geneid | 9457 |
---|---|
ensemblid | ENSG00000112214.11 |
hgncid | 17371 |
symbol | FHL5 |
name | four and a half LIM domains 5 |
refseq_nuc | NM_001322466.2 |
refseq_prot | NP_001309395.1 |
ensembl_nuc | ENST00000450218.6 |
ensembl_prot | ENSP00000396390.2 |
mane_status | MANE Select |
chr | chr6 |
start | 96563128 |
end | 96618626 |
strand | + |
ver | v1.2 |
region | chr6:96563128-96618626 |
region5000 | chr6:96558128-96623626 |
regionname0 | FHL5_chr6_96563128_96618626 |
regionname5000 | FHL5_chr6_96558128_96623626 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 284 | 198 | 48 | 25 | 94 | 7 | 23 | 80 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0002 | 0/0 | 284 | 97 | 3 | 27 | 53 | 4 | 10 | 39 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0003 | 1/0 | 284 | 71 | 26 | 16 | 14 | 3 | 11 | 14 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0004 | 0/0 | 284 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0005 | 0/0 | 284 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0006 | 0/0 | 284 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0007 | 0/0 | 284 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 855 | 141 | 38 | 12 | 73 | 2 | 15 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0002 | 0/0 | 855 | 97 | 3 | 27 | 53 | 4 | 10 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0003 | 1/0 | 855 | 71 | 26 | 16 | 14 | 3 | 11 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0004 | 0/0 | 855 | 55 | 9 | 13 | 20 | 5 | 8 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0005 | 0/0 | 855 | 5 | 5 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0006 | 0/0 | 855 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0007 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0008 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0009 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0010 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0011 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0012 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
c0013 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3095 | 136 | 23 | 26 | 65 | 5 | 16 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0002 | 0/1 | 3093 | 82 | 6 | 6 | 60 | 0 | 9 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0003 | 0/0 | 3093 | 55 | 9 | 13 | 20 | 5 | 8 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0004 | 0/0 | 3093 | 55 | 33 | 2 | 14 | 0 | 6 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0005 | 0/0 | 3093 | 9 | 0 | 5 | 2 | 0 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0006 | 0/0 | 3095 | 7 | 0 | 7 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0007 | 0/0 | 3093 | 6 | 1 | 3 | 0 | 2 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0008 | 0/0 | 3095 | 5 | 0 | 2 | 0 | 1 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0009 | 0/0 | 3093 | 5 | 4 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0010 | 0/0 | 3095 | 3 | 3 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0011 | 0/0 | 3095 | 3 | 0 | 2 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0012 | 0/0 | 3093 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0013 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0014 | 0/0 | 3095 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0015 | 0/0 | 3095 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0016 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0017 | 0/0 | 3095 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0018 | 0/0 | 3095 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0019 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0020 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0021 | 0/0 | 3093 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
t0022 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0002 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0004 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0009 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 855 | 141 | 38 | 12 | 73 | 2 | 15 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0004 | 0/0 | 855 | 55 | 9 | 13 | 20 | 5 | 8 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0007 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0012 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0002c0002 | 0/0 | 855 | 97 | 3 | 27 | 53 | 4 | 10 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0003c0003 | 1/0 | 855 | 71 | 26 | 16 | 14 | 3 | 11 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0004c0005 | 0/0 | 855 | 5 | 5 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0004c0010 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0004c0013 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0005c0006 | 0/0 | 855 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0005c0008 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0006c0011 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0007c0009 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/1 | 3947 | 82 | 6 | 6 | 60 | 0 | 9 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0001t0004 | 0/0 | 3947 | 42 | 22 | 1 | 13 | 0 | 6 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0001t0007 | 0/0 | 3947 | 6 | 1 | 3 | 0 | 2 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0001t0009 | 0/0 | 3947 | 5 | 4 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0001t0012 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0001t0013 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0001t0014 | 0/0 | 3949 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0001t0016 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0001t0019 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0001t0021 | 0/0 | 3947 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0004t0003 | 0/0 | 3947 | 55 | 9 | 13 | 20 | 5 | 8 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0007t0004 | 0/0 | 3947 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0001c0012t0020 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0002c0002t0001 | 0/0 | 3949 | 83 | 2 | 18 | 53 | 3 | 7 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0002c0002t0004 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0002c0002t0005 | 0/0 | 3947 | 2 | 0 | 0 | 0 | 0 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0002c0002t0006 | 0/0 | 3949 | 7 | 0 | 7 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0002c0002t0011 | 0/0 | 3949 | 3 | 0 | 2 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0002c0002t0015 | 0/0 | 3949 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0003c0003t0001 | 1/0 | 3949 | 49 | 18 | 8 | 11 | 2 | 9 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0003c0003t0004 | 0/0 | 3947 | 6 | 5 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0003c0003t0005 | 0/0 | 3947 | 7 | 0 | 5 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0003c0003t0008 | 0/0 | 3949 | 5 | 0 | 2 | 0 | 1 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0003c0003t0010 | 0/0 | 3949 | 3 | 3 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0003c0003t0017 | 0/0 | 3949 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0004c0005t0001 | 0/0 | 3949 | 3 | 3 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0004c0005t0004 | 0/0 | 3947 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0004c0010t0022 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0004c0013t0018 | 0/0 | 3949 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0005c0006t0004 | 0/0 | 3947 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0005c0008t0012 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0006c0011t0001 | 0/0 | 3949 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
a0007c0009t0004 | 0/0 | 3947 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | copy fasta | chr6 | 96558128 | 96623626 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0007g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0007g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0007g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0009g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0013g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0014g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0016g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0019g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0001t0021g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0004 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0009 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0004t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0007t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0001c0012t0020g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0005g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0005g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0006g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0006g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0011g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0011g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0011g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0002c0002t0015g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0004g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0008g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0008g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0008g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0008g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0010g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0010g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0003c0003t0017g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0004c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0004c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0004c0005t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0004c0005t0004g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0004c0010t0022g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0004c0013t0018g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0005c0006t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0005c0006t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0005c0008t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0006c0011t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
a0007c0009t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0011 | g0175 | EUR | GBR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0120 | EUR | GBR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0197 | EUR | FIN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00280 | hp2 | a0001 | c0004 | t0003 | g0004 | EUR | FIN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00323 | hp1 | a0001 | c0004 | t0003 | g0004 | EUR | FIN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00323 | hp2 | a0003 | c0003 | t0001 | g0106 | EUR | FIN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00642 | hp1 | a0003 | c0003 | t0005 | g0130 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00642 | hp2 | a0002 | c0002 | t0006 | g0183 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | CHS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00733 | hp2 | a0001 | c0001 | t0009 | g0056 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00741 | hp1 | a0001 | c0004 | t0003 | g0038 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0323 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01069 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01070 | hp1 | a0003 | c0003 | t0005 | g0125 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01070 | hp2 | a0001 | c0001 | t0007 | g0044 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01071 | hp1 | a0001 | c0001 | t0007 | g0041 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01071 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01074 | hp1 | a0002 | c0002 | t0011 | g0154 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01074 | hp2 | a0001 | c0004 | t0003 | g0290 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01081 | hp1 | a0001 | c0004 | t0003 | g0293 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0011 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01099 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0224 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01106 | hp2 | a0003 | c0003 | t0001 | g0107 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01167 | hp1 | a0002 | c0002 | t0006 | g0184 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01167 | hp2 | a0003 | c0003 | t0005 | g0133 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01168 | hp1 | a0002 | c0002 | t0011 | g0155 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01169 | hp1 | a0002 | c0002 | t0006 | g0185 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01192 | hp1 | a0001 | c0004 | t0003 | g0305 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01192 | hp2 | a0002 | c0002 | t0006 | g0007 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0246 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0218 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01255 | hp2 | a0001 | c0004 | t0003 | g0034 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01256 | hp2 | a0001 | c0004 | t0003 | g0292 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0178 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01257 | hp2 | a0003 | c0003 | t0008 | g0021 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01258 | hp2 | a0003 | c0003 | t0008 | g0021 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01346 | hp2 | a0003 | c0003 | t0001 | g0020 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01358 | hp1 | a0003 | c0003 | t0005 | g0126 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01358 | hp2 | a0001 | c0004 | t0003 | g0034 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01433 | hp2 | a0001 | c0004 | t0003 | g0033 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01496 | hp2 | a0003 | c0003 | t0004 | g0029 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01515 | hp1 | a0001 | c0004 | t0003 | g0304 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01516 | hp1 | a0001 | c0001 | t0007 | g0042 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01516 | hp2 | a0003 | c0003 | t0008 | g0143 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01517 | hp1 | a0001 | c0001 | t0007 | g0011 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01517 | hp2 | a0001 | c0004 | t0003 | g0303 | EUR | IBS | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0321 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01952 | hp1 | a0001 | c0004 | t0003 | g0291 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0219 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01981 | hp1 | a0003 | c0003 | t0001 | g0118 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01981 | hp2 | a0002 | c0002 | t0006 | g0007 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02004 | hp1 | a0002 | c0002 | t0006 | g0226 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02055 | hp1 | a0003 | c0003 | t0001 | g0233 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02145 | hp1 | a0003 | c0003 | t0001 | g0204 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0043 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0228 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02148 | hp2 | a0003 | c0003 | t0001 | g0192 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | CDX | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02257 | hp1 | a0005 | c0008 | t0012 | g0058 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02257 | hp2 | a0001 | c0004 | t0003 | g0036 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02258 | hp1 | a0003 | c0003 | t0004 | g0270 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0275 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02280 | hp2 | a0001 | c0001 | t0019 | g0249 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02293 | hp1 | a0001 | c0001 | t0021 | g0064 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02293 | hp2 | a0003 | c0003 | t0001 | g0026 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02300 | hp1 | a0001 | c0004 | t0003 | g0009 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02300 | hp2 | a0002 | c0002 | t0006 | g0189 | AMR | PEL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0054 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02572 | hp2 | a0003 | c0003 | t0001 | g0200 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02602 | hp1 | a0001 | c0004 | t0003 | g0009 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0020 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0277 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02622 | hp1 | a0003 | c0003 | t0004 | g0199 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02630 | hp1 | a0004 | c0005 | t0001 | g0059 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0273 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02698 | hp2 | a0001 | c0004 | t0003 | g0298 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0324 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02723 | hp2 | a0004 | c0005 | t0001 | g0057 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0221 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02735 | hp2 | a0003 | c0003 | t0008 | g0135 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02738 | hp1 | a0001 | c0004 | t0003 | g0312 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02809 | hp1 | a0001 | c0004 | t0003 | g0309 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02809 | hp2 | a0003 | c0003 | t0010 | g0237 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02886 | hp1 | a0001 | c0001 | t0013 | g0063 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02895 | hp1 | a0004 | c0005 | t0004 | g0031 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02895 | hp2 | a0003 | c0003 | t0010 | g0236 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02896 | hp1 | a0002 | c0002 | t0004 | g0149 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02897 | hp2 | a0004 | c0005 | t0004 | g0031 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0274 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02922 | hp2 | a0003 | c0003 | t0001 | g0151 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0046 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02970 | hp1 | a0001 | c0001 | t0009 | g0240 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02976 | hp1 | a0001 | c0004 | t0003 | g0307 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0205 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03017 | hp2 | a0001 | c0004 | t0003 | g0299 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03041 | hp1 | a0003 | c0003 | t0001 | g0320 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03041 | hp2 | a0005 | c0006 | t0004 | g0286 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03130 | hp1 | a0004 | c0013 | t0018 | g0040 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03130 | hp2 | a0001 | c0004 | t0003 | g0318 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03139 | hp2 | a0003 | c0003 | t0001 | g0232 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | ESN | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03209 | hp1 | a0001 | c0004 | t0003 | g0035 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03209 | hp2 | a0003 | c0003 | t0001 | g0322 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03225 | hp1 | a0003 | c0003 | t0001 | g0238 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03225 | hp2 | a0003 | c0003 | t0001 | g0203 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03453 | hp1 | a0004 | c0010 | t0022 | g0047 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03490 | hp2 | a0003 | c0003 | t0001 | g0132 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03491 | hp2 | a0002 | c0002 | t0005 | g0227 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03540 | hp1 | a0001 | c0001 | t0012 | g0062 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | GWD | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03579 | hp1 | a0003 | c0003 | t0001 | g0202 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03579 | hp2 | a0005 | c0006 | t0004 | g0285 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0262 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03669 | hp1 | a0003 | c0003 | t0008 | g0142 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0266 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03688 | hp1 | a0003 | c0003 | t0001 | g0121 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0256 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03704 | hp2 | a0002 | c0002 | t0015 | g0169 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03710 | hp2 | a0003 | c0003 | t0001 | g0127 | SAS | PJL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03831 | hp2 | a0002 | c0002 | t0005 | g0028 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03834 | hp1 | a0003 | c0003 | t0001 | g0134 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03942 | hp1 | a0001 | c0004 | t0003 | g0302 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03942 | hp2 | a0003 | c0003 | t0001 | g0136 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG04115 | hp1 | a0001 | c0004 | t0003 | g0295 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0124 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG04184 | hp2 | a0001 | c0004 | t0003 | g0310 | SAS | BEB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG04199 | hp1 | a0003 | c0003 | t0001 | g0128 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG04204 | hp1 | a0003 | c0003 | t0001 | g0137 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG04204 | hp2 | a0001 | c0004 | t0003 | g0033 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0258 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0186 | SAS | STU | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18522 | hp1 | a0003 | c0003 | t0004 | g0206 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18522 | hp2 | a0007 | c0009 | t0004 | g0280 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | CHB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18906 | hp1 | a0001 | c0001 | t0016 | g0279 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18906 | hp2 | a0001 | c0004 | t0003 | g0296 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18944 | hp1 | a0001 | c0004 | t0003 | g0315 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18950 | hp1 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18952 | hp1 | a0001 | c0004 | t0003 | g0009 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18952 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18957 | hp2 | a0001 | c0004 | t0003 | g0317 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18959 | hp1 | a0001 | c0004 | t0003 | g0316 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18964 | hp1 | a0001 | c0004 | t0003 | g0313 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18967 | hp1 | a0001 | c0004 | t0003 | g0306 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18968 | hp2 | a0003 | c0003 | t0017 | g0198 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18969 | hp1 | a0003 | c0003 | t0005 | g0026 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18972 | hp1 | a0001 | c0004 | t0003 | g0287 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18973 | hp1 | a0001 | c0004 | t0003 | g0037 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18975 | hp1 | a0001 | c0004 | t0003 | g0297 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18979 | hp1 | a0003 | c0003 | t0001 | g0190 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18979 | hp2 | a0001 | c0004 | t0003 | g0045 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18981 | hp2 | a0001 | c0004 | t0003 | g0301 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18986 | hp2 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18989 | hp2 | a0003 | c0003 | t0005 | g0229 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18998 | hp1 | a0001 | c0004 | t0003 | g0300 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18998 | hp2 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19002 | hp1 | a0006 | c0011 | t0001 | g0161 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19002 | hp2 | a0001 | c0004 | t0003 | g0037 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19006 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19030 | hp1 | a0003 | c0003 | t0001 | g0119 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19030 | hp2 | a0001 | c0004 | t0003 | g0311 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0278 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19043 | hp2 | a0003 | c0003 | t0004 | g0029 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19058 | hp1 | a0001 | c0004 | t0003 | g0294 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19060 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19065 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0141 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19067 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19072 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19075 | hp1 | a0001 | c0007 | t0004 | g0251 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19076 | hp1 | a0001 | c0004 | t0003 | g0308 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19077 | hp1 | a0003 | c0003 | t0001 | g0193 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19078 | hp2 | a0001 | c0004 | t0003 | g0288 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19079 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19085 | hp1 | a0001 | c0004 | t0003 | g0314 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19088 | hp2 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | YRI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA20129 | hp1 | a0001 | c0001 | t0014 | g0061 | AFR | ASW | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA20129 | hp2 | a0001 | c0001 | t0009 | g0053 | AFR | ASW | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA20752 | hp1 | a0001 | c0004 | t0003 | g0039 | EUR | TSI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0225 | EUR | TSI | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01123 | hp1 | a0001 | c0004 | t0003 | g0289 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG01123 | hp2 | a0003 | c0003 | t0005 | g0129 | AMR | CLM | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0272 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02109 | hp2 | a0004 | c0005 | t0001 | g0055 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02486 | hp1 | a0001 | c0004 | t0003 | g0035 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02486 | hp2 | a0003 | c0003 | t0001 | g0123 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG02559 | hp2 | a0001 | c0004 | t0003 | g0036 | AFR | ACB | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03471 | hp1 | a0003 | c0003 | t0010 | g0235 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG03471 | hp2 | a0003 | c0003 | t0001 | g0201 | AFR | MSL | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG06807 | hp1 | a0003 | c0003 | t0001 | g0325 | AFR | USA | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0177 | AFR | USA | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA20300 | hp1 | a0003 | c0003 | t0004 | g0234 | AFR | USA | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA20300 | hp2 | a0003 | c0003 | t0001 | g0319 | AFR | USA | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
NA21309 | hp2 | a0001 | c0012 | t0020 | g0116 | AFR | LWK | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0109 | REF | REF | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0122 | REF | REF | FHL5_chr6_96558128_96623626 | FHL5 | chr6 | 96558128 | 96623626 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:96610671
|
A | C | 1 | a0006 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.604A>C | p.Met202Leu | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 844/3949 | 604/855 | 202/284 | chr6 | 96610671 | ||
chr6:96610677
|
A | G | 3 | a0001a0004a0007 | 206 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(203): Show |
missense_variant | MODERATE | c.610A>G | p.Arg204Gly | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 850/3949 | 610/855 | 204/284 | chr6 | 96610677 | ||
chr6:96610698
|
G | A | 2 | a0002a0006 | 98 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(95): Show |
missense_variant | MODERATE | c.631G>A | p.Val211Met | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 871/3949 | 631/855 | 211/284 | chr6 | 96610698 | ||
chr6:96610741
|
G | T | 1 | a0007 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.674G>T | p.Cys225Phe | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 914/3949 | 674/855 | 225/284 | chr6 | 96610741 | ||
chr6:96615646
|
C | G | 3 | a0001a0005a0007 | 202 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(199): Show |
missense_variant | MODERATE | c.729C>G | p.Ser243Arg | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 969/3949 | 729/855 | 243/284 | chr6 | 96615646 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:96604821
|
G | C | 1 | a0005c0006 | 2 | HG03041.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.231G>C | p.Val77Val | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/6 | 471/3949 | 231/855 | 77/284 | chr6 | 96604821 | ||
chr6:96604878
|
C | T | 3 | a0001c0004a0001c0012a0004c0013 | 57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
synonymous_variant | LOW | c.288C>T | p.Asn96Asn | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/6 | 528/3949 | 288/855 | 96/284 | chr6 | 96604878 | ||
chr6:96610601
|
T | C | 1 | a0001c0007 | 1 | NA19075.hp1 | synonymous_variant | LOW | c.534T>C | p.Cys178Cys | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 774/3949 | 534/855 | 178/284 | chr6 | 96610601 | ||
chr6:96610691
|
A | G | 3 | a0001c0004a0004c0010a0004c0013 | 57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
synonymous_variant | LOW | c.624A>G | p.Pro208Pro | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/6 | 864/3949 | 624/855 | 208/284 | chr6 | 96610691 | ||
chr6:96615679
|
A | G | 8 | a0001c0001a0001c0004a0001c0007others(5): Show | 203 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
synonymous_variant | LOW | c.762A>G | p.Lys254Lys | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1002/3949 | 762/855 | 254/284 | chr6 | 96615679 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:96615848
|
T | G | 1 | a0001c0001t0002 | 82 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*76T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 76 | chr6 | 96615848 | |||||
chr6:96615960
|
A | G | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 188 | chr6 | 96615960 | |||||
chr6:96615987
|
T | C | 4 | a0001c0001t0012a0001c0001t0013a0001c0001t0014others(1): Show | 4 | HG02257.hp1 HG02886.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*215T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 215 | chr6 | 96615987 | |||||
chr6:96616044
|
C | G | 1 | a0001c0001t0021 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 272 | chr6 | 96616044 | |||||
chr6:96616108
|
T | C | 1 | a0002c0002t0015 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*336T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 336 | chr6 | 96616108 | |||||
chr6:96616146
|
G | A | 1 | a0001c0001t0013 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*374G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 374 | chr6 | 96616146 | |||||
chr6:96616350
|
T | C | 1 | a0001c0001t0016 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 578 | chr6 | 96616350 | |||||
chr6:96616603
|
G | A | 1 | a0002c0002t0006 | 7 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*831G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 831 | chr6 | 96616603 | |||||
chr6:96616929
|
CCA | C | 21 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(18): Show | 220 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1161_*1162delAC | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1161 | INFO_REALIGN_3_PRIME | chr6 | 96616929 | ||||
chr6:96616937
|
C | A | 21 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(18): Show | 220 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1165C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1165 | chr6 | 96616937 | |||||
chr6:96617255
|
C | T | 19 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(16): Show | 211 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*1483C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1483 | chr6 | 96617255 | |||||
chr6:96617263
|
T | C | 1 | a0001c0001t0007 | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1491T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1491 | chr6 | 96617263 | |||||
chr6:96617336
|
G | A | 2 | a0001c0001t0007a0001c0004t0003 | 61 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1564G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1564 | chr6 | 96617336 | |||||
chr6:96617392
|
A | C | 1 | a0003c0003t0017 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1620A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1620 | chr6 | 96617392 | |||||
chr6:96617460
|
G | A | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1688G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1688 | chr6 | 96617460 | |||||
chr6:96617627
|
T | C | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1855T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1855 | chr6 | 96617627 | |||||
chr6:96617727
|
T | C | 1 | a0003c0003t0010 | 3 | HG02809.hp2 HG02895.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1955T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 1955 | chr6 | 96617727 | |||||
chr6:96617785
|
A | G | 19 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(16): Show | 211 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*2013A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2013 | chr6 | 96617785 | |||||
chr6:96617807
|
C | T | 1 | a0001c0012t0020 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2035C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2035 | chr6 | 96617807 | |||||
chr6:96617818
|
G | C | 1 | a0002c0002t0011 | 3 | HG00140.hp1 HG01074.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2046G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2046 | chr6 | 96617818 | |||||
chr6:96617875
|
G | A | 2 | a0001c0001t0007a0001c0004t0003 | 61 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2103G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2103 | chr6 | 96617875 | |||||
chr6:96617985
|
G | A | 2 | a0001c0001t0002a0003c0003t0008 | 87 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2213G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2213 | chr6 | 96617985 | |||||
chr6:96617989
|
G | T | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2217G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2217 | chr6 | 96617989 | |||||
chr6:96618033
|
G | C | 1 | a0001c0001t0009 | 5 | HG00733.hp2 HG02572.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2261G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2261 | chr6 | 96618033 | |||||
chr6:96618056
|
C | T | 1 | a0001c0001t0019 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2284C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2284 | chr6 | 96618056 | |||||
chr6:96618144
|
C | T | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2372C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2372 | chr6 | 96618144 | |||||
chr6:96618160
|
T | C | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2388T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2388 | chr6 | 96618160 | |||||
chr6:96618322
|
A | T | 1 | a0002c0002t0015 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2550A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2550 | chr6 | 96618322 | |||||
chr6:96618366
|
C | T | 1 | a0001c0004t0003 | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2594C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2594 | chr6 | 96618366 | |||||
chr6:96618406
|
T | C | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2634T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2634 | chr6 | 96618406 | |||||
chr6:96618447
|
C | T | 1 | a0004c0010t0022 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2675C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2675 | chr6 | 96618447 | |||||
chr6:96618453
|
C | G | 19 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(16): Show | 211 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*2681C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2681 | chr6 | 96618453 | |||||
chr6:96618479
|
A | T | 19 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(16): Show | 211 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*2707A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2707 | chr6 | 96618479 | |||||
chr6:96618506
|
T | C | 19 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(16): Show | 211 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*2734T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2734 | chr6 | 96618506 | |||||
chr6:96618561
|
C | T | 1 | a0004c0013t0018 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2789C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 6/6 | 2789 | chr6 | 96618561 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:96563383
|
T | A | 2 | a0001c0004t0003g0038a0001c0004t0003g0039 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-13+28T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96563383 | ||||||
chr6:96563430
|
T | A | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+75T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96563430 | ||||||
chr6:96564216
|
T | G | 1 | a0001c0004t0003g0045 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-13+861T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96564216 | ||||||
chr6:96564577
|
CTG | C | 7 | a0003c0003t0001g0319a0003c0003t0001g0320a0003c0003t0001g0321others(4): Show | 7 | HG00741.hp2 HG01884.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+1226_-13+1227d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96564577 | |||||
chr6:96564744
|
G | C | 2 | a0001c0001t0009g0046a0004c0010t0022g0047 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-13+1389G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96564744 | ||||||
chr6:96564870
|
C | T | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-13+1515C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96564870 | ||||||
chr6:96564879
|
G | A | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+1524G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96564879 | ||||||
chr6:96564942
|
A | T | 2 | a0005c0006t0004g0285a0005c0006t0004g0286 | 2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-13+1587A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96564942 | ||||||
chr6:96565048
|
G | C | 1 | a0001c0001t0002g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-13+1693G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565048 | ||||||
chr6:96565073
|
A | G | 2 | a0001c0001t0009g0046a0004c0010t0022g0047 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-13+1718A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565073 | ||||||
chr6:96565094
|
AAAAT | A | 49 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(46): Show | 50 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.-13+1746_-13+1749d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96565094 | |||||
chr6:96565103
|
A | T | 1 | a0001c0001t0004g0241 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-13+1748A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565103 | ||||||
chr6:96565463
|
A | G | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+2108A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565463 | ||||||
chr6:96565486
|
C | T | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13+2131C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565486 | ||||||
chr6:96565552
|
G | A | 1 | a0001c0001t0004g0242 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-13+2197G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565552 | ||||||
chr6:96565641
|
A | G | 1 | a0003c0003t0001g0325 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-13+2286A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565641 | ||||||
chr6:96565661
|
G | T | 1 | a0002c0002t0001g0239 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-13+2306G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565661 | ||||||
chr6:96565750
|
C | T | 1 | a0001c0001t0002g0030 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-13+2395C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565750 | ||||||
chr6:96565938
|
T | C | 180 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(177): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.-13+2583T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96565938 | ||||||
chr6:96566315
|
C | T | 1 | a0001c0004t0003g0318 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-13+2960C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566315 | ||||||
chr6:96566357
|
C | T | 2 | a0001c0001t0009g0046a0004c0010t0022g0047 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-13+3002C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566357 | ||||||
chr6:96566379
|
T | G | 46 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(43): Show | 47 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13+3024T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566379 | ||||||
chr6:96566530
|
G | A | 2 | a0001c0001t0009g0046a0004c0010t0022g0047 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-13+3175G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566530 | ||||||
chr6:96566535
|
A | G | 6 | a0001c0004t0003g0045a0001c0004t0003g0313a0001c0004t0003g0314others(3): Show | 6 | NA18944.hp1 NA18957.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+3180A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566535 | ||||||
chr6:96566541
|
C | T | 14 | a0001c0001t0004g0268a0001c0001t0004g0269a0001c0001t0004g0271others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+3186C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566541 | ||||||
chr6:96566612
|
T | C | 10 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(7): Show | 10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+3257T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566612 | ||||||
chr6:96566649
|
C | T | 1 | a0003c0003t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-13+3294C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566649 | ||||||
chr6:96566661
|
T | A | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-13+3306T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566661 | ||||||
chr6:96566720
|
G | A | 2 | a0001c0001t0002g0060a0002c0002t0001g0117 | 2 | HG00735.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-13+3365G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566720 | ||||||
chr6:96566755
|
T | A | 1 | a0001c0001t0009g0053 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-13+3400T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566755 | ||||||
chr6:96566971
|
C | T | 314 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(311): Show | 363 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(360): Show |
intron_variant | MODIFIER | c.-13+3616C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96566971 | ||||||
chr6:96567071
|
A | G | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13+3716A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567071 | ||||||
chr6:96567096
|
G | T | 7 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(4): Show | 7 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+3741G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567096 | ||||||
chr6:96567429
|
C | T | 10 | a0003c0003t0001g0319a0003c0003t0001g0320a0003c0003t0001g0321others(7): Show | 10 | HG00741.hp2 HG01884.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+4074C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567429 | ||||||
chr6:96567545
|
C | T | 1 | a0003c0003t0004g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-13+4190C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567545 | ||||||
chr6:96567643
|
T | C | 46 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(43): Show | 47 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13+4288T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567643 | ||||||
chr6:96567666
|
T | A | 1 | a0002c0002t0001g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-13+4311T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567666 | ||||||
chr6:96567694
|
A | G | 2 | a0003c0003t0001g0232a0003c0003t0001g0233 | 2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-13+4339A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96567694 | ||||||
chr6:96567731
|
CT | C | 46 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(43): Show | 47 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13+4383delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567731 | |||||
chr6:96567769
|
AT | A | 179 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(176): Show | 211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-13+4422delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567769 | |||||
chr6:96567825
|
C | CT | 65 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(62): Show | 81 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-13+4487dupT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567825 | |||||
chr6:96567825
|
C | CTT | 12 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0112others(9): Show | 13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13+4486_-13+4487d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567825 | |||||
chr6:96567825
|
C | CTTTT | 70 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0241others(67): Show | 83 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.-13+4484_-13+4487d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567825 | |||||
chr6:96567825
|
C | CTTTTT | 10 | a0001c0001t0004g0049a0001c0001t0004g0050a0001c0001t0004g0051others(7): Show | 10 | HG02280.hp1 HG02738.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+4483_-13+4487d others(7): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567825 | |||||
chr6:96567825
|
CT | C | 18 | a0001c0001t0002g0030a0001c0001t0009g0046a0001c0001t0012g0062others(15): Show | 20 | HG01167.hp2 HG01257.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13+4487delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96567825 | |||||
chr6:96568423
|
T | C | 7 | a0001c0004t0003g0033a0001c0004t0003g0034a0001c0004t0003g0289others(4): Show | 9 | HG01074.hp2 HG01081.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+5068T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568423 | ||||||
chr6:96568634
|
G | A | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-13+5279G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568634 | ||||||
chr6:96568729
|
G | A | 1 | a0001c0001t0004g0269 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-13+5374G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568729 | ||||||
chr6:96568804
|
G | A | 10 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(7): Show | 10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+5449G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568804 | ||||||
chr6:96568845
|
C | T | 46 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(43): Show | 47 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13+5490C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568845 | ||||||
chr6:96568889
|
A | G | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-13+5534A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568889 | ||||||
chr6:96568925
|
T | C | 1 | a0003c0003t0004g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-13+5570T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568925 | ||||||
chr6:96568976
|
C | T | 2 | a0003c0003t0005g0129a0003c0003t0005g0130 | 2 | HG00642.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-13+5621C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568976 | ||||||
chr6:96568993
|
T | G | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+5638T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96568993 | ||||||
chr6:96569038
|
G | T | 1 | a0001c0001t0002g0109 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-13+5683G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569038 | ||||||
chr6:96569305
|
T | C | 1 | a0003c0003t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-13+5950T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569305 | ||||||
chr6:96569449
|
T | C | 1 | a0001c0001t0019g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-13+6094T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569449 | ||||||
chr6:96569650
|
G | A | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+6295G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569650 | ||||||
chr6:96569794
|
A | AGTGAGTT others(314): Show |
1 | a0001c0004t0003g0294 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-13+6452_-13+6453i others(323): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96569794 | |||||
chr6:96569794
|
A | AGTGAGTT others(315): Show |
37 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(34): Show | 48 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.-13+6452_-13+6453i others(324): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96569794 | |||||
chr6:96569794
|
A | AGTGAGTT others(315): Show |
1 | a0001c0004t0003g0308 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-13+6452_-13+6453i others(324): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96569794 | |||||
chr6:96569794
|
A | AGTGAGTT others(316): Show |
4 | a0001c0004t0003g0037a0001c0004t0003g0045a0001c0004t0003g0309others(1): Show | 5 | HG02738.hp1 HG02809.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+6452_-13+6453i others(325): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96569794 | |||||
chr6:96569824
|
G | T | 1 | a0001c0001t0002g0284 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-13+6469G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569824 | ||||||
chr6:96569825
|
G | T | 1 | a0001c0001t0002g0284 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-13+6470G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569825 | ||||||
chr6:96569827
|
CT | C | 43 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(40): Show | 44 | HG00408.hp1 HG00544.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.-13+6484delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96569827 | |||||
chr6:96569855
|
T | C | 5 | a0001c0001t0004g0244a0001c0001t0004g0245a0001c0001t0004g0246others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+6500T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96569855 | ||||||
chr6:96570315
|
C | T | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13+6960C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96570315 | ||||||
chr6:96570528
|
C | G | 6 | a0002c0002t0001g0117a0002c0002t0001g0224a0002c0002t0001g0225others(3): Show | 6 | HG00735.hp2 HG01106.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+7173C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96570528 | ||||||
chr6:96570944
|
T | C | 1 | a0001c0001t0021g0064 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-13+7589T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96570944 | ||||||
chr6:96571301
|
G | A | 2 | a0002c0002t0001g0146a0002c0002t0001g0147 | 2 | HG01952.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-13+7946G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571301 | ||||||
chr6:96571313
|
G | A | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+7958G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571313 | ||||||
chr6:96571595
|
G | T | 44 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(41): Show | 56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13+8240G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571595 | ||||||
chr6:96571599
|
C | T | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+8244C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571599 | ||||||
chr6:96571766
|
C | T | 1 | a0002c0002t0001g0223 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-13+8411C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571766 | ||||||
chr6:96571872
|
A | G | 1 | a0002c0002t0001g0222 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-13+8517A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571872 | ||||||
chr6:96571912
|
C | T | 1 | a0001c0001t0002g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-13+8557C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571912 | ||||||
chr6:96571962
|
G | A | 1 | a0002c0002t0001g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-13+8607G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96571962 | ||||||
chr6:96572214
|
G | A | 4 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+8859G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572214 | ||||||
chr6:96572244
|
G | T | 4 | a0002c0002t0001g0218a0002c0002t0001g0219a0002c0002t0001g0220others(1): Show | 4 | HG01081.hp2 HG01255.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+8889G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572244 | ||||||
chr6:96572422
|
A | G | 2 | a0003c0003t0001g0106a0003c0003t0001g0107 | 2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-13+9067A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572422 | ||||||
chr6:96572601
|
T | C | 1 | a0002c0002t0004g0149 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-13+9246T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572601 | ||||||
chr6:96572710
|
G | T | 1 | a0001c0001t0021g0064 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-13+9355G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572710 | ||||||
chr6:96572732
|
T | C | 1 | a0001c0001t0004g0250 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-13+9377T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572732 | ||||||
chr6:96572778
|
C | G | 1 | a0001c0001t0002g0105 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-13+9423C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572778 | ||||||
chr6:96572845
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-13+9490A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572845 | ||||||
chr6:96572978
|
C | T | 3 | a0003c0003t0008g0021a0003c0003t0008g0142a0003c0003t0008g0143 | 4 | HG01257.hp2 HG01258.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+9623C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96572978 | ||||||
chr6:96573028
|
AAAG | A | 41 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(38): Show | 42 | HG00408.hp1 HG00544.hp2 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.-13+9678_-13+9680d others(5): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96573028 | |||||
chr6:96573041
|
C | A | 60 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(57): Show | 73 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.-13+9686C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573041 | ||||||
chr6:96573146
|
G | A | 2 | a0001c0004t0003g0295a0001c0004t0003g0310 | 2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-13+9791G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573146 | ||||||
chr6:96573217
|
T | G | 9 | a0003c0003t0001g0132a0003c0003t0001g0134a0003c0003t0001g0136others(6): Show | 10 | HG01167.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+9862T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573217 | ||||||
chr6:96573527
|
A | AT | 46 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(43): Show | 49 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-13+10196dupT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96573527 | |||||
chr6:96573527
|
A | ATT | 11 | a0001c0001t0004g0268a0001c0001t0004g0273a0001c0001t0004g0274others(8): Show | 11 | HG01106.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+10195_-13+1019 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96573527 | |||||
chr6:96573527
|
AT | A | 19 | a0001c0001t0002g0052a0001c0001t0002g0065a0001c0001t0002g0066others(16): Show | 20 | HG01109.hp2 HG01981.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13+10196delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96573527 | |||||
chr6:96573527
|
ATT | A | 9 | a0001c0001t0004g0250a0001c0001t0007g0011a0001c0001t0007g0041others(6): Show | 10 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+10195_-13+1019 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96573527 | |||||
chr6:96573577
|
A | G | 1 | a0003c0003t0004g0206 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-13+10222A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573577 | ||||||
chr6:96573582
|
C | T | 50 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(47): Show | 51 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.-13+10227C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573582 | ||||||
chr6:96573593
|
C | T | 4 | a0001c0004t0003g0034a0001c0004t0003g0291a0001c0004t0003g0292others(1): Show | 5 | HG01081.hp1 HG01255.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+10238C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573593 | ||||||
chr6:96573615
|
G | A | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13+10260G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573615 | ||||||
chr6:96573635
|
C | A | 50 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(47): Show | 51 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.-13+10280C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573635 | ||||||
chr6:96573743
|
G | A | 1 | a0001c0001t0021g0064 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-13+10388G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573743 | ||||||
chr6:96573749
|
C | G | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13+10394C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573749 | ||||||
chr6:96573811
|
G | A | 2 | a0001c0001t0002g0067a0002c0002t0001g0131 | 2 | HG00673.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.-13+10456G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573811 | ||||||
chr6:96573839
|
G | T | 4 | a0001c0004t0003g0036a0001c0004t0003g0305a0001c0004t0003g0307others(1): Show | 5 | HG01192.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+10484G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96573839 | ||||||
chr6:96574083
|
A | G | 44 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(41): Show | 56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13+10728A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574083 | ||||||
chr6:96574141
|
G | A | 1 | a0002c0002t0001g0152 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-13+10786G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574141 | ||||||
chr6:96574164
|
G | T | 7 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(4): Show | 7 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+10809G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574164 | ||||||
chr6:96574592
|
C | T | 180 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(177): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.-13+11237C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574592 | ||||||
chr6:96574776
|
T | A | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+11421T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574776 | ||||||
chr6:96574838
|
T | G | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13+11483T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574838 | ||||||
chr6:96574853
|
C | G | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13+11498C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574853 | ||||||
chr6:96574939
|
A | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+11584A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96574939 | ||||||
chr6:96575062
|
C | G | 204 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(201): Show | 237 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.-13+11707C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575062 | ||||||
chr6:96575150
|
G | A | 204 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(201): Show | 237 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.-13+11795G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575150 | ||||||
chr6:96575194
|
G | A | 104 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(101): Show | 123 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.-13+11839G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575194 | ||||||
chr6:96575232
|
C | A | 1 | a0003c0003t0001g0132 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-13+11877C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575232 | ||||||
chr6:96575383
|
T | G | 1 | a0003c0003t0001g0153 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-13+12028T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575383 | ||||||
chr6:96575385
|
C | T | 22 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(19): Show | 25 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-13+12030C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575385 | ||||||
chr6:96575403
|
C | T | 5 | a0001c0001t0004g0241a0001c0001t0004g0242a0001c0001t0004g0243others(2): Show | 5 | HG00544.hp2 NA18970.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+12048C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575403 | ||||||
chr6:96575565
|
C | T | 1 | a0001c0001t0004g0263 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-13+12210C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575565 | ||||||
chr6:96575568
|
A | G | 9 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(6): Show | 9 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+12213A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575568 | ||||||
chr6:96575589
|
G | A | 2 | a0002c0002t0011g0154a0002c0002t0011g0155 | 2 | HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-13+12234G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575589 | ||||||
chr6:96575590
|
G | T | 2 | a0005c0006t0004g0285a0005c0006t0004g0286 | 2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-13+12235G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575590 | ||||||
chr6:96575656
|
G | T | 1 | a0002c0002t0001g0228 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-13+12301G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575656 | ||||||
chr6:96575756
|
T | C | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-13+12401T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575756 | ||||||
chr6:96575795
|
G | A | 4 | a0001c0001t0004g0252a0001c0001t0004g0253a0001c0001t0004g0265others(1): Show | 4 | HG02280.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+12440G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575795 | ||||||
chr6:96575908
|
T | C | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13+12553T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575908 | ||||||
chr6:96575911
|
G | T | 1 | a0001c0001t0004g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-13+12556G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96575911 | ||||||
chr6:96576030
|
C | G | 1 | a0001c0004t0003g0309 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13+12675C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576030 | ||||||
chr6:96576063
|
A | G | 4 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+12708A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576063 | ||||||
chr6:96576073
|
C | T | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13+12718C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576073 | ||||||
chr6:96576289
|
G | A | 1 | a0004c0013t0018g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-13+12934G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576289 | ||||||
chr6:96576460
|
C | T | 1 | a0003c0003t0001g0233 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-13+13105C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576460 | ||||||
chr6:96576527
|
C | A | 1 | a0005c0006t0004g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-13+13172C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576527 | ||||||
chr6:96576812
|
A | G | 2 | a0001c0004t0003g0004a0001c0004t0003g0312 | 5 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+13457A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576812 | ||||||
chr6:96576941
|
C | T | 1 | a0003c0003t0017g0198 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-13+13586C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96576941 | ||||||
chr6:96577368
|
C | T | 12 | a0001c0001t0004g0268a0001c0001t0004g0269a0001c0001t0004g0271others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13+14013C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96577368 | ||||||
chr6:96577588
|
T | A | 1 | a0001c0001t0004g0254 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-13+14233T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96577588 | ||||||
chr6:96577620
|
C | T | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-13+14265C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96577620 | ||||||
chr6:96577868
|
A | G | 3 | a0001c0001t0002g0016a0001c0001t0002g0084a0001c0001t0002g0108 | 4 | NA18948.hp2 NA18962.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+14513A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96577868 | ||||||
chr6:96577941
|
C | CA | 6 | a0001c0004t0003g0297a0001c0004t0003g0306a0003c0003t0001g0106others(3): Show | 6 | HG00323.hp2 HG01106.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+14603dupA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96577941 | |||||
chr6:96577941
|
CA | C | 9 | a0001c0001t0002g0108a0001c0001t0004g0051a0001c0001t0004g0278others(6): Show | 9 | HG00280.hp1 HG01070.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+14603delA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96577941 | |||||
chr6:96577945
|
A | C | 1 | a0002c0002t0001g0217 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-13+14590A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96577945 | ||||||
chr6:96578109
|
T | C | 9 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(6): Show | 9 | HG00733.hp2 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+14754T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578109 | ||||||
chr6:96578313
|
T | A | 1 | a0001c0001t0002g0085 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-13+14958T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578313 | ||||||
chr6:96578408
|
G | T | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+15053G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578408 | ||||||
chr6:96578553
|
G | A | 44 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(41): Show | 56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13+15198G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578553 | ||||||
chr6:96578580
|
G | A | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+15225G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578580 | ||||||
chr6:96578714
|
C | T | 1 | a0001c0001t0004g0277 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-13+15359C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578714 | ||||||
chr6:96578736
|
G | A | 4 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+15381G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578736 | ||||||
chr6:96578906
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-13+15551T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96578906 | ||||||
chr6:96579086
|
C | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+15731C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579086 | ||||||
chr6:96579154
|
T | A | 1 | a0001c0001t0002g0108 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-13+15799T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579154 | ||||||
chr6:96579504
|
C | T | 180 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(177): Show | 212 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.-13+16149C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579504 | ||||||
chr6:96579643
|
C | T | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+16288C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579643 | ||||||
chr6:96579829
|
GA | G | 46 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(43): Show | 47 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.-13+16475delA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579829 | ||||||
chr6:96579983
|
C | G | 1 | a0003c0003t0001g0232 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-13+16628C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96579983 | ||||||
chr6:96580016
|
A | G | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-13+16661A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580016 | ||||||
chr6:96580066
|
C | T | 45 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(42): Show | 57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13+16711C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580066 | ||||||
chr6:96580067
|
G | A | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+16712G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580067 | ||||||
chr6:96580311
|
G | T | 1 | a0003c0003t0001g0137 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-13+16956G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580311 | ||||||
chr6:96580499
|
G | T | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-13+17144G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580499 | ||||||
chr6:96580551
|
C | T | 44 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(41): Show | 56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-13+17196C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580551 | ||||||
chr6:96580581
|
C | G | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-13+17226C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580581 | ||||||
chr6:96580733
|
T | A | 1 | a0001c0001t0004g0250 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-13+17378T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96580733 | ||||||
chr6:96581203
|
T | C | 4 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+17848T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581203 | ||||||
chr6:96581389
|
A | G | 41 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(38): Show | 42 | HG00408.hp1 HG00544.hp2 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.-13+18034A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581389 | ||||||
chr6:96581429
|
G | A | 62 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(59): Show | 78 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-13+18074G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581429 | ||||||
chr6:96581469
|
T | C | 3 | a0001c0001t0012g0062a0001c0001t0013g0063a0001c0001t0014g0061 | 3 | HG02886.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-13+18114T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581469 | ||||||
chr6:96581590
|
G | A | 4 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+18235G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581590 | ||||||
chr6:96581995
|
G | A | 99 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(96): Show | 114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-13+18640G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96581995 | ||||||
chr6:96582078
|
T | C | 1 | a0001c0001t0002g0085 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-13+18723T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582078 | ||||||
chr6:96582114
|
G | T | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+18759G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582114 | ||||||
chr6:96582315
|
C | T | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-13+18960C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582315 | ||||||
chr6:96582332
|
A | T | 4 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+18977A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582332 | ||||||
chr6:96582730
|
C | T | 2 | a0005c0006t0004g0285a0005c0006t0004g0286 | 2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-13+19375C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582730 | ||||||
chr6:96582735
|
A | G | 10 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(7): Show | 10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+19380A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582735 | ||||||
chr6:96582837
|
G | A | 2 | a0001c0001t0002g0017a0001c0001t0002g0113 | 3 | HG02738.hp2 HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-13+19482G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582837 | ||||||
chr6:96582866
|
C | T | 1 | a0001c0001t0002g0030 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-13+19511C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96582866 | ||||||
chr6:96583093
|
C | T | 4 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+19738C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583093 | ||||||
chr6:96583211
|
C | T | 13 | a0003c0003t0001g0003a0003c0003t0001g0025a0003c0003t0001g0026others(10): Show | 18 | HG01099.hp2 HG01978.hp1 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13+19856C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583211 | ||||||
chr6:96583250
|
C | T | 8 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(5): Show | 8 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+19895C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583250 | ||||||
chr6:96583329
|
T | C | 1 | a0002c0002t0001g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-13+19974T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583329 | ||||||
chr6:96583613
|
G | A | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-19989G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583613 | ||||||
chr6:96583627
|
A | G | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-19975A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583627 | ||||||
chr6:96583869
|
C | A | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-19733C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96583869 | ||||||
chr6:96584074
|
T | C | 1 | a0001c0004t0003g0298 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-12-19528T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584074 | ||||||
chr6:96584110
|
G | A | 1 | a0003c0003t0001g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12-19492G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584110 | ||||||
chr6:96584202
|
A | G | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-19400A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584202 | ||||||
chr6:96584435
|
A | ATG | 49 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(46): Show | 62 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.-12-19143_-12-1914 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584435 | |||||
chr6:96584435
|
A | ATGTG | 9 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(6): Show | 10 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-19145_-12-1914 others(8): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584435 | |||||
chr6:96584435
|
ATGTGTG | A | 105 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(102): Show | 122 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-12-19147_-12-1914 others(10): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584435 | |||||
chr6:96584435
|
ATGTGTGT others(19): Show |
A | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-19141_-12-1911 others(30): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584435 | |||||
chr6:96584455
|
G | T | 8 | a0001c0001t0002g0068a0001c0001t0002g0102a0001c0001t0004g0252others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-19147G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584455 | ||||||
chr6:96584457
|
GTGTT | G | 8 | a0001c0001t0002g0068a0001c0001t0002g0102a0001c0001t0004g0252others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-19141_-12-1913 others(8): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584457 | |||||
chr6:96584461
|
T | G | 9 | a0001c0001t0004g0242a0001c0001t0009g0053a0001c0001t0009g0054others(6): Show | 9 | HG00544.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-19141T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584461 | ||||||
chr6:96584461
|
T | TTG | 4 | a0002c0002t0001g0218a0003c0003t0001g0120a0003c0003t0001g0200others(1): Show | 4 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-19115_-12-1911 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584461 | |||||
chr6:96584461
|
TTG | T | 3 | a0001c0001t0009g0056a0002c0002t0011g0155a0003c0003t0001g0205 | 3 | HG00733.hp2 HG01168.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-12-19115_-12-1911 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584461 | |||||
chr6:96584461
|
TTGTGTGT others(3): Show |
T | 1 | a0002c0002t0001g0131 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-12-19123_-12-1911 others(14): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584461 | |||||
chr6:96584463
|
G | GTT | 5 | a0001c0001t0009g0053a0001c0001t0009g0054a0004c0005t0001g0055others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-19138_-12-1913 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96584463 | |||||
chr6:96584463
|
G | T | 3 | a0001c0001t0002g0030a0001c0004t0003g0317a0005c0008t0012g0058 | 4 | HG02257.hp1 HG02965.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-19139G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584463 | ||||||
chr6:96584909
|
G | T | 1 | a0002c0002t0001g0148 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-12-18693G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96584909 | ||||||
chr6:96585093
|
C | T | 1 | a0001c0001t0002g0093 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-12-18509C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585093 | ||||||
chr6:96585321
|
A | G | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-18281A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585321 | ||||||
chr6:96585382
|
T | C | 1 | a0001c0001t0002g0030 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-12-18220T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585382 | ||||||
chr6:96585385
|
A | G | 27 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0013others(24): Show | 37 | HG00544.hp1 HG00621.hp2 HG02015.hp2 others(34): Show |
intron_variant | MODIFIER | c.-12-18217A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585385 | ||||||
chr6:96585422
|
A | G | 3 | a0003c0003t0004g0029a0003c0003t0004g0206a0003c0003t0004g0234 | 4 | HG01496.hp2 NA18522.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-18180A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585422 | ||||||
chr6:96585457
|
A | G | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-18145A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585457 | ||||||
chr6:96585494
|
A | G | 50 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(47): Show | 63 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.-12-18108A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585494 | ||||||
chr6:96585904
|
G | A | 101 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(98): Show | 116 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-12-17698G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585904 | ||||||
chr6:96585937
|
C | A | 1 | a0001c0001t0002g0074 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-12-17665C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96585937 | ||||||
chr6:96586228
|
G | C | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-17374G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586228 | ||||||
chr6:96586267
|
T | C | 179 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(176): Show | 211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-12-17335T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586267 | ||||||
chr6:96586357
|
T | A | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-17245T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586357 | ||||||
chr6:96586450
|
A | G | 1 | a0001c0001t0002g0068 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-17152A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586450 | ||||||
chr6:96586454
|
GTC | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-17144_-12-1714 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96586454 | |||||
chr6:96586598
|
T | G | 1 | a0003c0003t0004g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-12-17004T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586598 | ||||||
chr6:96586839
|
G | A | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-16763G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586839 | ||||||
chr6:96586998
|
C | T | 62 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(59): Show | 78 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-12-16604C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96586998 | ||||||
chr6:96587038
|
A | T | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-16564A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587038 | ||||||
chr6:96587057
|
C | A | 7 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(4): Show | 7 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-16545C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587057 | ||||||
chr6:96587219
|
T | C | 1 | a0002c0002t0001g0146 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-12-16383T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587219 | ||||||
chr6:96587245
|
CAA | C | 4 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-16356_-12-1635 others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587245 | ||||||
chr6:96587264
|
A | G | 23 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(20): Show | 24 | HG00408.hp1 HG00544.hp2 HG02886.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12-16338A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587264 | ||||||
chr6:96587325
|
C | T | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-16277C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587325 | ||||||
chr6:96587355
|
A | G | 16 | a0002c0002t0001g0007a0002c0002t0001g0024a0002c0002t0001g0138others(13): Show | 18 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-16247A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587355 | ||||||
chr6:96587506
|
T | TA | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-16093dupA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96587506 | |||||
chr6:96587542
|
C | T | 89 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(86): Show | 104 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-12-16060C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587542 | ||||||
chr6:96587568
|
T | C | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-16034T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587568 | ||||||
chr6:96587641
|
C | A | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-15961C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587641 | ||||||
chr6:96587780
|
T | C | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-15822T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587780 | ||||||
chr6:96587856
|
G | A | 1 | a0002c0002t0001g0182 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-12-15746G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96587856 | ||||||
chr6:96587892
|
AG | A | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-15707delG | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96587892 | |||||
chr6:96588019
|
C | T | 1 | a0002c0002t0006g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-12-15583C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588019 | ||||||
chr6:96588020
|
G | A | 1 | a0001c0004t0003g0289 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-12-15582G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588020 | ||||||
chr6:96588119
|
T | C | 1 | a0001c0001t0021g0064 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-12-15483T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588119 | ||||||
chr6:96588192
|
G | A | 40 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(37): Show | 53 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.-12-15410G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588192 | ||||||
chr6:96588266
|
A | G | 194 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(191): Show | 227 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.-12-15336A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588266 | ||||||
chr6:96588280
|
G | A | 1 | a0003c0003t0001g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-12-15322G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588280 | ||||||
chr6:96588325
|
C | T | 44 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(41): Show | 56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-12-15277C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588325 | ||||||
chr6:96588337
|
A | G | 1 | a0001c0001t0002g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-12-15265A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588337 | ||||||
chr6:96588504
|
T | G | 1 | a0001c0001t0009g0053 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-15098T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588504 | ||||||
chr6:96588534
|
T | A | 1 | a0001c0001t0004g0255 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-12-15068T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588534 | ||||||
chr6:96588589
|
G | A | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-15013G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588589 | ||||||
chr6:96588590
|
T | G | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-15012T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588590 | ||||||
chr6:96588663
|
C | A | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-14939C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588663 | ||||||
chr6:96588672
|
A | C | 1 | a0003c0003t0001g0232 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-12-14930A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588672 | ||||||
chr6:96588683
|
T | C | 89 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(86): Show | 104 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-12-14919T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588683 | ||||||
chr6:96588684
|
T | A | 89 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(86): Show | 104 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-12-14918T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588684 | ||||||
chr6:96588687
|
G | A | 89 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(86): Show | 104 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-12-14915G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588687 | ||||||
chr6:96588706
|
T | A | 1 | a0002c0002t0001g0224 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-12-14896T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96588706 | ||||||
chr6:96588850
|
TTAAA | T | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-14749_-12-1474 others(8): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96588850 | |||||
chr6:96588881
|
T | TA | 91 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(88): Show | 105 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-12-14712dupA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96588881 | |||||
chr6:96589067
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-12-14535T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589067 | ||||||
chr6:96589465
|
T | C | 2 | a0002c0002t0001g0028a0002c0002t0005g0028 | 2 | HG03831.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-12-14137T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589465 | ||||||
chr6:96589607
|
T | C | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-13995T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589607 | ||||||
chr6:96589654
|
A | G | 1 | a0001c0001t0002g0109 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-12-13948A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589654 | ||||||
chr6:96589685
|
T | C | 5 | a0001c0001t0004g0244a0001c0001t0004g0245a0001c0001t0004g0246others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-13917T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589685 | ||||||
chr6:96589797
|
T | C | 1 | a0002c0002t0001g0158 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-12-13805T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589797 | ||||||
chr6:96589801
|
C | G | 5 | a0002c0002t0001g0006a0002c0002t0001g0178a0002c0002t0001g0179others(2): Show | 7 | HG00733.hp1 HG01256.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-13801C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589801 | ||||||
chr6:96589984
|
G | A | 1 | a0001c0001t0004g0266 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-12-13618G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96589984 | ||||||
chr6:96590342
|
A | T | 1 | a0002c0002t0001g0209 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-12-13260A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96590342 | ||||||
chr6:96590527
|
G | T | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-13075G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96590527 | ||||||
chr6:96590817
|
C | A | 3 | a0001c0004t0003g0035a0001c0004t0003g0296a0001c0004t0003g0311 | 4 | HG02486.hp1 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-12785C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96590817 | ||||||
chr6:96590981
|
G | T | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-12621G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96590981 | ||||||
chr6:96591006
|
T | C | 1 | a0002c0002t0001g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-12-12596T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591006 | ||||||
chr6:96591072
|
C | A | 2 | a0001c0001t0002g0094a0001c0001t0002g0095 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-12-12530C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591072 | ||||||
chr6:96591080
|
T | G | 1 | a0001c0001t0007g0041 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-12-12522T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591080 | ||||||
chr6:96591123
|
T | C | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-12479T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591123 | ||||||
chr6:96591141
|
G | A | 4 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0075others(1): Show | 6 | HG00621.hp2 HG02165.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-12461G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591141 | ||||||
chr6:96591428
|
C | T | 1 | a0004c0013t0018g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-12-12174C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591428 | ||||||
chr6:96591462
|
A | G | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12-12140A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591462 | ||||||
chr6:96591498
|
T | G | 1 | a0003c0003t0004g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-12-12104T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591498 | ||||||
chr6:96591545
|
A | T | 45 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(42): Show | 57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-12-12057A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591545 | ||||||
chr6:96591638
|
C | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-11964C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591638 | ||||||
chr6:96591745
|
G | A | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-11857G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591745 | ||||||
chr6:96591788
|
C | T | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-11814C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591788 | ||||||
chr6:96591789
|
A | G | 99 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(96): Show | 114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-12-11813A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591789 | ||||||
chr6:96591844
|
C | G | 31 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(28): Show | 41 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.-12-11758C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591844 | ||||||
chr6:96591865
|
G | A | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-11737G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591865 | ||||||
chr6:96591881
|
T | C | 99 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(96): Show | 114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-12-11721T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591881 | ||||||
chr6:96591887
|
G | A | 2 | a0005c0006t0004g0285a0005c0006t0004g0286 | 2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-12-11715G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591887 | ||||||
chr6:96591942
|
G | A | 44 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(41): Show | 56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-12-11660G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591942 | ||||||
chr6:96591945
|
T | C | 2 | a0002c0002t0001g0158a0002c0002t0001g0159 | 2 | NA18994.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-12-11657T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591945 | ||||||
chr6:96591973
|
T | C | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12-11629T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591973 | ||||||
chr6:96591981
|
A | G | 179 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(176): Show | 211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-12-11621A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96591981 | ||||||
chr6:96592068
|
C | T | 3 | a0001c0001t0002g0091a0001c0001t0002g0092a0002c0002t0001g0231 | 3 | NA18984.hp1 NA19056.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-12-11534C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592068 | ||||||
chr6:96592120
|
A | T | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-11482A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592120 | ||||||
chr6:96592138
|
T | C | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-11464T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592138 | ||||||
chr6:96592143
|
G | T | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-11459G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592143 | ||||||
chr6:96592177
|
C | G | 2 | a0002c0002t0001g0139a0002c0002t0001g0140 | 2 | NA19066.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-12-11425C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592177 | ||||||
chr6:96592189
|
C | A | 79 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(76): Show | 96 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-12-11413C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592189 | ||||||
chr6:96592208
|
T | C | 2 | a0001c0001t0021g0064a0001c0004t0003g0036 | 3 | HG02257.hp2 HG02293.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-12-11394T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592208 | ||||||
chr6:96592252
|
G | C | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-11350G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592252 | ||||||
chr6:96592369
|
C | T | 1 | a0003c0003t0001g0141 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-12-11233C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592369 | ||||||
chr6:96592372
|
C | A | 10 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(7): Show | 10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-11230C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592372 | ||||||
chr6:96592376
|
C | T | 1 | a0001c0001t0009g0053 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-11226C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592376 | ||||||
chr6:96592385
|
G | A | 1 | a0003c0003t0001g0132 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-12-11217G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592385 | ||||||
chr6:96592418
|
T | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0284 | 2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-12-11184T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592418 | ||||||
chr6:96592466
|
A | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-11136A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592466 | ||||||
chr6:96592478
|
C | A | 1 | a0001c0001t0021g0064 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-12-11124C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592478 | ||||||
chr6:96592597
|
A | G | 1 | a0002c0002t0001g0217 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-12-11005A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592597 | ||||||
chr6:96592640
|
T | C | 2 | a0001c0004t0003g0303a0001c0004t0003g0304 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-12-10962T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592640 | ||||||
chr6:96592797
|
C | T | 1 | a0001c0001t0021g0064 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-12-10805C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592797 | ||||||
chr6:96592798
|
G | A | 28 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(25): Show | 32 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.-12-10804G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592798 | ||||||
chr6:96592833
|
G | T | 1 | a0001c0001t0004g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-12-10769G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592833 | ||||||
chr6:96592838
|
T | C | 1 | a0001c0004t0003g0291 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-12-10764T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592838 | ||||||
chr6:96592840
|
G | A | 2 | a0002c0002t0001g0160a0006c0011t0001g0161 | 2 | HG00408.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-12-10762G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96592840 | ||||||
chr6:96593016
|
T | G | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-10586T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593016 | ||||||
chr6:96593018
|
T | C | 10 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(7): Show | 10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-10584T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593018 | ||||||
chr6:96593470
|
G | C | 1 | a0002c0002t0001g0156 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-12-10132G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593470 | ||||||
chr6:96593520
|
A | G | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-10082A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593520 | ||||||
chr6:96593706
|
A | T | 2 | a0001c0001t0004g0260a0001c0001t0004g0261 | 2 | NA18963.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-12-9896A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593706 | ||||||
chr6:96593759
|
C | T | 45 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(42): Show | 48 | HG00408.hp1 HG00544.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.-12-9843C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593759 | ||||||
chr6:96593798
|
G | A | 1 | a0002c0002t0001g0144 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-12-9804G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593798 | ||||||
chr6:96593955
|
T | G | 1 | a0002c0002t0006g0183 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-12-9647T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96593955 | ||||||
chr6:96594102
|
C | T | 1 | a0007c0009t0004g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-12-9500C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594102 | ||||||
chr6:96594224
|
AATTTATA others(11): Show |
A | 1 | a0003c0003t0001g0325 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-12-9375_-12-9358d others(20): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594224 | |||||
chr6:96594226
|
TTTATA | T | 3 | a0001c0001t0004g0049a0003c0003t0001g0319a0003c0003t0004g0234 | 3 | HG02886.hp2 NA20300.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-12-9374_-12-9370d others(7): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594226 | |||||
chr6:96594227
|
T | TTA | 26 | a0001c0001t0004g0244a0001c0001t0004g0257a0001c0001t0004g0262others(23): Show | 26 | HG00408.hp2 HG00621.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.-12-9329_-12-9328d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
T | TTATA | 6 | a0001c0001t0004g0256a0001c0001t0004g0272a0001c0001t0009g0240others(3): Show | 6 | HG02109.hp1 HG02970.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-9331_-12-9328d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTA | T | 42 | a0001c0001t0002g0104a0001c0001t0004g0246a0001c0001t0004g0247others(39): Show | 46 | HG00673.hp2 HG00733.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.-12-9329_-12-9328d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTATA | T | 28 | a0001c0001t0002g0030a0001c0001t0004g0048a0001c0001t0004g0051others(25): Show | 34 | HG00597.hp2 HG00642.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12-9331_-12-9328d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTATATA | T | 18 | a0001c0001t0002g0086a0001c0001t0004g0050a0001c0001t0004g0258others(15): Show | 18 | HG01070.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-12-9333_-12-9328d others(8): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTATATAT others(1): Show |
T | 6 | a0001c0004t0003g0038a0002c0002t0001g0028a0002c0002t0005g0028others(3): Show | 6 | HG00140.hp1 HG00741.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-9335_-12-9328d others(10): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTATATAT others(3): Show |
T | 15 | a0001c0001t0002g0067a0001c0001t0002g0076a0001c0001t0002g0087others(12): Show | 16 | HG00597.hp1 HG00673.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-12-9337_-12-9328d others(12): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTATATAT others(5): Show |
T | 17 | a0001c0001t0002g0018a0001c0001t0002g0070a0001c0001t0002g0077others(14): Show | 19 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12-9339_-12-9328d others(14): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTATATAT others(7): Show |
T | 29 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(26): Show | 38 | HG00423.hp1 HG01074.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12-9341_-12-9328d others(16): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTATATAT others(9): Show |
T | 59 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0015others(56): Show | 77 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-12-9343_-12-9328d others(18): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTATATAT others(11): Show |
T | 4 | a0001c0001t0002g0073a0001c0001t0002g0101a0002c0002t0001g0179others(1): Show | 4 | HG00280.hp1 HG03239.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-9345_-12-9328d others(20): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTATATAT others(13): Show |
T | 12 | a0001c0001t0002g0052a0001c0001t0002g0284a0001c0001t0004g0241others(9): Show | 14 | HG00408.hp1 HG00544.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-9347_-12-9328d others(22): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTATATAT others(15): Show |
T | 8 | a0001c0001t0004g0267a0002c0002t0001g0007a0002c0002t0006g0007others(5): Show | 9 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-9349_-12-9328d others(24): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594227
|
TTATATAT others(17): Show |
T | 2 | a0002c0002t0001g0146a0004c0013t0018g0040 | 2 | HG01952.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-12-9351_-12-9328d others(26): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594227 | |||||
chr6:96594229
|
A | T | 1 | a0002c0002t0001g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-12-9373A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594229 | ||||||
chr6:96594245
|
A | T | 1 | a0001c0001t0002g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-12-9357A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594245 | ||||||
chr6:96594259
|
A | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-9343A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594259 | ||||||
chr6:96594261
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0074 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-12-9337_-12-9324d others(16): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594261 | |||||
chr6:96594271
|
A | T | 50 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(47): Show | 63 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.-12-9331A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594271 | ||||||
chr6:96594273
|
A | G | 1 | a0003c0003t0001g0204 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-12-9329A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594273 | ||||||
chr6:96594582
|
T | C | 1 | a0003c0003t0001g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-12-9020T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594582 | ||||||
chr6:96594616
|
T | C | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-8986T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594616 | ||||||
chr6:96594743
|
T | TA | 10 | a0001c0004t0003g0045a0001c0004t0003g0287a0001c0004t0003g0288others(7): Show | 10 | NA18944.hp1 NA18957.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-8858dupA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96594743 | |||||
chr6:96594971
|
T | C | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-8631T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96594971 | ||||||
chr6:96595041
|
G | A | 1 | a0003c0003t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-12-8561G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595041 | ||||||
chr6:96595094
|
G | T | 38 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(35): Show | 39 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.-12-8508G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595094 | ||||||
chr6:96595149
|
C | G | 99 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(96): Show | 114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.-12-8453C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595149 | ||||||
chr6:96595167
|
T | C | 10 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(7): Show | 10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-8435T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595167 | ||||||
chr6:96595276
|
G | A | 1 | a0001c0004t0003g0290 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-12-8326G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595276 | ||||||
chr6:96595394
|
C | T | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-8208C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595394 | ||||||
chr6:96595565
|
A | C | 1 | a0004c0013t0018g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-12-8037A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595565 | ||||||
chr6:96595627
|
C | T | 10 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(7): Show | 10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-7975C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595627 | ||||||
chr6:96595987
|
G | T | 4 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-7615G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96595987 | ||||||
chr6:96596018
|
GA | G | 3 | a0001c0001t0012g0062a0001c0001t0013g0063a0001c0001t0014g0061 | 3 | HG02886.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-12-7583delA | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596018 | ||||||
chr6:96596349
|
A | G | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-7253A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596349 | ||||||
chr6:96596449
|
A | T | 1 | a0004c0013t0018g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-12-7153A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596449 | ||||||
chr6:96596559
|
C | T | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-7043C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596559 | ||||||
chr6:96596601
|
T | C | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-7001T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596601 | ||||||
chr6:96596613
|
CT | C | 179 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(176): Show | 211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-12-6980delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96596613 | |||||
chr6:96596724
|
G | A | 34 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(31): Show | 35 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.-12-6878G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596724 | ||||||
chr6:96596774
|
A | C | 1 | a0001c0001t0009g0053 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-6828A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596774 | ||||||
chr6:96596908
|
G | A | 2 | a0005c0006t0004g0285a0005c0006t0004g0286 | 2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-12-6694G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596908 | ||||||
chr6:96596928
|
ACT | A | 4 | a0002c0002t0001g0024a0002c0002t0001g0138a0002c0002t0001g0186others(1): Show | 5 | HG02015.hp1 HG02027.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-6660_-12-6659d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96596928 | |||||
chr6:96596941
|
C | T | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-6661C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596941 | ||||||
chr6:96596955
|
C | A | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12-6647C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596955 | ||||||
chr6:96596981
|
C | T | 1 | a0002c0002t0001g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12-6621C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96596981 | ||||||
chr6:96597366
|
A | C | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-6236A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597366 | ||||||
chr6:96597367
|
C | A | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-6235C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597367 | ||||||
chr6:96597374
|
A | AC | 171 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(168): Show | 201 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.-12-6228_-12-6227i others(3): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597374 | ||||||
chr6:96597374
|
A | C | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-6228A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597374 | ||||||
chr6:96597429
|
A | G | 79 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(76): Show | 96 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-12-6173A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597429 | ||||||
chr6:96597458
|
G | A | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-6144G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597458 | ||||||
chr6:96597501
|
T | C | 1 | a0002c0002t0001g0228 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-12-6101T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597501 | ||||||
chr6:96597605
|
C | G | 1 | a0002c0002t0001g0170 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-12-5997C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597605 | ||||||
chr6:96597672
|
C | G | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-5930C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597672 | ||||||
chr6:96597888
|
C | T | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-12-5714C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597888 | ||||||
chr6:96597965
|
C | T | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-5637C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96597965 | ||||||
chr6:96598038
|
A | T | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-5564A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598038 | ||||||
chr6:96598088
|
G | A | 4 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-5514G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598088 | ||||||
chr6:96598099
|
C | T | 1 | a0002c0002t0001g0228 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-12-5503C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598099 | ||||||
chr6:96598189
|
C | T | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-5413C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598189 | ||||||
chr6:96598249
|
T | C | 1 | a0001c0001t0002g0015 | 2 | NA19063.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-12-5353T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598249 | ||||||
chr6:96598388
|
G | C | 10 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(7): Show | 10 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-5214G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598388 | ||||||
chr6:96598578
|
G | C | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-5024G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598578 | ||||||
chr6:96598693
|
A | G | 1 | a0002c0002t0001g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-12-4909A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598693 | ||||||
chr6:96598701
|
A | C | 1 | a0002c0002t0015g0169 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-12-4901A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598701 | ||||||
chr6:96598733
|
T | A | 1 | a0001c0001t0004g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12-4869T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598733 | ||||||
chr6:96598776
|
G | A | 79 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(76): Show | 96 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-12-4826G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598776 | ||||||
chr6:96598894
|
C | T | 1 | a0001c0004t0003g0316 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-12-4708C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96598894 | ||||||
chr6:96599042
|
AAATGTTA others(2): Show |
A | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-4550_-12-4542d others(11): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96599042 | |||||
chr6:96599141
|
C | T | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-4461C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599141 | ||||||
chr6:96599160
|
G | C | 11 | a0001c0001t0004g0268a0001c0001t0004g0269a0001c0001t0004g0271others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-4442G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599160 | ||||||
chr6:96599191
|
C | CT | 8 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(5): Show | 8 | HG01109.hp2 HG02258.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-4390dupT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96599191 | |||||
chr6:96599191
|
CT | C | 166 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(163): Show | 195 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.-12-4390delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96599191 | |||||
chr6:96599191
|
CTT | C | 11 | a0001c0001t0002g0019a0001c0001t0002g0085a0001c0001t0002g0089others(8): Show | 12 | HG00423.hp1 HG01517.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12-4391_-12-4390d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96599191 | |||||
chr6:96599232
|
G | T | 1 | a0007c0009t0004g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-12-4370G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599232 | ||||||
chr6:96599258
|
C | T | 4 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-4344C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599258 | ||||||
chr6:96599270
|
A | G | 179 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(176): Show | 211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-12-4332A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599270 | ||||||
chr6:96599324
|
T | C | 1 | a0001c0001t0002g0111 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-12-4278T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599324 | ||||||
chr6:96599342
|
T | C | 7 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(4): Show | 9 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-4260T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599342 | ||||||
chr6:96599382
|
C | G | 1 | a0001c0004t0003g0307 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-12-4220C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599382 | ||||||
chr6:96599446
|
T | C | 179 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(176): Show | 211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-12-4156T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599446 | ||||||
chr6:96599470
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-12-4132C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599470 | ||||||
chr6:96599474
|
C | T | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-4128C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599474 | ||||||
chr6:96599575
|
A | G | 1 | a0001c0001t0002g0090 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-12-4027A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599575 | ||||||
chr6:96599687
|
C | T | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-3915C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599687 | ||||||
chr6:96599749
|
G | A | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-3853G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599749 | ||||||
chr6:96599761
|
A | C | 2 | a0003c0003t0001g0151a0003c0003t0001g0201 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-12-3841A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599761 | ||||||
chr6:96599870
|
T | C | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-3732T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96599870 | ||||||
chr6:96600088
|
G | A | 1 | a0001c0001t0002g0284 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-12-3514G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600088 | ||||||
chr6:96600126
|
A | T | 1 | a0001c0001t0002g0091 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-12-3476A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600126 | ||||||
chr6:96600242
|
T | C | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-12-3360T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600242 | ||||||
chr6:96600364
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-12-3238C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600364 | ||||||
chr6:96600499
|
C | T | 1 | a0001c0001t0002g0030 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-12-3103C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600499 | ||||||
chr6:96600549
|
T | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-3053T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600549 | ||||||
chr6:96600593
|
G | A | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-3009G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600593 | ||||||
chr6:96600612
|
T | C | 1 | a0001c0001t0002g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-12-2990T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600612 | ||||||
chr6:96600632
|
T | C | 6 | a0001c0001t0004g0241a0001c0001t0004g0242a0001c0001t0004g0243others(3): Show | 6 | HG00408.hp1 HG00544.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-2970T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600632 | ||||||
chr6:96600649
|
A | T | 1 | a0001c0004t0003g0302 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-12-2953A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96600649 | ||||||
chr6:96601050
|
C | A | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-2552C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601050 | ||||||
chr6:96601106
|
T | C | 204 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(201): Show | 237 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.-12-2496T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601106 | ||||||
chr6:96601157
|
A | T | 2 | a0001c0001t0009g0056a0005c0008t0012g0058 | 2 | HG00733.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-12-2445A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601157 | ||||||
chr6:96601283
|
G | A | 1 | a0002c0002t0001g0207 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-12-2319G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601283 | ||||||
chr6:96601315
|
T | C | 179 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(176): Show | 211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-12-2287T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601315 | ||||||
chr6:96601322
|
G | A | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-2280G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601322 | ||||||
chr6:96601414
|
A | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-2188A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601414 | ||||||
chr6:96601440
|
G | A | 5 | a0001c0001t0004g0244a0001c0001t0004g0245a0001c0001t0004g0246others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-2162G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601440 | ||||||
chr6:96601478
|
A | G | 2 | a0005c0006t0004g0285a0005c0006t0004g0286 | 2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-12-2124A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601478 | ||||||
chr6:96601656
|
G | A | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1946G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601656 | ||||||
chr6:96601710
|
C | T | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1892C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601710 | ||||||
chr6:96601711
|
G | A | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-12-1891G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601711 | ||||||
chr6:96601777
|
T | G | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-1825T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601777 | ||||||
chr6:96601783
|
G | A | 1 | a0001c0001t0004g0259 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-12-1819G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96601783 | ||||||
chr6:96602023
|
C | A | 45 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(42): Show | 57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.-12-1579C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602023 | ||||||
chr6:96602228
|
C | T | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1374C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602228 | ||||||
chr6:96602299
|
T | C | 1 | a0004c0005t0001g0055 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-12-1303T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602299 | ||||||
chr6:96602387
|
A | G | 5 | a0002c0002t0001g0024a0002c0002t0001g0138a0002c0002t0001g0186others(2): Show | 6 | HG02015.hp1 HG02027.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-1215A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602387 | ||||||
chr6:96602389
|
T | C | 179 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(176): Show | 211 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-12-1213T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602389 | ||||||
chr6:96602422
|
G | GTTCCTTT others(3): Show |
1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-1178_-12-1177i others(12): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602422 | |||||
chr6:96602425
|
T | C | 9 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(6): Show | 9 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-1177T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602425 | ||||||
chr6:96602426
|
C | CT | 66 | a0001c0001t0004g0269a0001c0001t0004g0272a0001c0001t0004g0273others(63): Show | 73 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.-12-1138dupT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | |||||
chr6:96602426
|
C | CTT | 24 | a0002c0002t0001g0146a0002c0002t0001g0167a0002c0002t0001g0168others(21): Show | 24 | HG00642.hp1 HG00642.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-12-1139_-12-1138d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | |||||
chr6:96602426
|
C | T | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-1176C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602426 | ||||||
chr6:96602426
|
CT | C | 6 | a0001c0001t0012g0062a0001c0001t0013g0063a0001c0001t0021g0064others(3): Show | 6 | HG01074.hp1 HG01167.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1138delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | |||||
chr6:96602426
|
CTTTTT | C | 13 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(10): Show | 14 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-1142_-12-1138d others(7): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | |||||
chr6:96602426
|
CTTTTTT | C | 43 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0067others(40): Show | 47 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-12-1143_-12-1138d others(8): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | |||||
chr6:96602426
|
CTTTTTTT | C | 81 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(78): Show | 106 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-12-1144_-12-1138d others(9): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | |||||
chr6:96602426
|
CTTTTTTT others(1): Show |
C | 13 | a0001c0001t0002g0017a0001c0001t0002g0066a0001c0001t0002g0077others(10): Show | 14 | HG01081.hp1 HG01169.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.-12-1145_-12-1138d others(10): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | |||||
chr6:96602426
|
CTTTTTTT others(4): Show |
C | 1 | a0003c0003t0001g0118 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-12-1148_-12-1138d others(13): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | |||||
chr6:96602426
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0009g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-12-1157_-12-1138d others(22): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | |||||
chr6:96602426
|
CTTTTTTT others(14): Show |
C | 8 | a0001c0001t0009g0053a0001c0001t0009g0056a0004c0005t0001g0055others(5): Show | 8 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-1158_-12-1138d others(23): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | |||||
chr6:96602426
|
CTTTTTTT others(15): Show |
C | 1 | a0003c0003t0010g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-12-1159_-12-1138d others(24): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602426 | |||||
chr6:96602432
|
T | C | 1 | a0001c0001t0002g0284 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-12-1170T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602432 | ||||||
chr6:96602434
|
T | C | 8 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(5): Show | 8 | HG03453.hp2 NA18906.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-1168T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602434 | ||||||
chr6:96602435
|
T | C | 24 | a0001c0001t0004g0032a0001c0001t0004g0049a0001c0001t0004g0050others(21): Show | 25 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-12-1167T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602435 | ||||||
chr6:96602436
|
T | C | 7 | a0001c0001t0004g0048a0001c0001t0004g0253a0001c0004t0003g0033others(4): Show | 8 | HG01433.hp2 HG02622.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-1166T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602436 | ||||||
chr6:96602437
|
T | C | 37 | a0001c0001t0004g0252a0001c0001t0004g0265a0001c0004t0003g0004others(34): Show | 48 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.-12-1165T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602437 | ||||||
chr6:96602438
|
T | C | 5 | a0001c0004t0003g0292a0001c0004t0003g0293a0001c0004t0003g0303others(2): Show | 5 | HG01081.hp1 HG01256.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-1164T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602438 | ||||||
chr6:96602441
|
T | C | 1 | a0001c0004t0003g0297 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-12-1161T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602441 | ||||||
chr6:96602488
|
CCAGGCTG others(67): Show |
C | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-1110_-12-1037d others(76): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602488 | |||||
chr6:96602506
|
G | A | 1 | a0001c0001t0004g0246 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-12-1096G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602506 | ||||||
chr6:96602520
|
C | T | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-1082C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602520 | ||||||
chr6:96602927
|
A | G | 2 | a0003c0003t0001g0132a0003c0003t0001g0134 | 2 | HG03490.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-12-675A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96602927 | ||||||
chr6:96602983
|
CAG | C | 3 | a0001c0001t0002g0018a0001c0001t0002g0086a0001c0001t0002g0093 | 4 | HG02074.hp2 HG02083.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-615_-12-614del others(2): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr6 | 96602983 | |||||
chr6:96603084
|
T | C | 1 | a0002c0002t0001g0182 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-12-518T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96603084 | ||||||
chr6:96603591
|
G | T | 1 | a0007c0009t0004g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-12-11G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 1/5 | chr6 | 96603591 | ||||||
chr6:96604037
|
A | C | 2 | a0002c0002t0001g0171a0002c0002t0001g0195 | 2 | NA18957.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.159+265A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604037 | ||||||
chr6:96604074
|
C | T | 1 | a0003c0003t0001g0191 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.159+302C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604074 | ||||||
chr6:96604227
|
T | G | 36 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(33): Show | 37 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.159+455T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604227 | ||||||
chr6:96604239
|
C | G | 5 | a0001c0001t0002g0019a0001c0001t0002g0085a0001c0001t0002g0089others(2): Show | 6 | HG00423.hp1 NA18967.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+467C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604239 | ||||||
chr6:96604242
|
ATTCT | A | 7 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(4): Show | 7 | HG00733.hp2 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-486_160-483del others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 96604242 | |||||
chr6:96604288
|
C | T | 45 | a0001c0001t0004g0252a0001c0001t0004g0265a0001c0004t0003g0004others(42): Show | 57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.160-462C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604288 | ||||||
chr6:96604307
|
T | TTC | 28 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(25): Show | 31 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.160-419_160-418dup others(2): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 96604307 | |||||
chr6:96604307
|
TTCTC | T | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-421_160-418del others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr6 | 96604307 | |||||
chr6:96604377
|
T | C | 1 | a0004c0005t0004g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160-373T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604377 | ||||||
chr6:96604410
|
G | A | 47 | a0001c0001t0004g0252a0001c0001t0004g0265a0001c0004t0003g0004others(44): Show | 59 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.160-340G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604410 | ||||||
chr6:96604476
|
A | G | 1 | a0001c0001t0004g0244 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.160-274A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 2/5 | chr6 | 96604476 | ||||||
chr6:96605029
|
A | C | 9 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(6): Show | 9 | HG00733.hp2 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.334+105A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605029 | ||||||
chr6:96605229
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.334+305C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605229 | ||||||
chr6:96605277
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.334+353T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605277 | ||||||
chr6:96605327
|
G | A | 1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.334+403G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605327 | ||||||
chr6:96605423
|
A | G | 1 | a0003c0003t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.335-479A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605423 | ||||||
chr6:96605605
|
A | C | 38 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(35): Show | 39 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.335-297A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605605 | ||||||
chr6:96605638
|
C | T | 44 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(41): Show | 56 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.335-264C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | chr6 | 96605638 | ||||||
chr6:96605725
|
AT | A | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.335-168delT | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr6 | 96605725 | |||||
chr6:96606155
|
T | C | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.504+84T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606155 | ||||||
chr6:96606234
|
G | T | 4 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(1): Show | 4 | HG01109.hp2 HG03453.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+163G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606234 | ||||||
chr6:96606253
|
T | C | 1 | a0003c0003t0001g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.504+182T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606253 | ||||||
chr6:96606288
|
T | A | 5 | a0001c0001t0004g0244a0001c0001t0004g0245a0001c0001t0004g0246others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+217T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606288 | ||||||
chr6:96606342
|
T | G | 38 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(35): Show | 39 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.504+271T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606342 | ||||||
chr6:96606343
|
T | G | 1 | a0004c0013t0018g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.504+272T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606343 | ||||||
chr6:96606345
|
G | T | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+274G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606345 | ||||||
chr6:96606382
|
C | T | 1 | a0002c0002t0001g0223 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.504+311C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606382 | ||||||
chr6:96606387
|
T | A | 38 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(35): Show | 39 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.504+316T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606387 | ||||||
chr6:96606438
|
G | T | 45 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(42): Show | 57 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.504+367G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606438 | ||||||
chr6:96606475
|
C | G | 1 | a0003c0003t0004g0199 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.504+404C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606475 | ||||||
chr6:96606497
|
G | A | 1 | a0002c0002t0004g0149 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.504+426G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606497 | ||||||
chr6:96606499
|
G | A | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+428G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606499 | ||||||
chr6:96606509
|
G | A | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+438G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606509 | ||||||
chr6:96606542
|
G | C | 2 | a0004c0005t0001g0057a0004c0005t0001g0059 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.504+471G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606542 | ||||||
chr6:96606617
|
A | G | 176 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(173): Show | 208 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.504+546A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606617 | ||||||
chr6:96606940
|
T | C | 38 | a0001c0001t0002g0052a0001c0001t0002g0282a0001c0001t0002g0283others(35): Show | 39 | HG00408.hp1 HG00544.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.504+869T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96606940 | ||||||
chr6:96607041
|
T | C | 1 | a0001c0004t0003g0039 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.504+970T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96607041 | ||||||
chr6:96607206
|
G | A | 1 | a0002c0002t0001g0228 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.504+1135G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96607206 | ||||||
chr6:96607286
|
T | TTCAAAGT others(830): Show |
2 | a0005c0006t0004g0285a0005c0006t0004g0286 | 2 | HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.504+1229_504+1230i others(839): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607286 | |||||
chr6:96607286
|
T | TTCAAAGT others(837): Show |
1 | a0001c0001t0009g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.504+1229_504+1230i others(846): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607286 | |||||
chr6:96607286
|
T | TTCAAAGT others(836): Show |
2 | a0001c0001t0009g0054a0004c0005t0001g0055 | 2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.504+1229_504+1230i others(845): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607286 | |||||
chr6:96607286
|
T | TTCAAAGT others(837): Show |
4 | a0001c0001t0009g0053a0001c0001t0009g0056a0004c0005t0001g0057others(1): Show | 4 | HG00733.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+1229_504+1230i others(846): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607286 | |||||
chr6:96607406
|
T | TAC | 49 | a0001c0001t0012g0062a0001c0001t0013g0063a0001c0001t0014g0061others(46): Show | 62 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.504+1354_504+1355d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607406 | |||||
chr6:96607406
|
TAC | T | 7 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+1354_504+1355d others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607406 | |||||
chr6:96607406
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.504+1346_504+1355d others(12): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr6 | 96607406 | |||||
chr6:96607587
|
A | T | 1 | a0002c0002t0001g0194 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.504+1516A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96607587 | ||||||
chr6:96607987
|
C | A | 1 | a0002c0002t0001g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.504+1916C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96607987 | ||||||
chr6:96608169
|
C | T | 1 | a0004c0013t0018g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.504+2098C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96608169 | ||||||
chr6:96608178
|
G | A | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.504+2107G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96608178 | ||||||
chr6:96608379
|
T | C | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.505-2193T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96608379 | ||||||
chr6:96608529
|
G | A | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0096 | 3 | HG01168.hp2 HG01169.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.505-2043G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96608529 | ||||||
chr6:96608547
|
A | G | 1 | a0001c0001t0009g0053 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.505-2025A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96608547 | ||||||
chr6:96609103
|
C | T | 176 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(173): Show | 208 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.505-1469C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609103 | ||||||
chr6:96609511
|
T | A | 6 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(3): Show | 6 | HG00733.hp2 HG02109.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-1061T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609511 | ||||||
chr6:96609582
|
C | G | 1 | a0002c0002t0001g0220 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.505-990C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609582 | ||||||
chr6:96609787
|
G | A | 1 | a0004c0013t0018g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.505-785G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609787 | ||||||
chr6:96609868
|
G | A | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.505-704G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609868 | ||||||
chr6:96609949
|
G | A | 6 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(3): Show | 6 | HG00733.hp2 HG02109.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-623G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609949 | ||||||
chr6:96609953
|
G | A | 1 | a0002c0002t0004g0149 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.505-619G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96609953 | ||||||
chr6:96610064
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0081 | 3 | NA19063.hp2 NA19070.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.505-508C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96610064 | ||||||
chr6:96610268
|
A | G | 1 | a0001c0001t0002g0030 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.505-304A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96610268 | ||||||
chr6:96610274
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(62): Show | 82 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.505-298T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96610274 | ||||||
chr6:96610476
|
T | A | 1 | a0002c0002t0001g0176 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.505-96T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 4/5 | chr6 | 96610476 | ||||||
chr6:96610836
|
A | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+78A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96610836 | ||||||
chr6:96610862
|
C | T | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.691+104C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96610862 | ||||||
chr6:96610883
|
A | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+125A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96610883 | ||||||
chr6:96610921
|
C | T | 3 | a0003c0003t0001g0321a0003c0003t0001g0322a0003c0003t0001g0323 | 3 | HG00741.hp2 HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.691+163C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96610921 | ||||||
chr6:96610954
|
T | G | 3 | a0002c0002t0001g0131a0002c0002t0001g0163a0002c0002t0001g0165 | 3 | NA18951.hp2 NA18992.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.691+196T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96610954 | ||||||
chr6:96611055
|
T | C | 67 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(64): Show | 70 | HG00408.hp1 HG00544.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.691+297T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611055 | ||||||
chr6:96611068
|
G | A | 6 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.691+310G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611068 | ||||||
chr6:96611086
|
C | T | 1 | a0004c0013t0018g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.691+328C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611086 | ||||||
chr6:96611249
|
T | C | 50 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(47): Show | 52 | HG00408.hp1 HG00544.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.691+491T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611249 | ||||||
chr6:96611285
|
G | A | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+527G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611285 | ||||||
chr6:96611556
|
A | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+798A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611556 | ||||||
chr6:96611578
|
C | A | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+820C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611578 | ||||||
chr6:96611668
|
C | T | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.691+910C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611668 | ||||||
chr6:96611694
|
T | C | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+936T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611694 | ||||||
chr6:96611697
|
G | A | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.691+939G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611697 | ||||||
chr6:96611790
|
A | G | 165 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(162): Show | 197 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.691+1032A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611790 | ||||||
chr6:96611893
|
A | C | 165 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(162): Show | 197 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.691+1135A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96611893 | ||||||
chr6:96612078
|
C | T | 6 | a0002c0002t0001g0144a0002c0002t0001g0150a0002c0002t0001g0171others(3): Show | 6 | NA18948.hp1 NA18957.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.691+1320C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612078 | ||||||
chr6:96612248
|
G | A | 105 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(102): Show | 119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.691+1490G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612248 | ||||||
chr6:96612321
|
C | A | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.691+1563C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612321 | ||||||
chr6:96612349
|
T | C | 3 | a0002c0002t0001g0131a0002c0002t0001g0163a0002c0002t0001g0165 | 3 | NA18951.hp2 NA18992.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.691+1591T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612349 | ||||||
chr6:96612408
|
C | T | 1 | a0002c0002t0004g0149 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.691+1650C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612408 | ||||||
chr6:96612443
|
A | T | 67 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(64): Show | 84 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.691+1685A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612443 | ||||||
chr6:96612657
|
T | C | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.691+1899T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612657 | ||||||
chr6:96612812
|
C | A | 124 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(121): Show | 154 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.691+2054C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612812 | ||||||
chr6:96612823
|
T | A | 1 | a0001c0001t0004g0258 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.691+2065T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612823 | ||||||
chr6:96612823
|
T | C | 1 | a0003c0003t0001g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.691+2065T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612823 | ||||||
chr6:96612889
|
G | A | 1 | a0002c0002t0001g0188 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.691+2131G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96612889 | ||||||
chr6:96613095
|
G | C | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.691+2337G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613095 | ||||||
chr6:96613183
|
G | C | 1 | a0002c0002t0001g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.691+2425G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613183 | ||||||
chr6:96613224
|
TTTTA | T | 172 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(169): Show | 203 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.692-2381_692-2378d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 96613224 | |||||
chr6:96613260
|
T | A | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-2349T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613260 | ||||||
chr6:96613283
|
C | T | 174 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(171): Show | 206 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.692-2326C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613283 | ||||||
chr6:96613293
|
C | G | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-2316C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613293 | ||||||
chr6:96613296
|
G | C | 9 | a0001c0001t0009g0053a0001c0001t0009g0054a0001c0001t0009g0056others(6): Show | 9 | HG00733.hp2 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.692-2313G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613296 | ||||||
chr6:96613349
|
A | T | 1 | a0001c0004t0003g0298 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.692-2260A>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613349 | ||||||
chr6:96613436
|
G | A | 3 | a0004c0005t0004g0031a0004c0010t0022g0047a0004c0013t0018g0040 | 4 | HG02895.hp1 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.692-2173G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613436 | ||||||
chr6:96613611
|
A | C | 2 | a0001c0001t0002g0104a0004c0010t0022g0047 | 2 | HG03453.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.692-1998A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613611 | ||||||
chr6:96613619
|
T | C | 1 | a0001c0004t0003g0299 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.692-1990T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613619 | ||||||
chr6:96613648
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.692-1961C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613648 | ||||||
chr6:96613874
|
C | T | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-1735C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613874 | ||||||
chr6:96613914
|
C | T | 1 | a0002c0002t0001g0211 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.692-1695C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96613914 | ||||||
chr6:96614064
|
T | C | 43 | a0001c0004t0003g0004a0001c0004t0003g0009a0001c0004t0003g0010others(40): Show | 55 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.692-1545T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614064 | ||||||
chr6:96614082
|
A | C | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-1527A>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614082 | ||||||
chr6:96614149
|
T | A | 19 | a0001c0001t0004g0032a0001c0001t0004g0241a0001c0001t0004g0242others(16): Show | 20 | HG00408.hp1 HG00544.hp2 HG03490.hp1 others(17): Show |
intron_variant | MODIFIER | c.692-1460T>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614149 | ||||||
chr6:96614151
|
C | T | 1 | a0002c0002t0001g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.692-1458C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614151 | ||||||
chr6:96614152
|
C | T | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-1457C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614152 | ||||||
chr6:96614241
|
ATAAT | A | 48 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(45): Show | 61 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.692-1365_692-1362d others(6): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr6 | 96614241 | |||||
chr6:96614301
|
C | A | 1 | a0004c0013t0018g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.692-1308C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614301 | ||||||
chr6:96614344
|
T | C | 5 | a0001c0001t0007g0011a0001c0001t0007g0041a0001c0001t0007g0042others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-1265T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614344 | ||||||
chr6:96614355
|
C | T | 1 | a0001c0001t0004g0256 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.692-1254C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614355 | ||||||
chr6:96614444
|
G | C | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-1165G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614444 | ||||||
chr6:96614630
|
G | A | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-979G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614630 | ||||||
chr6:96614677
|
A | G | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-932A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614677 | ||||||
chr6:96614687
|
G | C | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.692-922G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614687 | ||||||
chr6:96614736
|
C | T | 3 | a0001c0001t0004g0243a0001c0001t0004g0264a0001c0001t0004g0267 | 3 | NA18970.hp2 NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.692-873C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614736 | ||||||
chr6:96614748
|
C | T | 1 | a0002c0002t0005g0227 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.692-861C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614748 | ||||||
chr6:96614756
|
A | G | 1 | a0001c0012t0020g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.692-853A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614756 | ||||||
chr6:96614832
|
A | G | 1 | a0001c0001t0004g0259 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.692-777A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614832 | ||||||
chr6:96614916
|
G | T | 23 | a0001c0001t0004g0032a0001c0001t0004g0048a0001c0001t0004g0049others(20): Show | 24 | HG00408.hp1 HG00544.hp2 HG02886.hp2 others(21): Show |
intron_variant | MODIFIER | c.692-693G>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614916 | ||||||
chr6:96614917
|
T | G | 327 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(324): Show | 377 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.692-692T>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614917 | ||||||
chr6:96614959
|
C | T | 172 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(169): Show | 203 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.692-650C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614959 | ||||||
chr6:96614989
|
C | A | 1 | a0006c0011t0001g0161 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.692-620C>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614989 | ||||||
chr6:96614990
|
G | A | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-619G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614990 | ||||||
chr6:96614998
|
G | A | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-611G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96614998 | ||||||
chr6:96615029
|
GTTAT | G | 172 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(169): Show | 203 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.692-579_692-576del others(4): Show |
FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615029 | ||||||
chr6:96615129
|
C | G | 172 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0012others(169): Show | 203 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.692-480C>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615129 | ||||||
chr6:96615216
|
T | C | 1 | a0007c0009t0004g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.692-393T>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615216 | ||||||
chr6:96615273
|
C | T | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-336C>T | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615273 | ||||||
chr6:96615353
|
A | G | 1 | a0001c0001t0009g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.692-256A>G | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615353 | ||||||
chr6:96615554
|
G | A | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-55G>A | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615554 | ||||||
chr6:96615563
|
G | C | 1 | a0004c0010t0022g0047 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.692-46G>C | FHL5 | ENSG00000112214.11 | transcript | ENST00000450218.6 | protein_coding | 5/5 | chr6 | 96615563 |