573G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201340797 | ||||||
chr2:201341226
|
A | G | 3 | a0001c0001t0004g0289a0001c0001t0004g0290a0001c0001t0004g0291 | 3 | HG02970.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.524+1144T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341226 | ||||||
chr2:201341239
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.524+1131A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341239 | ||||||
chr2:201341392
|
C | CAT | 5 | a0002c0002t0002g0164a0002c0002t0002g0200a0002c0002t0002g0201others(2): Show | 5 | HG00323.hp1 HG01099.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.524+976_524+977dup others(2): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341392 | ||||||
chr2:201341392
|
C | CATAT | 3 | a0002c0002t0002g0020a0002c0002t0002g0163a0002c0002t0002g0213 | 4 | HG00423.hp2 HG02071.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+974_524+977dup others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341392 | ||||||
chr2:201341392
|
CAT | C | 194 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(191): Show | 215 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.524+976_524+977del others(2): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341392 | ||||||
chr2:201341392
|
CATAT | C | 16 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(13): Show | 17 | HG01433.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.524+974_524+977del others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341392 | ||||||
chr2:201341486
|
TAC | T | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.524+882_524+883del others(2): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341486 | ||||||
chr2:201341535
|
G | GTA | 2 | a0002c0002t0002g0008a0002c0002t0002g0199 | 4 | HG00544.hp2 HG02040.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+833_524+834dup others(2): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341535 | ||||||
chr2:201341535
|
G | GTATA | 4 | a0001c0001t0003g0310a0001c0001t0013g0315a0003c0004t0005g0311others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.524+831_524+834dup others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341535 | ||||||
chr2:201341597
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(127): Show | 142 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.524+773C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341597 | ||||||
chr2:201341622
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.524+748T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341622 | ||||||
chr2:201341849
|
T | C | 1 | a0001c0007t0001g0126 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.524+521A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201341849 | ||||||
chr2:201342014
|
C | T | 1 | a0002c0002t0002g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.524+356G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201342014 | ||||||
chr2:201342141
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.524+229A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201342141 | ||||||
chr2:201342212
|
T | A | 3 | a0001c0001t0006g0127a0001c0001t0006g0128a0001c0001t0007g0129 | 3 | HG02976.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.524+158A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 7/14 | chr2 | 201342212 | ||||||
chr2:201342514
|
T | A | 1 | a0001c0001t0004g0301 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.463-83A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201342514 | ||||||
chr2:201342529
|
G | A | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.463-98C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201342529 | ||||||
chr2:201342541
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | NA18979.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.463-110T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201342541 | ||||||
chr2:201342993
|
A | C | 1 | a0001c0001t0003g0272 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.463-562T>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201342993 | ||||||
chr2:201343063
|
G | A | 1 | a0002c0002t0002g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.463-632C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343063 | ||||||
chr2:201343270
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(125): Show | 140 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.463-839A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343270 | ||||||
chr2:201343329
|
T | C | 2 | a0001c0001t0004g0306a0001c0001t0004g0308 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.462+841A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343329 | ||||||
chr2:201343436
|
C | T | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.462+734G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343436 | ||||||
chr2:201343515
|
T | C | 1 | a0006c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.462+655A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343515 | ||||||
chr2:201343672
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.462+498A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343672 | ||||||
chr2:201343813
|
C | T | 1 | a0006c0010t0004g0156 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.462+357G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201343813 | ||||||
chr2:201344087
|
G | A | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+83C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 6/14 | chr2 | 201344087 | ||||||
chr2:201344327
|
G | C | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.369-64C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201344327 | ||||||
chr2:201344380
|
T | G | 1 | a0001c0001t0004g0305 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.369-117A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201344380 | ||||||
chr2:201345059
|
A | G | 4 | a0001c0001t0003g0310a0001c0001t0013g0315a0003c0004t0005g0311others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-796T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345059 | ||||||
chr2:201345254
|
C | T | 5 | a0001c0001t0006g0014a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 6 | HG01109.hp1 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.369-991G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345254 | ||||||
chr2:201345450
|
T | TTG | 9 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0004g0033others(6): Show | 10 | HG01167.hp2 HG01175.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.368+1090_368+1091d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | ||||||
chr2:201345450
|
T | TTGTG | 3 | a0002c0002t0002g0198a0002c0002t0002g0199a0002c0002t0002g0203 | 3 | HG01255.hp2 NA18970.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.368+1088_368+1091d others(6): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | ||||||
chr2:201345450
|
T | TTGTGTG | 7 | a0001c0001t0001g0133a0001c0001t0004g0004a0001c0001t0004g0286others(4): Show | 10 | HG01515.hp2 HG01891.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.368+1086_368+1091d others(8): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | ||||||
chr2:201345450
|
TTG | T | 22 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(19): Show | 23 | HG01074.hp1 HG01081.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.368+1090_368+1091d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | ||||||
chr2:201345450
|
TTGTG | T | 5 | a0001c0001t0001g0134a0001c0001t0002g0271a0001c0001t0003g0269others(2): Show | 5 | HG01346.hp2 HG01884.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.368+1088_368+1091d others(6): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | ||||||
chr2:201345450
|
TTGTGTG | T | 76 | a0001c0001t0003g0010a0001c0001t0003g0028a0001c0001t0003g0029others(73): Show | 86 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.368+1086_368+1091d others(8): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | ||||||
chr2:201345450
|
TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0003g0310a0001c0001t0005g0235a0001c0001t0013g0315 | 3 | HG02083.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.368+1084_368+1091d others(10): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | ||||||
chr2:201345450
|
TTGTGTGT others(3): Show |
T | 3 | a0001c0001t0003g0234a0003c0004t0005g0311a0003c0004t0005g0312 | 3 | HG02630.hp1 HG02818.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.368+1082_368+1091d others(12): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345450 | ||||||
chr2:201345484
|
GTA | G | 3 | a0001c0001t0001g0050a0001c0001t0004g0005a0001c0001t0004g0306 | 6 | HG02886.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.368+1056_368+1057d others(4): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345484 | ||||||
chr2:201345486
|
A | G | 3 | a0001c0001t0004g0307a0001c0001t0004g0308a0001c0001t0004g0309 | 3 | HG02055.hp1 HG02293.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.368+1056T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345486 | ||||||
chr2:201345486
|
A | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.368+1056T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345486 | ||||||
chr2:201345663
|
A | G | 1 | a0001c0001t0005g0278 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.368+879T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345663 | ||||||
chr2:201345829
|
C | T | 1 | a0002c0003t0005g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.368+713G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345829 | ||||||
chr2:201345891
|
G | A | 15 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(12): Show | 16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.368+651C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345891 | ||||||
chr2:201345933
|
G | A | 1 | a0001c0001t0004g0034 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.368+609C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201345933 | ||||||
chr2:201346184
|
A | G | 1 | a0001c0001t0004g0293 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.368+358T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201346184 | ||||||
chr2:201346200
|
T | A | 15 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(12): Show | 16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.368+342A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201346200 | ||||||
chr2:201346339
|
C | T | 1 | a0001c0001t0005g0277 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.368+203G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 5/14 | chr2 | 201346339 | ||||||
chr2:201346720
|
C | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(134): Show | 153 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.235-45G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201346720 | ||||||
chr2:201346735
|
ATCT | A | 4 | a0002c0002t0002g0200a0002c0002t0002g0201a0002c0002t0002g0202others(1): Show | 4 | HG01099.hp2 HG01109.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.235-63_235-61delAG others(1): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201346735 | ||||||
chr2:201346841
|
C | T | 1 | a0001c0001t0003g0273 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.235-166G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201346841 | ||||||
chr2:201346972
|
G | A | 138 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(135): Show | 154 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.235-297C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201346972 | ||||||
chr2:201347152
|
CT | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(125): Show | 139 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.235-478delA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347152 | ||||||
chr2:201347377
|
C | T | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.235-702G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347377 | ||||||
chr2:201347477
|
A | G | 2 | a0002c0002t0005g0158a0002c0002t0005g0159 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.234+777T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347477 | ||||||
chr2:201347642
|
C | CA | 15 | a0001c0001t0002g0271a0001c0001t0003g0270a0002c0002t0004g0216others(12): Show | 15 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.234+611dupT | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347642 | ||||||
chr2:201347642
|
C | CAAA | 129 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(126): Show | 142 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.234+609_234+611dup others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347642 | ||||||
chr2:201347651
|
G | A | 208 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(205): Show | 234 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.234+603C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347651 | ||||||
chr2:201347803
|
A | T | 1 | a0001c0001t0004g0284 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.234+451T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347803 | ||||||
chr2:201347817
|
G | A | 1 | a0002c0002t0002g0204 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.234+437C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347817 | ||||||
chr2:201347824
|
G | A | 4 | a0001c0001t0003g0273a0001c0001t0003g0274a0001c0001t0003g0275others(1): Show | 4 | HG00438.hp2 NA18941.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.234+430C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347824 | ||||||
chr2:201347830
|
G | A | 1 | a0002c0002t0003g0157 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.234+424C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347830 | ||||||
chr2:201347866
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.234+388C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201347866 | ||||||
chr2:201348226
|
C | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0042others(2): Show | 6 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+28G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201348226 | ||||||
chr2:201348227
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0042others(2): Show | 6 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.234+27G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 4/14 | chr2 | 201348227 | ||||||
chr2:201348338
|
C | G | 105 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(102): Show | 118 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.186-36G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348338 | ||||||
chr2:201348424
|
A | AT | 9 | a0001c0001t0004g0004a0001c0001t0004g0033a0001c0001t0004g0284others(6): Show | 13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-123dupA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348424 | ||||||
chr2:201348437
|
T | C | 3 | a0002c0003t0005g0225a0002c0003t0005g0226a0002c0003t0005g0227 | 3 | HG01069.hp1 HG01192.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.186-135A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348437 | ||||||
chr2:201348635
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.186-333G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348635 | ||||||
chr2:201348659
|
C | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(140): Show | 160 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.186-357G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348659 | ||||||
chr2:201348745
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.186-443A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348745 | ||||||
chr2:201348792
|
C | T | 9 | a0001c0001t0004g0004a0001c0001t0004g0033a0001c0001t0004g0284others(6): Show | 13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-490G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201348792 | ||||||
chr2:201349112
|
T | C | 15 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(12): Show | 16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.186-810A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349112 | ||||||
chr2:201349131
|
G | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0042others(2): Show | 6 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-829C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349131 | ||||||
chr2:201349211
|
G | A | 9 | a0001c0001t0004g0004a0001c0001t0004g0033a0001c0001t0004g0284others(6): Show | 13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-909C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349211 | ||||||
chr2:201349247
|
G | T | 7 | a0001c0001t0003g0028a0001c0001t0003g0228a0001c0001t0003g0229others(4): Show | 8 | HG00621.hp1 NA18950.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-945C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349247 | ||||||
chr2:201349425
|
C | T | 229 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(226): Show | 259 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.186-1123G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349425 | ||||||
chr2:201349442
|
C | T | 1 | a0001c0001t0007g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.186-1140G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349442 | ||||||
chr2:201349782
|
G | A | 13 | a0001c0001t0003g0310a0001c0001t0004g0004a0001c0001t0004g0033others(10): Show | 17 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.185+929C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349782 | ||||||
chr2:201349945
|
C | A | 2 | a0003c0004t0005g0311a0003c0004t0005g0312 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.185+766G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201349945 | ||||||
chr2:201350123
|
C | A | 8 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0140others(5): Show | 8 | HG00558.hp1 HG03927.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+588G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350123 | ||||||
chr2:201350216
|
C | T | 5 | a0001c0001t0004g0005a0001c0001t0004g0306a0001c0001t0004g0307others(2): Show | 8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+495G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350216 | ||||||
chr2:201350321
|
G | A | 1 | a0001c0001t0003g0272 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.185+390C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350321 | ||||||
chr2:201350445
|
C | G | 158 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(155): Show | 176 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.185+266G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350445 | ||||||
chr2:201350573
|
C | T | 9 | a0001c0001t0004g0004a0001c0001t0004g0033a0001c0001t0004g0284others(6): Show | 13 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.185+138G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350573 | ||||||
chr2:201350633
|
G | T | 1 | a0001c0001t0001g0040 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.185+78C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350633 | ||||||
chr2:201350686
|
C | CAAAACAA others(10): Show |
143 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(140): Show | 160 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.185+8_185+24dupTTG others(14): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 3/14 | chr2 | 201350686 | ||||||
chr2:201350844
|
A | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0038 | 3 | HG01496.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.114-62T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/14 | chr2 | 201350844 | ||||||
chr2:201351096
|
T | C | 64 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(61): Show | 73 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.113+196A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/14 | chr2 | 201351096 | ||||||
chr2:201351116
|
G | C | 1 | a0001c0001t0007g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.113+176C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/14 | chr2 | 201351116 | ||||||
chr2:201351117
|
C | A | 4 | a0001c0001t0003g0273a0001c0001t0003g0274a0001c0001t0003g0275others(1): Show | 4 | HG00438.hp2 NA18941.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+175G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/14 | chr2 | 201351117 | ||||||
chr2:201351274
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.113+18T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 2/14 | chr2 | 201351274 | ||||||
chr2:201351883
|
G | A | 1 | a0002c0011t0005g0205 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-47-432C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201351883 | ||||||
chr2:201351938
|
G | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(140): Show | 160 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.-47-487C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201351938 | ||||||
chr2:201352101
|
G | A | 4 | a0002c0002t0002g0207a0002c0002t0002g0208a0002c0002t0002g0209others(1): Show | 4 | HG00642.hp2 HG00738.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-650C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352101 | ||||||
chr2:201352193
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(127): Show | 143 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.-47-742C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352193 | ||||||
chr2:201352242
|
G | T | 1 | a0001c0001t0004g0292 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-47-791C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352242 | ||||||
chr2:201352258
|
T | C | 2 | a0002c0002t0004g0210a0002c0002t0004g0211 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-47-807A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352258 | ||||||
chr2:201352262
|
G | C | 65 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(62): Show | 74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-47-811C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352262 | ||||||
chr2:201352277
|
C | G | 1 | a0001c0001t0004g0284 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-47-826G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352277 | ||||||
chr2:201352338
|
C | A | 13 | a0001c0001t0003g0310a0001c0001t0004g0004a0001c0001t0004g0033others(10): Show | 17 | HG01167.hp2 HG01175.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47-887G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352338 | ||||||
chr2:201352442
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-47-991T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352442 | ||||||
chr2:201352529
|
C | T | 1 | a0002c0002t0002g0155 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-47-1078G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352529 | ||||||
chr2:201352643
|
G | C | 1 | a0002c0002t0002g0009 | 3 | NA18986.hp2 NA19009.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-47-1192C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352643 | ||||||
chr2:201352788
|
A | G | 3 | a0001c0001t0004g0289a0001c0001t0004g0290a0001c0001t0004g0291 | 3 | HG02970.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-47-1337T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352788 | ||||||
chr2:201352863
|
G | A | 1 | a0001c0001t0006g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-47-1412C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201352863 | ||||||
chr2:201353063
|
C | G | 1 | a0001c0001t0001g0035 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-47-1612G>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201353063 | ||||||
chr2:201353624
|
G | A | 4 | a0001c0001t0003g0310a0001c0001t0013g0315a0003c0004t0005g0311others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-2173C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201353624 | ||||||
chr2:201353795
|
G | A | 1 | a0001c0001t0003g0032 | 2 | HG00423.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-47-2344C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201353795 | ||||||
chr2:201354248
|
G | A | 1 | a0001c0001t0009g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-48+2734C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354248 | ||||||
chr2:201354301
|
G | C | 1 | a0001c0001t0004g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-48+2681C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354301 | ||||||
chr2:201354316
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(141): Show | 161 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.-48+2666T>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354316 | ||||||
chr2:201354415
|
A | T | 1 | a0001c0001t0013g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-48+2567T>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354415 | ||||||
chr2:201354596
|
G | A | 64 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(61): Show | 73 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-48+2386C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354596 | ||||||
chr2:201354604
|
C | A | 1 | a0001c0001t0007g0149 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-48+2378G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354604 | ||||||
chr2:201354897
|
G | A | 1 | a0002c0002t0002g0212 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-48+2085C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354897 | ||||||
chr2:201354929
|
T | C | 6 | a0001c0001t0004g0005a0001c0001t0004g0306a0001c0001t0004g0307others(3): Show | 9 | HG02055.hp1 HG02293.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+2053A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201354929 | ||||||
chr2:201355055
|
C | A | 1 | a0001c0001t0001g0150 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-48+1927G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355055 | ||||||
chr2:201355072
|
G | A | 64 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(61): Show | 73 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-48+1910C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355072 | ||||||
chr2:201355317
|
C | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01099.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-48+1665G>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355317 | ||||||
chr2:201355358
|
G | T | 56 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(53): Show | 63 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-48+1624C>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355358 | ||||||
chr2:201355737
|
G | C | 15 | a0001c0001t0004g0034a0001c0001t0004g0289a0001c0001t0004g0290others(12): Show | 16 | HG02258.hp2 HG02280.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.-48+1245C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355737 | ||||||
chr2:201355895
|
C | T | 65 | a0001c0001t0002g0271a0001c0001t0003g0010a0001c0001t0003g0028others(62): Show | 74 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-48+1087G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355895 | ||||||
chr2:201355900
|
T | C | 230 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(227): Show | 260 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.-48+1082A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201355900 | ||||||
chr2:201356042
|
G | C | 6 | a0001c0001t0004g0005a0001c0001t0004g0306a0001c0001t0004g0307others(3): Show | 9 | HG02055.hp1 HG02293.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+940C>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356042 | ||||||
chr2:201356082
|
G | A | 1 | a0001c0001t0003g0303 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-48+900C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356082 | ||||||
chr2:201356120
|
G | A | 1 | a0005c0006t0003g0304 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-48+862C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356120 | ||||||
chr2:201356252
|
C | T | 1 | a0001c0001t0003g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-48+730G>A | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356252 | ||||||
chr2:201356264
|
G | A | 1 | a0001c0001t0004g0305 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-48+718C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356264 | ||||||
chr2:201356321
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-48+661A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356321 | ||||||
chr2:201356515
|
GCTT | G | 14 | a0002c0002t0004g0216a0002c0002t0004g0217a0002c0003t0005g0214others(11): Show | 14 | HG00140.hp2 HG00738.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-48+464_-48+466del others(3): Show |
FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356515 | ||||||
chr2:201356583
|
T | C | 5 | a0001c0001t0004g0005a0001c0001t0004g0306a0001c0001t0004g0307others(2): Show | 8 | HG02055.hp1 HG02293.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-48+399A>G | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356583 | ||||||
chr2:201356645
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-48+337A>C | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356645 | ||||||
chr2:201356656
|
G | A | 4 | a0001c0001t0003g0310a0001c0001t0013g0315a0003c0004t0005g0311others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+326C>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356656 | ||||||
chr2:201356718
|
T | A | 229 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(226): Show | 259 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.-48+264A>T | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356718 | ||||||
chr2:201356812
|
AT | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(127): Show | 143 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.-48+169delA | FLACC1 | ENSG00000155749.13 | transcript | ENST00000392257.8 | protein_coding | 1/14 | chr2 | 201356812 |