geneid | 6596 |
---|---|
ensemblid | ENSG00000071794.16 |
hgncid | 11099 |
symbol | HLTF |
name | helicase like transcription factor |
refseq_nuc | NM_003071.4 |
refseq_prot | NP_003062.2 |
ensembl_nuc | ENST00000310053.10 |
ensembl_prot | ENSP00000308944.5 |
mane_status | MANE Select |
chr | chr3 |
start | 149030127 |
end | 149086533 |
strand | - |
ver | v1.2 |
region | chr3:149030127-149086533 |
region5000 | chr3:149025127-149091533 |
regionname0 | HLTF_chr3_149030127_149086533 |
regionname5000 | HLTF_chr3_149025127_149091533 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1009 | 354 | 71 | 54 | 170 | 16 | 41 | 135 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0002 | 0/0 | 1009 | 15 | 0 | 2 | 10 | 2 | 1 | 9 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0003 | 0/0 | 1009 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0004 | 0/0 | 1009 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0005 | 0/0 | 1009 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0006 | 0/0 | 1009 | 4 | 0 | 3 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0007 | 0/0 | 1009 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0008 | 0/0 | 1009 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0009 | 0/0 | 1009 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0010 | 0/0 | 1009 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0011 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0012 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0013 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0014 | 0/0 | 1009 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0015 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0016 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3030 | 123 | 26 | 15 | 65 | 6 | 11 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0002 | 0/0 | 3030 | 112 | 20 | 23 | 57 | 3 | 9 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0003 | 1/1 | 3030 | 97 | 11 | 10 | 47 | 6 | 21 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0004 | 0/0 | 3030 | 15 | 0 | 2 | 10 | 2 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0005 | 0/0 | 3030 | 13 | 12 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0006 | 0/0 | 3030 | 8 | 8 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0007 | 0/0 | 3030 | 6 | 1 | 4 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0008 | 0/0 | 3030 | 5 | 4 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0009 | 0/0 | 3030 | 4 | 0 | 3 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0010 | 0/0 | 3030 | 4 | 4 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0011 | 0/0 | 3030 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0012 | 0/0 | 3030 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0013 | 0/0 | 3030 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0014 | 0/0 | 3030 | 2 | 0 | 2 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0015 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0016 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0017 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0018 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0019 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0020 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0021 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0022 | 0/0 | 3030 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
c0023 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2291 | 134 | 24 | 16 | 76 | 7 | 11 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0002 | 1/1 | 2291 | 118 | 25 | 17 | 46 | 6 | 22 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0003 | 0/0 | 2294 | 94 | 1 | 26 | 56 | 3 | 8 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0004 | 0/0 | 2291 | 16 | 13 | 2 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0005 | 0/0 | 2291 | 8 | 8 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0006 | 0/0 | 2291 | 6 | 6 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0007 | 0/0 | 2292 | 4 | 4 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0008 | 0/0 | 2291 | 3 | 3 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0009 | 0/0 | 2291 | 3 | 0 | 1 | 0 | 1 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0010 | 0/0 | 2295 | 3 | 2 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0011 | 0/0 | 2289 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0012 | 0/0 | 2294 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0013 | 0/0 | 2294 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0014 | 0/0 | 2291 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0015 | 0/0 | 2289 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0016 | 0/0 | 2291 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0017 | 0/0 | 2291 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0018 | 0/0 | 2291 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0019 | 0/0 | 2291 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0020 | 0/0 | 2291 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
t0021 | 0/0 | 2294 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 5 | 0 | 0 | 0 | 2 | 2 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0008 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0329 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3030 | 123 | 26 | 15 | 65 | 6 | 11 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0002 | 0/0 | 3030 | 112 | 20 | 23 | 57 | 3 | 9 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0003 | 1/1 | 3030 | 97 | 11 | 10 | 47 | 6 | 21 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0005 | 0/0 | 3030 | 13 | 12 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0007 | 0/0 | 3030 | 6 | 1 | 4 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0017 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0021 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0023 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0002c0004 | 0/0 | 3030 | 15 | 0 | 2 | 10 | 2 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0003c0006 | 0/0 | 3030 | 8 | 8 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0004c0008 | 0/0 | 3030 | 5 | 4 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0005c0010 | 0/0 | 3030 | 4 | 4 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0006c0009 | 0/0 | 3030 | 4 | 0 | 3 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0007c0013 | 0/0 | 3030 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0008c0011 | 0/0 | 3030 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0009c0014 | 0/0 | 3030 | 2 | 0 | 2 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0010c0012 | 0/0 | 3030 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0011c0016 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0012c0020 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0013c0019 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0014c0022 | 0/0 | 3030 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0015c0018 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0016c0015 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5320 | 116 | 22 | 14 | 63 | 6 | 11 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0001t0011 | 0/0 | 5318 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0001t0014 | 0/0 | 5320 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0001t0015 | 0/0 | 5318 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0001t0018 | 0/0 | 5320 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0001t0020 | 0/0 | 5320 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0002t0003 | 0/0 | 5323 | 85 | 0 | 20 | 55 | 2 | 8 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0002t0004 | 0/0 | 5320 | 16 | 13 | 2 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0002t0006 | 0/0 | 5320 | 5 | 5 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0002t0010 | 0/0 | 5324 | 3 | 2 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0002t0013 | 0/0 | 5323 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0002t0021 | 0/0 | 5323 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0003t0002 | 1/1 | 5320 | 94 | 11 | 10 | 45 | 6 | 20 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0003t0012 | 0/0 | 5323 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0003t0016 | 0/0 | 5320 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0005t0002 | 0/0 | 5320 | 12 | 11 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0005t0019 | 0/0 | 5320 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0007t0003 | 0/0 | 5323 | 6 | 1 | 4 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0017t0001 | 0/0 | 5320 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0021t0002 | 0/0 | 5320 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0001c0023t0002 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0002c0004t0001 | 0/0 | 5320 | 12 | 0 | 1 | 10 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0002c0004t0009 | 0/0 | 5320 | 3 | 0 | 1 | 0 | 1 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0003c0006t0005 | 0/0 | 5320 | 8 | 8 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0004c0008t0002 | 0/0 | 5320 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0004c0008t0008 | 0/0 | 5320 | 3 | 3 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0004c0008t0017 | 0/0 | 5320 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0005c0010t0007 | 0/0 | 5321 | 4 | 4 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0006c0009t0002 | 0/0 | 5320 | 4 | 0 | 3 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0007c0013t0002 | 0/0 | 5320 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0008c0011t0001 | 0/0 | 5320 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0009c0014t0002 | 0/0 | 5320 | 2 | 0 | 2 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0010c0012t0001 | 0/0 | 5320 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0011c0016t0003 | 0/0 | 5323 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0012c0020t0003 | 0/0 | 5323 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0013c0019t0003 | 0/0 | 5323 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0014c0022t0002 | 0/0 | 5320 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0015c0018t0001 | 0/0 | 5320 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
a0016c0015t0006 | 0/0 | 5320 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | copy fasta | chr3 | 149025127 | 149091533 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0014g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0014g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0018g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0001t0020g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0003g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0010g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0013g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0013g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0002t0021g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0001 | 1/0 | 5 | 0 | 0 | 0 | 2 | 2 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0329 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0012g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0012g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0003t0016g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0005t0019g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0007t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0017t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0021t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0001c0023t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0009g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0002c0004t0009g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0003c0006t0005g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0004c0008t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0004c0008t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0004c0008t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0004c0008t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0004c0008t0017g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0005c0010t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0005c0010t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0005c0010t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0005c0010t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0006c0009t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0006c0009t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0006c0009t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0006c0009t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0007c0013t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0007c0013t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0008c0011t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0008c0011t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0009c0014t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0009c0014t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0010c0012t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0010c0012t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0011c0016t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0012c0020t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0013c0019t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0014c0022t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0015c0018t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
a0016c0015t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0065 | EUR | GBR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00099 | hp2 | a0001 | c0003 | t0002 | g0308 | EUR | GBR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00140 | hp2 | a0001 | c0003 | t0002 | g0290 | EUR | GBR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00280 | hp2 | a0002 | c0004 | t0001 | g0201 | EUR | FIN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00323 | hp1 | a0001 | c0003 | t0002 | g0336 | EUR | FIN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00323 | hp2 | a0002 | c0004 | t0009 | g0016 | EUR | FIN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00423 | hp1 | a0001 | c0002 | t0003 | g0100 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00438 | hp1 | a0001 | c0002 | t0003 | g0110 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00438 | hp2 | a0001 | c0003 | t0002 | g0348 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00558 | hp2 | a0001 | c0003 | t0002 | g0345 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00597 | hp2 | a0001 | c0002 | t0003 | g0058 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00621 | hp1 | a0001 | c0003 | t0002 | g0298 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00621 | hp2 | a0001 | c0002 | t0003 | g0102 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00673 | hp1 | a0001 | c0002 | t0003 | g0086 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00733 | hp2 | a0001 | c0002 | t0003 | g0124 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00735 | hp2 | a0001 | c0002 | t0003 | g0123 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00738 | hp1 | a0001 | c0002 | t0003 | g0070 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG00738 | hp2 | a0001 | c0002 | t0010 | g0048 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01069 | hp1 | a0009 | c0014 | t0002 | g0282 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01070 | hp2 | a0001 | c0003 | t0002 | g0331 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01071 | hp1 | a0009 | c0014 | t0002 | g0281 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0072 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01074 | hp2 | a0001 | c0003 | t0002 | g0339 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01081 | hp1 | a0002 | c0004 | t0009 | g0016 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01106 | hp1 | a0001 | c0002 | t0003 | g0069 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01106 | hp2 | a0001 | c0003 | t0002 | g0332 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01109 | hp1 | a0001 | c0007 | t0003 | g0108 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01167 | hp1 | a0001 | c0002 | t0004 | g0256 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01167 | hp2 | a0006 | c0009 | t0002 | g0032 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01169 | hp1 | a0001 | c0002 | t0003 | g0255 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01169 | hp2 | a0001 | c0007 | t0003 | g0097 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01175 | hp1 | a0001 | c0002 | t0003 | g0091 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01175 | hp2 | a0001 | c0003 | t0002 | g0316 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01243 | hp1 | a0001 | c0003 | t0002 | g0272 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01243 | hp2 | a0001 | c0005 | t0002 | g0145 | AMR | PUR | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01255 | hp1 | a0001 | c0003 | t0002 | g0312 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01255 | hp2 | a0004 | c0008 | t0002 | g0029 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01256 | hp1 | a0001 | c0002 | t0004 | g0262 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01256 | hp2 | a0001 | c0007 | t0003 | g0095 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0087 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0113 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01261 | hp2 | a0013 | c0019 | t0003 | g0116 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01346 | hp2 | a0006 | c0009 | t0002 | g0031 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01358 | hp1 | a0001 | c0007 | t0003 | g0093 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01358 | hp2 | a0006 | c0009 | t0002 | g0033 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01433 | hp1 | a0001 | c0003 | t0002 | g0271 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01433 | hp2 | a0001 | c0003 | t0002 | g0311 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01496 | hp2 | a0001 | c0002 | t0003 | g0111 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01515 | hp1 | a0001 | c0007 | t0003 | g0066 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01515 | hp2 | a0001 | c0003 | t0002 | g0001 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01516 | hp1 | a0001 | c0002 | t0004 | g0259 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01517 | hp2 | a0001 | c0003 | t0002 | g0001 | EUR | IBS | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01891 | hp1 | a0010 | c0012 | t0001 | g0183 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01891 | hp2 | a0004 | c0008 | t0008 | g0028 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01928 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01952 | hp2 | a0001 | c0002 | t0003 | g0106 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01975 | hp1 | a0012 | c0020 | t0003 | g0083 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01975 | hp2 | a0001 | c0003 | t0002 | g0304 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01978 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01978 | hp2 | a0001 | c0017 | t0001 | g0158 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0090 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0063 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02055 | hp1 | a0010 | c0012 | t0001 | g0238 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02055 | hp2 | a0003 | c0006 | t0005 | g0043 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02074 | hp1 | a0001 | c0003 | t0012 | g0300 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02080 | hp1 | a0001 | c0003 | t0002 | g0291 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02080 | hp2 | a0001 | c0002 | t0003 | g0081 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02083 | hp1 | a0001 | c0003 | t0002 | g0352 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02129 | hp1 | a0002 | c0004 | t0001 | g0199 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02129 | hp2 | a0001 | c0003 | t0002 | g0292 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0059 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02135 | hp1 | a0001 | c0002 | t0003 | g0109 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02135 | hp2 | a0001 | c0003 | t0012 | g0324 | EAS | KHV | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02145 | hp1 | a0001 | c0002 | t0006 | g0042 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02148 | hp1 | a0001 | c0003 | t0002 | g0315 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02155 | hp2 | a0001 | c0002 | t0003 | g0067 | EAS | CDX | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02165 | hp1 | a0001 | c0002 | t0003 | g0062 | EAS | CDX | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02257 | hp1 | a0001 | c0002 | t0004 | g0355 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0129 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02273 | hp1 | a0001 | c0001 | t0018 | g0163 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02280 | hp1 | a0007 | c0013 | t0002 | g0035 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02280 | hp2 | a0001 | c0005 | t0002 | g0137 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02293 | hp1 | a0001 | c0002 | t0003 | g0084 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02300 | hp1 | a0001 | c0002 | t0003 | g0085 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0112 | AMR | PEL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02451 | hp2 | a0001 | c0002 | t0010 | g0047 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02572 | hp1 | a0001 | c0002 | t0006 | g0050 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02572 | hp2 | a0005 | c0010 | t0007 | g0040 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02602 | hp1 | a0002 | c0004 | t0009 | g0153 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02602 | hp2 | a0001 | c0003 | t0002 | g0296 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02615 | hp1 | a0001 | c0001 | t0011 | g0131 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02615 | hp2 | a0001 | c0002 | t0006 | g0052 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02622 | hp1 | a0001 | c0003 | t0002 | g0268 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02622 | hp2 | a0001 | c0005 | t0019 | g0136 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02630 | hp1 | a0001 | c0002 | t0004 | g0267 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02647 | hp1 | a0001 | c0005 | t0002 | g0142 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02647 | hp2 | a0001 | c0001 | t0015 | g0130 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02683 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02717 | hp1 | a0001 | c0003 | t0002 | g0279 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02717 | hp2 | a0001 | c0002 | t0004 | g0261 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02723 | hp1 | a0005 | c0010 | t0007 | g0039 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02723 | hp2 | a0004 | c0008 | t0008 | g0027 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0120 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02738 | hp2 | a0001 | c0003 | t0002 | g0288 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02809 | hp1 | a0001 | c0002 | t0004 | g0265 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02809 | hp2 | a0001 | c0002 | t0006 | g0051 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02818 | hp1 | a0001 | c0002 | t0006 | g0046 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02886 | hp1 | a0004 | c0008 | t0017 | g0026 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02886 | hp2 | a0001 | c0002 | t0004 | g0264 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0253 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02895 | hp2 | a0001 | c0005 | t0002 | g0140 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02922 | hp1 | a0003 | c0006 | t0005 | g0012 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02965 | hp1 | a0003 | c0006 | t0005 | g0362 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02965 | hp2 | a0001 | c0005 | t0002 | g0143 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02970 | hp1 | a0007 | c0013 | t0002 | g0036 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02970 | hp2 | a0003 | c0006 | t0005 | g0012 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02976 | hp2 | a0001 | c0021 | t0002 | g0254 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03041 | hp1 | a0001 | c0003 | t0002 | g0356 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03041 | hp2 | a0001 | c0007 | t0003 | g0064 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03098 | hp1 | a0001 | c0005 | t0002 | g0135 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03130 | hp1 | a0001 | c0005 | t0002 | g0015 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03130 | hp2 | a0001 | c0002 | t0010 | g0049 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03139 | hp1 | a0003 | c0006 | t0005 | g0053 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03195 | hp1 | a0001 | c0002 | t0004 | g0257 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03209 | hp2 | a0001 | c0002 | t0004 | g0266 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03225 | hp1 | a0001 | c0002 | t0004 | g0260 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03239 | hp1 | a0006 | c0009 | t0002 | g0034 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03239 | hp2 | a0001 | c0003 | t0002 | g0001 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03453 | hp2 | a0003 | c0006 | t0005 | g0045 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03486 | hp1 | a0001 | c0002 | t0004 | g0263 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03486 | hp2 | a0016 | c0015 | t0006 | g0041 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03491 | hp1 | a0001 | c0002 | t0003 | g0014 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03491 | hp2 | a0001 | c0003 | t0002 | g0001 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03492 | hp1 | a0001 | c0002 | t0003 | g0014 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03516 | hp2 | a0003 | c0006 | t0005 | g0054 | AFR | ESN | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03540 | hp1 | a0001 | c0003 | t0002 | g0277 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03540 | hp2 | a0001 | c0005 | t0002 | g0138 | AFR | GWD | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03579 | hp1 | a0003 | c0006 | t0005 | g0044 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03654 | hp1 | a0001 | c0002 | t0021 | g0365 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03654 | hp2 | a0001 | c0003 | t0002 | g0286 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03669 | hp1 | a0001 | c0003 | t0002 | g0360 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03669 | hp2 | a0001 | c0003 | t0002 | g0278 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0094 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0317 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03704 | hp1 | a0001 | c0003 | t0002 | g0128 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03704 | hp2 | a0001 | c0003 | t0002 | g0335 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03710 | hp1 | a0001 | c0003 | t0002 | g0310 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03710 | hp2 | a0001 | c0003 | t0002 | g0269 | SAS | PJL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03834 | hp1 | a0001 | c0003 | t0002 | g0327 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03927 | hp1 | a0001 | c0003 | t0002 | g0346 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03927 | hp2 | a0001 | c0003 | t0002 | g0354 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03942 | hp1 | a0001 | c0002 | t0003 | g0361 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03942 | hp2 | a0001 | c0003 | t0002 | g0284 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0337 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04184 | hp2 | a0001 | c0003 | t0002 | g0295 | SAS | BEB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04199 | hp1 | a0001 | c0003 | t0002 | g0322 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04199 | hp2 | a0001 | c0002 | t0003 | g0114 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04204 | hp2 | a0001 | c0002 | t0003 | g0013 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04228 | hp1 | a0001 | c0003 | t0002 | g0273 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG04228 | hp2 | a0014 | c0022 | t0002 | g0325 | SAS | STU | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18522 | hp1 | a0001 | c0002 | t0004 | g0023 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18522 | hp2 | a0001 | c0005 | t0002 | g0144 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18612 | hp2 | a0001 | c0003 | t0002 | g0299 | EAS | CHB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0088 | EAS | CHB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0274 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18906 | hp2 | a0005 | c0010 | t0007 | g0038 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18939 | hp1 | a0001 | c0003 | t0002 | g0306 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18941 | hp1 | a0001 | c0002 | t0003 | g0098 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18943 | hp2 | a0001 | c0001 | t0014 | g0363 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18944 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18944 | hp2 | a0001 | c0003 | t0002 | g0330 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18945 | hp2 | a0001 | c0002 | t0013 | g0077 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18947 | hp1 | a0001 | c0003 | t0002 | g0347 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18948 | hp1 | a0001 | c0003 | t0002 | g0302 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18948 | hp2 | a0001 | c0002 | t0003 | g0068 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18951 | hp1 | a0001 | c0003 | t0002 | g0353 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0115 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18952 | hp1 | a0002 | c0004 | t0001 | g0200 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18952 | hp2 | a0001 | c0002 | t0003 | g0078 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18953 | hp1 | a0002 | c0004 | t0001 | g0197 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18953 | hp2 | a0011 | c0016 | t0003 | g0056 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18954 | hp1 | a0002 | c0004 | t0001 | g0229 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18954 | hp2 | a0001 | c0003 | t0002 | g0305 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18956 | hp1 | a0001 | c0002 | t0003 | g0118 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18957 | hp1 | a0001 | c0002 | t0003 | g0107 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18960 | hp1 | a0001 | c0023 | t0002 | g0357 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18961 | hp2 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18962 | hp1 | a0001 | c0003 | t0002 | g0307 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18963 | hp1 | a0001 | c0002 | t0003 | g0104 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18964 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18964 | hp2 | a0001 | c0003 | t0002 | g0321 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18965 | hp2 | a0001 | c0003 | t0002 | g0340 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18967 | hp1 | a0001 | c0002 | t0003 | g0127 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18967 | hp2 | a0001 | c0003 | t0002 | g0343 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18968 | hp1 | a0001 | c0003 | t0002 | g0319 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18969 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18970 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18971 | hp2 | a0001 | c0003 | t0002 | g0289 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18972 | hp1 | a0001 | c0003 | t0002 | g0313 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18972 | hp2 | a0001 | c0002 | t0003 | g0103 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18973 | hp1 | a0015 | c0018 | t0001 | g0155 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18973 | hp2 | a0001 | c0002 | t0003 | g0122 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18974 | hp1 | a0001 | c0003 | t0002 | g0318 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18978 | hp1 | a0001 | c0001 | t0014 | g0364 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18978 | hp2 | a0001 | c0002 | t0003 | g0101 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18979 | hp1 | a0001 | c0003 | t0002 | g0344 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18979 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18980 | hp1 | a0001 | c0002 | t0003 | g0071 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18980 | hp2 | a0002 | c0004 | t0001 | g0196 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18984 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18984 | hp2 | a0001 | c0003 | t0002 | g0293 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18985 | hp1 | a0001 | c0003 | t0002 | g0351 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18986 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18986 | hp2 | a0008 | c0011 | t0001 | g0133 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18989 | hp1 | a0002 | c0004 | t0001 | g0202 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18989 | hp2 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18990 | hp1 | a0001 | c0003 | t0002 | g0297 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18991 | hp2 | a0002 | c0004 | t0001 | g0241 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18992 | hp2 | a0001 | c0003 | t0002 | g0349 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18993 | hp1 | a0001 | c0003 | t0002 | g0342 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18998 | hp1 | a0001 | c0003 | t0002 | g0024 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18998 | hp2 | a0001 | c0002 | t0003 | g0126 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18999 | hp1 | a0001 | c0002 | t0003 | g0060 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18999 | hp2 | a0001 | c0003 | t0002 | g0350 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19000 | hp1 | a0001 | c0003 | t0002 | g0341 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19002 | hp1 | a0001 | c0002 | t0003 | g0075 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19005 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19006 | hp1 | a0001 | c0003 | t0002 | g0303 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19006 | hp2 | a0001 | c0002 | t0003 | g0105 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19007 | hp1 | a0001 | c0002 | t0013 | g0080 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19007 | hp2 | a0001 | c0003 | t0002 | g0309 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19009 | hp1 | a0001 | c0003 | t0002 | g0338 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19010 | hp2 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19012 | hp2 | a0001 | c0003 | t0002 | g0333 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19030 | hp2 | a0001 | c0003 | t0002 | g0287 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19043 | hp1 | a0001 | c0005 | t0002 | g0141 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19043 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19056 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19057 | hp1 | a0001 | c0003 | t0002 | g0301 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19057 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19058 | hp2 | a0001 | c0003 | t0002 | g0323 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19059 | hp1 | a0001 | c0003 | t0002 | g0326 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19060 | hp2 | a0001 | c0003 | t0002 | g0328 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19063 | hp1 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19064 | hp1 | a0001 | c0002 | t0003 | g0061 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19064 | hp2 | a0002 | c0004 | t0001 | g0204 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19066 | hp2 | a0001 | c0003 | t0002 | g0025 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19074 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19076 | hp1 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19077 | hp1 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19078 | hp1 | a0002 | c0004 | t0001 | g0242 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19078 | hp2 | a0001 | c0002 | t0003 | g0057 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19079 | hp1 | a0002 | c0004 | t0001 | g0205 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19082 | hp1 | a0001 | c0002 | t0003 | g0099 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19083 | hp1 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19083 | hp2 | a0008 | c0011 | t0001 | g0194 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19085 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19086 | hp1 | a0001 | c0003 | t0002 | g0024 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19088 | hp2 | a0001 | c0003 | t0002 | g0314 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19090 | hp2 | a0001 | c0003 | t0002 | g0334 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19091 | hp1 | a0001 | c0003 | t0002 | g0358 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19240 | hp1 | a0001 | c0005 | t0002 | g0015 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20752 | hp2 | a0001 | c0003 | t0002 | g0283 | EUR | TSI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20805 | hp2 | a0001 | c0002 | t0003 | g0119 | EUR | TSI | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20905 | hp1 | a0001 | c0003 | t0016 | g0285 | SAS | GIH | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | GIH | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG01123 | hp2 | a0002 | c0004 | t0001 | g0203 | AMR | CLM | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02109 | hp1 | a0005 | c0010 | t0007 | g0037 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02109 | hp2 | a0004 | c0008 | t0008 | g0030 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02486 | hp1 | a0001 | c0003 | t0002 | g0275 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG02559 | hp2 | a0001 | c0005 | t0002 | g0139 | AFR | ACB | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG03471 | hp2 | a0001 | c0003 | t0002 | g0280 | AFR | MSL | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG06807 | hp1 | a0001 | c0001 | t0020 | g0221 | AFR | USA | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0258 | AFR | USA | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18955 | hp1 | a0001 | c0003 | t0002 | g0294 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20300 | hp1 | a0001 | c0003 | t0002 | g0270 | AFR | USA | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA20300 | hp2 | a0001 | c0003 | t0002 | g0320 | AFR | USA | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
NA21309 | hp2 | a0001 | c0003 | t0002 | g0276 | AFR | LWK | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0002 | g0329 | REF | REF | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0001 | REF | REF | HLTF_chr3_149025127_149091533 | HLTF | chr3 | 149025127 | 149091533 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149040077
|
C | T | 1 | a0006 | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
missense_variant | MODERATE | c.2456G>A | p.Arg819His | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 21/25 | 2653/5320 | 2456/3030 | 819/1009 | chr3 | 149040077 | ||
chr3:149040122
|
A | G | 1 | a0012 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.2411T>C | p.Ile804Thr | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 21/25 | 2608/5320 | 2411/3030 | 804/1009 | chr3 | 149040122 | ||
chr3:149041582
|
T | C | 1 | a0010 | 2 | HG01891.hp1 HG02055.hp1 |
missense_variant | MODERATE | c.2284A>G | p.Ile762Val | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/25 | 2481/5320 | 2284/3030 | 762/1009 | chr3 | 149041582 | ||
chr3:149042174
|
C | T | 1 | a0009 | 2 | HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.2189G>A | p.Gly730Asp | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 19/25 | 2386/5320 | 2189/3030 | 730/1009 | chr3 | 149042174 | ||
chr3:149046257
|
C | T | 1 | a0008 | 2 | NA18986.hp2 NA19083.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1895G>A | p.Arg632His | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/25 | 2092/5320 | 1895/3030 | 632/1009 | chr3 | 149046257 | ||
chr3:149063459
|
A | T | 1 | a0013 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.1132T>A | p.Ser378Thr | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/25 | 1329/5320 | 1132/3030 | 378/1009 | chr3 | 149063459 | ||
chr3:149063464
|
C | T | 1 | a0005 | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
missense_variant | MODERATE | c.1127G>A | p.Arg376His | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/25 | 1324/5320 | 1127/3030 | 376/1009 | chr3 | 149063464 | ||
chr3:149063507
|
C | G | 1 | a0003 | 8 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(5): Show |
missense_variant | MODERATE | c.1084G>C | p.Glu362Gln | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/25 | 1281/5320 | 1084/3030 | 362/1009 | chr3 | 149063507 | ||
chr3:149063522
|
C | T | 1 | a0014 | 1 | HG04228.hp2 | missense_variant&splice_region_variant | MODERATE | c.1069G>A | p.Ala357Thr | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/25 | 1266/5320 | 1069/3030 | 357/1009 | chr3 | 149063522 | ||
chr3:149064862
|
T | C | 2 | a0005a0007 | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
missense_variant | MODERATE | c.995A>G | p.Tyr332Cys | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/25 | 1192/5320 | 995/3030 | 332/1009 | chr3 | 149064862 | ||
chr3:149068298
|
T | C | 1 | a0002 | 15 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(12): Show |
missense_variant | MODERATE | c.932A>G | p.Asn311Ser | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/25 | 1129/5320 | 932/3030 | 311/1009 | chr3 | 149068298 | ||
chr3:149071340
|
T | C | 1 | a0004 | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
missense_variant | MODERATE | c.806A>G | p.Asp269Gly | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/25 | 1003/5320 | 806/3030 | 269/1009 | chr3 | 149071340 | ||
chr3:149071341
|
C | T | 1 | a0015 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.805G>A | p.Asp269Asn | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/25 | 1002/5320 | 805/3030 | 269/1009 | chr3 | 149071341 | ||
chr3:149084684
|
C | T | 1 | a0011 | 1 | NA18953.hp2 | missense_variant&splice_region_variant | MODERATE | c.226G>A | p.Val76Ile | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/25 | 423/5320 | 226/3030 | 76/1009 | chr3 | 149084684 | ||
chr3:149084782
|
A | G | 1 | a0016 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.128T>C | p.Ile43Thr | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/25 | 325/5320 | 128/3030 | 43/1009 | chr3 | 149084782 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149041538
|
T | C | 6 | a0001c0001a0001c0017a0002c0004others(3): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
synonymous_variant | LOW | c.2328A>G | p.Ala776Ala | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/25 | 2525/5320 | 2328/3030 | 776/1009 | chr3 | 149041538 | ||
chr3:149048879
|
T | C | 1 | a0001c0007 | 6 | HG01109.hp1 HG01169.hp2 HG01256.hp2 others(3): Show |
synonymous_variant | LOW | c.1740A>G | p.Arg580Arg | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/25 | 1937/5320 | 1740/3030 | 580/1009 | chr3 | 149048879 | ||
chr3:149048882
|
T | C | 1 | a0001c0021 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1737A>G | p.Glu579Glu | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/25 | 1934/5320 | 1737/3030 | 579/1009 | chr3 | 149048882 | ||
chr3:149050343
|
T | C | 1 | a0001c0005 | 13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
synonymous_variant | LOW | c.1506A>G | p.Val502Val | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/25 | 1703/5320 | 1506/3030 | 502/1009 | chr3 | 149050343 | ||
chr3:149068321
|
C | T | 19 | a0001c0001a0001c0002a0001c0005others(16): Show | 303 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(300): Show |
synonymous_variant | LOW | c.909G>A | p.Thr303Thr | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/25 | 1106/5320 | 909/3030 | 303/1009 | chr3 | 149068321 | ||
chr3:149073279
|
A | T | 1 | a0001c0017 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.573T>A | p.Ala191Ala | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/25 | 770/5320 | 573/3030 | 191/1009 | chr3 | 149073279 | ||
chr3:149084739
|
G | A | 1 | a0001c0023 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.171C>T | p.Ser57Ser | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/25 | 368/5320 | 171/3030 | 57/1009 | chr3 | 149084739 | ||
chr3:149084826
|
G | A | 1 | a0004c0008 | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
synonymous_variant | LOW | c.84C>T | p.Leu28Leu | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/25 | 281/5320 | 84/3030 | 28/1009 | chr3 | 149084826 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149030292
|
C | CT | 1 | a0005c0010t0007 | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1927dupA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1927 | chr3 | 149030292 | |||||
chr3:149030415
|
A | AACTT | 1 | a0001c0002t0010 | 3 | HG00738.hp2 HG02451.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1801_*1804dupAAGT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1804 | chr3 | 149030415 | |||||
chr3:149030453
|
A | C | 1 | a0004c0008t0017 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1767T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1767 | chr3 | 149030453 | |||||
chr3:149030475
|
T | TGTC | 8 | a0001c0002t0003a0001c0002t0013a0001c0002t0021others(5): Show | 99 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1742_*1744dupGAC | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1744 | chr3 | 149030475 | |||||
chr3:149030579
|
C | T | 1 | a0003c0006t0005 | 8 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1641G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1641 | chr3 | 149030579 | |||||
chr3:149030593
|
T | C | 10 | a0001c0001t0001a0001c0001t0014a0001c0001t0018others(7): Show | 141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1627A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1627 | chr3 | 149030593 | |||||
chr3:149030681
|
G | A | 1 | a0001c0001t0018 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1539C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1539 | chr3 | 149030681 | |||||
chr3:149030713
|
C | G | 1 | a0002c0004t0009 | 3 | HG00323.hp2 HG01081.hp1 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1507G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1507 | chr3 | 149030713 | |||||
chr3:149030729
|
T | C | 4 | a0001c0002t0006a0001c0002t0010a0003c0006t0005others(1): Show | 17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1491A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1491 | chr3 | 149030729 | |||||
chr3:149030894
|
A | G | 1 | a0004c0008t0008 | 3 | HG01891.hp2 HG02109.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1326T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 1326 | chr3 | 149030894 | |||||
chr3:149031224
|
T | G | 1 | a0001c0003t0016 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 996 | chr3 | 149031224 | |||||
chr3:149031252
|
A | G | 1 | a0001c0003t0016 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*968T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 968 | chr3 | 149031252 | |||||
chr3:149031379
|
T | G | 1 | a0001c0001t0015 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*841A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 841 | chr3 | 149031379 | |||||
chr3:149031418
|
TTA | T | 2 | a0001c0001t0011a0001c0001t0015 | 3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*800_*801delTA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 800 | chr3 | 149031418 | |||||
chr3:149031421
|
T | C | 1 | a0001c0005t0019 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 799 | chr3 | 149031421 | |||||
chr3:149031566
|
A | G | 1 | a0001c0002t0013 | 2 | NA18945.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*654T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 654 | chr3 | 149031566 | |||||
chr3:149031834
|
T | C | 8 | a0001c0002t0003a0001c0002t0004a0001c0002t0013others(5): Show | 113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*386A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 386 | chr3 | 149031834 | |||||
chr3:149032000
|
T | C | 1 | a0001c0001t0020 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*220A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 25/25 | 220 | chr3 | 149032000 | |||||
chr3:149086458
|
T | A | 1 | a0001c0001t0014 | 2 | NA18943.hp2 NA18978.hp1 |
5_prime_UTR_variant | MODIFIER | c.-122A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/25 | 122 | chr3 | 149086458 | |||||
chr3:149086493
|
G | C | 1 | a0001c0001t0014 | 2 | NA18943.hp2 NA18978.hp1 |
5_prime_UTR_variant | MODIFIER | c.-157C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/25 | 157 | chr3 | 149086493 | |||||
chr3:149086507
|
C | A | 1 | a0001c0002t0021 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-171G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/25 | 171 | chr3 | 149086507 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149032513
|
A | T | 6 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2878-141T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032513 | ||||||
chr3:149032571
|
G | A | 4 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(1): Show | 4 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2878-199C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032571 | ||||||
chr3:149032734
|
G | A | 2 | a0001c0002t0006g0042a0016c0015t0006g0041 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2878-362C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032734 | ||||||
chr3:149032909
|
G | A | 2 | a0001c0002t0006g0042a0016c0015t0006g0041 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2878-537C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032909 | ||||||
chr3:149032957
|
C | CA | 44 | a0001c0002t0006g0042a0001c0003t0002g0128a0001c0003t0002g0268others(41): Show | 45 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.2878-586dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032957 | ||||||
chr3:149032957
|
C | CAA | 7 | a0001c0003t0002g0271a0001c0003t0002g0273a0003c0006t0005g0045others(4): Show | 7 | HG01255.hp2 HG01433.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2878-587_2878-586d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032957 | ||||||
chr3:149032967
|
A | C | 12 | a0001c0005t0002g0015a0001c0005t0002g0135a0001c0005t0002g0137others(9): Show | 13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2878-595T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032967 | ||||||
chr3:149032968
|
A | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0247 | 2 | NA19076.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2878-596T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032968 | ||||||
chr3:149032971
|
A | AC | 3 | a0001c0002t0003g0118a0001c0002t0003g0125a0001c0002t0003g0361 | 3 | HG03942.hp1 NA18956.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.2878-600_2878-599i others(3): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032971 | ||||||
chr3:149032971
|
A | C | 95 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(92): Show | 110 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2878-599T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032971 | ||||||
chr3:149032974
|
A | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2878-602T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032974 | ||||||
chr3:149032975
|
A | C | 11 | a0001c0001t0001g0134a0001c0001t0001g0146a0001c0001t0001g0173others(8): Show | 11 | HG02818.hp2 HG03225.hp2 HG03516.hp1 others(8): Show |
intron_variant | MODIFIER | c.2878-603T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032975 | ||||||
chr3:149032976
|
AAC | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 146 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.2878-606_2878-605d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032976 | ||||||
chr3:149032977
|
AC | A | 11 | a0001c0001t0001g0134a0001c0001t0001g0146a0001c0001t0001g0173others(8): Show | 11 | HG02818.hp2 HG03225.hp2 HG03516.hp1 others(8): Show |
intron_variant | MODIFIER | c.2878-606delG | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032977 | ||||||
chr3:149032978
|
C | A | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2878-606G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149032978 | ||||||
chr3:149033026
|
C | T | 22 | a0001c0003t0002g0128a0001c0003t0002g0268a0001c0003t0002g0269others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.2878-654G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033026 | ||||||
chr3:149033109
|
A | G | 1 | a0001c0002t0013g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2878-737T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033109 | ||||||
chr3:149033217
|
G | A | 4 | a0001c0003t0002g0321a0001c0003t0002g0340a0001c0003t0002g0342others(1): Show | 4 | NA18964.hp2 NA18965.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.2878-845C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033217 | ||||||
chr3:149033328
|
C | G | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2878-956G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033328 | ||||||
chr3:149033370
|
TA | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.2878-999delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033370 | ||||||
chr3:149033468
|
C | A | 293 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(290): Show | 326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2878-1096G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033468 | ||||||
chr3:149033816
|
C | T | 1 | a0001c0003t0002g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2877+1102G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033816 | ||||||
chr3:149033893
|
CT | C | 3 | a0001c0003t0002g0269a0001c0003t0002g0278a0001c0003t0002g0286 | 3 | HG03654.hp2 HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2877+1024delA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149033893 | ||||||
chr3:149034043
|
G | A | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2877+875C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034043 | ||||||
chr3:149034186
|
T | A | 1 | a0001c0001t0001g0234 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2877+732A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034186 | ||||||
chr3:149034354
|
A | G | 1 | a0001c0003t0002g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2877+564T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034354 | ||||||
chr3:149034363
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.2877+555A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034363 | ||||||
chr3:149034395
|
A | G | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2877+523T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034395 | ||||||
chr3:149034620
|
T | A | 1 | a0001c0005t0002g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2877+298A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034620 | ||||||
chr3:149034651
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.2877+267C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034651 | ||||||
chr3:149034728
|
A | C | 2 | a0002c0004t0009g0016a0002c0004t0009g0153 | 3 | HG00323.hp2 HG01081.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.2877+190T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034728 | ||||||
chr3:149034764
|
A | G | 2 | a0007c0013t0002g0035a0007c0013t0002g0036 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2877+154T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 24/24 | chr3 | 149034764 | ||||||
chr3:149035095
|
T | C | 1 | a0001c0003t0002g0323 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2797-97A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035095 | ||||||
chr3:149035146
|
G | C | 2 | a0001c0002t0006g0042a0016c0015t0006g0041 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2797-148C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035146 | ||||||
chr3:149035298
|
A | T | 2 | a0001c0002t0003g0014a0001c0002t0003g0114 | 3 | HG03491.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2797-300T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035298 | ||||||
chr3:149035435
|
G | GAAATAAA others(5): Show |
1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2797-449_2797-438d others(14): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035435 | ||||||
chr3:149035523
|
T | A | 4 | a0001c0002t0006g0050a0001c0002t0010g0047a0001c0002t0010g0048others(1): Show | 4 | HG00738.hp2 HG02451.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797-525A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035523 | ||||||
chr3:149035576
|
T | G | 1 | a0006c0009t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2797-578A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035576 | ||||||
chr3:149035607
|
C | G | 12 | a0001c0005t0002g0015a0001c0005t0002g0135a0001c0005t0002g0137others(9): Show | 13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2797-609G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035607 | ||||||
chr3:149035614
|
G | C | 1 | a0001c0002t0006g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2797-616C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035614 | ||||||
chr3:149035656
|
C | CA | 13 | a0001c0003t0002g0288a0001c0003t0002g0289a0001c0003t0002g0290others(10): Show | 13 | HG00140.hp2 HG01175.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.2797-659dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | ||||||
chr3:149035656
|
CAAA | C | 10 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0001g0184others(7): Show | 10 | HG00423.hp2 HG00597.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.2797-661_2797-659d others(5): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | ||||||
chr3:149035656
|
CAAAA | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 160 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.2797-662_2797-659d others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | ||||||
chr3:149035656
|
CAAAAA | C | 76 | a0001c0001t0001g0149a0001c0001t0011g0129a0001c0001t0011g0131others(73): Show | 87 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.2797-663_2797-659d others(7): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | ||||||
chr3:149035656
|
CAAAAAA | C | 42 | a0001c0002t0003g0087a0001c0002t0003g0125a0001c0002t0004g0253others(39): Show | 42 | HG00738.hp2 HG01071.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.2797-664_2797-659d others(8): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | ||||||
chr3:149035656
|
CAAAAAAA | C | 7 | a0001c0002t0006g0051a0004c0008t0002g0029a0004c0008t0008g0027others(4): Show | 7 | HG01069.hp1 HG01255.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.2797-665_2797-659d others(9): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035656 | ||||||
chr3:149035673
|
A | G | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2797-675T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035673 | ||||||
chr3:149035674
|
A | G | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2797-676T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035674 | ||||||
chr3:149035675
|
A | G | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2797-677T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035675 | ||||||
chr3:149035676
|
A | T | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2797-678T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035676 | ||||||
chr3:149035677
|
A | T | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2797-679T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035677 | ||||||
chr3:149035678
|
A | AGGGGGTT others(1): Show |
12 | a0001c0002t0003g0006a0001c0002t0003g0013a0001c0002t0003g0059others(9): Show | 13 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.2797-681_2797-680i others(10): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035678 | ||||||
chr3:149035678
|
A | T | 4 | a0001c0002t0003g0361a0001c0002t0004g0260a0001c0002t0004g0262others(1): Show | 4 | HG01256.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797-680T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035678 | ||||||
chr3:149035679
|
A | T | 16 | a0001c0002t0003g0006a0001c0002t0003g0013a0001c0002t0003g0059others(13): Show | 17 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2797-681T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035679 | ||||||
chr3:149035682
|
A | G | 18 | a0001c0002t0003g0006a0001c0002t0003g0013a0001c0002t0003g0059others(15): Show | 19 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797-684T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035682 | ||||||
chr3:149035683
|
A | G | 5 | a0001c0001t0001g0210a0001c0002t0006g0050a0001c0002t0010g0047others(2): Show | 5 | HG00738.hp2 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2797-685T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035683 | ||||||
chr3:149035685
|
G | T | 18 | a0001c0002t0003g0006a0001c0002t0003g0013a0001c0002t0003g0059others(15): Show | 19 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797-687C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035685 | ||||||
chr3:149035686
|
G | C | 18 | a0001c0002t0003g0006a0001c0002t0003g0013a0001c0002t0003g0059others(15): Show | 19 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797-688C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035686 | ||||||
chr3:149035687
|
G | A | 18 | a0001c0002t0003g0006a0001c0002t0003g0013a0001c0002t0003g0059others(15): Show | 19 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797-689C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035687 | ||||||
chr3:149035690
|
T | C | 18 | a0001c0002t0003g0006a0001c0002t0003g0013a0001c0002t0003g0059others(15): Show | 19 | HG01169.hp1 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2797-692A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035690 | ||||||
chr3:149035690
|
T | TTTAAGAG others(6): Show |
81 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(78): Show | 93 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.2797-693_2797-692i others(15): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035690 | ||||||
chr3:149035776
|
G | C | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797-778C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035776 | ||||||
chr3:149035840
|
A | G | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797-842T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035840 | ||||||
chr3:149035874
|
G | A | 12 | a0001c0002t0003g0011a0001c0002t0003g0061a0001c0002t0003g0072others(9): Show | 13 | HG00621.hp2 HG01074.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.2797-876C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035874 | ||||||
chr3:149035971
|
T | C | 1 | a0001c0002t0006g0050 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2797-973A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035971 | ||||||
chr3:149035993
|
G | T | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2797-995C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149035993 | ||||||
chr3:149036035
|
T | C | 1 | a0001c0002t0003g0085 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2797-1037A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036035 | ||||||
chr3:149036177
|
T | G | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2797-1179A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036177 | ||||||
chr3:149036196
|
G | T | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797-1198C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036196 | ||||||
chr3:149036297
|
G | GTTTTTTT others(3): Show |
6 | a0001c0002t0003g0060a0001c0002t0003g0073a0001c0002t0003g0255others(3): Show | 7 | HG01167.hp1 HG01169.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.2797-1309_2797-130 others(14): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036297 | ||||||
chr3:149036297
|
G | GTTTTTTT others(4): Show |
92 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(89): Show | 104 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.2797-1300_2797-129 others(15): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036297 | ||||||
chr3:149036297
|
G | GTTTTTTT others(5): Show |
127 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(124): Show | 143 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.2797-1300_2797-129 others(16): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036297 | ||||||
chr3:149036297
|
G | GTTTTTTT others(6): Show |
40 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0132others(37): Show | 44 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2797-1300_2797-129 others(17): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036297 | ||||||
chr3:149036297
|
G | GTTTTTTT others(7): Show |
5 | a0001c0001t0018g0163a0003c0006t0005g0044a0003c0006t0005g0053others(2): Show | 5 | HG02273.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2797-1300_2797-129 others(18): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036297 | ||||||
chr3:149036376
|
C | T | 3 | a0001c0002t0003g0060a0001c0002t0003g0112a0001c0002t0003g0113 | 3 | HG01261.hp1 HG02300.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2797-1378G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036376 | ||||||
chr3:149036378
|
TCCTGGGT others(5): Show |
T | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797-1392_2797-138 others(16): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036378 | ||||||
chr3:149036578
|
C | T | 1 | a0001c0002t0021g0365 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2797-1580G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036578 | ||||||
chr3:149036579
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2797-1581C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036579 | ||||||
chr3:149036581
|
G | A | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797-1583C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036581 | ||||||
chr3:149036619
|
T | C | 1 | a0001c0003t0002g0346 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2797-1621A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036619 | ||||||
chr3:149036692
|
T | C | 98 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(95): Show | 113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2797-1694A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036692 | ||||||
chr3:149036756
|
A | G | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2797-1758T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036756 | ||||||
chr3:149036757
|
G | A | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2797-1759C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036757 | ||||||
chr3:149036767
|
T | A | 2 | a0007c0013t0002g0035a0007c0013t0002g0036 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2797-1769A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036767 | ||||||
chr3:149036829
|
G | A | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0248 | 3 | NA18992.hp1 NA19002.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2797-1831C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149036829 | ||||||
chr3:149037134
|
A | C | 1 | a0001c0005t0002g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2796+1915T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037134 | ||||||
chr3:149037171
|
A | T | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2796+1878T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037171 | ||||||
chr3:149037327
|
C | A | 1 | a0001c0003t0002g0278 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2796+1722G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037327 | ||||||
chr3:149037372
|
G | A | 114 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(111): Show | 130 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.2796+1677C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037372 | ||||||
chr3:149037447
|
G | A | 2 | a0001c0003t0002g0284a0001c0003t0002g0333 | 2 | HG03942.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2796+1602C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037447 | ||||||
chr3:149037460
|
T | C | 9 | a0001c0005t0002g0015a0001c0005t0002g0137a0001c0005t0002g0138others(6): Show | 10 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2796+1589A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037460 | ||||||
chr3:149037467
|
C | CA | 142 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.2796+1581dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037467 | ||||||
chr3:149037477
|
A | G | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2796+1572T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037477 | ||||||
chr3:149037685
|
T | C | 2 | a0001c0002t0003g0014a0001c0002t0003g0114 | 3 | HG03491.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2796+1364A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037685 | ||||||
chr3:149037784
|
G | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(62): Show | 73 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.2796+1265C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037784 | ||||||
chr3:149037840
|
G | C | 1 | a0001c0002t0004g0265 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2796+1209C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149037840 | ||||||
chr3:149038074
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.2796+975C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038074 | ||||||
chr3:149038125
|
T | C | 1 | a0001c0003t0002g0307 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2796+924A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038125 | ||||||
chr3:149038133
|
C | T | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2796+916G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038133 | ||||||
chr3:149038147
|
C | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(145): Show | 165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.2796+902G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038147 | ||||||
chr3:149038216
|
G | A | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2796+833C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038216 | ||||||
chr3:149038398
|
C | A | 2 | a0003c0006t0005g0043a0003c0006t0005g0362 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2796+651G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038398 | ||||||
chr3:149038436
|
A | G | 1 | a0003c0006t0005g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2796+613T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038436 | ||||||
chr3:149038563
|
C | T | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2796+486G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038563 | ||||||
chr3:149038592
|
T | C | 1 | a0006c0009t0002g0032 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2796+457A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038592 | ||||||
chr3:149038664
|
A | T | 1 | a0001c0001t0001g0019 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2796+385T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038664 | ||||||
chr3:149038698
|
A | C | 1 | a0001c0005t0002g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2796+351T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038698 | ||||||
chr3:149038739
|
C | G | 12 | a0001c0005t0002g0015a0001c0005t0002g0135a0001c0005t0002g0137others(9): Show | 13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2796+310G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038739 | ||||||
chr3:149038759
|
C | T | 1 | a0002c0004t0009g0016 | 2 | HG00323.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2796+290G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038759 | ||||||
chr3:149038877
|
T | G | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2796+172A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038877 | ||||||
chr3:149038974
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2796+75A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149038974 | ||||||
chr3:149039015
|
C | T | 2 | a0001c0002t0006g0042a0016c0015t0006g0041 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2796+34G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149039015 | ||||||
chr3:149039038
|
G | A | 359 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(356): Show | 394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.2796+11C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 23/24 | chr3 | 149039038 | ||||||
chr3:149039294
|
G | A | 1 | a0001c0007t0003g0097 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2616-65C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 22/24 | chr3 | 149039294 | ||||||
chr3:149039381
|
T | G | 1 | a0001c0002t0003g0125 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2616-152A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 22/24 | chr3 | 149039381 | ||||||
chr3:149039503
|
G | GT | 9 | a0001c0002t0006g0051a0001c0002t0006g0052a0003c0006t0005g0012others(6): Show | 10 | HG02055.hp2 HG02615.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2615+77dupA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 22/24 | chr3 | 149039503 | ||||||
chr3:149039940
|
T | C | 1 | a0001c0003t0002g0338 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2502+91A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 21/24 | chr3 | 149039940 | ||||||
chr3:149040162
|
T | TAAGAAAG others(342): Show |
1 | a0006c0009t0002g0034 | 1 | HG03239.hp1 | splice_region_variant&intron_variant | LOW | c.2377-7_2377-6insTT others(347): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040162 | ||||||
chr3:149040172
|
C | G | 1 | a0001c0003t0002g0309 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2377-16G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040172 | ||||||
chr3:149040173
|
G | A | 1 | a0001c0002t0003g0113 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2377-17C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040173 | ||||||
chr3:149040348
|
C | T | 293 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(290): Show | 326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2377-192G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040348 | ||||||
chr3:149040435
|
T | TA | 127 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.2377-280dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040435 | ||||||
chr3:149040915
|
C | T | 1 | a0001c0003t0002g0313 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2376+575G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149040915 | ||||||
chr3:149041282
|
G | A | 3 | a0001c0002t0004g0253a0001c0002t0004g0261a0001c0002t0004g0263 | 3 | HG02717.hp2 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2376+208C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149041282 | ||||||
chr3:149041320
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2376+170G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149041320 | ||||||
chr3:149041342
|
A | T | 1 | a0006c0009t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2376+148T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149041342 | ||||||
chr3:149041472
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2376+18T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 20/24 | chr3 | 149041472 | ||||||
chr3:149041755
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0222 | 3 | HG01070.hp1 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2198-87G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 19/24 | chr3 | 149041755 | ||||||
chr3:149041773
|
A | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.2198-105T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 19/24 | chr3 | 149041773 | ||||||
chr3:149042498
|
C | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2073-208G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042498 | ||||||
chr3:149042559
|
C | T | 16 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(13): Show | 17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.2073-269G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042559 | ||||||
chr3:149042592
|
G | T | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2073-302C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042592 | ||||||
chr3:149042640
|
T | C | 1 | a0001c0003t0002g0322 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2073-350A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042640 | ||||||
chr3:149042689
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0236 | 2 | NA18955.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2073-399C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042689 | ||||||
chr3:149042881
|
T | C | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2073-591A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042881 | ||||||
chr3:149042901
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2073-611T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149042901 | ||||||
chr3:149043059
|
T | A | 1 | a0001c0001t0001g0165 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2073-769A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043059 | ||||||
chr3:149043272
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2073-982T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043272 | ||||||
chr3:149043275
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2073-985C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043275 | ||||||
chr3:149043277
|
T | A | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2073-987A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043277 | ||||||
chr3:149043283
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2073-993G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043283 | ||||||
chr3:149043524
|
A | G | 161 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2073-1234T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043524 | ||||||
chr3:149043547
|
G | GA | 40 | a0001c0001t0001g0162a0001c0001t0001g0171a0001c0001t0001g0190others(37): Show | 41 | HG00621.hp2 HG00738.hp2 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.2073-1258dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043547 | ||||||
chr3:149043547
|
GA | G | 16 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0150others(13): Show | 16 | HG01255.hp2 HG01515.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2073-1258delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043547 | ||||||
chr3:149043548
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2073-1258T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043548 | ||||||
chr3:149043558
|
A | C | 22 | a0001c0003t0002g0128a0001c0003t0002g0268a0001c0003t0002g0269others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.2073-1268T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043558 | ||||||
chr3:149043699
|
G | T | 2 | a0001c0002t0006g0051a0001c0002t0006g0052 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2073-1409C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043699 | ||||||
chr3:149043703
|
A | G | 2 | a0001c0002t0003g0014a0001c0002t0003g0114 | 3 | HG03491.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2073-1413T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043703 | ||||||
chr3:149043813
|
T | C | 98 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(95): Show | 113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2073-1523A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043813 | ||||||
chr3:149043854
|
T | C | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2073-1564A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043854 | ||||||
chr3:149043889
|
T | C | 4 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(1): Show | 4 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2073-1599A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043889 | ||||||
chr3:149043891
|
C | T | 2 | a0003c0006t0005g0043a0003c0006t0005g0362 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2073-1601G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149043891 | ||||||
chr3:149044021
|
A | G | 1 | a0001c0002t0003g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2073-1731T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044021 | ||||||
chr3:149044028
|
A | C | 88 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(85): Show | 103 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2073-1738T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044028 | ||||||
chr3:149044032
|
A | G | 1 | a0001c0003t0002g0335 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2073-1742T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044032 | ||||||
chr3:149044042
|
C | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0236 | 2 | NA18955.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2073-1752G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044042 | ||||||
chr3:149044054
|
C | T | 2 | a0001c0005t0002g0015a0001c0005t0002g0139 | 3 | HG02559.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2073-1764G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044054 | ||||||
chr3:149044073
|
T | C | 6 | a0001c0002t0006g0050a0004c0008t0002g0029a0004c0008t0008g0027others(3): Show | 6 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2073-1783A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044073 | ||||||
chr3:149044486
|
C | CT | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0237 | 3 | HG02258.hp2 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2072+1593dupA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044486 | ||||||
chr3:149044501
|
G | C | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2072+1579C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044501 | ||||||
chr3:149044564
|
C | G | 292 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(289): Show | 325 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.2072+1516G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044564 | ||||||
chr3:149044576
|
T | G | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2072+1504A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044576 | ||||||
chr3:149044640
|
T | C | 1 | a0001c0017t0001g0158 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2072+1440A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044640 | ||||||
chr3:149044643
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2072+1437T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044643 | ||||||
chr3:149044727
|
G | T | 1 | a0001c0003t0002g0327 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2072+1353C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044727 | ||||||
chr3:149044849
|
T | C | 1 | a0001c0003t0002g0330 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2072+1231A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044849 | ||||||
chr3:149044862
|
T | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 6 | HG00558.hp1 HG02165.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2072+1218A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044862 | ||||||
chr3:149044927
|
G | A | 1 | a0001c0003t0002g0335 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2072+1153C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149044927 | ||||||
chr3:149045043
|
A | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.2072+1037T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045043 | ||||||
chr3:149045076
|
C | T | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.2072+1004G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045076 | ||||||
chr3:149045077
|
G | A | 1 | a0001c0002t0006g0042 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2072+1003C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045077 | ||||||
chr3:149045196
|
G | C | 6 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2072+884C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045196 | ||||||
chr3:149045196
|
G | T | 54 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0019others(51): Show | 62 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.2072+884C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045196 | ||||||
chr3:149045412
|
G | C | 6 | a0001c0002t0006g0050a0004c0008t0002g0029a0004c0008t0008g0027others(3): Show | 6 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2072+668C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045412 | ||||||
chr3:149045618
|
G | T | 1 | a0001c0003t0002g0297 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2072+462C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045618 | ||||||
chr3:149045669
|
T | C | 3 | a0001c0003t0002g0308a0001c0003t0002g0331a0001c0003t0002g0332 | 3 | HG00099.hp2 HG01070.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2072+411A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045669 | ||||||
chr3:149045703
|
G | A | 1 | a0001c0002t0003g0107 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2072+377C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045703 | ||||||
chr3:149045719
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.2072+361C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045719 | ||||||
chr3:149045822
|
T | C | 1 | a0005c0010t0007g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2072+258A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 18/24 | chr3 | 149045822 | ||||||
chr3:149046303
|
C | T | 171 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1893-44G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046303 | ||||||
chr3:149046498
|
T | G | 3 | a0001c0001t0011g0129a0001c0001t0011g0131a0001c0001t0015g0130 | 3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1893-239A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046498 | ||||||
chr3:149046515
|
T | C | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1893-256A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046515 | ||||||
chr3:149046519
|
G | C | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1893-260C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046519 | ||||||
chr3:149046756
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1893-497T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046756 | ||||||
chr3:149046883
|
A | G | 15 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0051others(12): Show | 16 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1893-624T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149046883 | ||||||
chr3:149047012
|
C | T | 1 | a0004c0008t0008g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1893-753G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047012 | ||||||
chr3:149047149
|
C | T | 7 | a0003c0006t0005g0012a0003c0006t0005g0043a0003c0006t0005g0044others(4): Show | 8 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1892+879G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047149 | ||||||
chr3:149047162
|
C | G | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1892+866G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047162 | ||||||
chr3:149047211
|
T | TTAGTC | 292 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(289): Show | 325 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1892+816_1892+817i others(7): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047211 | ||||||
chr3:149047598
|
C | T | 2 | a0007c0013t0002g0035a0007c0013t0002g0036 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1892+430G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047598 | ||||||
chr3:149047634
|
T | C | 2 | a0001c0003t0002g0342a0001c0003t0002g0343 | 2 | NA18967.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1892+394A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047634 | ||||||
chr3:149047659
|
A | C | 2 | a0001c0002t0003g0061a0001c0002t0003g0073 | 2 | NA18970.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1892+369T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 17/24 | chr3 | 149047659 | ||||||
chr3:149048439
|
C | T | 2 | a0001c0002t0006g0042a0016c0015t0006g0041 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1757-276G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048439 | ||||||
chr3:149048494
|
G | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1757-331C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048494 | ||||||
chr3:149048636
|
G | T | 2 | a0001c0002t0006g0042a0016c0015t0006g0041 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1756+227C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048636 | ||||||
chr3:149048675
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0222 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1756+188T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048675 | ||||||
chr3:149048698
|
C | A | 1 | a0001c0001t0001g0216 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1756+165G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048698 | ||||||
chr3:149048836
|
T | C | 6 | a0001c0002t0006g0042a0001c0002t0006g0050a0001c0002t0010g0047others(3): Show | 6 | HG00738.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1756+27A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 16/24 | chr3 | 149048836 | ||||||
chr3:149049171
|
C | T | 2 | a0001c0003t0002g0273a0001c0003t0016g0285 | 2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1618-170G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049171 | ||||||
chr3:149049193
|
C | T | 99 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(96): Show | 114 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1618-192G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049193 | ||||||
chr3:149049329
|
C | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1618-328G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049329 | ||||||
chr3:149049370
|
G | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1618-369C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049370 | ||||||
chr3:149049599
|
A | C | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1618-598T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049599 | ||||||
chr3:149049993
|
G | A | 6 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1617+239C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149049993 | ||||||
chr3:149050023
|
G | T | 5 | a0001c0003t0002g0301a0001c0003t0002g0318a0001c0003t0002g0341others(2): Show | 5 | HG00438.hp2 HG00558.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1617+209C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149050023 | ||||||
chr3:149050221
|
A | G | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1617+11T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 15/24 | chr3 | 149050221 | ||||||
chr3:149050444
|
A | C | 1 | a0001c0002t0010g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1474-69T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050444 | ||||||
chr3:149050526
|
A | T | 2 | a0005c0010t0007g0037a0005c0010t0007g0038 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1474-151T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050526 | ||||||
chr3:149050634
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1474-259A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050634 | ||||||
chr3:149050687
|
G | A | 1 | a0001c0002t0006g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1474-312C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050687 | ||||||
chr3:149050836
|
C | T | 3 | a0001c0005t0002g0138a0001c0005t0002g0140a0001c0005t0002g0143 | 3 | HG02895.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1474-461G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050836 | ||||||
chr3:149050847
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0251 | 2 | HG02074.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1474-472A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050847 | ||||||
chr3:149050955
|
A | C | 1 | a0006c0009t0002g0033 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1474-580T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149050955 | ||||||
chr3:149051133
|
G | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0239 | 3 | HG02273.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1474-758C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051133 | ||||||
chr3:149051235
|
TA | T | 20 | a0001c0001t0001g0147a0001c0001t0001g0169a0001c0001t0001g0233others(17): Show | 20 | HG00140.hp1 HG00558.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.1474-861delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051235 | ||||||
chr3:149051236
|
A | T | 95 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(92): Show | 110 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1474-861T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051236 | ||||||
chr3:149051237
|
A | T | 1 | a0001c0007t0003g0066 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1474-862T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051237 | ||||||
chr3:149051259
|
A | T | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1474-884T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051259 | ||||||
chr3:149051280
|
A | G | 1 | a0001c0003t0002g0296 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1474-905T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051280 | ||||||
chr3:149051364
|
T | C | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1474-989A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051364 | ||||||
chr3:149051609
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1474-1234G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051609 | ||||||
chr3:149051695
|
T | C | 22 | a0001c0003t0002g0128a0001c0003t0002g0268a0001c0003t0002g0269others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1474-1320A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051695 | ||||||
chr3:149051740
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0166 | 2 | NA18965.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1474-1365G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051740 | ||||||
chr3:149051799
|
G | A | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1474-1424C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149051799 | ||||||
chr3:149052077
|
C | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1474-1702G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052077 | ||||||
chr3:149052148
|
T | TA | 44 | a0001c0001t0001g0184a0001c0001t0001g0195a0001c0001t0001g0211others(41): Show | 45 | HG00738.hp1 HG00738.hp2 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.1474-1774dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052148 | ||||||
chr3:149052148
|
TA | T | 10 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0168others(7): Show | 10 | HG01515.hp1 HG01516.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-1774delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052148 | ||||||
chr3:149052289
|
A | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1474-1914T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052289 | ||||||
chr3:149052642
|
A | C | 2 | a0001c0002t0006g0051a0001c0002t0006g0052 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1474-2267T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052642 | ||||||
chr3:149052965
|
A | G | 1 | a0004c0008t0017g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1473+2338T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149052965 | ||||||
chr3:149053153
|
A | AG | 3 | a0001c0001t0011g0129a0001c0001t0011g0131a0001c0001t0015g0130 | 3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1473+2149dupC | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053153 | ||||||
chr3:149053405
|
T | A | 1 | a0010c0012t0001g0238 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1473+1898A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053405 | ||||||
chr3:149053447
|
C | T | 6 | a0001c0002t0006g0042a0001c0002t0006g0050a0001c0002t0010g0047others(3): Show | 6 | HG00738.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+1856G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053447 | ||||||
chr3:149053525
|
C | T | 88 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(85): Show | 103 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1473+1778G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053525 | ||||||
chr3:149053913
|
A | T | 1 | a0001c0002t0003g0071 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1473+1390T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053913 | ||||||
chr3:149053939
|
C | A | 3 | a0001c0001t0001g0184a0010c0012t0001g0183a0010c0012t0001g0238 | 3 | HG01891.hp1 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1473+1364G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149053939 | ||||||
chr3:149054086
|
G | A | 1 | a0001c0003t0002g0338 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1473+1217C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149054086 | ||||||
chr3:149054135
|
A | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(267): Show | 303 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1473+1168T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149054135 | ||||||
chr3:149054481
|
G | A | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1473+822C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149054481 | ||||||
chr3:149054668
|
T | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 157 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1473+635A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149054668 | ||||||
chr3:149054982
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1473+321T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149054982 | ||||||
chr3:149055075
|
G | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0159a0001c0001t0001g0182 | 4 | HG00597.hp1 NA18941.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1473+228C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 14/24 | chr3 | 149055075 | ||||||
chr3:149055476
|
T | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0159others(3): Show | 8 | HG00597.hp1 HG02293.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376-76A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149055476 | ||||||
chr3:149055793
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1376-393G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149055793 | ||||||
chr3:149056106
|
G | A | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1376-706C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056106 | ||||||
chr3:149056176
|
C | T | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1376-776G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056176 | ||||||
chr3:149056183
|
G | A | 8 | a0002c0004t0001g0197a0002c0004t0001g0199a0002c0004t0001g0201others(5): Show | 8 | HG00280.hp2 HG01123.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.1376-783C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056183 | ||||||
chr3:149056267
|
T | C | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1376-867A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056267 | ||||||
chr3:149056269
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1376-869C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056269 | ||||||
chr3:149056491
|
A | G | 3 | a0001c0001t0011g0129a0001c0001t0011g0131a0001c0001t0015g0130 | 3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1376-1091T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056491 | ||||||
chr3:149056629
|
A | C | 1 | a0001c0002t0013g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1376-1229T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056629 | ||||||
chr3:149056787
|
C | T | 1 | a0004c0008t0002g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1376-1387G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056787 | ||||||
chr3:149056807
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1376-1407C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056807 | ||||||
chr3:149056862
|
C | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1376-1462G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056862 | ||||||
chr3:149056891
|
C | T | 6 | a0001c0002t0003g0255a0001c0002t0004g0256a0005c0010t0007g0037others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1376-1491G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056891 | ||||||
chr3:149056950
|
A | T | 9 | a0001c0005t0002g0015a0001c0005t0002g0137a0001c0005t0002g0138others(6): Show | 10 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1376-1550T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149056950 | ||||||
chr3:149057012
|
G | A | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1376-1612C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057012 | ||||||
chr3:149057026
|
G | A | 6 | a0001c0003t0002g0349a0004c0008t0002g0029a0004c0008t0008g0027others(3): Show | 6 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376-1626C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057026 | ||||||
chr3:149057035
|
A | G | 1 | a0001c0003t0002g0349 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1376-1635T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057035 | ||||||
chr3:149057107
|
C | CA | 44 | a0001c0002t0003g0058a0001c0002t0003g0060a0001c0002t0003g0070others(41): Show | 44 | HG00597.hp2 HG00621.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1376-1708dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | ||||||
chr3:149057107
|
CA | C | 60 | a0001c0001t0001g0022a0001c0001t0001g0055a0001c0001t0001g0134others(57): Show | 63 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.1376-1708delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | ||||||
chr3:149057107
|
CAA | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(105): Show | 123 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1376-1709_1376-170 others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | ||||||
chr3:149057107
|
CAAA | C | 6 | a0001c0001t0001g0198a0004c0008t0002g0029a0004c0008t0008g0027others(3): Show | 6 | HG01069.hp1 HG01255.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1376-1710_1376-170 others(7): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | ||||||
chr3:149057107
|
CAAAAAAA others(4): Show |
C | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0040others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1376-1718_1376-170 others(15): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | ||||||
chr3:149057107
|
CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0001g0154a0001c0001t0001g0166a0001c0002t0003g0072others(1): Show | 4 | HG01074.hp1 HG02723.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1376-1719_1376-170 others(16): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | ||||||
chr3:149057107
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0005t0002g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1376-1722_1376-170 others(19): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057107 | ||||||
chr3:149057191
|
A | C | 3 | a0001c0001t0011g0129a0001c0001t0011g0131a0001c0001t0015g0130 | 3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1376-1791T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057191 | ||||||
chr3:149057283
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1376-1883C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057283 | ||||||
chr3:149057315
|
A | G | 2 | a0001c0002t0006g0051a0001c0002t0006g0052 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1376-1915T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057315 | ||||||
chr3:149057413
|
G | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1376-2013C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057413 | ||||||
chr3:149057426
|
A | AAAAC | 8 | a0001c0001t0001g0162a0001c0001t0001g0164a0001c0001t0001g0165others(5): Show | 8 | HG01109.hp2 HG01257.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1376-2030_1376-202 others(8): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057426 | ||||||
chr3:149057456
|
G | A | 1 | a0001c0003t0002g0313 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1376-2056C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057456 | ||||||
chr3:149057515
|
C | A | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1376-2115G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057515 | ||||||
chr3:149057593
|
A | C | 2 | a0007c0013t0002g0035a0007c0013t0002g0036 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1375+2125T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057593 | ||||||
chr3:149057602
|
G | A | 2 | a0003c0006t0005g0043a0003c0006t0005g0362 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1375+2116C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057602 | ||||||
chr3:149057700
|
G | A | 1 | a0001c0002t0004g0262 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1375+2018C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149057700 | ||||||
chr3:149058224
|
A | C | 1 | a0001c0003t0002g0283 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1375+1494T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058224 | ||||||
chr3:149058224
|
A | G | 2 | a0001c0002t0006g0042a0016c0015t0006g0041 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1375+1494T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058224 | ||||||
chr3:149058310
|
G | C | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1375+1408C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058310 | ||||||
chr3:149058348
|
ATGCCTGC | A | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1375+1363_1375+136 others(11): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058348 | ||||||
chr3:149058457
|
T | C | 2 | a0007c0013t0002g0035a0007c0013t0002g0036 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1375+1261A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058457 | ||||||
chr3:149058501
|
T | C | 1 | a0001c0002t0004g0261 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1375+1217A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058501 | ||||||
chr3:149058520
|
A | G | 1 | a0001c0003t0002g0269 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1375+1198T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058520 | ||||||
chr3:149058606
|
C | T | 7 | a0003c0006t0005g0012a0003c0006t0005g0043a0003c0006t0005g0044others(4): Show | 8 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1375+1112G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058606 | ||||||
chr3:149058689
|
C | T | 6 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0184others(3): Show | 6 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1375+1029G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058689 | ||||||
chr3:149058774
|
T | C | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0240others(2): Show | 5 | HG00673.hp2 NA18986.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375+944A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058774 | ||||||
chr3:149058824
|
G | A | 98 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(95): Show | 113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1375+894C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058824 | ||||||
chr3:149058899
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0195 | 2 | NA19012.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1375+819C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058899 | ||||||
chr3:149058944
|
A | C | 1 | a0001c0001t0001g0243 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1375+774T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149058944 | ||||||
chr3:149059130
|
A | G | 1 | a0001c0003t0002g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1375+588T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059130 | ||||||
chr3:149059185
|
C | CTAT | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1375+532_1375+533i others(5): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059185 | ||||||
chr3:149059341
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1375+377T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059341 | ||||||
chr3:149059395
|
C | T | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1375+323G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059395 | ||||||
chr3:149059511
|
C | A | 1 | a0001c0001t0001g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1375+207G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059511 | ||||||
chr3:149059597
|
T | G | 1 | a0001c0003t0002g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1375+121A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059597 | ||||||
chr3:149059677
|
G | GA | 9 | a0001c0001t0001g0215a0001c0001t0001g0230a0001c0002t0003g0071others(6): Show | 9 | HG00423.hp1 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1375+40dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 13/24 | chr3 | 149059677 | ||||||
chr3:149060025
|
TGAG | T | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1286-221_1286-219d others(5): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 12/24 | chr3 | 149060025 | ||||||
chr3:149060303
|
A | G | 98 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(95): Show | 113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1285+340T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 12/24 | chr3 | 149060303 | ||||||
chr3:149060372
|
T | C | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0237 | 3 | HG02258.hp2 HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1285+271A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 12/24 | chr3 | 149060372 | ||||||
chr3:149061130
|
C | A | 1 | a0016c0015t0006g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1161-272G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061130 | ||||||
chr3:149061233
|
C | T | 1 | a0003c0006t0005g0044 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1161-375G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061233 | ||||||
chr3:149061268
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1161-410C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061268 | ||||||
chr3:149061277
|
G | C | 3 | a0001c0001t0011g0129a0001c0001t0011g0131a0001c0001t0015g0130 | 3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1161-419C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061277 | ||||||
chr3:149061284
|
G | A | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1161-426C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061284 | ||||||
chr3:149061294
|
C | G | 16 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(13): Show | 17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1161-436G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061294 | ||||||
chr3:149061370
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1161-512G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061370 | ||||||
chr3:149061413
|
A | AAAAAT | 22 | a0001c0002t0006g0050a0001c0002t0010g0047a0001c0002t0010g0048others(19): Show | 23 | HG00738.hp2 HG01243.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.1161-560_1161-556d others(7): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061413 | ||||||
chr3:149061413
|
A | AAAAATAA others(3): Show |
1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1161-565_1161-556d others(12): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061413 | ||||||
chr3:149061413
|
AAAAATAA others(3): Show |
A | 98 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(95): Show | 113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1161-565_1161-556d others(12): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061413 | ||||||
chr3:149061729
|
A | T | 1 | a0001c0002t0003g0103 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1161-871T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061729 | ||||||
chr3:149061759
|
C | A | 1 | a0001c0002t0003g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1161-901G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061759 | ||||||
chr3:149061785
|
G | A | 1 | a0001c0002t0003g0094 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1161-927C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061785 | ||||||
chr3:149061836
|
C | CA | 8 | a0001c0003t0002g0311a0001c0003t0002g0313a0002c0004t0001g0242others(5): Show | 8 | HG01255.hp2 HG01433.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1161-979dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061836 | ||||||
chr3:149061837
|
A | C | 1 | a0003c0006t0005g0362 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1161-979T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061837 | ||||||
chr3:149061914
|
G | A | 16 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(13): Show | 17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1161-1056C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061914 | ||||||
chr3:149061959
|
A | G | 4 | a0001c0003t0002g0289a0001c0003t0002g0304a0001c0003t0002g0315others(1): Show | 4 | HG01975.hp2 HG02148.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161-1101T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061959 | ||||||
chr3:149061983
|
C | T | 1 | a0001c0002t0004g0253 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1161-1125G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149061983 | ||||||
chr3:149062102
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1161-1244A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062102 | ||||||
chr3:149062251
|
T | G | 1 | a0001c0003t0002g0335 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1160+1180A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062251 | ||||||
chr3:149062276
|
T | C | 2 | a0007c0013t0002g0035a0007c0013t0002g0036 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1160+1155A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062276 | ||||||
chr3:149062307
|
GT | G | 12 | a0001c0005t0002g0015a0001c0005t0002g0135a0001c0005t0002g0137others(9): Show | 13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1160+1123delA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062307 | ||||||
chr3:149062482
|
G | C | 7 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0220others(4): Show | 7 | HG00408.hp2 HG00673.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.1160+949C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062482 | ||||||
chr3:149062501
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1160+930G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062501 | ||||||
chr3:149062581
|
T | C | 1 | a0002c0004t0001g0204 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1160+850A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062581 | ||||||
chr3:149062722
|
C | T | 1 | a0001c0002t0010g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1160+709G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062722 | ||||||
chr3:149062808
|
T | C | 1 | a0001c0005t0002g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1160+623A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062808 | ||||||
chr3:149062817
|
A | G | 1 | a0001c0002t0004g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1160+614T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062817 | ||||||
chr3:149062862
|
A | G | 22 | a0001c0003t0002g0128a0001c0003t0002g0268a0001c0003t0002g0269others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1160+569T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062862 | ||||||
chr3:149062900
|
C | T | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1160+531G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149062900 | ||||||
chr3:149063051
|
C | T | 4 | a0001c0003t0002g0302a0001c0003t0002g0303a0001c0003t0002g0314others(1): Show | 4 | NA18948.hp1 NA19006.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160+380G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 10/24 | chr3 | 149063051 | ||||||
chr3:149063668
|
C | G | 12 | a0001c0005t0002g0015a0001c0005t0002g0135a0001c0005t0002g0137others(9): Show | 13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1067-144G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149063668 | ||||||
chr3:149063733
|
G | C | 1 | a0001c0001t0020g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1067-209C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149063733 | ||||||
chr3:149063752
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1067-228G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149063752 | ||||||
chr3:149063874
|
T | C | 22 | a0001c0003t0002g0128a0001c0003t0002g0268a0001c0003t0002g0269others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1067-350A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149063874 | ||||||
chr3:149064046
|
G | A | 4 | a0001c0005t0002g0015a0001c0005t0002g0139a0001c0005t0002g0144others(1): Show | 5 | HG01243.hp2 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1067-522C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064046 | ||||||
chr3:149064070
|
T | C | 1 | a0001c0003t0002g0280 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1067-546A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064070 | ||||||
chr3:149064160
|
G | C | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066+631C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064160 | ||||||
chr3:149064162
|
T | C | 1 | a0001c0003t0002g0322 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1066+629A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064162 | ||||||
chr3:149064271
|
T | A | 1 | a0001c0003t0002g0353 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1066+520A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064271 | ||||||
chr3:149064313
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 6 | HG00558.hp1 HG02165.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.1066+478G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064313 | ||||||
chr3:149064432
|
C | T | 1 | a0001c0002t0003g0071 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1066+359G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064432 | ||||||
chr3:149064459
|
A | G | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1066+332T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064459 | ||||||
chr3:149064713
|
C | T | 1 | a0001c0003t0002g0286 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1066+78G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 9/24 | chr3 | 149064713 | ||||||
chr3:149064988
|
T | C | 1 | a0001c0002t0004g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.991-122A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149064988 | ||||||
chr3:149065066
|
C | CA | 8 | a0001c0003t0002g0312a0001c0003t0002g0336a0001c0003t0002g0337others(5): Show | 8 | HG00323.hp1 HG01255.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.991-201dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065066 | ||||||
chr3:149065076
|
A | T | 16 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(13): Show | 16 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.991-210T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065076 | ||||||
chr3:149065109
|
C | T | 22 | a0001c0003t0002g0128a0001c0003t0002g0268a0001c0003t0002g0269others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.991-243G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065109 | ||||||
chr3:149065156
|
G | A | 99 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(96): Show | 114 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.991-290C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065156 | ||||||
chr3:149065260
|
T | C | 2 | a0001c0003t0002g0321a0001c0003t0002g0340 | 2 | NA18964.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.991-394A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065260 | ||||||
chr3:149065272
|
C | T | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.991-406G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065272 | ||||||
chr3:149065288
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.991-422G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065288 | ||||||
chr3:149065428
|
T | G | 1 | a0001c0001t0001g0148 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.991-562A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065428 | ||||||
chr3:149065565
|
G | A | 2 | a0001c0002t0006g0051a0001c0002t0006g0052 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.991-699C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065565 | ||||||
chr3:149065599
|
G | A | 2 | a0001c0002t0006g0042a0016c0015t0006g0041 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.991-733C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065599 | ||||||
chr3:149065605
|
G | A | 1 | a0001c0002t0004g0355 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.991-739C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065605 | ||||||
chr3:149065666
|
C | T | 1 | a0001c0002t0004g0355 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.991-800G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065666 | ||||||
chr3:149065685
|
C | G | 22 | a0001c0003t0002g0128a0001c0003t0002g0268a0001c0003t0002g0269others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.991-819G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065685 | ||||||
chr3:149065698
|
C | T | 87 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(84): Show | 102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.991-832G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065698 | ||||||
chr3:149065779
|
A | G | 1 | a0002c0004t0001g0199 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.991-913T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065779 | ||||||
chr3:149065787
|
G | A | 1 | a0003c0006t0005g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.991-921C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149065787 | ||||||
chr3:149066023
|
T | G | 1 | a0001c0002t0003g0065 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.991-1157A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066023 | ||||||
chr3:149066099
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.991-1233A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066099 | ||||||
chr3:149066104
|
C | T | 3 | a0001c0003t0002g0349a0001c0003t0002g0350a0001c0003t0002g0351 | 3 | NA18985.hp1 NA18992.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.991-1238G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066104 | ||||||
chr3:149066105
|
G | A | 6 | a0001c0003t0002g0313a0004c0008t0002g0029a0004c0008t0008g0027others(3): Show | 6 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.991-1239C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066105 | ||||||
chr3:149066116
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.991-1250C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066116 | ||||||
chr3:149066129
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0181 | 2 | HG00733.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.991-1263G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066129 | ||||||
chr3:149066195
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.991-1329G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066195 | ||||||
chr3:149066204
|
A | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(267): Show | 303 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.991-1338T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066204 | ||||||
chr3:149066293
|
G | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0188others(23): Show | 29 | HG00408.hp2 HG00558.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.991-1427C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066293 | ||||||
chr3:149066529
|
AT | A | 18 | a0001c0001t0001g0147a0001c0001t0001g0181a0001c0001t0001g0222others(15): Show | 18 | HG01069.hp1 HG01070.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.991-1664delA | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066529 | ||||||
chr3:149066553
|
C | T | 6 | a0001c0002t0006g0042a0001c0002t0006g0050a0001c0002t0010g0047others(3): Show | 6 | HG00738.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.990+1687G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066553 | ||||||
chr3:149066678
|
T | A | 1 | a0006c0009t0002g0032 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.990+1562A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066678 | ||||||
chr3:149066775
|
G | A | 1 | a0001c0007t0003g0095 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.990+1465C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066775 | ||||||
chr3:149066822
|
G | T | 87 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(84): Show | 102 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.990+1418C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066822 | ||||||
chr3:149066953
|
C | A | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.990+1287G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066953 | ||||||
chr3:149066986
|
T | A | 1 | a0001c0003t0002g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.990+1254A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149066986 | ||||||
chr3:149067145
|
C | T | 1 | a0001c0005t0002g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.990+1095G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067145 | ||||||
chr3:149067186
|
G | A | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.990+1054C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067186 | ||||||
chr3:149067197
|
C | T | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+1043G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067197 | ||||||
chr3:149067200
|
A | G | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.990+1040T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067200 | ||||||
chr3:149067286
|
A | G | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.990+954T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067286 | ||||||
chr3:149067384
|
A | G | 6 | a0001c0001t0001g0055a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 6 | HG00423.hp2 NA18992.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.990+856T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067384 | ||||||
chr3:149067388
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.990+852A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067388 | ||||||
chr3:149067462
|
G | T | 1 | a0001c0001t0015g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.990+778C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067462 | ||||||
chr3:149067540
|
T | G | 1 | a0001c0002t0003g0102 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.990+700A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067540 | ||||||
chr3:149067547
|
A | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.990+693T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067547 | ||||||
chr3:149067693
|
A | T | 2 | a0001c0001t0001g0148a0001c0005t0002g0142 | 2 | HG02647.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.990+547T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067693 | ||||||
chr3:149067708
|
A | T | 2 | a0001c0002t0006g0051a0001c0002t0006g0052 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.990+532T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067708 | ||||||
chr3:149067744
|
CTGGTAAC others(70): Show |
C | 2 | a0001c0002t0003g0096a0001c0002t0003g0098 | 2 | NA18941.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.990+419_990+495del others(77): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067744 | ||||||
chr3:149067887
|
T | C | 5 | a0001c0001t0001g0359a0006c0009t0002g0031a0006c0009t0002g0032others(2): Show | 5 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.990+353A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149067887 | ||||||
chr3:149068109
|
A | G | 2 | a0001c0002t0006g0051a0001c0002t0006g0052 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.990+131T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 8/24 | chr3 | 149068109 | ||||||
chr3:149068981
|
A | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(290): Show | 326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.895-646T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149068981 | ||||||
chr3:149069002
|
A | C | 2 | a0007c0013t0002g0035a0007c0013t0002g0036 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.895-667T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069002 | ||||||
chr3:149069158
|
T | TA | 129 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.895-824dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069158 | ||||||
chr3:149069292
|
T | A | 3 | a0001c0001t0001g0184a0010c0012t0001g0183a0010c0012t0001g0238 | 3 | HG01891.hp1 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.895-957A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069292 | ||||||
chr3:149069403
|
G | A | 6 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.895-1068C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069403 | ||||||
chr3:149069472
|
G | GA | 45 | a0001c0001t0001g0231a0001c0002t0006g0042a0001c0002t0006g0046others(42): Show | 47 | HG00738.hp2 HG01167.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.895-1138dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069472 | ||||||
chr3:149069472
|
G | GAA | 127 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.895-1139_895-1138d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069472 | ||||||
chr3:149069494
|
G | A | 2 | a0001c0002t0003g0255a0001c0002t0004g0256 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.895-1159C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069494 | ||||||
chr3:149069556
|
T | A | 1 | a0001c0002t0003g0112 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.895-1221A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069556 | ||||||
chr3:149069858
|
T | G | 119 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 135 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.894+1394A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069858 | ||||||
chr3:149069976
|
T | C | 1 | a0001c0003t0002g0339 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.894+1276A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149069976 | ||||||
chr3:149070092
|
CAG | C | 13 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(10): Show | 13 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.894+1158_894+1159d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070092 | ||||||
chr3:149070249
|
C | T | 1 | a0001c0003t0002g0360 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.894+1003G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070249 | ||||||
chr3:149070642
|
A | C | 4 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(1): Show | 4 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+610T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070642 | ||||||
chr3:149070711
|
A | G | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+541T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070711 | ||||||
chr3:149070816
|
G | A | 2 | a0001c0001t0011g0129a0001c0001t0011g0131 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.894+436C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070816 | ||||||
chr3:149070841
|
T | A | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.894+411A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149070841 | ||||||
chr3:149071017
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.894+235G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149071017 | ||||||
chr3:149071044
|
CA | C | 8 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.894+207delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149071044 | ||||||
chr3:149071052
|
A | AT | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.894+199_894+200ins others(1): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149071052 | ||||||
chr3:149071106
|
C | T | 293 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(290): Show | 326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.894+146G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149071106 | ||||||
chr3:149071154
|
G | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.894+98C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 7/24 | chr3 | 149071154 | ||||||
chr3:149071467
|
G | A | 2 | a0001c0002t0003g0255a0001c0002t0004g0256 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.703-24C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 6/24 | chr3 | 149071467 | ||||||
chr3:149071502
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.703-59A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 6/24 | chr3 | 149071502 | ||||||
chr3:149071751
|
G | A | 5 | a0001c0002t0003g0113a0006c0009t0002g0031a0006c0009t0002g0032others(2): Show | 5 | HG01167.hp2 HG01261.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-94C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149071751 | ||||||
chr3:149071838
|
G | A | 1 | a0001c0005t0002g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.628-181C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149071838 | ||||||
chr3:149071875
|
C | T | 1 | a0002c0004t0009g0153 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.628-218G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149071875 | ||||||
chr3:149072136
|
A | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(290): Show | 326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.628-479T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072136 | ||||||
chr3:149072172
|
C | G | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-515G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072172 | ||||||
chr3:149072247
|
A | T | 6 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02273.hp2 HG02683.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-590T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072247 | ||||||
chr3:149072471
|
C | T | 5 | a0001c0003t0002g0301a0001c0003t0002g0318a0001c0003t0002g0341others(2): Show | 5 | HG00438.hp2 HG00558.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+754G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072471 | ||||||
chr3:149072516
|
T | C | 15 | a0001c0005t0002g0015a0001c0005t0002g0135a0001c0005t0002g0137others(12): Show | 17 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.627+709A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072516 | ||||||
chr3:149072626
|
G | A | 1 | a0001c0002t0003g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.627+599C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072626 | ||||||
chr3:149072744
|
T | C | 1 | a0002c0004t0001g0205 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.627+481A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072744 | ||||||
chr3:149072971
|
C | A | 1 | a0001c0003t0002g0354 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.627+254G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072971 | ||||||
chr3:149072972
|
G | A | 1 | a0006c0009t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.627+253C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149072972 | ||||||
chr3:149073072
|
T | C | 2 | a0001c0002t0003g0057a0001c0002t0003g0058 | 2 | HG00597.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.627+153A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 5/24 | chr3 | 149073072 | ||||||
chr3:149073333
|
C | G | 15 | a0001c0005t0002g0015a0001c0005t0002g0135a0001c0005t0002g0137others(12): Show | 17 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.530-11G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073333 | ||||||
chr3:149073454
|
G | T | 1 | a0005c0010t0007g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.530-132C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073454 | ||||||
chr3:149073515
|
G | A | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.530-193C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073515 | ||||||
chr3:149073559
|
T | C | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG03490.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.530-237A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073559 | ||||||
chr3:149073564
|
T | G | 2 | a0001c0002t0003g0121a0001c0002t0003g0125 | 2 | NA18947.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.530-242A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073564 | ||||||
chr3:149073669
|
C | T | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-347G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073669 | ||||||
chr3:149073844
|
C | G | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.529+371G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073844 | ||||||
chr3:149073854
|
G | A | 2 | a0001c0003t0002g0273a0001c0003t0016g0285 | 2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.529+361C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073854 | ||||||
chr3:149073917
|
A | G | 1 | a0001c0001t0011g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.529+298T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073917 | ||||||
chr3:149073953
|
T | C | 1 | a0001c0003t0002g0298 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.529+262A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149073953 | ||||||
chr3:149074013
|
C | T | 6 | a0001c0003t0002g0293a0001c0003t0002g0299a0001c0003t0002g0323others(3): Show | 6 | HG02074.hp1 HG02135.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+202G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149074013 | ||||||
chr3:149074155
|
G | A | 1 | a0001c0002t0003g0122 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.529+60C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 4/24 | chr3 | 149074155 | ||||||
chr3:149074514
|
C | A | 8 | a0001c0002t0004g0253a0001c0002t0004g0260a0001c0002t0004g0261others(5): Show | 8 | HG02630.hp1 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.396-166G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074514 | ||||||
chr3:149074666
|
C | T | 1 | a0001c0002t0021g0365 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.396-318G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074666 | ||||||
chr3:149074684
|
T | C | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-336A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074684 | ||||||
chr3:149074723
|
G | A | 1 | a0001c0007t0003g0097 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.396-375C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074723 | ||||||
chr3:149074737
|
T | C | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-389A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074737 | ||||||
chr3:149074797
|
T | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0239 | 3 | HG02273.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.396-449A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074797 | ||||||
chr3:149074819
|
A | G | 1 | a0001c0002t0004g0264 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.396-471T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074819 | ||||||
chr3:149074943
|
T | C | 1 | a0001c0005t0002g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.396-595A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149074943 | ||||||
chr3:149075072
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.396-724A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075072 | ||||||
chr3:149075092
|
A | G | 4 | a0003c0006t0005g0043a0003c0006t0005g0044a0003c0006t0005g0045others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-744T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075092 | ||||||
chr3:149075097
|
T | A | 15 | a0001c0005t0002g0015a0001c0005t0002g0135a0001c0005t0002g0137others(12): Show | 17 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.396-749A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075097 | ||||||
chr3:149075195
|
G | A | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.395+686C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075195 | ||||||
chr3:149075247
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.395+634C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075247 | ||||||
chr3:149075291
|
G | A | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+590C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075291 | ||||||
chr3:149075315
|
G | A | 1 | a0001c0003t0002g0277 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.395+566C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075315 | ||||||
chr3:149075426
|
G | A | 1 | a0001c0001t0011g0129 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.395+455C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075426 | ||||||
chr3:149075500
|
C | T | 6 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.395+381G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075500 | ||||||
chr3:149075544
|
AAAAT | A | 15 | a0001c0005t0002g0015a0001c0005t0002g0135a0001c0005t0002g0137others(12): Show | 17 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.395+333_395+336del others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075544 | ||||||
chr3:149075544
|
AAAATAAA others(1): Show |
A | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+329_395+336del others(8): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075544 | ||||||
chr3:149075613
|
G | A | 1 | a0006c0009t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.395+268C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075613 | ||||||
chr3:149075648
|
A | C | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+233T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075648 | ||||||
chr3:149075712
|
GGTA | G | 15 | a0001c0001t0001g0198a0002c0004t0001g0196a0002c0004t0001g0197others(12): Show | 16 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.395+166_395+168del others(3): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075712 | ||||||
chr3:149075809
|
C | G | 1 | a0001c0001t0001g0190 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.395+72G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075809 | ||||||
chr3:149075869
|
A | C | 1 | a0002c0004t0001g0241 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.395+12T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 3/24 | chr3 | 149075869 | ||||||
chr3:149076067
|
G | A | 22 | a0001c0003t0002g0128a0001c0003t0002g0268a0001c0003t0002g0269others(19): Show | 22 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.229-20C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076067 | ||||||
chr3:149076183
|
C | G | 1 | a0002c0004t0001g0196 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.229-136G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076183 | ||||||
chr3:149076294
|
T | C | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-247A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076294 | ||||||
chr3:149076304
|
C | A | 1 | a0001c0002t0003g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.229-257G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076304 | ||||||
chr3:149076412
|
T | C | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-365A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076412 | ||||||
chr3:149076444
|
G | A | 1 | a0001c0003t0002g0278 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.229-397C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076444 | ||||||
chr3:149076642
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.229-595A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076642 | ||||||
chr3:149076679
|
T | C | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-632A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076679 | ||||||
chr3:149076914
|
T | C | 1 | a0001c0002t0003g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.229-867A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149076914 | ||||||
chr3:149077031
|
G | A | 2 | a0001c0002t0006g0051a0001c0002t0006g0052 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.229-984C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077031 | ||||||
chr3:149077112
|
G | T | 1 | a0001c0003t0002g0322 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.229-1065C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077112 | ||||||
chr3:149077121
|
G | A | 1 | a0003c0006t0005g0362 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.229-1074C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077121 | ||||||
chr3:149077204
|
T | C | 269 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(266): Show | 302 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.229-1157A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077204 | ||||||
chr3:149077204
|
T | G | 1 | a0001c0002t0003g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.229-1157A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077204 | ||||||
chr3:149077233
|
C | T | 3 | a0001c0002t0004g0253a0001c0002t0004g0261a0001c0002t0004g0263 | 3 | HG02717.hp2 HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.229-1186G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077233 | ||||||
chr3:149077247
|
A | AAAAT | 25 | a0001c0001t0011g0129a0001c0001t0011g0131a0001c0001t0015g0130others(22): Show | 25 | HG00621.hp1 HG01167.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.229-1204_229-1201d others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077247 | ||||||
chr3:149077247
|
AAAAT | A | 53 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0190others(50): Show | 55 | HG00140.hp2 HG00738.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.229-1204_229-1201d others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077247 | ||||||
chr3:149077247
|
AAAATAAA others(1): Show |
A | 117 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 133 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.229-1208_229-1201d others(10): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077247 | ||||||
chr3:149077247
|
AAAATAAA others(5): Show |
A | 2 | a0001c0002t0006g0042a0016c0015t0006g0041 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.229-1212_229-1201d others(14): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077247 | ||||||
chr3:149077251
|
T | C | 3 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0040 | 3 | HG02109.hp1 HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.229-1204A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077251 | ||||||
chr3:149077255
|
T | C | 1 | a0005c0010t0007g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.229-1208A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077255 | ||||||
chr3:149077260
|
A | T | 2 | a0001c0002t0003g0069a0001c0002t0003g0070 | 2 | HG00738.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.229-1213T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077260 | ||||||
chr3:149077264
|
A | T | 19 | a0001c0002t0003g0013a0001c0002t0003g0061a0001c0002t0003g0067others(16): Show | 20 | HG00621.hp2 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.229-1217T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077264 | ||||||
chr3:149077268
|
A | T | 70 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(67): Show | 81 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.229-1221T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077268 | ||||||
chr3:149077270
|
A | T | 1 | a0001c0007t0003g0066 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.229-1223T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077270 | ||||||
chr3:149077272
|
A | T | 85 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(82): Show | 100 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.229-1225T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077272 | ||||||
chr3:149077274
|
A | T | 1 | a0001c0007t0003g0066 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.229-1227T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077274 | ||||||
chr3:149077276
|
A | T | 97 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(94): Show | 112 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.229-1229T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077276 | ||||||
chr3:149077278
|
A | T | 1 | a0001c0007t0003g0066 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.229-1231T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077278 | ||||||
chr3:149077280
|
A | C | 1 | a0001c0007t0003g0066 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.229-1233T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077280 | ||||||
chr3:149077280
|
A | T | 97 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(94): Show | 112 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.229-1233T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077280 | ||||||
chr3:149077284
|
A | T | 98 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(95): Show | 113 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.229-1237T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077284 | ||||||
chr3:149077288
|
A | T | 18 | a0001c0002t0003g0006a0001c0002t0003g0068a0001c0002t0003g0099others(15): Show | 21 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.229-1241T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077288 | ||||||
chr3:149077429
|
A | C | 1 | a0001c0002t0003g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.229-1382T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077429 | ||||||
chr3:149077488
|
A | G | 1 | a0001c0001t0015g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.229-1441T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077488 | ||||||
chr3:149077496
|
C | G | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.229-1449G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077496 | ||||||
chr3:149077505
|
T | G | 1 | a0001c0001t0001g0186 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.229-1458A>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077505 | ||||||
chr3:149077592
|
C | T | 1 | a0001c0003t0002g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.229-1545G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077592 | ||||||
chr3:149077738
|
C | A | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-1691G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077738 | ||||||
chr3:149077739
|
C | T | 2 | a0001c0003t0002g0296a0001c0003t0002g0316 | 2 | HG01175.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.229-1692G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077739 | ||||||
chr3:149077930
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.229-1883C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149077930 | ||||||
chr3:149078071
|
T | C | 16 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(13): Show | 17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.229-2024A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078071 | ||||||
chr3:149078102
|
A | G | 3 | a0001c0002t0003g0060a0001c0002t0003g0112a0001c0002t0003g0113 | 3 | HG01261.hp1 HG02300.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.229-2055T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078102 | ||||||
chr3:149078167
|
A | G | 1 | a0001c0002t0003g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.229-2120T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078167 | ||||||
chr3:149078205
|
T | C | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-2158A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078205 | ||||||
chr3:149078210
|
G | A | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-2163C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078210 | ||||||
chr3:149078285
|
C | T | 1 | a0001c0003t0002g0315 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.229-2238G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078285 | ||||||
chr3:149078323
|
A | T | 99 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(96): Show | 114 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.229-2276T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078323 | ||||||
chr3:149078363
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.229-2316A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078363 | ||||||
chr3:149078497
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0240 | 2 | HG00673.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.229-2450G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078497 | ||||||
chr3:149078507
|
G | A | 1 | a0001c0003t0002g0314 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.229-2460C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078507 | ||||||
chr3:149078615
|
T | C | 54 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0019others(51): Show | 62 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.229-2568A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078615 | ||||||
chr3:149078726
|
G | A | 1 | a0001c0002t0003g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.229-2679C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078726 | ||||||
chr3:149078741
|
C | T | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.229-2694G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078741 | ||||||
chr3:149078763
|
A | G | 1 | a0001c0003t0002g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.229-2716T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078763 | ||||||
chr3:149078851
|
C | T | 1 | a0001c0002t0003g0067 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.229-2804G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078851 | ||||||
chr3:149078856
|
CA | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.229-2810delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078856 | ||||||
chr3:149078916
|
C | A | 5 | a0001c0002t0003g0255a0001c0002t0004g0023a0001c0002t0004g0256others(2): Show | 6 | HG01167.hp1 HG01169.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.229-2869G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078916 | ||||||
chr3:149078936
|
G | A | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.229-2889C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078936 | ||||||
chr3:149078938
|
C | T | 6 | a0001c0001t0001g0152a0004c0008t0002g0029a0004c0008t0008g0027others(3): Show | 6 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.229-2891G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078938 | ||||||
chr3:149078985
|
G | T | 16 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(13): Show | 17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.229-2938C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149078985 | ||||||
chr3:149079028
|
G | A | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.229-2981C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079028 | ||||||
chr3:149079102
|
A | C | 2 | a0001c0002t0006g0051a0001c0002t0006g0052 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.229-3055T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079102 | ||||||
chr3:149079107
|
A | G | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.229-3060T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079107 | ||||||
chr3:149079162
|
A | G | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.229-3115T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079162 | ||||||
chr3:149079248
|
C | T | 4 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(1): Show | 4 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.229-3201G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079248 | ||||||
chr3:149079373
|
T | C | 1 | a0001c0002t0003g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.229-3326A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
T | TA | 36 | a0001c0002t0010g0047a0001c0002t0010g0048a0001c0003t0002g0024others(33): Show | 37 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.229-3327dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
T | TAA | 14 | a0001c0002t0010g0049a0001c0003t0002g0025a0001c0003t0002g0288others(11): Show | 15 | HG00558.hp2 HG02723.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.229-3328_229-3327d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
T | TAAAA | 5 | a0001c0003t0002g0348a0001c0003t0002g0352a0001c0005t0002g0015others(2): Show | 6 | HG00438.hp2 HG01243.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.229-3330_229-3327d others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0015g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.229-3336_229-3327d others(12): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
T | TAAAAAAA others(6): Show |
1 | a0001c0001t0011g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.229-3339_229-3327d others(15): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TA | T | 16 | a0001c0002t0003g0119a0001c0002t0003g0120a0001c0002t0003g0121others(13): Show | 16 | HG01167.hp2 HG01346.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.229-3327delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAA | T | 14 | a0001c0002t0003g0118a0001c0002t0003g0125a0001c0002t0004g0023others(11): Show | 15 | HG01256.hp1 HG02486.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.229-3328_229-3327d others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAA | T | 23 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0014others(20): Show | 28 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.229-3329_229-3327d others(5): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(2): Show |
T | 15 | a0001c0002t0003g0099a0001c0002t0003g0100a0001c0002t0003g0101others(12): Show | 15 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.229-3335_229-3327d others(11): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(3): Show |
T | 53 | a0001c0001t0001g0055a0001c0001t0001g0134a0001c0001t0001g0245others(50): Show | 62 | HG00423.hp2 HG00597.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.229-3336_229-3327d others(12): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(4): Show |
T | 26 | a0001c0001t0001g0022a0001c0001t0001g0146a0001c0001t0001g0230others(23): Show | 27 | HG00099.hp1 HG00735.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.229-3337_229-3327d others(13): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(5): Show |
T | 95 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.229-3338_229-3327d others(14): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0001g0154 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.229-3339_229-3327d others(15): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(8): Show |
T | 1 | a0001c0003t0002g0290 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.229-3341_229-3327d others(17): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(9): Show |
T | 1 | a0001c0003t0002g0289 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.229-3342_229-3327d others(18): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(10): Show |
T | 2 | a0001c0021t0002g0254a0003c0006t0005g0054 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.229-3343_229-3327d others(19): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(11): Show |
T | 6 | a0003c0006t0005g0012a0003c0006t0005g0043a0003c0006t0005g0044others(3): Show | 7 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.229-3344_229-3327d others(20): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(12): Show |
T | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-3345_229-3327d others(21): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(15): Show |
T | 3 | a0001c0002t0004g0256a0007c0013t0002g0035a0007c0013t0002g0036 | 3 | HG01167.hp1 HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.229-3348_229-3327d others(24): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079373
|
TAAAAAAA others(16): Show |
T | 1 | a0001c0002t0003g0255 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.229-3349_229-3327d others(25): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079373 | ||||||
chr3:149079374
|
A | T | 1 | a0001c0002t0003g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.229-3327T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079374 | ||||||
chr3:149079401
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0251 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.229-3366_229-3355d others(14): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079401 | ||||||
chr3:149079426
|
T | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-3379A>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079426 | ||||||
chr3:149079463
|
CTATCTCA others(47): Show |
C | 128 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 144 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.229-3470_229-3417d others(56): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079463 | ||||||
chr3:149079468
|
T | C | 4 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-3421A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079468 | ||||||
chr3:149079522
|
A | C | 1 | a0001c0003t0002g0288 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.229-3475T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079522 | ||||||
chr3:149079602
|
T | C | 1 | a0003c0006t0005g0362 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.229-3555A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079602 | ||||||
chr3:149079634
|
C | T | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.229-3587G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079634 | ||||||
chr3:149079836
|
T | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.229-3789A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079836 | ||||||
chr3:149079975
|
C | G | 1 | a0001c0005t0019g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.229-3928G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149079975 | ||||||
chr3:149080118
|
C | T | 7 | a0003c0006t0005g0012a0003c0006t0005g0043a0003c0006t0005g0044others(4): Show | 8 | HG02055.hp2 HG02922.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.229-4071G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080118 | ||||||
chr3:149080134
|
G | A | 3 | a0001c0001t0011g0129a0001c0001t0011g0131a0001c0001t0015g0130 | 3 | HG02258.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.229-4087C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080134 | ||||||
chr3:149080240
|
G | A | 21 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(18): Show | 22 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.229-4193C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080240 | ||||||
chr3:149080398
|
AACCT | A | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.228+4280_228+4283d others(6): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080398 | ||||||
chr3:149080407
|
C | T | 1 | a0001c0021t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.228+4275G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080407 | ||||||
chr3:149080411
|
A | ATC | 171 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.228+4270_228+4271i others(4): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080411 | ||||||
chr3:149080585
|
G | C | 2 | a0001c0002t0003g0123a0001c0002t0003g0124 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.228+4097C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080585 | ||||||
chr3:149080711
|
C | T | 1 | a0001c0002t0006g0042 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.228+3971G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080711 | ||||||
chr3:149080769
|
G | C | 1 | a0001c0002t0006g0050 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.228+3913C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080769 | ||||||
chr3:149080805
|
G | GA | 4 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(1): Show | 4 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+3876dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080805 | ||||||
chr3:149080893
|
C | T | 43 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(40): Show | 45 | HG00738.hp2 HG01167.hp2 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.228+3789G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080893 | ||||||
chr3:149080928
|
C | T | 270 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(267): Show | 303 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.228+3754G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149080928 | ||||||
chr3:149081214
|
C | T | 1 | a0003c0006t0005g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.228+3468G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081214 | ||||||
chr3:149081260
|
C | T | 2 | a0002c0004t0009g0016a0002c0004t0009g0153 | 3 | HG00323.hp2 HG01081.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.228+3422G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081260 | ||||||
chr3:149081265
|
TA | T | 133 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(130): Show | 148 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.228+3416delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081265 | ||||||
chr3:149081274
|
A | T | 1 | a0001c0005t0002g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.228+3408T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081274 | ||||||
chr3:149081279
|
C | A | 1 | a0001c0001t0001g0252 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.228+3403G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081279 | ||||||
chr3:149081502
|
A | C | 1 | a0001c0002t0003g0060 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.228+3180T>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081502 | ||||||
chr3:149081527
|
C | T | 2 | a0007c0013t0002g0035a0007c0013t0002g0036 | 2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.228+3155G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081527 | ||||||
chr3:149081833
|
G | A | 4 | a0001c0003t0002g0349a0001c0003t0002g0350a0001c0003t0002g0351others(1): Show | 4 | HG02083.hp1 NA18985.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+2849C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149081833 | ||||||
chr3:149082180
|
C | T | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.228+2502G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082180 | ||||||
chr3:149082184
|
C | T | 1 | a0001c0002t0003g0059 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.228+2498G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082184 | ||||||
chr3:149082233
|
C | T | 1 | a0001c0003t0002g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.228+2449G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082233 | ||||||
chr3:149082408
|
G | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.228+2274C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082408 | ||||||
chr3:149082414
|
C | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(290): Show | 326 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.228+2268G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082414 | ||||||
chr3:149082454
|
G | A | 12 | a0001c0005t0002g0015a0001c0005t0002g0135a0001c0005t0002g0137others(9): Show | 13 | HG01243.hp2 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.228+2228C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082454 | ||||||
chr3:149082494
|
G | A | 10 | a0001c0002t0004g0253a0001c0002t0004g0259a0001c0002t0004g0260others(7): Show | 10 | HG01256.hp1 HG01516.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.228+2188C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082494 | ||||||
chr3:149082571
|
G | C | 1 | a0001c0003t0002g0353 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.228+2111C>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082571 | ||||||
chr3:149082665
|
C | A | 1 | a0001c0003t0002g0354 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.228+2017G>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082665 | ||||||
chr3:149082673
|
A | G | 1 | a0001c0002t0004g0253 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.228+2009T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082673 | ||||||
chr3:149082690
|
A | G | 21 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(18): Show | 22 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.228+1992T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082690 | ||||||
chr3:149082722
|
CA | C | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.228+1959delT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082722 | ||||||
chr3:149082894
|
GAAGAT | G | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.228+1783_228+1787d others(7): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149082894 | ||||||
chr3:149083108
|
G | A | 1 | a0006c0009t0002g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.228+1574C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083108 | ||||||
chr3:149083165
|
C | G | 6 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.228+1517G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083165 | ||||||
chr3:149083232
|
T | C | 2 | a0001c0002t0006g0051a0001c0002t0006g0052 | 2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.228+1450A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083232 | ||||||
chr3:149083253
|
A | G | 2 | a0001c0002t0003g0057a0001c0002t0003g0058 | 2 | HG00597.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.228+1429T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083253 | ||||||
chr3:149083285
|
A | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(267): Show | 303 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.228+1397T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083285 | ||||||
chr3:149083411
|
G | A | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.228+1271C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083411 | ||||||
chr3:149083507
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.228+1175G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083507 | ||||||
chr3:149083680
|
C | T | 13 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(10): Show | 13 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.228+1002G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083680 | ||||||
chr3:149083749
|
C | CA | 16 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(13): Show | 16 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.228+932dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083749 | ||||||
chr3:149083749
|
C | CAA | 135 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.228+931_228+932dup others(2): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083749 | ||||||
chr3:149083758
|
A | AC | 4 | a0006c0009t0002g0031a0006c0009t0002g0032a0006c0009t0002g0033others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+923_228+924ins others(1): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083758 | ||||||
chr3:149083830
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.228+852T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083830 | ||||||
chr3:149083842
|
C | G | 1 | a0001c0002t0006g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.228+840G>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083842 | ||||||
chr3:149083928
|
G | GA | 122 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.228+753dupT | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149083928 | ||||||
chr3:149084128
|
G | T | 171 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(168): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.228+554C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149084128 | ||||||
chr3:149084356
|
A | G | 4 | a0003c0006t0005g0043a0003c0006t0005g0044a0003c0006t0005g0045others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.228+326T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149084356 | ||||||
chr3:149084457
|
A | G | 2 | a0001c0002t0006g0042a0016c0015t0006g0041 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.228+225T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149084457 | ||||||
chr3:149084661
|
A | ATTTAG | 21 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(18): Show | 22 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.228+20_228+21insCT others(3): Show |
HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 2/24 | chr3 | 149084661 | ||||||
chr3:149085422
|
T | C | 16 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(13): Show | 17 | HG00738.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.21-533A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085422 | ||||||
chr3:149085518
|
T | C | 1 | a0001c0003t0002g0358 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.21-629A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085518 | ||||||
chr3:149085721
|
G | A | 1 | a0001c0001t0001g0359 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.20+596C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085721 | ||||||
chr3:149085795
|
T | C | 1 | a0001c0003t0002g0360 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.20+522A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085795 | ||||||
chr3:149085818
|
G | T | 1 | a0001c0003t0002g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.20+499C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085818 | ||||||
chr3:149085892
|
A | G | 82 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0005others(79): Show | 96 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.20+425T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085892 | ||||||
chr3:149085892
|
A | T | 1 | a0001c0001t0001g0055 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.20+425T>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085892 | ||||||
chr3:149085972
|
A | G | 21 | a0001c0002t0006g0042a0001c0002t0006g0046a0001c0002t0006g0050others(18): Show | 22 | HG00738.hp2 HG01255.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.20+345T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149085972 | ||||||
chr3:149086034
|
T | C | 1 | a0001c0002t0003g0361 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.20+283A>G | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149086034 | ||||||
chr3:149086048
|
G | A | 1 | a0003c0006t0005g0362 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.20+269C>T | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149086048 | ||||||
chr3:149086068
|
A | G | 1 | a0001c0002t0003g0011 | 2 | NA18968.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.20+249T>C | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149086068 | ||||||
chr3:149086082
|
C | T | 10 | a0005c0010t0007g0037a0005c0010t0007g0038a0005c0010t0007g0039others(7): Show | 10 | HG01167.hp2 HG01346.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.20+235G>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149086082 | ||||||
chr3:149086226
|
G | T | 5 | a0004c0008t0002g0029a0004c0008t0008g0027a0004c0008t0008g0028others(2): Show | 5 | HG01255.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.20+91C>A | HLTF | ENSG00000071794.16 | transcript | ENST00000310053.10 | protein_coding | 1/24 | chr3 | 149086226 |